Relevant bibliographies by topics / MND

Academic literature on the topic 'MND'

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Published: 4 June 2021
Last updated: 10 March 2023

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Journal articles on the topic "MND"

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Turner, Martin R. "MND plus." Practical Neurology 19, no. 5 (May 21, 2019): 376–77. http://dx.doi.org/10.1136/practneurol-2019-002213.

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Soltani, Nader, Christy Shropshire, and Peter Sikkema. "Short Communication: Influence of manganese on efficacy of glyphosate in glyphosate-resistant soybean." Canadian Journal of Plant Science 91, no. 6 (November 1, 2011): 1061–64. http://dx.doi.org/10.4141/cjps2011-035.

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Soltani, N., Shropshire, C. and Sikkema, P. H. 2011. Short Communication: Influence of manganese on efficacy of glyphosate in glyphosate-resistant soybean. Can. J. Plant Sci. 91: 1061–1064. Four field trials were conducted from 2007 to 2010 in Ontario to evaluate the effect of various manganese (Mn) formulations (Mn1, Ecoman 5% Mn; Mn2, MangaMax 5.5% Mn; Mn3, ManMax 5.5% Mn; Mn4, Superman 5% Mn; Mn5, Stoller This 5% Mn; Mn6, Nortrace 6% Mn-EDTA (ethylenediaminetetraacetate); Mn7, Nortrace 22% Mn and Mn8, WolfTrax 33% Mn) applied at 2.0 kg actual Mn ha−1 on glyphosate efficacy at 900 g a.e. ha−1 in glyphosate-resistant soybean. The tank mix of glyphosate plus Mn4, Mn6 or Mn8 caused as much as 6, 17 and 4% injury in soybean, respectively. There was minimal crop injury (0–1.4%) with other Mn tank mixes. The addition of Mn4 or Mn6 to glyphosate did not antagonize glyphosate efficacy on the weeds evaluated (AMARE, AMBEL, CHEAL and SETVI). The other Mn formulations antagonized glyphosate efficacy for the control of AMARE, AMBEL, CHEAL or SETVI under some environments. The addition of Mn3 or Mn6 to glyphosate reduced soybean yield as much as 15 and 10% compared with glyphosate alone, respectively. Based on these results, it is recommended that glyphosate and manganese applications be applied sequentially to avoid weed control antagonism and maximize soybean yield.
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Robertson, Adrian. "MND Resource File." Physiotherapy 87, no. 1 (January 2001): 48. http://dx.doi.org/10.1016/s0031-9406(05)61194-7.

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Dysch, Leon. "MND research request." Neuropsychologist 1, no. 9 (April 2020): 13. http://dx.doi.org/10.53841/bpsneur.2020.1.9.13.

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Higashihara, Mana, Parvathi Menon, Nimeshan Geevasinga, Mehdi AJVan den Bos, Matthew C. Kiernan, and Steve Vucic. "092 Motor neuron disease with malignancy: clinical and pathophysiological insights." Journal of Neurology, Neurosurgery & Psychiatry 90, e7 (July 2019): A29.3—A30. http://dx.doi.org/10.1136/jnnp-2019-anzan.80.

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IntroductionWhile some regard an association between motor neuron disease (MND) and malignancy as co-incidental, others have argued that it could represent a distinct clinical entity. The present study undertook in depth phenotyping along with assessment of cortical function to further explore disease pathophysiology in MND with malignancy (MND-M) patients.MethodsClinical features along with assessment of peripheral and cortical function was undertaken in 13 MND-M and results were compared to sporadic and familial MND cohorts.ResultsFrom a cohort 13 patients (10 males; aged 65.2±2.0 years), 30.8% were diagnosed with a haematological malignancy. The lower motor neuron phenotype predominated in the in the MND-M patients (χ2=10.8, P<0.01), with the upper motor neuron (UMN) score being significantly reduced in MND-M patients compared to sporadic and familial MND cohorts (χ2=6.84, P<0.01). The neurological deficits did not respond to treatment of the underlying malignancy in the majority of MND-M (92%) patients, and as such there were no significant differences in survival between the cohorts. Despite a paucity of UMN signs, cortical hyperexcitability was evident in MND-M patients, as indicated by reduction in short interval intracortical inhibition (P<0.01) and increase in motor evoked potential amplitude (P<0.01), that were similar to findings in sporadic and familial MND cohorts.ConclusionsThe present study suggests that MND-M falls within the spectrum of MND. A co-incidental association between MND and malignancy is underscored by cortical dysfunction and clinical findings which seems within the spectrum of abnormality evident in classical MND phenotypes.
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Pei, Yan Li, Tatsuro Hiraki, Toshiya Kojima, Takafumi Fukushima, Mitsumasa Koyanagi, and Tetsu Tanaka. "Energy Band Engineering of Metal Nanodots for High Performance Nonvolatile Memory Application." Key Engineering Materials 470 (February 2011): 140–45. http://dx.doi.org/10.4028/www.scientific.net/kem.470.140.

