Tesis sobre el tema "Neurological Disorder"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 50 mejores tesis para su investigación sobre el tema "Neurological Disorder".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Explore tesis sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.
Coy, G. "Emotion processing in functional neurological disorder". Thesis, Canterbury Christ Church University, 2018. http://create.canterbury.ac.uk/17707/.
Texto completoWilliams, Isobel Anne. "Emotion regulation in patients with Functional Neurological Disorder". Thesis, University of Sheffield, 2018. http://etheses.whiterose.ac.uk/21430/.
Texto completoShaw, P. J. "Neurological and neurophysiological complications of coronary artery bypass graft surgery". Thesis, University of Newcastle Upon Tyne, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380746.
Texto completoIchikawa, Shoji. "The molecular genetic analysis of three human neurological disorders". free online free to MU campus, others may purchase, 2002. http://wwwlib.umi.com/cr/mo/preview?3074409.
Texto completoPhoenix, Danielle. "Exploring how males who encounter phenomena they identify as 'Conversion Disorder'/'Functional Neurological Disorder' experience agency in their lives". Thesis, Middlesex University, 2017. http://eprints.mdx.ac.uk/21822/.
Texto completoBeckh, Johanna [Verfasser]. "Is Functional Neurological Symptom Disorder (FNSD) a (somatic) stress disorder with altered emotion processing? : An approach to an answer via different methods, disorders an over time / Johanna Beckh". Konstanz : KOPS Universität Konstanz, 2019. http://d-nb.info/1206096772/34.
Texto completoBeasley, Brooke, Aubrey Sciara, Tiffani Carrasco, Gregory Dr Ordway y Michelle Dr Chandley. "Laser Capture Microdissection Analysis of Inflammatory-Related Alterations in Postmortem Brain Tissue of Autism Spectrum Disorder". Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/asrf/2019/schedule/34.
Texto completoChetram, Sursatie. "Neurodevelopmental Basis of Autism Spectrum Disorder based on Age and Gender". ScholarWorks, 2018. https://scholarworks.waldenu.edu/dissertations/4720.
Texto completoLaw, Cecilia. "Everyday Memory Difficulties in Children and Adults with Neurological Disorders: Mixed Method Studies". Thesis, The University of Sydney, 2022. https://hdl.handle.net/2123/29743.
Texto completoColson, Natalie y n/a. "The Role of Hormonal and Vascular Genes in Migraine". Griffith University. School of Medical Science, 2007. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20071121.104112.
Texto completoColson, Natalie. "The Role of Hormonal and Vascular Genes in Migraine". Thesis, Griffith University, 2007. http://hdl.handle.net/10072/365958.
Texto completoThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Medical Science
Full Text
Tomioka, Maiko. "Expression of ABCA13 in the brain and the effect of neurological disorder-related SNPs on the function". Kyoto University, 2013. http://hdl.handle.net/2433/175051.
Texto completo0048
新制・課程博士
博士(農学)
甲第17622号
農博第1984号
新制||農||1010(附属図書館)
学位論文||H25||N4743(農学部図書室)
30388
京都大学大学院農学研究科応用生命科学専攻
(主査)教授 植田 和光, 教授 植田 充美, 教授 阪井 康能
学位規則第4条第1項該当
Hölscher, Sara, Barbara Leinweber, Harald Hefter, Ulrike Reuner, Peter Günther, Karl Heinz Weiss, Wolfgang H. Oertel y Jens Carsten Möller. "Evaluation of the Symptomatic Treatment of Residual Neurological Symptoms in Wilson Disease". Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-133378.
Texto completoDieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
Ahmed, Fida Al Noor. "Rhodiola Rosea L.- An Evaluation of Safety and Efficacy in the Context of a Neurological Disorder, Alzheimer Disease". Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/33374.
Texto completoKwan, Cheung Keith A. "Monitoring of cannabinoid-based medicines for the treatment of neurological disorders to improve clinical outcomes in minors". Thesis, Queensland University of Technology, 2022. https://eprints.qut.edu.au/228475/1/Keith_Kwan%20Cheung_Thesis.pdf.
