Gotowe bibliografie tematyczne / Clumsiness in literature

Gotowa bibliografia na temat „Clumsiness in literature”

Autor: Grafiati
Data publikacji: 26 lipca 2024
Data aktualizacji: 28 lipca 2024

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Spis treści

Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Clumsiness in literature”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Artykuły w czasopismach na temat "Clumsiness in literature"

1

Ivry, Richard B. "Cerebellar Involvement in Clumsiness and Other Developmental Disorders". Neural Plasticity 10, nr 1-2 (2003): 141–53. http://dx.doi.org/10.1155/np.2003.141.

Pełny tekst źródła
Streszczenie:
Cerebellar abnormalities have been linked to a number of developmental disorders. Much evidence is based on the analysis of highresolution MRI scans. Imaging and behavioral studies have led researchers to consider functional contributions of the cerebellum beyond that associated with motor control. I review this literature, providing an analysis of different ways to consider the relation between cerebellar abnormalities and developmental disorders. Interestingly, although clumsiness is a problem of coordination, the contribution of cerebellar dysfunction to this developmental problem has received little attention. Select studies indicate that some clumsy children have difficulties on tasks requiring precise timing, similar to that observed in adult patients with cerebellar lesions. I suggest that the underlying neural bases of clumsiness are heterogeneous, with cerebellar dysfunction likely a major contributor for a subpopulation of such children.
Style APA, Harvard, Vancouver, ISO itp.
2

Sannareddy, Rajesh, Rahul Lath, Michelle de Padua i Alok Ranjan. "Meningioma with Intra- and Peritumoral Abscess". Indian Journal of Neurosurgery 07, nr 03 (4.10.2017): 220–22. http://dx.doi.org/10.1055/s-0037-1606820.

Pełny tekst źródła
Streszczenie:
AbstractThe association of meningioma with intra- and peritumoral brain abscess is rare. All cases reported in literature had some focus of infection in the body. We report a 56-year-old man with well-controlled diabetes mellitus found to have a space-occupying lesion upon evaluation for headache, vomiting, and clumsiness of right upper limb. Perioperatively, pus was found intra- and perilesionally around a thick, capsulated, dural-based, vascular lesion. Histopathology was suggestive of meningioma, and Escherichia coli was isolated upon culture.
Style APA, Harvard, Vancouver, ISO itp.
3

Kresojevic, Nikola, Igor Petrovic, Natasa Dragasevic­Miskovic i Vladimir Kostic. "Superficial siderosis: Case report and literature review". Srpski arhiv za celokupno lekarstvo 141, nr 3-4 (2013): 219–22. http://dx.doi.org/10.2298/sarh1304219k.

Pełny tekst źródła
Streszczenie:
Introduction. Superficial siderosis (SS) is caused by chronic subarachnoid bleeding and is characterized by free iron and hemosiderin deposition along the pial and subpial structures of central nervous system. SS leads to progressive and irreversible CNS damage. The most common causes of chronic subarachnoidal bleeding are tumors, head and spinal cord trauma, arteriovenous malformations and aneurysms. SS is characterized by clinical triad: sensorineural hearing loss, cerebellar ataxia and piramydal signs. Brain MR imaging is the investigation of choice for the diagnosis of SS. Typical findings include hypointensities seen on T2?weighted MR imaging around the brain, cerebellum, brain stem, spinal cord, VIII cranial nerve and atrophy of cerebellum and medulla. Case Outline. A 71-year?old female patient noticed hand tremor in the middle of the third decade of life, and later slowly progressive bilateral hearing loss. At the age of 64 she developed un? steady gate, hand clumsiness and dysarthria, to became incapable of independent walking and standing five years later. Clinical course and brain MRI findings were typical for SS, but additional investigation did not reveal the couse of subarahnoidal bleeding. Conclusion. SS represents a rare and under?recognized condition that must be considered in all patients with cerebellar syndrome of unknown cause. Early diagnosis of SS in some cases with identified cause of chronic bleeding allowes therapeutic interventions that may prevent further progression of the disease.
Style APA, Harvard, Vancouver, ISO itp.
4