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In this work, high density and small size metal nanodots (MND) with different work-functions were fabricated as a floating gate of nonvolatile memory (NVM) devices by self-assembled nanodot deposition (SAND). The energy band engineering of NVM was demonstrated through controlling MND work-function. For single MND layer floating gate NVM, the retention time was improved by choosing high work-function MND. Furthermore, we proposed a new type NVM with a double stacked MND floating gate. Here, the high work-function MND are placed on the top layer and the low work-function MND are placed on the bottom layer. A large memory window and long retention time were obtained. However, the thermal electron excitation is dominant for the electron discharge process during retention. How to reduce the defects in MND layer is important for further improving of memory characteristics.
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Danielle, Leighton, and Chandran Siddharthan. "WED 225 Changing epidemiology of motor neurone disease in scotland." Journal of Neurology, Neurosurgery & Psychiatry 89, no. 10 (September 13, 2018): A33.1—A33. http://dx.doi.org/10.1136/jnnp-2018-abn.114.

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Clinical Audit Research and Evaluation for Motor Neurone Disease (CARE-MND) (formerly the Scottish MND Register) is an electronic platform for prospective, population-based research in Scotland. We present the results of recent epidemiological analyses.Capture-recapture methods were adopted to determine incidence of MND in 2015–2016: 1) notifications via CARE-MND, 2) Information Services Division (ISD) data i) hospital admissions, ii) death data, iii) riluzole prescriptions.Crude prevalence of MND in Scotland is 7.61–7.64/100,000 of the population. Direct age standardised incidence in 2015 was 3.42/100,000 (95% CI: 2.99 to 3.91); in 2016, 2.89/100,000 (95% CI: 2.50 to 3.34). Using maximum likelihood estimates, coverage of the CARE-MND platform was 99.6% (2015) and 98.1% (2016). In view of high coverage, CARE-MND estimates alone will be presented for 2017.Previous Scottish MND Register capture-recapture annual incidence estimates were 2.32/100,000 (95% CI: 2.26 to 2.37) in 1989–1998 (direct standardised). Our data suggest a changing landscape of MND in Scotland, with a rise in incidence by 36%. This could be attributed to improved neurological services in Scotland. Incidence is also 67% higher than Northern European estimates, which perhaps reflects our robust ascertainment methods. However, further work using population CARE-MND data aims to determine if genetic or environmental variables account for these findings.
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Camarero, J. Julio, and Andrea Hevia. "Links between climate, drought and minimum wood density in conifers." IAWA Journal 41, no. 2 (May 12, 2020): 236–55. http://dx.doi.org/10.1163/22941932-bja10005.

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Abstract As the global climate warms, increased aridity is expected to become a major determinant of forest productivity and tree growth. In gymnosperms, wood density quantified at seasonal to annual scales can be related to changes in tracheid lumen size due to alterations in soil water availability. In this way, minimum wood density (MND) has been shown to respond negatively to early growing-season precipitation in several conifers because dry conditions reduce tracheid lumen size and consequently increase MND. We investigated if this relationship between spring precipitation and MND applies to four conifer species (Abies alba, Pinus sylvestris, Pinus nigra, Juniperus thurifera) in NE Spain from mesic (A. alba, P. sylvestris) to xeric (P. nigra, J. thurifera) conditions. We further assessed how climate, precipitation, and drought-affected tree-ring width (TRW) and MND at several time scales to test if water shortage in spring increases MND and decreases TRW over time and seasonally. Lastly, we quantified the post-drought MND recovery. We found the strongest negative correlations between MND and spring precipitation in P. nigra followed by J. thurifera. In these two species, the associations between MND and 9-month long droughts peaked in early spring (P. nigra, ; J. thurifera, ). Juniperus thurifera presented a better post-drought recovery (decrease in MND), followed by P. nigra and P. sylvestris. We conclude that MND is a reliable and accurate proxy of drought severity during spring in conifers subjected to seasonal water shortage. MND can be used as an early-warning indicator of short- and long-term changes in the responses of trees to water shortage.
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Pearce, Lynne. "New guidance targets MND." Nursing Standard 30, no. 36 (May 4, 2016): 20–21. http://dx.doi.org/10.7748/ns.30.36.20.s22.

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Trueland, Jennifer. "Fighting for MND specialists." Nursing Standard 29, no. 30 (March 25, 2015): 24–25. http://dx.doi.org/10.7748/ns.29.30.24.s22.

