Littérature scientifique sur le sujet « Posterior insula »
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Articles de revues sur le sujet "Posterior insula"
Türe, Uğur, Dianne C. H. Yaşargil, Ossama Al-Mefty et M. Gazi Yaşargil. « Topographic anatomy of the insular region ». Journal of Neurosurgery 90, no 4 (avril 1999) : 720–33. http://dx.doi.org/10.3171/jns.1999.90.4.0720.
Texte intégralTanriover, Necmettin, Albert L. Rhoton, Masatou Kawashima, Arthur J. Ulm et Alexandre Yasuda. « Microsurgical anatomy of the insula and the sylvian fissure ». Journal of Neurosurgery 100, no 5 (mai 2004) : 891–922. http://dx.doi.org/10.3171/jns.2004.100.5.0891.
Texte intégralRachidi, Inès, Lorella Minotti, Guillaume Martin, Dominique Hoffmann, Julien Bastin, Olivier David et Philippe Kahane. « The Insula : A Stimulating Island of the Brain ». Brain Sciences 11, no 11 (19 novembre 2021) : 1533. http://dx.doi.org/10.3390/brainsci11111533.
Texte intégralKaneko, Nobuyuki, Warren W. Boling, Takaharu Shonai, Kazumi Ohmori, Yoshiaki Shiokawa, Hiroki Kurita et Takanori Fukushima. « Delineation of the Safe Zone in Surgery of Sylvian Insular Triangle : Morphometric Analysis and Magnetic Resonance Imaging Study ». Operative Neurosurgery 70, suppl_2 (9 août 2011) : ons290—ons299. http://dx.doi.org/10.1227/neu.0b013e3182315112.
Texte intégralMartino, Juan, Francesco Vergani, Santiago Gil Robles et Hugues Duffau. « New Insights Into the Anatomic Dissection of the Temporal Stem With Special Emphasis on the Inferior Fronto-occipital Fasciculus : Implications in Surgical Approach to Left Mesiotemporal and Temporoinsular Structures ». Operative Neurosurgery 66, suppl_1 (1 mars 2010) : ons—4—ons—12. http://dx.doi.org/10.1227/01.neu.0000348564.28415.fa.
Texte intégralAfif, Afif, Guillaume Becq et Patrick Mertens. « Definition of a Stereotactic 3-Dimensional Magnetic Resonance Imaging Template of the Human Insula ». Operative Neurosurgery 72, no 1 (14 septembre 2012) : ons35—ons46. http://dx.doi.org/10.1227/neu.0b013e31826cdc57.
Texte intégralParellada, M., L. Pina-Camacho, C. Moreno, Y. Aleman, M. O. Krebs, M. Desco, J. Merchán-Naranjo et al. « Insular pathology in young people with high-functioning autism and first-episode psychosis ». Psychological Medicine 47, no 14 (24 avril 2017) : 2472–82. http://dx.doi.org/10.1017/s0033291717000988.
Texte intégralTüre, Uğur, M. Gazi Yaşargil, Ossama Al-Mefty et Dianne C. H. Yaşargil. « Arteries of the insula ». Journal of Neurosurgery 92, no 4 (avril 2000) : 676–87. http://dx.doi.org/10.3171/jns.2000.92.4.0676.
Texte intégralLiang, Despoina, et Charalampos Labrakakis. « Multiple Posterior Insula Projections to the Brainstem Descending Pain Modulatory System ». International Journal of Molecular Sciences 25, no 17 (24 août 2024) : 9185. http://dx.doi.org/10.3390/ijms25179185.
Texte intégralDesai, Atman, Kimon Bekelis, Terrance M. Darcey et David W. Roberts. « Surgical techniques for investigating the role of the insula in epilepsy : a review ». Neurosurgical Focus 32, no 3 (mars 2012) : E6. http://dx.doi.org/10.3171/2012.1.focus11325.