Texto completoBuervenich, Silvia. "Candidate genes and the dopamine system : possible implications in complex neurological and psychiatric disease /". Stockholm, 2002. http://diss.kib.ki.se/2002/91-7349-202-7.
Texto completoHölscher, Sara, Barbara Leinweber, Harald Hefter, Ulrike Reuner, Peter Günther, Karl Heinz Weiss, Wolfgang H. Oertel y Jens Carsten Möller. "Evaluation of the Symptomatic Treatment of Residual Neurological Symptoms in Wilson Disease". Karger, 2010. https://tud.qucosa.de/id/qucosa%3A27508.
Texto completoDieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.
Gitchel, George Thomas Jr. "Development of an Accurate Differential Diagnostic Tool for Neurological Movement Disorders Utilizing Eye Movements". VCU Scholars Compass, 2015. http://scholarscompass.vcu.edu/etd/4109.
Texto completoRothman, David J. "An Investigation of Neurological soft signs as a discriminating factor between Veterans with Post-traumatic Stress Disorder, mild Traumatic Brain Injury, and co-occurring Post-traumatic Stress Disorder and mild Traumatic Brain Injury". VCU Scholars Compass, 2019. https://scholarscompass.vcu.edu/etd/5915.
Texto completoShafran, Rosamund Lucy. "An investigation into the cognitive-behavioural model of obsessive-compulsive disorder (O.C.D.) : can this be reconciled with a neurological deficit model?" Thesis, King's College London (University of London), 1995. https://kclpure.kcl.ac.uk/portal/en/theses/an-investigation-into-the-cognitivebehavioural-model-of-obsessivecompulsive-disorder-ocd--can-this-be-reconciled-with-a-neurological-deficit-model(825d532c-226d-486e-ba58-c8f7c114f0f6).html.
Texto completoO'Connell, Nicola. "Functional neurological disorder in acute stroke and mental health services : a mixed methods assessment of experiences, prevalence, associated clinical factors, and treatment". Thesis, King's College London (University of London), 2018. https://kclpure.kcl.ac.uk/portal/en/theses/functional-neurological-disorder-in-acute-stroke-and-mental-health-services(c6f40fea-3c02-40ac-aed3-2f662107589d).html.
Texto completoMartorano, Lisa. "Analysis of Brain Structure in a Community Sample of Women with Posttraumatic Stress Disorder as a Result of Chile Abuse Exposure". Wittenberg University Honors Theses / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=wuhonors1239029267.
Texto completoNegash, Alemayehu. "Bipolar disorder in rural Ethiopia : community-based studies in Butajira for screening, epidemiology, follow-up, and the burden of care". Doctoral thesis, Umeå universitet, Psykiatri, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-21743.
Texto completoChikhani, Sherin. "The Potential Role of GATA4, ESR1, GRIA3 and SCN1A Genes in Migraine Susceptibility". Thesis, Griffith University, 2009. http://hdl.handle.net/10072/366267.
Texto completoThesis (Masters)
Master of Philosophy (MPhil)
School of Medical Science
Griffith Health
Full Text
Mackay, Gillian Moira. "Kynurenines in neurological disorders". Thesis, University of Glasgow, 2007. http://theses.gla.ac.uk/39/.
Texto completoHammarlund, Silje. "An Occupational Therapy Needs Assessment for an organization attending to children with autism spectrum disorder in Addis Ababa, Ethiopia : To identify the occupational therapy needs for an organization attending to children with autism spectrum disorder in Addis Ababa, Ethiopia". Thesis, Hälsohögskolan, Högskolan i Jönköping, HHJ, Avd. för rehabilitering, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-27964.