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Dissertations / Theses on the topic "MND"

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Mutton, Simon Philip. "Catalytic cascades applied to MND inhibitors." Thesis, University of Leeds, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493612.

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Lloyd, Catherine Margaret. "Aspects of cortical function in motor neurone disease." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243835.

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Hanley, Bridget. "Loss and transcendence in couples living with MND : an interpretative phenomenological analysis." Thesis, Edge Hill University, 2012. http://repository.edgehill.ac.uk/6168/.

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The aim of this qualitative study was to explore couples’ experiences of living with MND (MND). Previous research has not focussed on the experiences of both people with the disease and their partners, but tended to look at each separately. In examining the experiences of both side by side and reflecting on each other, the aim of this study was to explore an overlooked aspect of the experience of living with MND and make an original type of contribution to the extant literature. Method Most previous research into MND has relied upon quantitative methods. The study used a qualitative method and collected two types of data. The longitudinal case study comprised analysis of one couple’s journal of their experiences of MND, spanning the period of one year, from the diagnosis to death of the individual with the disease. It also incorporated a narrative interview of the couple. Narrative interviews were also carried out with 12 couples. Interpretative Phenomenological Analysis was used to analyse the data. Results From the analysis utilizing Interpretative Phenomenology, themes were derived from the data. The super-ordinate themes of altered body, diminishing self, altered temporality and transcending embodiment were established, with many subordinate themes deriving from these. The study reveals that although couples experienced significant physical deterioration and emotional and social losses, they developed new understandings of themselves and each other, in relation to the abstractions time and embodiment, which enabled them to cope with living with the disease. Conclusion The study suggests that living with MND can be understood as something individuals with the disease and their partners respond to in ways that intimately link them together. The study proposes that couples may be better supported by psychological services and considers how this might occur.
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Wicks, Paul Jon Andrew. "The profile of cognitive, behehavioural and emotional change within MND [motor neurone disease]." Thesis, King's College London (University of London), 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.430936.

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Yip, J. "Harnessing the heat shock response as a therapeutic approach in models of MND." Thesis, University College London (University of London), 2012. http://discovery.ucl.ac.uk/1356296/.

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Amyotrophic Lateral Sclerosis (ALS) is an untreatable and fatal neurodegenerative disease that leads to muscle atrophy, paralysis of voluntary muscles and death. ALS is characterized by the selective degeneration of upper and lower motoneurons in the spinal cord, brain stem and motor cortex. The maJority of ALS cases are sporadic, whereas 10 - 20Z of cases have a genetic component and are familial. The causes for most cases of ALS are unknown and the clinical course is highly variable, suggesting that multiple factors underlie the disease mechanism. Recent experimental evidence has illustrated that selective motoneurons degeneration in ALS does not arise solely within motoneurons. The involvement of non-neuronal cells, such as astrocytes, in the pathogenesis of ALS have recently been shown with convincing data supporting the hypothesis of non-cell autonomous mechanism in which motoneuron degenerations is influenced by the toxicity of non-neuronal cells surrounding the motoneurons. In view of this crucial interaction between astrocytes and motoneurons and the implication of astrocytes in ALS disease progression, the role of astrocytes will be examined. An in vitro approach is employed in order to examine the role of mutant SOD1 protein expression in primary astrocyte cells. Motoneurons have an unusually high threshold for induction of heat shock proteins (Hsps), which may contribute to their susceptibility in ALS compared to astrocytes. Thus by increasing the heat shock response (HSR), the cytoprotective mechanism in astrocytes, as a result of up-regulation of Hsp expression within these cells, is a potential therapeutic target. This neuroprotective effect of manipulating the HSR system is investigated in vitro in SOD1G93A transgenic mice. Furthermore, characterization of astrocytes was also carried out in vivo of the cortex and spinal cord in SOD1G93A transgenic mice. Finally, the effect of co- inducing the HSR system in astrocytes by pharmacological manipulation is assessed. The data of the present study clearly indicate that expression of mutant SOD1 protein in astrocytes causes a stress response, and successful manipulation of the increased HSR system in primary astrocytes causes an increase in primary motoneurons survival. Thus targeting the HSR in astrocytes in proximity of motoneurons may be a successful therapeutic approach by circumventing motoneuron degenerations in ALS.
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Jones, Ross Alexander. "Comparative anatomy of the human neuromuscular junction." Thesis, University of Edinburgh, 2018. http://hdl.handle.net/1842/29629.