Texte intégralThèses sur le sujet "Posterior insula"
Paiva, Joselisa Péres Queiroz de. « Efeitos da inativação temporária do córtex insular anterior e posterior no condicionamento de medo ao contexto e ao som em ratos ». reponame:Repositório Institucional da UFABC, 2015.
Trouver le texte intégralDissertação (mestrado) - Universidade Federal do ABC, Programa de Pós-Graduação em Neurociência e Cognição, 2015.
O cortex insular (CI), ou insula, conquistou nos ultimos anos um lugar de destaque na area cientifica por seu suposto envolvimento em processos emocionais e cognitivos. No rato, como nos seres humanos, o CI pode ser dividido em duas sub-regioes funcionalmente heterogeneas. Embora a maioria dos estudos realizados em animais tenha mostrado um envolvimento da regiao mais rostral (CI anterior) na memoria gustativa, outros sugerem um papel mais amplo, abrangendo desde o reconhecimento de objetos ate o processamento de memorias espaciais e aversivas. A regiao mais caudal (CI posterior), por sua vez, recebe aferencias multissensoriais e supoe-se que esteja envolvida em processamento multissensorial e nociceptivo. Entretanto, pouquissimos trabalhos avaliaram a participacao dessa sub-regiao posterior em tarefas de memoria, com resultados inconclusivos. Nao havia, ate o momento, nenhum trabalho que tivesse investigado isoladamente o papel de ambas as sub-regioes do CI na consolidacao da memoria emocional. Portanto, o objetivo deste estudo foi investigar os efeitos da inativacao temporaria do CI anterior e posterior sobre a consolidacao da memoria de medo de tarefas de condicionamento de medo ao contexto e ao som. Ratos Wistar de 3 meses de idade passaram por cirurgia estereotaxica para implante de canulas-guia bilaterais no CI anterior ou posterior. Os animais tiveram pelo menos 7 dias de recuperacao e foram manipulados por 3 dias antes do inicio do procedimento comportamental. Para o treino de condicionamento de medo ao contexto e ao som, os ratos foram colocados individualmente em um caixa de condicionamento. Apos 120 segundos de livre exploracao, um som (90 decibeis, 2 kHz) foi emitido por 30 segundos, co-terminando com um choque nas patas (0,7 mA, 1s). Imediatamente apos, cada rato recebeu uma microinfusao bilateral de muscimol (agonista gabaergico, 0,5¿Êg/0,5¿ÊL por hemisferio) ou salina (grupo controle). O teste de condicionamento de medo ao contexto (CMC) ocorreu 48 horas apos o treino e consistiu na re-exposicao a caixa de condicionamento por 5 minutos, sem apresentacao de som ou choque. 24 horas depois, os mesmos animais foram submetidos ao teste de condicionamento de medo ao som (CMS), o qual ocorreu em uma caixa modificada, com duracao de 5 minutos. Ao final do segundo e terceiro minutos, o mesmo estimulo sonoro apresentado no treino foi emitido por 30 segundos. O tempo de congelamento e o comportamento motor foram utilizados como medidas de condicionamento. No CMS, os ratos que receberam a microinfusao de muscimol no CI anterior e posterior apresentaram uma media de tempo de congelamento menor durante o periodo pos-som. Entretanto, no CMC nao houve diferencas entre grupos para ambas as subregioes do CI. Portanto, os resultados deste estudo indicam que a inativacao pos-treino do CI como um todo prejudica exclusivamente o CMS. Entretanto, o prejuizo deste tipo de memoria, provocado pela inativacao do CI posterior, foi maior, evidenciando, portanto, que esta subregiao esta mais importantemente envolvida na circuitaria neural responsavel pela consolidacao do medo condicionado a um estimulo sonoro discreto.
