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Jean-Pierre Lin

Showing results (121-130 of 139) with videos related to

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Journal of Medical Genetics|November 23, 2013
A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1John H Livingston, Jean-Pierre Lin, Russell C Dale, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|April 14, 2021
Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2Mario Sa, Luwaiza Mirza, Michael Carter, et al.
Neuromuscular Disorders : NMD|March 9, 2010
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutationsFatemeh Geranmayeh, Emma Clement, Lucy H Feng, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 12, 2026
Transition from paediatric to adult care in paediatric-onset neurological disorders in Europe: A survey and scoping reviewDana Craiu, Maria T Papadopoulou, Jasna Orazem Mrak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 2012
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigensYael Hacohen, Sukhvir Wright, Patrick Waters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 23, 2018
The Movement disorder associated with NMDAR antibody-encephalitis is complex and characteristic: an expert video-rating studyJames A Varley, Alastair J S Webb, Bettina Balint, et al.
Movement Disorders Clinical Practice|May 19, 2023
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on PediatricsTamara Pringsheim, Amit Batla, Ali Shalash, et al.
Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Pageof 14

Showing results (121-130 of 139) with videos related to

Sort By:
Pageof 14
Journal of Medical Genetics|November 23, 2013
A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1John H Livingston, Jean-Pierre Lin, Russell C Dale, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|April 14, 2021
Systemic Inflammation Is Associated With Neurologic Involvement in Pediatric Inflammatory Multisystem Syndrome Associated With SARS-CoV-2Mario Sa, Luwaiza Mirza, Michael Carter, et al.
Neuromuscular Disorders : NMD|March 9, 2010
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutationsFatemeh Geranmayeh, Emma Clement, Lucy H Feng, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 12, 2026
Transition from paediatric to adult care in paediatric-onset neurological disorders in Europe: A survey and scoping reviewDana Craiu, Maria T Papadopoulou, Jasna Orazem Mrak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 2012
Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigensYael Hacohen, Sukhvir Wright, Patrick Waters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 23, 2018
The Movement disorder associated with NMDAR antibody-encephalitis is complex and characteristic: an expert video-rating studyJames A Varley, Alastair J S Webb, Bettina Balint, et al.
Movement Disorders Clinical Practice|May 19, 2023
Transitional Care for Young People with Movement Disorders: Consensus-Based Recommendations from the MDS Task Force on PediatricsTamara Pringsheim, Amit Batla, Ali Shalash, et al.
Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Pageof 14