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Neuromuscular Disorders : NMD
|
August 12, 2018
Respiratory insight to congenital muscular dystrophies and congenital myopathies and its relation to clinical trial
Brigitte Fauroux, Alessandro Amaddeo, Susana Quijano-Roy, et al.
Clinical Genetics
|
June 7, 2019
Exome sequencing findings in 27 patients with myoclonic-atonic epilepsy: Is there a major genetic factor?
Laura Routier, Florine Verny, Giulia Barcia, et al.
Kidney International Reports
|
July 31, 2024
Thrombotic Microangiopathy as an Emerging Complication of Viral Vector-Based Gene Therapy
Nora Schwotzer, Carine El Sissy, Isabelle Desguerre, et al.
Sleep Medicine
|
May 15, 2024
Polysomnography findings and respiratory muscle function in infants with early onset spinal muscular atrophy after gene replacement as monotherapy: A prospective study
Rémi Barrois, Lucie Griffon, Christine Barnerias, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 21, 2015
Benign intermittent upbeat nystagmus in infancy: a new clinical entity
Matthieu P Robert, Sarah Michel, Elias Adjadj, et al.
Journal of Neuropathology and Experimental Neurology
|
June 19, 2009
Endomysial fibrosis in Duchenne muscular dystrophy: a marker of poor outcome associated with macrophage alternative activation
Isabelle Desguerre, Michelle Mayer, France Leturcq, et al.
Epilepsy Research
|
June 10, 2008
An unexpected EEG course in Dravet syndrome
Rima Nabbout, Isabelle Desguerre, Sandra Sabbagh, et al.
Epilepsia
|
May 17, 2011
Ketogenic diet also benefits Dravet syndrome patients receiving stiripentol: a prospective pilot study
Rima Nabbout, Cristiana Copioli, Mathilde Chipaux, et al.
Epilepsy & Behavior Case Reports
|
March 29, 2017
Unilateral predominance of abnormal movements: A characteristic feature of the pediatric anti-NMDA receptor encephalitis?
Vanessa Benjumea-Cuartas, Monika Eisermann, Hina Simonnet, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
February 26, 2021
Jerking during absences: video-EEG and polygraphy of epileptic myoclonus associated with two paediatric epilepsy syndromes
Marc Abi Aoun, Monika Eisermann, Nicole Chemaly, et al.
Page
of 24
Search research articles
Search
Showing results (11-20 of 235) with videos related to
Sort By:
Page
of 24
Neuromuscular Disorders : NMD
|
August 12, 2018
Respiratory insight to congenital muscular dystrophies and congenital myopathies and its relation to clinical trial
Brigitte Fauroux, Alessandro Amaddeo, Susana Quijano-Roy, et al.
Clinical Genetics
|
June 7, 2019
Exome sequencing findings in 27 patients with myoclonic-atonic epilepsy: Is there a major genetic factor?
Laura Routier, Florine Verny, Giulia Barcia, et al.
Kidney International Reports
|
July 31, 2024
Thrombotic Microangiopathy as an Emerging Complication of Viral Vector-Based Gene Therapy
Nora Schwotzer, Carine El Sissy, Isabelle Desguerre, et al.
Sleep Medicine
|
May 15, 2024
Polysomnography findings and respiratory muscle function in infants with early onset spinal muscular atrophy after gene replacement as monotherapy: A prospective study
Rémi Barrois, Lucie Griffon, Christine Barnerias, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 21, 2015
Benign intermittent upbeat nystagmus in infancy: a new clinical entity
Matthieu P Robert, Sarah Michel, Elias Adjadj, et al.
Journal of Neuropathology and Experimental Neurology
|
June 19, 2009
Endomysial fibrosis in Duchenne muscular dystrophy: a marker of poor outcome associated with macrophage alternative activation
Isabelle Desguerre, Michelle Mayer, France Leturcq, et al.
Epilepsy Research
|
June 10, 2008
An unexpected EEG course in Dravet syndrome
Rima Nabbout, Isabelle Desguerre, Sandra Sabbagh, et al.
Epilepsia
|
May 17, 2011
Ketogenic diet also benefits Dravet syndrome patients receiving stiripentol: a prospective pilot study
Rima Nabbout, Cristiana Copioli, Mathilde Chipaux, et al.
Epilepsy & Behavior Case Reports
|
March 29, 2017
Unilateral predominance of abnormal movements: A characteristic feature of the pediatric anti-NMDA receptor encephalitis?
Vanessa Benjumea-Cuartas, Monika Eisermann, Hina Simonnet, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
February 26, 2021
Jerking during absences: video-EEG and polygraphy of epileptic myoclonus associated with two paediatric epilepsy syndromes
Marc Abi Aoun, Monika Eisermann, Nicole Chemaly, et al.
Page
of 24