The insular cortex (IC), or insula, has achieved over the last years an eminent position in the scientific literature due to its involvement in emotional and cognitive processes. In the rat, as in humans, the IC can be divided into two functionally heterogeneous sub-regions. Although most animal studies have shown an involvement of the rostral subregion (anterior IC) in gustatory memory, others suggest a broader role in memory, ranging from object recognition to the processing of spatial and aversive memories. In addition, even though the most caudal area (posterior IC) seems to be involved in multisensory and nociceptive processing, very few studies have evaluated its role in mnemonic processes and the results so far are unclear. Nevertheless, no work, to the best of our knowledge, had investigated the specific role of both sub-regions of the IC on consolidation of fear conditioning tasks. Thus, the aim of the present study was to investigate the effects of temporary inactivation of the anterior and posterior IC on memory consolidation of contextual and tone fear conditioning tasks. 3-month-old male Wistar rats underwent stereotaxic surgery for implantation of bilateral guide cannulae aimed directly above the anterior or posterior IC. The animals were allowed at least 7 days of recovery and were handled once a day for 3 days prior to behavioral sessions. For the contextual and tone fear conditioning training session, the rats were individually placed in the conditioning box. After 120 seconds of free exploration, a tone (90 decibels, 2 kHz) was delivered for 30 seconds, coterminating with a footshock (0.7 mA, 1 s). Immediately after, each rat received a bilateral microinjection of muscimol (GABAergic agonist, 0.5 ìg/0.5ìL by hemisphere) or saline (control group) into the intended IC subregion. The contextual fear conditioning test (CFC) was performed 48 hours after training and consisted in the re-exposure to the conditioning box for 5 minutes, without delivery of tone and shock. After 24 hours, the same animals were submitted to tone fear conditioning test (TFC), which occurred in a modified chamber, for 5 minutes. At the end of the second and third minutes, the same tone stimulus presented in the training session was delivered for 30 seconds. Freezing time and motion behavior were used as measures of conditioning. In TFC, the rats that had received muscimol microinfusion into the anterior and posterior IC displayed a lower freezing time during the post-tone period. However, for both IC subregions, there were no differences between groups in the CFC. Thus, our findings indicate that the posttraining inactivation of both IC subregions impaired the TFC. However, the impairment in this kind of memory, caused by the the inactivation of the posterior IC, was higher, thus, highlighting that this subregion is more importantly involved in the neural circuitry related to the consolidation of the discrete tone conditioned fear.
Sawamoto, Nobukatsu. « Expectation of pain enhances responses to nonpainful somatosensory stimulation in the anterior cingulate cortex and parietal operculum/posterior insula : an event-related functional magnetic resonance imaging study ». Kyoto University, 2001. http://hdl.handle.net/2433/150507.
Texte intégralBouchatta, Otmane. « Sensibilisation à la douleur chez un modèle murin de troubles du déficit de l'attention et de l'hyperactivité ». Thesis, Bordeaux, 2018. http://www.theses.fr/2018BORD0356/document.
Texte intégralAttention deficit hyperactivity disorder (ADHD) is characterized by the core symptoms of inattention, hyperactivity and impulsivity. Neural pathways underlying these deficits point to deficits within frontal-subcortical catecholaminergic networks, involving dopaminergic and noradrenergic innervation. Hence, impairment of the dopaminergic neurotransmission is a frequent target of ADHD medication. Low-dose psychostimulants, including methylphenidate (MpH) and amphetamines (AMP) are the most widely used treatments of ADHD. Recent evidence pointed to pain hypersensitivity in subjects with ADHD history, and suggests possible comorbidity of ADHD with pain. However, the mechanisms and neural circuits involved in these interactions are unknown. In order to understand this comorbidity, the first objective was to create a good animal model of ADHD. We generated a mouse model at P5 by neonatal disruption of central dopaminergic pathways with 6-Hydroxydopamine (6-OHDA) and we demonstrated the validity of the model to mimic ADHD syndrome. Next, we analyzed nociceptive responses in the 6-OHDA mouse model of ADHD. We found that 6-OHDA mice exhibited a marked decrease of withdrawal thresholds, suggesting that ADHD increase nociceptive sensitivity. Interestingly, by using in vivo electrophysiological recordings, we demonstrated that allodynia and hyperalgesia may be caused by neuronal hyperexcitability in the dorsal spinal cord. Moreover, we found that both lowered wihdrawal threshold and increased activity of nociceptive neurons in ADHD-like mice was not normalized by MpH. We tested the hypothesis that descending controls are responsible for pain alterations through the modulation of spinal circuits. The ‘anterior cingulate cortex (ACC) – posterior insular (PI)’ connectivity is at the cross-road of ADHD and pain, being involved in executive functions and emotions, as well as sending projections to the dorsal horn of the spinal cord. By combining electrophysiological, optogenetic and behavioral analyzes, we have shown that the effects of ADHD on painful sensitization involve the implication of ACC and the ACC - PI pathway. In conclusion, we showed that ADHD conditions induce spinal cord nociceptive neurons hyperactivation and pain hypersensitivity. We also suggest that the ACC - PI circuit may trigger dysfunction of spinal cord neurons in ADHD conditions
Bou, Sader Nehme Sarah. « Cortical mechanisms of comorbidity between pain sensitization and attention-deficit/hyperactivity disorder (ADHD) in a mouse model ». Electronic Thesis or Diss., Bordeaux, 2024. http://www.theses.fr/2024BORD0488.