Texto completoAim: To identify the occupational therapy needs at the Nehemiah Autism Center by completing a needs assessment. Method: A mixed-methods design was adopted to construct a comprehensive needs assessment to identify the occupational therapy needs. Result: All areas of what an occupational therapist could assist with were selected as an area of need. Communication and social skills were most frequently reported and behavior management was ranked as most important among caregivers. Among staff members, leisure and play was reported most frequently and stress management was ranked as most important. Training opportunities, communication among staff members, and co-worker relationship were identified to be supporting factors in achieving the goal at Nehemiah Autism Center. Stigma, religion, and cultural diversity were reported to be unsupportive factors in achieving the goal at Nehemiah Autism Center. Conclusion: There is a great need for occupational therapy services to attend to children with autism spectrum disorder at Nehemiah Autism Center in Addis Ababa, Ethiopia.
Griffiths, Timothy D. "Neurological and physical abnormalities in familial and sporadic schizophrenia : a study of the phenotype of schizophrenic subjects and their relatives from populations with a high or a low genetic risk of the disorder". Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.364042.
Texto completoDomarski, Shannon. "Neurological disorders: A model for parsimony". Honors in the Major Thesis, University of Central Florida, 2005. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/752.
Texto completoBachelors
Arts and Sciences
Psychology
Manole, A. A. "Functional genetics of rare neurological disorders". Thesis, University College London (University of London), 2017. http://discovery.ucl.ac.uk/1572333/.
Texto completoFedele, Laura. "Dysfunctional NMDA receptors in neurological disorders". Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10043277/.
Texto completoSmertenko, Tetyana. "Exome sequencing in rare neurological disorders". Thesis, University of Newcastle upon Tyne, 2016. http://hdl.handle.net/10443/3359.
Texto completoPashkovskyy, V. M. "Comorbidity in neurological and mental disorders". Thesis, БДМУ, 2020. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/17640.
Texto completoHulter, Birgitta. "Sexual function in women with neurological disorders". Doctoral thesis, Uppsala University, Department of Neuroscience, 1999. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-379.
Texto completoThe purpose of this investigation was to study sexual function in women with neurological disorders at fairly distinct and separate locations. The dissertation comprises descriptive, retrospective, quantitative studies on sexual functioning in women with hypothalamo-pituitary disorders (HPD) (n:48), multiple sclerosis (MS)(n:47), and insulin-dependent diabetes mellitus (IDDM) (n:42). The results werecompared with those in an age-matched control group (C) (n:42), and as reported by representative Swedish women (n:742) in the Swedish sex survey SiS). The studies were based on comprehensive interviews, neurological examinations, incl. Vibration Perception Thresholds (IDDM), concentrations of prolactin and testosterone in serum (HPD), and a checklist on life satisfaction (IDDM, C, and SiS).
Sexual dysfunction was prevalent in almost all women with HPD and MS, and in 40% of the IDDM group. The problem of insufficient vaginal lubrication was more common in those with neurological disorders than among women in the SiS group. Sexual problems caused by reduced libido and orgasmic difficulties were more commonin the HPD and MS groups than in the SiS group. In the HPD group, women with intrasellar adenomas had better sexual function than women having expansively growing pituitary adenomas with both intra- and suprasellar extension. Normal serum testosterone values correlated to masturbation activity. Amenorrhea and older age werecorrelated with sexual problems in all groups. In the MS group, symptoms of a weak pelvic floor and of bladder and bowel dysfunction were correlated with reduced lubrication and orgasmic ability. In the IDDM group, signs of autonomic neuropathy were correlated with sexual dysfunction. Concerning life satisfaction generally,proportionately fewer women with IDDM were satisfied or very satisfied, though differing significantly from the other two groups in only two domains of life: contacts with friends, and physical health.
Picardi, Chiara. "Characterization of neurological disorders using evolutionary algorithms". Thesis, University of York, 2018. http://etheses.whiterose.ac.uk/21702/.
Texto completoKitchener, Erin Grace. "Selective disorders of memory in neurological patients". Thesis, University of Cambridge, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.627365.
Texto completoBilous, Iryna Ivanivna. "Neurological disorders of patients with endocrine pathology". Thesis, Буковинський деравний медичний університет, 2018. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/14444.