Elvebakk, Kristine, Ingrid Elisabeth Johnsen, Cecilie Bendiksen Wold, Thomas Finsen, Harald Russwurm i Vilhjalmur Finsen. "Simple Trapeziectomy for Arthrosis of the Basal Joint of the Thumb: 49 Thumbs Reviewed After Two Years". Hand Surgery 20, nr 03 (21.09.2015): 435–39. http://dx.doi.org/10.1142/s0218810415500367.

Pełny tekst źródła
Streszczenie:
Background: Many different surgical strategies for arthrosis of the carpometacarpal joint of the thumb are described in the literature. In 2010 we changed our routine procedure from an interposition arthroplasty using the abductor pollicis longus (APL) tendon to simple trapeziectomy without suspension or interposition. The purpose of this study was to review the clinical outcome after trapeziectomy and to compare it to those we had achieved with the APL procedure. Methods: We examined 49 hands operated with simple trapeziectomy during 2011-2012. Time between operation and review was 26 (15-26) months. Subjective estimation of pain before and after surgery and satisfaction with the general results were evaluated with visual analogue scales. The ability to participate in various activities of daily living before and after the operation were noted and patients completed the Quick-DASH and the PRWHE questionnaires. The mobility of the thumb and wrist were recorded and grip and key pinch strength were measured. The distance between the base of the first metacarpal and the scaphoid was noted on radiographs. Results: There were no significant differences between the present results and those we had achieved with the APL procedure regarding subjective estimation of pain and satisfaction, activities of daily living, mobility, strength and radiographic carpometacarpal distance. For many outcome parameters there was a non-significant trend for better results among the trapeziectomy patients, but increased clumsiness was reported by 20 of them. Conclusions: We conclude that our results with simple trapeziectomy are at least as good as with the APL procedure. However, the considerable number of patients complaining of clumsiness is worrying.
Style APA, Harvard, Vancouver, ISO itp.
5

Zaver, Dhillon B., i Nathan T. Douthit. "A Novel Mutation in the Adult-Onset Alexander’s Disease GFAP Gene". Case Reports in Medicine 2019 (10.01.2019): 1–4. http://dx.doi.org/10.1155/2019/2986538.

Pełny tekst źródła
Streszczenie:
The case describes a 25-year-old Caucasian female diagnosed with Alexander’s disease (AxD) as an outpatient after extensive inpatient workup. Her presenting complaints included incontinence, clumsiness, seizures, dysphagia, and dysarthria. She was also found to have pancytopenia and dysautonomia. A full neurologic and hematologic workup yielded very little results, until a thorough literature search of her presenting complaints and radiologic findings pointed to adult-onset Alexander’s Disease. Alexander’s disease is a rare genetic leukodystrophy with a broad variety of presentations. Despite its infrequency in adults and the difficulty in diagnosis, the prevalence of AxD has been increasing due to ease of genetic analysis and identification of key clinical and radiological findings. This case illustrates the necessity of vigilance and persistence in the face of unusual patient presentations; occasionally, the sound of hoofbeats is zebras.
Style APA, Harvard, Vancouver, ISO itp.
6

Mastrolilli, F., A. Benvenga, L. Di Biase, F. Giambattistelli, L. Trotta, G. Salomone, L. Quintiliani, D. Landi, J. M. Melgari i F. Vernieri. "An Unusual Cause of Dementia: Essential Diagnostic Elements of Corticobasal Degeneration—A Case Report and Review of the Literature". International Journal of Alzheimer's Disease 2011 (2011): 1–6. http://dx.doi.org/10.4061/2011/536141.