Texte intégralAttention deficit/hyperactivity disorder (ADHD) and chronic pain are two complex conditions of multifactorial origins. Clinical and preclinical studies support an association between these two syndromes. However, the mechanisms underlying their comorbidity are not well understood. Previous findings from our team demonstrated a hyperactivity of the neurons of the anterior cingulate cortex (ACC) and a deregulation of the ACC-posterior insula (PI) pathway in ADHD-like conditions. Growing evidence also suggests a role for neuroinflammation in this concomitance. Our hypothesis thus suggests that neuroinflammation triggers an enhanced neuronal activity in the ACC that sensitizes pathways involved in ADHD symptoms and pain perception. Therefore, this Ph.D. work aims to elucidate the inflammatory mechanisms that may underlie ADHD and its associated pain sensitization, with an interest in the role of the purinergic P2X4 receptor.To address this question, we generated an ADHD-like mouse model through the unilateral intracerebroventricular injection of 6-hydroxydopamine (6-OHDA) at P5. Two-month-old wild-type male and female mice were sacrificed, their brains were extracted, and their ACC and PI were dissected. Fixed tissues were used to study microglial and astrocytic morphology while fresh tissues were utilized for transcriptomic, proteomic, and phosphoproteomic investigations. Moreover, mice with a total knock-out of the P2X4 receptor were tested for thermal and mechanical pain sensitization, in addition to hyperactivity. Fixed tissues of the ACC were used to study changes in microglial morphology while fresh tissues of the ACC and PI were utilized for transcriptomic analyses.Regarding the identification of inflammatory mechanisms in our ADHD-like mouse model, our results report (i) changes in microglial and astrocytic morphology, associated with cellular reactivity, in the ACC of 6-OHDA mice, (ii) the presence of a pro-inflammatory environment in the ACC and PI of 6-OHDA mice, (iii) modifications in protein expression and kinase (serine-threonine and tyrosine) activity in the ACC and PI of 6-OHDA mice, and correlated with impairments in axon guidance, apoptosis, cytoskeleton dynamics, signaling cascades, neurotrophins, and neurotransmitter systems, and (iv) alterations in protein interactions and, therefore, neuronal-astrocytic communication in the ACC of 6-OHDA mice. Finally, data integration identified four processes impaired in the ACC and PI of 6-OHDA males and females: apoptosis, axon guidance, synaptic plasticity (long-term potentiation), and growth of neuronal components. Interestingly, alterations in these processes were not only linked to ADHD and chronic pain conditions but also associated with Eph/ephrin bidirectional signaling cascades. Our findings also indicate a role for the P2X4 receptor in the worsening of ADHD hyperactivity symptom and the induction of morphological changes in microglial cells that correlate with cellular reactivity. However, it exerts a protective effect by limiting the expression of pro-inflammatory molecules, possibly from non-microglial cells.In conclusion, our work provides interesting insights into the inflammatory mechanisms that may underpin the comorbidity between ADHD and pain sensitization. A mild and sustained pro-inflammatory environment in the ACC and PI drives changes in synaptic-related (long-term potentiation, axon guidance, outgrowth of neuronal components) and apoptotic processes. These impairments alter cell-cell connectivity and neuronal activity, thus participating in ADHD and chronic pain pathogenesis
Thiaucourt, Margot [Verfasser], et Gabriele [Akademischer Betreuer] Ende. « Magnetresonanzspektroskopie der posterioren Insula - Korrelation von GABA und Glutamat mit der Schmerzsensibilität bei Patientinnen mit Borderline Persönlichkeitsstörung und gesunden Kontrollen / Margot Thiaucourt ; Betreuer : Gabriele Ende ». Heidelberg : Universitätsbibliothek Heidelberg, 2019. http://d-nb.info/119910907X/34.