Texto completoSvedberg, Lena. "Cold feet in children with neurological disorders /". Gothenburg : Institute of Neuroscience and Physiology, Clinical Neuroscience and Rehabilitation, Sahlgrenska Academy, University of Gothenburg, 2009. http://hdl.handle.net/2077/21042.
Texto completoCasanova, Manuela Amaral Mucci. "Estudo da marcha da distrofia miotonica tipo 1 : parametros espaciais, temporais e cinematica". [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/313862.
Texto completoDissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciencias Medicas
Made available in DSpace on 2018-08-11T03:23:57Z (GMT). No. of bitstreams: 1 Casanova_ManuelaAmaralMucci_M.pdf: 2345728 bytes, checksum: f66ccc6bdf60b6250a95b5911fe73602 (MD5) Previous issue date: 2008
Resumo: A Distrofia Miotônica tipo 1 é doença multisistêmica que afeta com freqüência o músculo estriado, repercutindo na marcha, a qual pode apresentar-se em um espectro, desde muito anormal a sutis alterações de difícil caracterização através da visão humana. O objetivo deste trabalho foi analisar as variáveis espaciais, temporais e cinemáticas da marcha de afetados pela doença. Desenhou-se estudo prospectivo do tipo caso (n = 10) e controles (n = 20); os sujeitos foram investigados quanto à clínica da marcha e submetidos ao teste de força muscular. Marcadores reflexivos foram fixados em membros superiores, inferiores, tronco e pelve. A marcha, com pés descalços, ocorreu em passarela de 6 metros, capturada por 6 câmeras. Foram coletadas e analisadas 3 amostras de cada participante através do Sistema Qualisys®. Utilizou-se o Teste Exato de Fisher e o Teste de Mann-Whitney para a comparação das variáveis demográficas entre os grupos e a estatística descritiva dos casos. Encontrou-se alterações laboratoriais nos 10 pacientes, embora 04 não tivessem clínica de marcha anormal. O comprimento da passada foi diminuído em 80% dos casos, cadência menor em 30% e velocidade lenta em 40%. Anormalidade no movimento do quadril foi observada em 100% dos pacientes, da pelve em 90% e do tornozelo em 70%. O exame laboratorial da marcha permitiu diagnosticar alterações precoces, antes do aparecimento de déficit muscular à oposição de força, como ocorreu em 2 casos. A disfunção da marcha em laboratório esteve associada à fraqueza muscular distal isoladamente em 40%; e em associação com déficit proximal e distal em outros 40%
Abstract: Myotonic Dystrophy type 1 is a multisystemic disease that frequently affects the striated muscle with repercussion on gait. Gait function may be very abnormal or exhibit subtle alterations of difficult characterization by the human eyes. With objective to analyse the spatiotemporal and kinematics variables parameters of gait in patients affected by the disease, a prospective study of type case (n = 10) and controls (n = 20) was designed. The subjects were investigated in relation to clinical aspects of gait and submitted to the muscular force test. Reflexive markers were affixed in the upper and lower extremities, trunk and pelvis. A barefooted gait was performed in a 6-meter runway and captured by 6 ProReflex cameras. Three samples of each patient were collected and analyzed by the Qualisys® System. The Exact Test of Fisher and the Mann-Whitney Test were used for comparison of demographic variables between the groups and a descriptive statistic for cases. Abnormalities were found in all 10 patients, although 4 had no clinical evidence of gait problems. Stride was diminished in 80% of the cases, cadence in 30% and slow speed in 40%. Gait dysfunction was observed in 100% of the patients¿ hips, 90% of pelvis and 70% of ankles. The laboratory examination of gait allows early detection of alterations, even before the appearance of muscular deficit by manual force opposition test as occurred in two cases. Gait dysfunction observed in the laboratory was associated with distal muscular weakness in 40% of the patients and in association with proximal and distal deficits in others 40%
Mestrado
Ciencias Biomedicas
Mestre em Ciências Médicas
Fu, Pengfei. "Causes of neurological disorders : associations of pm2.5 exposure and intestinal disorders". HKBU Institutional Repository, 2020. https://repository.hkbu.edu.hk/etd_oa/742.