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The neuromuscular junction (NMJ), the synapse formed between lower motor neuron and skeletal muscle fibre, is known to be a target in a number of neurodegenerative conditions, including motor neuron disease (MND). Located in an accessible part of the peripheral nervous system, the NMJ can be used as a ‘model synapse’ in the context of ‘connectomics’ – the study of synaptic connectivity throughout the nervous system as a whole. Although the NMJ has been studied in a number of species, relatively little is known about its structure in humans, complicating the translation of animal models of disease to the human condition. Described here is the first detailed cellular and molecular characterization of the human NMJ. A standardized methodology for comparative morphometric analysis of NMJs was developed and validated (‘NMJ-morph’). NMJ-morph was used to generate baseline data for 2160 NMJs from a single litter of wild type mice, representing 9 distinct muscles across 3 body regions. Principal components analysis (PCA) revealed synaptic size and fragmentation to be the key determinants of synaptic variability. Correlation data revealed the pre-synaptic cell (motor neuron) to be a stronger predictor of synaptic morphology than the post-synaptic cell (muscle fibre). Other factors influencing synaptic variability were in a clear hierarchy: muscle identity accounted for more variation in synaptic form than animal identity, with side having no effect. Human tissue was obtained from 20 patients (aged 34 to 92 years) undergoing lower limb amputation, primarily for the complications of peripheral vascular disease (PVD). Muscle samples were harvested from non-pathological regions of the surgical discard tissue. 2860 human NMJs were analyzed from 4 distinct muscles (extensor digitorum longus, soleus, peroneus longus and peroneus brevis), and compared with equivalent NMJs from wild type mice. Human NMJs displayed unique morphological characteristics, including small size, thin axons, rudimentary nerve terminals and distinctive ‘nummular’ endplates, all of which distinguished them from equivalent mouse NMJs. The previous notion of partial occupancy in human NMJs was disproved. As in mice, the pre-synaptic cell was shown to correlate more strongly with NMJ morphology; in contrast to mice, the human NMJ was found to be relatively stable throughout its 90+ year lifespan. In support of the tissue harvesting procedure, patient co-morbidities (diabetes mellitus and vascular disease) did not significantly impact NMJ morphology. Super-resolution imaging of the NMJ revealed significant differences in the functional architecture of human and mouse active zones. Despite the smaller synaptic size in humans, the total quantity of active zone material was conserved between the species, suggesting a homeostatic mechanism to preserve effective neurotransmission. Parallel proteomic profiling demonstrated further species-specific differences in the broader molecular composition of the NMJ. The cellular and molecular anatomy of the human NMJ is fundamentally different to that of other mammalian species. These differences must be taken into account when translating animal models of disease to the human condition.
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Maekawa, Satomi. "MND as a multisystem disorder : quantitative studies on selective vulnerability, cellular and molecular pathology." Thesis, King's College London (University of London), 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.430860.

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Watermeyer, Tamlyn Julie. "Emotional processing and social cognition in Amyotrophic Lateral Sclerosis (ALS)/Motor Neuron Disease (MND)." Thesis, King's College London (University of London), 2014. https://kclpure.kcl.ac.uk/portal/en/theses/emotional-processing-and-social-cognition-in-amyotrophic-lateral-sclerosis-als--motor-neuron-disease-mnd(e3552e39-2127-40a8-8035-357b66edd75d).html.

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Amyotrophic Lateral Sclerosis (ALS) is a debilitating and life–limiting neurodegenerative disorder that causes progressive muscle atrophy and spasticity. A small proportion of ALS patients experience co–morbid Frontotemporal Dementia (FTD). Milder cognitive–behavioural changes have been noted in ALS patients without dementia. In these patients, deficits in executive functioning, language, memory and behaviour have been documented. Recently, changes to emotional processing and social cognition (EMOSOC) in ALS have also been reported, albeit with inconsistent findings. The primary aims of the current thesis were i) to delineate the nature and extent of changes in EMOSOC in ALS and ii) to determine the relationship between such changes and interindividual differences in mood, behaviour, personality, empathy and ALS–related executive dysfunction. The results of the study indicate a profile of predominant executive dysfunction, with relative sparing of EMOSOC in non–demented ALS patients. However, the ALS patients did show impaired performance on a task requiring the attribution of thoughts and feelings to characters from cartoons and vignettes. ALS patients’ performance on EMOSOC tasks was predicted by their performance on tests of executive function, above and beyond mood, behaviour, personality and empathy variables. As a secondary aim, the impact of patients’ cognitive and behavioural changes on ALS caregivers’ outcomes (mood, perceived strain, burden and marital satisfaction) were examined. The data indicated patients’ behavioural dysfunction and functional impairment as key predictors of caregivers’ outcomes. Exploratory analyses revealed differences between patients’ and caregivers’ perceptions of patients’ personality, empathy and behaviour; these differences were associated with caregiver outcomes. In summary, the current thesis characterises the profile of EMOSOC changes in non–demented ALS and highlights the role of ALS–related executive dysfunction in these changes. It also assesses the relative impact of patients’ disease, cognitive and behavioural changes on ALS caregivers.
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Rewaj, Phillipa Jane. "Nature of language impairment in motor neurone disease." Thesis, University of Edinburgh, 2014. http://hdl.handle.net/1842/9744.