Texte intégralFerrier, Jeremy. « Douleurs neuropathiques induites par l'oxaliplatine. Physiopathologie et approches thérapeutiques ». Thesis, Clermont-Ferrand 1, 2013. http://www.theses.fr/2013CLF1PP06/document.
Texte intégralOxaliplatin, an anticancer drug used for the treatment of colorectal cancer, is responsible for a dose-limiting peripheral neurotoxicity in the majority of treated patients. This neurotoxicity appears with two components: a rapid-onset acute neurotoxicity manifesting as transient paresthesias and cold-induced dysesthesias; and a late-onset cumulative neurotoxicity characterized by the development of a painful chronic neuropathy. To date, the management of chemotherapy- induced neuropathic pain is still challenging because of the lack of effective treatments. In this context, a better understanding of the pathophysiological mechanisms underlying this neurotoxicity could lead to the identification of new therapeutic targets. Firstly, we aimed to assess the preventive effect of a polyamine deficient diet on the development of oxaliplatin-induced acute neurotoxicity. Exogenous polyamines, by positively modulating spinal NR2B-containing NMDA receptors, could facilitate pain sensitization. This study has shown that a polyamine deficient diet for 7 days totally prevented oxaliplatin-induced acute cold and mechanical hypersensitivity in rats. Although we observed no change in spinal NR2B expression or phosphorylation, intrathecal ifenprodil (a specific NR2B antagonist) reduced oxaliplatin-induced allodynia in a dose-dependent manner. Finally, proton NMR spectroscopy- based metabolomic analysis has revealed a regulation of spinal glutamate neurotransmission as the most likely mechanism underlying the preventive effect of the diet. Secondly, the metabolic variations associated with oxaliplatin-induced chronic neuropathy were assessed at the supraspinal level using a 1 H-NMR HRMAS-based metabolomic approach. Among the neurochemical changes evidenced in this study, we observed a significant increase in choline within the posterior insular cortex, significantly correlated with the mechanical pain thresholds. A transcriptomic and pharmacological approach have revealed an implication of cholinergic neurotransmission in this brain area. Targeting the cholinergic system using centrally active muscarinic agents could represent an interesting strategy for the treatment of oxaliplatin- induced neuropathic pain. These experimental results led to the identification of new molecular targets for the comprehension and the treatment of chemotherapy-associated painful neuropathy. In a translational approach, these preclinical data will be extended to the clinical setting. A phase II clinical trial (NEUROXAPOL, NCT01775449) is undergoing to confirm the therapeutic interest of a polyamine free diet in patients receiving oxaliplatin. A second clinical project (INSULOX) aiming at assessing the choline concentrations in the insula of patients suffering from oxaliplatin-induced neuropathy is in preparation
Yeh, Han-Yuan, et 葉瀚元. « The Role of Posterior Insular Cortex in Rat Model of Neuropathic Pain ». Thesis, 2013. http://ndltd.ncl.edu.tw/handle/42719224738618799550.