Texto completoDoran, Graeme Paul. "Functional and genetic analysis of human neurological disorders". Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543472.
Texto completoMorganbarry, Rosemarie A. "Phonetic and phonological aspects of neurological speech disorders". Thesis, University of Reading, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292502.
Texto completoChauvin, Joshua. "Temporal expectations in healthy ageing & neurological disorders". Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:79292953-64db-4b67-bc40-f7172b1994a2.
Texto completoVitale, Giuseppina. "Aminergic systems in sleep disorders of neurological diseases". Doctoral thesis, Università di Catania, 2014. http://hdl.handle.net/10761/1538.
Texto completoCalinescu, Catalin. "Outcomes of educational intervention with students with neurological disorders". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape16/PQDD_0014/MQ29148.pdf.
Texto completoSpyers-Ashby, Julia Mary. "The recording and analysis of tremor in neurological disorders". Thesis, Imperial College London, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286132.
Texto completoCandler, Paul Mark Edward. "Antigen identification in paraneoplastic and post-infectious neurological disorders". Thesis, University College London (University of London), 2008. http://discovery.ucl.ac.uk/1444133/.
Texto completoBoridy, Sebastien. "Nanocarriers to modulate glial cell responses in neurological disorders". Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=121198.
Texto completoLes systèmes macromoléculaires de délivrance médicamenteuse, ou les nanovecteurs, visent à améliorer la biodisponibilité des agents thérapeutiques et diagnostiques et sont des outils prometteurs pour le traitement des maladies du système nerveux central (SNC). En particulier, les nanovecteurs présentent une activité intrinsèque qui peut être utilisé pour moduler les réponses des cellules gliales aux stimulis du micro-environnement du SNC. Cependant, nos connaissances sur la façon dont ces nanovecteurs exercent leur effets sont limités; en particulier, nous connaissons peu sur le rôle par rapport à leur grandeur, leur morphologie et la chimie de surface. L'objectif principal de cette thèse était de définir comment les nanovecteurs régulent les réponses des cellules gliales.Nous avons d'abord examiné comment les nanovecteurs nanogel peuvent promouvoir les fonctions des chaperons moléculaires pour éviter la cytotoxicité des cellules gliales lors d'une insulte pathologique. Utilisant les formes oligomériques du peptide β-amyloïde (Aβ1-42) jouant un rôle central dans la maladie d' Alzheimer, nous montrons que les nanogels se lient facilement aux oligomères, en prevenant la toxicité dans les deux cultures de cellules microgliales et astroglials primaire. Entre autre, nous montrons que les nanogels avec une charge de surface positive sont plus cytotoxiques et moins efficaces pour inhiber la toxicité de Aβ1-42- par comparaison à leurs homologues neutres. Ces résultats soulignent l'importance de la caractérisation des nanovecteurs pour prédire l'influence qu'ils exercent sur la fonction des cellules gliales. Nous avons cherché à élucider la relation entre la conception des nanovecteurs et la réponse inflammatoire des cellules gliales. Nous étions particulièrement intéressés par un trait qui n'est pas très bien caractérisé: sa morphologie. Les nanoparticules d'or (nanosphères, nanobâtonnets, nanourchins) sont des nanovecteurs idéales pour une telle étude en raison de leur construction modifiable. En utilisant des souris transgéniques qui expriment la luciférase entraînée par le récepteur Toll-like 2 (TLR-2), nous avons observé un signal bioluminescente dans le bulbe olfactif après injection intra-nasale avec des nanorods et des nanourchins, mais pas avec les nanosphères, qui corrélait avec une augmentation de microglies positifs pour Iba-1. Des études portants sur les cultures microgliales ont révélé des profils de libération de cytokines pro-inflammatoires différentielles qui étaient dépendants de la morphologie de nanoparticules, mais indépendants de la chimie de surface. Nos résultats fournissent de nouvelles directives pour la