Pełny tekst źródła
Streszczenie:
Corticobasal degeneration (CBD) is an uncommon, sporadic, neurodegenerative disorder of mid- to late-adult life. We describe a further example of the pathologic heterogeneity of this condition. A 71-year-old woman initially presented dysarthria, clumsiness, progressive asymmetric bradykinesia, and rigidity in left arm. Rigidity gradually involved ipsilateral leg; postural instability with falls, blepharospasm, and dysphagia subsequently developed. She has been previously diagnosed as unresponsive Parkinson's Disease. At our clinical examination, she presented left upper-arm-fixed-dystonia, spasticity in left lower limb and pyramidal signs (Babinski and Hoffmann). Brain MRI showed asymmetric cortical atrophy in the right frontotemporal cortex. Neuropsychological examination showed an impairment in visuospatial functioning, frontal-executive dysfunction, and hemineglect. This case demonstrates that association of asymmetrical focal cortical and subcortical features remains the clinical hallmark of this condition. There are no absolute markers for the clinical diagnosis that is complicated by the variability of presentation involving also cognitive symptoms that are reviewed in the paper. Despite the difficulty of diagnosing CBD, somatosensory evoked potentials, motor evoked potentials, long latency reflexes, and correlations between results on electroencephalography (EEG) and electromyography (EMG) provide further support for a CBD diagnosis. These techniques are also used to identify neurophysiological correlates of the neurological signs of the disease.
Style APA, Harvard, Vancouver, ISO itp.
7

Nardecchia, Francesca, Anna Caciotti, Teresa Giovanniello, Sabrina De Leo, Lorenzo Ferri, Serena Galosi, Silvia Santagata i in. "3-Methylglutaconic Aciduria Type I Due to AUH Defect: The Case Report of a Diagnostic Odyssey and a Review of the Literature". International Journal of Molecular Sciences 23, nr 8 (16.04.2022): 4422. http://dx.doi.org/10.3390/ijms23084422.

Pełny tekst źródła
Streszczenie:
3-Methylglutaconic aciduria type I (MGCA1) is an inborn error of the leucine degradation pathway caused by pathogenic variants in the AUH gene, which encodes 3-methylglutaconyl-coenzyme A hydratase (MGH). To date, MGCA1 has been diagnosed in 19 subjects and has been associated with a variable clinical picture, ranging from no symptoms to severe encephalopathy with basal ganglia involvement. We report the case of a 31-month-old female child referred to our center after the detection of increased 3-hydroxyisovalerylcarnitine levels at newborn screening, which were associated with increased urinary excretion of 3-methylglutaconic acid, 3-hydroxyisovaleric acid, and 3-methylglutaric acid. A next-generation sequencing (NGS) panel for 3-methylglutaconic aciduria failed to establish a definitive diagnosis. To further investigate the strong biochemical indication, we measured MGH activity, which was markedly decreased. Finally, single nucleotide polymorphism array analysis disclosed the presence of two microdeletions in compound heterozygosity encompassing the AUH gene, which confirmed the diagnosis. The patient was then supplemented with levocarnitine and protein intake was slowly decreased. At the last examination, the patient showed mild clumsiness and an expressive language disorder. This case exemplifies the importance of the biochemical phenotype in the differential diagnosis of metabolic diseases and the importance of collaboration between clinicians, biochemists, and geneticists for an accurate diagnosis.
Style APA, Harvard, Vancouver, ISO itp.
8

Sakaura, Hironobu, Yukihiko Yasui, Toshitada Miwa, Tomoya Yamashita, Kenji Ohzono i Tetsuo Ohwada. "Cervical myelopathy caused by invagination of anomalous lamina of the axis". Journal of Neurosurgery: Spine 19, nr 6 (grudzień 2013): 694–96. http://dx.doi.org/10.3171/2013.8.spine13325.