Texte intégral國立臺灣大學
動物學研究所
101
Neuropathic pain is an intractable disease in daily life and clinical research. It can result in long-term changes in central nervous system. Insular cortex is a brain region participated in processing of different sensory modalities. Evidences have also shown that posterior insular cortex may be related to somatosensory perception especially in nociception. However, the role for how PIC contributes to the initiation or maintenance of neuropathic pain is less understood. In the present study, permanent lesion by NMDA excitotoxicity in PIC was used to assess the response to pain. Results showed that after PIC lesion in neuropathic rats, the mechanical threshold recovered gradually. The spontaneous paw lifting showed no improve, and withdrawal response to cold were transiently diminished. PIC pre-lesion resulted in less decreased mechanical threshold, and transient decrement of spontaneous paw lifting. However, there were faster development of cold allodynia. Tracer study revealed that PIC had a strong connection to posterior triangular thalamic nucleus and periaqueductal gray. These data suggested the partial role of PIC to maintain mechanical allodynia in neuropathic pain. Moreover, spontaneous pain, mechanical allodynia and cold allodynia of neuropathic pain might be differentially processed in the forebrain.
Livres sur le sujet "Posterior insula"
Wilshire, Carolyn E. Conduction Aphasia : Impaired Phonological Processing. Sous la direction de Anastasia M. Raymer et Leslie J. Gonzalez Rothi. Oxford University Press, 2015. http://dx.doi.org/10.1093/oxfordhb/9780199772391.013.8.
Texte intégralWittmann, Marc, et Karin Meissner. The embodiment of time : How interoception shapes the perception of time. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198811930.003.0004.
Texte intégralDixon, Sharon, et Sophie Roberts. Orthotics. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199533909.003.0017.
Texte intégralKendall, Tim. ‘Freely Proffered’ ? Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198806516.003.0008.
Texte intégralChapitres de livres sur le sujet "Posterior insula"
Allardyce, Thomas J., Giles R. Scuderi et John N. Insall. « The Insall-Burstein® Posterior Stabilized Condylar Knee Prosthesis ». Dans Surgical Techniques in Total Knee Arthroplasty, 67–74. New York, NY : Springer New York, 2002. http://dx.doi.org/10.1007/0-387-21714-2_8.
Texte intégralGerrans, Philip. « Depersonalization disorder ». Dans Anatomy of an Avatar, 91–110. Oxford University PressOxford, 2024. http://dx.doi.org/10.1093/9780191994395.003.0005.
Texte intégralCraig, A. D. (Bud). « Bodily Feelings Emerge in the Insular Cortex ». Dans How Do You Feel ? Princeton University Press, 2014. http://dx.doi.org/10.23943/princeton/9780691156767.003.0006.
Texte intégralJob-Chapron, Anne-Sophie, Lorella Minotti, Dominique Hoffmann et Philippe Kahane. « SEEG in Temporal Lobe Epilepsy ». Dans Invasive Studies of the Human Epileptic Brain, sous la direction de Samden D. Lhatoo, Philippe Kahane et Hans O. Lüders, 277–88. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198714668.003.0021.
Texte intégralBenarroch, Eduardo E. « Executive Control ». Dans Neuroscience for Clinicians, sous la direction de Eduardo E. Benarroch, 781–98. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190948894.003.0042.
Texte intégralLi, Xiujun, Zhenglong Lin et Jinglong Wu. « Language Processing in the Human Brain of Literate and Illiterate Subjects ». Dans Advances in Bioinformatics and Biomedical Engineering, 201–9. IGI Global, 2013. http://dx.doi.org/10.4018/978-1-4666-2113-8.ch021.
Texte intégral« 49 Posterior Peri-insular Quadrantotomy ». Dans Pediatric Epilepsy Surgery, sous la direction de Oğuz Çataltepe et George I. Jallo. Stuttgart : Georg Thieme Verlag, 2019. http://dx.doi.org/10.1055/b-0039-171681.
Texte intégralKeller, Thomas, et Mark Miller. « Posterior Cruciate Ligament Reconstruction ». Dans Insall & Scott Surgery of the Knee, 539–47. Elsevier, 2012. http://dx.doi.org/10.1016/b978-1-4377-1503-3.00056-1.