construction de nanovecteurs afin de manipuler le phénotype inflammatoire microgliale.La neuro-inflammation non contrôlée pourrait aggraver les troubles du SNC, tels que les maladies neurodégénératives et le glioblastome multiforme (GBM). Celastrol est un nouveau médicament ayant une activité thérapeutique connue contre la neuro-inflammation et le survie des gliomes, mais l'utilisation est limitée en raison de l'instabilité et de la faible solubilité. Nous avons cherché à élucider ses effets contre l'activité aberrante des cellules gliales en utilisant des nanovecteurs.Dans un modèle in vitro de la neuro-inflammation où le traitement avec lipopolysaccharide (LPS) polarise les cellules microgliales dans un état pro-inflammatoire, nous avons étudié la capacité de celastrol à inhiber le changement de son phénotype. Celastrol a bloqué la libération de médiateurs pro-inflammatoires induit par LPS dans les cellules microgliales polarisées, ce qui réduit la production d'oxyde nitrique, de facteur de nécrose tumorale alpha (TNFα), et de l'interleukine-6 (IL-6), mais a provoqué une cytotoxicité indésirable à la même concentration. En intégrant celastrol dans les polymères anti-inflammatoire (amidoamine) (PAMAM) nanovecteurs dendritiques, nous avons réussi à bloquer ses effets cytotoxiques sans compromettre[couper]
Gannicliffe, A. "Investigations into the role of viruses in neurological disorders". Thesis, University of Liverpool, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381334.
Texto completoBeal, Maryann. "Serving Students with Neurological Disorders: A Manual for Educators". Diss., The University of Arizona, 2006. http://hdl.handle.net/10150/194131.
Texto completoOskoui, Maryam. "STAND: study on the transition of adolescents with neurological disorders". Thesis, McGill University, 2011. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=96754.
Texto completoLa problématique: Les enfants souffrant de troubles neurologiques chroniques vivent de plus en plus jusqu'à l'âge adulte. Nos objectifs étaient de décrire, du point de vue du neurologue au Québec, la pratique courante et les opinions à l'égard de la transition de ces adolescents des soins pédiatriques aux soins adultes, incluant les barrières au processus, si les patients éprouvent un carence en soins durant cette période, et si les neurologues pour adultes ont la formation requise pour prendre soin de ces patients.Les méthodes: Nous avons fait une étude transversale par envoyant deux questionnaires par la poste à tous les neuropédiatres et neurologues pour adultes du Québec.Résultats: Notre taux de réponses à lènvoi des questionnaires était de 65.4%, avec un taux de participation de 51.5%. La plupart nàvaient pas de programme de transition sur place, mais plusieurs planifiaient développer un programme dans les deux prochaines années. Presque la moitié des neurologues croyaient que les patients éprouvent une carence en soins durant la période de transition aux soins adultes. La moitié des neurologues croyaient que les neurologues pour adultes n`ont peut être pas la formation requise pour prendre la relève des soins des jeunes adultes ayant un trouble neurologique chronique débutant en enfance. 60% des neuropédiatres éprouvaient des difficultés à trouver un médecin pour adultes pour prendre la relève des soins de leurs patients. La majorité des neurologues croyaient que la connaissance du patient de sa maladie et de ses médicaments, la conformité aux médicaments, la capacité de participer pleinement durant les visites chez me médecin, la présence dùn trouble de communication ou de comportement, et le besoin de soins multidisciplinaires étaient des facteurs jouant des rôles importantes durant la période de transition des soins.Conclusion: La moitié des neurologues croyaient que les patients éprouvent une carence en soins durant la période de transition. Les neurologues ont fait rapport de plusieurs obstacles à la transition des soins, soit des facteurs reliés aux patients et d'autres reliés aux médecins et services de soins. Presque la moitié des neurologues croyaient que les neurologues pour adultes n'ont pas la formation requise pour prendre soin de ce groupe croissant de patients.