Pełny tekst źródła
Streszczenie:
The authors report a case of cervical myelopathy caused by invagination of the bilaterally separated lamina of the axis. They also present a literature review. The patient was a previously healthy 68-year-old man with a 1-year history of slowly progressive gait disturbance, right-hand clumsiness, and right dominant sensory disturbance in his trunk and extremities. Both MRI and CT showed that the spinal cord was markedly compressed at the C2–3 level, on the right side, by a deeply invaginated anomalous lamina of the axis. A bilaterally separated lamina was also visible. The patient underwent removal of the anomalous invaginated fragment of the separated lamina and the spinous process of the axis. One year after surgery, his myelopathic symptoms had almost completely resolved. Here, the authors present the case of a patient with an extremely rare anomaly of the lamina of the axis. The underlying pathogenesis of this anomaly could be the failure of the 2 chondrification centers on either side to fuse into a single ossification center. Surgical removal of the anomalous invaginated lamina produced a satisfactory outcome.
Style APA, Harvard, Vancouver, ISO itp.
9

Antonio Jesús, Morales Moreno, Castro Rey, Margarita del Carmen, De Felipe Pérez, Morales Albertos Laura, Uribe Reina María del Pilar, Romero del Hombrebueno Gómez del Pulgar Yara i in. "A 19-Month-Old Spanish Boy with Anti-NMDAR Encephalitis: Case Report and Review of Literature". SVOA Neurology 5, nr 1 (8.01.2024): 21–25. http://dx.doi.org/10.58624/svoane.2024.05.0122.

Pełny tekst źródła
Streszczenie:
Background and Aim: The classic definition of acute encephalitis consists of altered consciousness associated with fever, seizures or focal neurological alterations on neuroimaging or electroencephalography. However, there are particularities that may provide a glimpse of the probably autoimmune versus infectious etiology of the same neurological picture. Case presentation: A 19-month-old male starts with motor clumsiness and refusal to ambulation and leg claudication in the context of febrile pharyngotonsillitis. Simultaneously, first episode of forced gaze’s lateralization and cephalic deviation with right tonic movements and sucking. On examination: intense irritability with no contact, denial-type stereotypies, hemiparetic gait, pronation and adduction of the right arm and foot with frequent stumbling. Results: Neuroimaging tests, electroencephalogram, laboratory tests and antistreptolysin-O were normal, no pathological clinical exome and detection of antibodies in cerebrospinal fluid paired with serum. Such as diagnosis: acute autoimmune encephalitis due to anti-NMDA-R (N-methyl-D-aspartate Receptor) antibodies and movement disorder (choreoathetosis, hemidystonia). We initiate treatment with intramuscular penicillin and oral clobazam with erratic response. Fortunately, high doses of intravenous (iv) corticosteroids and immunoglobulins, oral corticotherapy and iv rituximab on our patient were used. Months later, clear improvement with autonomous ambulation without assistance, adequate manual opening and entire disappearance of dystonic-myoclonic movements. Conclusions: Choreoathetoid movements accompanied by irritability in an infectious context should lead us to think of Sydenham's chorea. However, new developments in the analysis of biological samples and a high index of suspicion may lead us to autoimmune pathology and the consequent early use of immunotherapy with optimal results.
Style APA, Harvard, Vancouver, ISO itp.
10

Salman, Michael S., i Kristin M. Ikeda. "The Syndrome of Infantile-Onset Saccade Initiation Delay". Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 40, nr 2 (marzec 2013): 235–40. http://dx.doi.org/10.1017/s0317167100013792.