Texte intégralFanelli, Gregory C. « Posterior Cruciate Ligament Reconstruction ». Dans Insall & Scott Surgery of the Knee, 548–56. Elsevier, 2012. http://dx.doi.org/10.1016/b978-1-4377-1503-3.00057-3.
Texte intégralKim, Sung-Jae, et Sung-Hwan Kim. « Posterior Cruciate Ligament Reconstruction ». Dans Insall & Scott Surgery of the Knee, 557–64. Elsevier, 2012. http://dx.doi.org/10.1016/b978-1-4377-1503-3.00058-5.
Texte intégralActes de conférences sur le sujet "Posterior insula"
Dosualdo, Caique Alberto. « Reversible posterior encephalopathy syndrome as a rare complication of oxaliplatin chemotherapy : a case report ». Dans XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.399.
Texte intégralSodre, Maria Eduarda Japyassu, Maria Izabel Wanderley Bezerra, Juliana Oliveira Costa, Diego Shelman de souza Rosado Amaral, Vinicius Guedes Lima Bahia et Maria Isabel Dantas Bezerra Lyra. « Association between religious practices impact on cerebral neurophysiology and radiological expression : a systematic review ». Dans XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.667.
Texte intégralTeixeira, Igor de Lima e., Marina Battaglini, Tarcisio Alvarenga et Patrick Sousa Santos. « Descartes’ error” : evidences for the role of brain regions and their connections in introspective thoughts and self-identity ». Dans XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.668.
Texte intégralLemos, Ana Flavia Andrade Ana Flavia Andrade, Helio Aquaroni Farão Gomes, Patrick Emanuell Mesquita Sousa Santos, Maria Clara Foloni, Rebeca Aranha Barbosa Sousa, Yasmim Nadime José Frigo, Tarcísio Nunes Alvarenga et al. « PRES in the context of an infectious insult ». Dans XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.683.
Texte intégralPetrella, Anthony J., Alexandros Karmas, Richard C. Berger, Harry E. Rubash et Mark C. Miller. « The Effect of PCL Substitution on Patellofemoral Joint Forces and A/P Drawer in the Post-TKA Knee ». Dans ASME 1998 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1998. http://dx.doi.org/10.1115/imece1998-0146.
Texte intégralSigal, Ian A., Hongli Yang, Michael D. Roberts, Claude F. Burgoyne et J. Crawford Downs. « Biomechanics of the Posterior Pole During the Remodeling Progression From Normal to Early Experimental Glaucoma ». Dans ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206518.
Texte intégralKodiyalam, Sanjay, Michael D. Roberts, Ian A. Sigal, Richard T. Hart, Claude F. Burgoyne et J. Crawford Downs. « Large Scale Voxel-Based Finite Element Modeling of Normal and Early Glaucomatous Monkey Lamina Cribrosa ». Dans ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192984.
Texte intégralKiriakidis, Kiriakos. « Particle Filter for Plasma Insulin Estimation ». Dans ASME 2010 Dynamic Systems and Control Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/dscc2010-4179.
Texte intégralSosa García, Omar. « Fragmentos de identidad insular : paisaje y cultura local como herramientas para la planificación turística de Agaete y Alghero ». Dans Seminario Internacional de Investigación en Urbanismo. Barcelona : Curso de Arquitetura e Urbanismo. Universidade do Vale do Itajaí, 2016. http://dx.doi.org/10.5821/siiu.6351.
Texte intégralAversa, María, et Pablo Del Río. « PUESTA EN VALOR DEL ESPACIO RIBEREÑO EN LOCALIDADES RURALES : Proyectos de paisaje en el partido de Alberti, provincia de Buenos Aires, Argentina ». Dans Seminario Internacional de Investigación en Urbanismo. Universitat Politècnica de Catalunya, Grup de Recerca en Urbanisme, 2024. http://dx.doi.org/10.5821/siiu.12637.
Texte intégral