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Background: Language impairment associated with Motor Neurone Disease (MND) has been documented since the late 19th century, yet little is understood about the pervasiveness or nature of these deficits. The common clinical view among healthcare professionals is that communication difficulties can be attributed solely to the motor speech disorder dysarthria. Recent literature raises the possibility of more central processing deficits. Impairments in naming ability and comprehension of complex grammatical constructs have been frequently reported in some patients with MND. However, there is now growing evidence of spelling impairment, which could suggest the contribution of a more phonologically based deficit. In addition, the close relationship between MND and frontotemporal dementia (FTD) raises questions about the connection between the language impairments seen in MND patients and those documented in patients with the primary progressive aphasia (PPA) syndromes associated with FTD. Aims: This thesis examines the nature of speech and language deficits in people with MND and the extent to which expressive communication impairment can occur above and beyond dysarthria. In particular, the study explores: i) to what extent these language impairments can be attributed to deficits in working memory, executive functioning and/or disease severity; ii) what spelling errors can reveal about the integrity of lexical, phonological and orthographic processing; iii) whether similar patterns of impairment can be seen in PPA syndromes; iv) the relationship between language impairment and bulbar onset; and v) the impact these findings have on clinical management of MND patients. Methods: MND patients from across Scotland with changes in speech and/or language were tested using a neuropsychological battery of experimental and standardised tests of naming, spelling, syntactic comprehension, prosody and phonological and orthographical awareness. Patients were also screened for levels of dysarthria, executive functioning and working memory deficits, and results compared to those of matched controls. Findings: As a group, MND participants performed significantly worse than matched controls on measures of naming, spelling, orthographical awareness, grammatical comprehension, affective prosody and verbal fluency, but not working memory. However, based on patterns of individual impairment, of which spelling impairment formed a distinctive marker, the patient group divided into dichotomous subgroups, with 44% of participants categorised as ‘linguistically impaired’, while the remainder displayed little to no impairment. Those participants identified as linguistically impaired did not differ significantly from other MND participants on measures of disease severity, disease duration or dysarthria severity, although significantly more bulbar onset than limb onset participants were linguistically impaired. Spelling error patterns were suggestive of deficits at both a lexical and sublexical level, and were comparable to those reported in PPA literature. These findings suggest that dysarthria may be masking linguistic deficits in almost half of dysarthric MND patients, and highlight the importance of multidimensional assessment of language for effective clinical management.
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Carina, Engström, Ludvig Fogelström, and Granbom Julia. "ALS-En livsförändring i vardagen : -En litteraturöversikt." Thesis, Hälsohögskolan, Högskolan i Jönköping, HHJ, Avd. för omvårdnad, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-39580.

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Syfte: Att beskriva närståendes upplevelser av att leva med en person med ALS. Metod: En litteraturöversikt med kvalitativ metod och en induktiv ansats. Resultat: Sjukdomen ALS är ovanlig och de som drabbas av den är i stort behov av omvårdnad. Närstående till en anhörig som har fått diagnosen ALS, upplever att vårdpersonalen har kunskapsbrist angående sjukdomen och vårdandet. De upplever bristande information om sjukdomens förlopp. Egentiden tas ifrån dem, sådant som förr togs förgivet läggs istället åt sidan, då all fokus ligger på den anhöriges omvårdnad. Slutsats: Närstående väljer ofta att vårda den anhöriga i hemmet, trots det snabba sjukdomsförloppet. Vårdandet av den anhöriga leder till känslomässiga påfrestningar hos de närstående, både psykiska och fysiska.
Purpose: To describe next of kin experiences of living with person with ALS. Method: A literature review with qualitative method and an inductive approach. Result: The disease ALS is unusual and those who suffer from it are in great need of nursing. The next of kin those who has been diagnosed with ALS, find that healthcare professionals have a lack of knowledge regarding the disease and care. They experience insufficient information about the course of the disease. The true time is taken away from them, as was previously taking for granted, instead being put aside, as all focus is on the patient's nursing. Conclusion: Next of kin often choose to care for their relatives in spite of the progress of the ilness. The care of the relatives leads to emotional stresses of the related, both mental and physical.
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Books on the topic "MND"

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Hurlic, Susan. MND, mulheres no desenvolvimento. [Luanda]: Ler & Escrever, 1992.