Pełny tekst źródła
Streszczenie:
Introduction:Infantile-onset saccade initiation delay (ISID), also known as congenital ocular motor apraxia, is characterized by the inability to initiate volitional horizontal saccades. Other abnormalities including developmental delay and ataxia have been reported. The frequency of these abnormalities is unknown. We performed a detailed review of the medical literature to quantify features of ISID.Methods:We searched the English medical literature for articles related to ISID from 1952 to 2010. Whenever possible, patients were excluded if they had acquired SID, Joubert syndrome or neurodegenerative conditions. The minimum prevalence was calculated for each abnormality.Results:Sixty-six articles with information on 288 patients were included in the analysis. Head thrusts were reported in 84.7%. Blinks without head thrusts were used to initiate saccades in 41%. The fast phases of the optokinetic response and vestibulo-ocular reflex were impaired in 69.8% and 34.4% respectively. Smooth ocular pursuit was abnormal in 33%. Global developmental delay occurred in 41.3%, speech or language delay in 36.5%, cognitive delay in 17%, hypotonia in 35.8%, motor delay in 48.6%, and ataxia/clumsiness in 49.3% of patients. Neuroimaging was performed on 197 patients and was normal in 39.1%. Abnormalities involved the cerebellum (24.9%), cerebrum (15.7%), other infratentorial structures (11.7%), and corpus callosum (6.1%).Conclusions:Infantile-onset saccade initiation delay is frequently associated with deficits in reflexive saccades and less frequently with impaired smooth ocular pursuit. Developmental delay, hypotonia, and ataxia occur frequently in ISID, suggesting more global brain impairment and not just a saccadic disorder.
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Książki na temat "Clumsiness in literature"

1

Henning, Adeline. Je suis adroit, je suis maladroit. [Paris]: Haiter, 2000.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Roger, Hargreaves. Mr. Bump. Wyd. 4. New York: PSS! Price Stern Sloan, 2011.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Carle, Eric. The very clumsy click beetle. New York: Philomel Books, 1999.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Carle, Eric. The very clumsy click beetle. New York: Philomel Books, 1999.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Carle, Eric. The very clumsy click beetle. London: Hamish Hamilton, 1999.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Ungeschickt: Eine Fallgeschichte der deutschen Literatur. Paderborn: Brill, Wilhelm Fink, 2021.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Carle, Eric. KLICK musst du machen, kleiner Käfer. Gerstenberg, 2000.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Carle, Eric. Very Clumsy Beet Prem. Philomel, 2000.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Carle, Eric. The Very Clumsy Click Beetle's Favorite Words (The World of Eric Carle). Grosset & Dunlap, 2008.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Roger, Hargreaves. Mr. Bump (Mr. Men and Little Miss). Price Stern Sloan, 1998.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.

Części książek na temat "Clumsiness in literature"

1

Patterson, Jonathan. "‘Greatness going off’ in Renaissance Antony and Cleopatra Tragedies". W Literature, Learning, and Social Hierarchy in Early Modern Europe, 201–18. British Academy, 2022. http://dx.doi.org/10.5871/bacad/9780197267332.003.0010.

Pełny tekst źródła
Streszczenie:
The suicides of Antony and Cleopatra afforded the Renaissance dramatist various angles on what Shakespeare called ‘Greatness going off’. Renaissance Antony and Cleopatra tragedies in France and England pointedly thematised how the great failed to preserve the dignity of their rank and office in life, and how they fell short of securing personal posthumous renown in death. Antony and his Egyptian queen found themselves unexpectedly upstaged by social inferiors. Renaissance tragedians noted the irony of Antony’s incompetent imitation of his slave, Eros, who took his own life rather than his master’s in a ‘most noble acte’ of disobedience (Mary Sidney Herbert, Countess of Pembroke). Cleopatra’s death, meanwhile, is unceremoniously delayed by a rebel ‘serf’, her treasurer (Etienne Jodelle); it is then facilitated by a garrulous ‘clown’ and a pair of loyal maids, one of whom almost beats the queen out of ‘this vile world’ (Shakespeare). The incongruities are manifest: what is said about Antony’s magnanimity, or Cleopatra’s alluring charms, is noticeably at odds with what is shown of their remorse, clumsiness, even physical debility, as they struggle to prevent their greatness going off. Culturally, Renaissance Antony and Cleopatra tragedies were in tune with the political–religious crises of their day; but they also sounded deeper notes of an aristocracy in slow decline.
Style APA, Harvard, Vancouver, ISO itp.
Możesz być także zainteresowany rozszerzonymi bibliografiami na temat „Clumsiness in literature” dla poszczególnych typów źródeł:
Artykuły w czasopismach
Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!

Do bibliografii