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Cyril Mignot

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Cytometry. Part B, Clinical Cytometry|January 18, 2011
In memoriam. Professor Emeritus Jean Montreuil (1920-2010). A lifetime dedicated to the progress of science and educationDaniela Bratosin, Cyril Mignot
Handbook of Clinical Neurology|April 30, 2013
Gaucher diseaseCyril Mignot, Antoinette Gelot, Thierry Billette De Villemeur
Muscle & Nerve|January 27, 2021
Demyelinating motor neuropathy associated with a homozygous GPT2 pathogenic variantLyse Ruaud, Boris Keren, Rabab Debs, et al.
Brain & Development|February 18, 2006
Type 2 Gaucher disease: 15 new cases and review of the literatureCyril Mignot, Diana Doummar, Irène Maire, et al.
Developmental Medicine and Child Neurology|September 25, 2015
Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutationRodolphe Dard, Cyril Mignot, Alexandra Durr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 25, 2015
A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar InvolvementDiane Doummar, Cyril Mignot, Emmanuelle Apartis, et al.
Pediatric Radiology|May 29, 2025
Moyamoya syndrome in a patient with Aicardi-Goutières syndrome associated with a SAMHD1 mutation: a case reportKorentin Le Floch, Jeanne Barillon, Maria Chiara Bonanno, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2011
Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutationAurélie Méneret, Cyril Mignot, Isabelle An, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2004
Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutationAnne Roubergue, Emmanuelle Apartis, Marie Vidailhet, et al.
The Journal of Investigative Dermatology|February 2, 2016
Postzygotic BRAF p.Lys601Asn Mutation in Phacomatosis Pigmentokeratotica with Woolly Hair Nevus and Focal Cortical DysplasiaPaul Kuentz, Cyril Mignot, Judith St-Onge, et al.
Pageof 24

Showing results (1-10 of 236) with videos related to

Sort By:
Pageof 24
Cytometry. Part B, Clinical Cytometry|January 18, 2011
In memoriam. Professor Emeritus Jean Montreuil (1920-2010). A lifetime dedicated to the progress of science and educationDaniela Bratosin, Cyril Mignot
Handbook of Clinical Neurology|April 30, 2013
Gaucher diseaseCyril Mignot, Antoinette Gelot, Thierry Billette De Villemeur
Muscle & Nerve|January 27, 2021
Demyelinating motor neuropathy associated with a homozygous GPT2 pathogenic variantLyse Ruaud, Boris Keren, Rabab Debs, et al.
Brain & Development|February 18, 2006
Type 2 Gaucher disease: 15 new cases and review of the literatureCyril Mignot, Diana Doummar, Irène Maire, et al.
Developmental Medicine and Child Neurology|September 25, 2015
Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutationRodolphe Dard, Cyril Mignot, Alexandra Durr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 25, 2015
A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar InvolvementDiane Doummar, Cyril Mignot, Emmanuelle Apartis, et al.
Pediatric Radiology|May 29, 2025
Moyamoya syndrome in a patient with Aicardi-Goutières syndrome associated with a SAMHD1 mutation: a case reportKorentin Le Floch, Jeanne Barillon, Maria Chiara Bonanno, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2011
Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutationAurélie Méneret, Cyril Mignot, Isabelle An, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2004
Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutationAnne Roubergue, Emmanuelle Apartis, Marie Vidailhet, et al.
The Journal of Investigative Dermatology|February 2, 2016
Postzygotic BRAF p.Lys601Asn Mutation in Phacomatosis Pigmentokeratotica with Woolly Hair Nevus and Focal Cortical DysplasiaPaul Kuentz, Cyril Mignot, Judith St-Onge, et al.
Pageof 24