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Blank, Robert H., Jerome E. Kurent, and David Oliver, eds. Public Policy in ALS/MND Care. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-5840-5.

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S, Kazandjian Marta, and Communication Independence for the Neurologically Impaired, Inc., eds. Communication and swallowing solutions for the ALS/MND community: A CINI manual. San Diego: Singular Pub. Group, 1997.

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Association, Motor Neurone Disease, ed. MND resource file: A patient and carer centred approach for health & social care professionals. Northampton: Motor Neurone Disease Association, 2000.

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Payback: The case for revenge. Chicago: The University of Chicago Press, 2013.

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Ayob, Osman. Mad Mid Mod. 2nd ed. Kuala Lumpur: Fajar Pakeer, 2010.

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The insane train. New York: Minotaur Books, 2010.

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Tikkanen, Märta. Sofia vuxen med sitt MBD. 2nd ed. [Stockholm]: Forum, 1998.

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Cruces, Steven. A mind made mad: A poetic disturbance. Miami, Fla: S. Cruces, 1997.

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Appignanesi, Lisa. Mad, bad, and sad: Women and the mind doctors. New York: W. W. Norton & Co., 2008.

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Book chapters on the topic "MND"

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Oette, Mark, Marvin J. Stone, Hendrik P. N. Scholl, Peter Charbel Issa, Monika Fleckenstein, Steffen Schmitz-Valckenberg, Frank G. Holz, et al. "MND." In Encyclopedia of Molecular Mechanisms of Disease, 1337. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_8993.

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Dubowsky, Megan, Stephanie R. Shepheard, and Mary-Louise Rogers. "Neurotrophic Therapy for ALS/MND." In Handbook of Neurotoxicity, 1–37. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-71519-9_34-1.

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Rogers, Mary-Louise. "Neurotrophic Therapy for ALS/MND." In Handbook of Neurotoxicity, 1755–85. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-5836-4_34.

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Dubowsky, Megan, Stephanie R. Shepheard, and Mary-Louise Rogers. "Neurotrophic Therapy for ALS/MND." In Handbook of Neurotoxicity, 1893–929. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-15080-7_34.

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Dohrn, Maike F., and Roman Rolke. "German Perspective on ALS/MND Policy." In Public Policy in ALS/MND Care, 107–20. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5840-5_7.

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Kurent, Jerome E., David Oliver, and Robert H. Blank. "Introduction to Public Policy of ALS/MND." In Public Policy in ALS/MND Care, 1–28. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5840-5_1.

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Ogun, Yomi, and Babawale Arabambi. "Public Policy in MND Care: Nigerian Perspective." In Public Policy in ALS/MND Care, 201–8. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5840-5_14.

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Aoun, Samar, Carol Birks, Anne Hogden, and Susan Mathers. "Public Policy in MND Care: The Australian Perspective." In Public Policy in ALS/MND Care, 29–49. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5840-5_2.

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Oliver, David, and Christopher McDermott. "Public Policy in MND Care: The United Kingdom." In Public Policy in ALS/MND Care, 279–300. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5840-5_21.

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Reviers, Evy, Ludo Vanopdenbosch, Ludo Van Den Bosch, and Philip Van Damme. "Correction to: Public Policy in ALS/MND Care: The Belgian Perspective." In Public Policy in ALS/MND Care, C1. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-5840-5_24.

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Conference papers on the topic "MND"

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Panja, Rintu, and Sathish Vadhiyar. "MND-MST." In ICPP 2018: 47th International Conference on Parallel Processing. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3225058.3225146.

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Xu, Chu-Lian, and Chyi-Yeu Lin. "Eye-motion detection system for mnd patients." In 2017 IEEE 4th International Conference on Soft Computing & Machine Intelligence (ISCMI). IEEE, 2017. http://dx.doi.org/10.1109/iscmi.2017.8279606.

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Hemsley, Bronwyn, Stuart Palmer, Wendy Goonan, and Stephen Dann. "Motor Neurone Disease (MND) and Amyotrophic Lateral Sclerosis (ALS): Social Media Communication on Selected #MND and #ALS Tagged Tweets." In Hawaii International Conference on System Sciences. Hawaii International Conference on System Sciences, 2017. http://dx.doi.org/10.24251/hicss.2017.455.

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Veaux, Christophe, Junichi Yamagishi, and Simon King. "Voice banking and voice reconstruction for MND patients." In The proceedings of the 13th international ACM SIGACCESS conference. New York, New York, USA: ACM Press, 2011. http://dx.doi.org/10.1145/2049536.2049619.

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Ujwal, SS, Suhas N. Bhargav, Yasha Jyothi M. Shirur, Sana Anaum, and Zeeshan Saquib. "Blinkom: A Smart Solution for the MND Patients." In 2018 3rd IEEE International Conference on Recent Trends in Electronics, Information & Communication Technology (RTEICT). IEEE, 2018. http://dx.doi.org/10.1109/rteict42901.2018.9012147.

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Palmer, Jonathan, Bhuvaneswari Kathiresan, Ben Messer, and Michelle Ramsey. "Tracheostomy ventilation in MND: A snapshot of UK practice." In ERS Respiratory Failure and Mechanical Ventilation Conference 2020 abstracts. European Respiratory Society, 2020. http://dx.doi.org/10.1183/23120541.rfmvc-2020.52.

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Ballard, Emily, Mike Mackie, Samiha Ismail, Reegan Puthussery, Hina Pattani, Joerg Steier, Philip Marino, et al. "Ventilation in Motor Neurone Disease (MND): what happens in practice." In ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.pa2177.

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"Modified Normal Density (MND) Concrete for the Troll GBS Platform." In "SP-149: High-Performance Concrete - Proceedings, International Conference Singapore, 1994". American Concrete Institute, 1994. http://dx.doi.org/10.14359/4069.

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Rodrigues, Rafael Felipe Silva, Ana Luiza Soares Henriques de Almeida, Amanda Mansur Rosa, Suelen Darlane Vieira, Luciana Maria Campos e. Silva, Ana Catarini Lopes Baltazar, Isabela Guedes, and Melina Efraim Vieira Pinto. "Association between HIV infection and neurocognitive disorders: a review." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.150.

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Background: HIV-associated neurocognitive disorders (HAND) are characterized by impairment in at least two cognitive domains with a prevalence of up to 50% in people living with HIV (PLHIV). HAND is subdivided into asymptomatic neurocognitive impairment (ANI), mild neurocognitive disorder (MND) and HIV-associated dementia (HAD). Objectives: Demonstrate the impact of HAND and possible pathogenic mechanisms by relating them to the prevalence of subtypes Design and Setting: Review of the literature. Methods: Review made from PubMed with the descriptors “neurocognitive disorder”, “HIV”, “review”. Twelve articles were selected, among systematic reviews and meta-analysis published since 2017. Results: Before Highly Active Antiretroviral Therapy (HAART) HAD cases had a higher prevalence, probably due to the high viral load causing intense brain inflammation. Today the percentage of HAD has decreased, but the cases of ANI and MND continue to increase. HAART increases life expectancy and reduces viral load, but it may be related to the increase in ANI / MND associated with early brain aging and mild inflammatory processes resulting from primary infection. Conclusions: HAND is a concern for its impact on the quality of life and life expectancy of PLHIV. Therefore, neuropsychological assessment is an important tool for early diagnosis and disease management. The change in prevalence of different HAND subtypes raises doubts about the pathogenesis of these conditions and further studies are needed to elucidate this issue and develop therapeutic solutions.
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Palmer, Jonathan, Bhuvaneswari Kathiresan, Ben Messer, and Michelle Ramsay. "Does tracheostomy ventilation in MND in the UK lead to improved survival?" In ERS Respiratory Failure and Mechanical Ventilation Conference 2020 abstracts. European Respiratory Society, 2020. http://dx.doi.org/10.1183/23120541.rfmvc-2020.01.

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Reports on the topic "MND"

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John H. Cohen, Greg Deskins, William Motion, and Jay Martin. DEVELOPMENT OF A MUD-PULSE HIGH-TEMPERATURE MEASUREMENT-WHILE-DRILLING (MWD) SYSTEM. Office of Scientific and Technical Information (OSTI), January 2002. http://dx.doi.org/10.2172/828406.

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Petersen, Kirsten Elisa. Danske daginstitutioners indsatser og disses betydninger for pædagogisk personale, børn og familier under COVID-19 pandemien 2020/2021. Aarhus University Library, 2021. http://dx.doi.org/10.7146/aul.420.

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Denne rapport præsenterer en række centrale resultater af et forskningsprojekt med fokus på daginstitutioners indsatser og betydning for pædagogisk personale, børn og familier under COVID-19 pandemien i Danmark. Forskningsprojektet har indsamlet data i perioden april 2020 til august 2020, og særligt i perioden fra midt april til juni, hvor alle landets daginstitutioner genåbnede efter cirka en måneds nedlukning af landets offentlige institutioner som følge af regeringens retningslinjer. Der er ligeledes indsamlet data i perioden august til oktober 2020, og igen i perioden januar til februar 2021. Der er således tale om tre empiriske nedslag hen over cirka et år af pandemiens forløb i relation til daginstitutionsledere og pædagogisk personale i landets daginstitutioner. De data, der ligger til grund for denne rapport, omfatter en spørgeskemaundersøgelse rettet mod daginstitutionsledere og en spørgeskemaundersøgelse rettet mod pædagogisk personale i daginstitutioner, geografisk fordelt over hele landet. Fælles for spørgeskemaundersøgelserne er et fokus på at udforske, hvordan daginstitutioner har arbejdet under COVID-19 pandemien, dels under selve nedlukningen i marts-april, hvor flere af landets daginstitutioner har fungeret som nødpasning, særligt for forældre med kritiske samfundsfunktioner, og dels under genåbningsfaserne, der officielt blev påbegyndt i midten af april og især har forløbet hen over forår og tidlig sommer 2020. Derudover er der ad to omgange foretaget en række forskningsinterview med daginstitutionsledere. I første omgang blev der foretaget 10 forskningsinterview i perioden august til november 2020, og i anden omgang er der foretaget 8 forskningsinterview med daginstitutionsledere fordelt på landets daginstitutioner omfattende perioden januar til februar 2021. Formålet med dette forskningsprojekt har været at kortlægge og udforske, hvordan daginstitutionsledere og pædagogisk personale i en række danske daginstitutioner for 0-6-årige børn løfter den store samfundsmæssige udfordring at håndtere COVID-19 pandemien på landets daginstitutioner.
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Nelson, Gena, Angela Crawford, and Jessica Hunt. A Systematic Review of Research Syntheses for Students with Mathematics Learning Disabilities and Difficulties. Boise State University, Albertsons Library, January 2022. http://dx.doi.org/10.18122/sped.143.boisestate.

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The purpose of this document is to provide readers with the coding protocol that authors used to code 36 research syntheses (including meta-analyses, evidence-based reviews, and quantitative systematic reviews) focused on mathematics interventions for students with learning disabilities (LD), mathematics learning disabilities (MLD), and mathematics difficulties (MD). The purpose of the systematic review of mathematics intervention syntheses was to identify patterns and gaps in content areas, instructional strategies, effect sizes, and definitions of LD, MLD, and MD. We searched the literature for research syntheses published between 2000 and 2020 and used rigorous inclusion criteria in our literature review process. We evaluated 36 syntheses that included 836 studies with 32,495 participants. We coded each synthesis for variables across seven categories including: publication codes (authors, year, journal), inclusion and exclusion criteria, content area focus, instructional strategy focus, sample size, methodological information, and results. The mean interrater reliability across all codes using this coding protocol was 90.3%. Although each synthesis stated a focus on LD, MLD, or MD, very few students with LD or MLD were included, and authors’ operational definitions of disability and risk varied. Syntheses predominantly focused on word problem solving, fractions, computer- assisted learning, and schema-based instruction. Syntheses reported wide variation in effectiveness, content areas, and instructional strategies. Finally, our results indicate the majority of syntheses report achievement outcomes, but very few syntheses report on other outcomes (e.g., social validity, strategy use). We discuss how the results of this comprehensive review can guide researchers in expanding the knowledge base on mathematics interventions. The systematic review that results from this coding process is accepted for publication and in press at Learning Disabilities Research and Practice.
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Lee, Jung Soo, and Hyunji Roh. Ever-Changing Mind. Ames: Iowa State University, Digital Repository, November 2015. http://dx.doi.org/10.31274/itaa_proceedings-180814-1271.

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Anderson, Rachel, and Donny Guerra. Free the Mind. Ames: Iowa State University, Digital Repository, November 2016. http://dx.doi.org/10.31274/itaa_proceedings-180814-1654.

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Plummer, Brianna. Parisian Mad Men. Ames: Iowa State University, Digital Repository, 2013. http://dx.doi.org/10.31274/itaa_proceedings-180814-726.

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Bityurin, Valentin A. MHD Flow Control. Fort Belvoir, VA: Defense Technical Information Center, September 2006. http://dx.doi.org/10.21236/ada473536.

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Coleman, Renita, Esther Thorson, Cinthia Jimenez, and Kami Vinton. Mind your language. Edited by Charis Palmer. Monash University, July 2022. http://dx.doi.org/10.54377/f63d-40ce.

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Rousculp, Christopher L. MHD For NRL Visit. Office of Scientific and Technical Information (OSTI), August 2017. http://dx.doi.org/10.2172/1377387.

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Garasi, Christopher Joseph, Thomas A. Haill, and Allen Conrad Robinson. ALEGRA-MHD : Version 4.0. Office of Scientific and Technical Information (OSTI), November 2003. http://dx.doi.org/10.2172/918373.

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