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Brain & Development
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February 5, 2008
Unusual magnetic resonance imaging features in Menkes disease
Christine Barnerias, Nathalie Boddaert, Pascale Guiraud, et al.
Epilepsia Open
|
March 15, 2019
Autism spectrum disorder and cognitive profile in children with Dravet syndrome: Delineation of a specific phenotype
Lisa Ouss, Dorothee Leunen, Jacques Laschet, et al.
Pediatric Neurology
|
May 11, 2024
Safety of Obinutuzumab in Children With Autoimmune Encephalitis and Early B-Cell Repopulation on Rituximab
Ai-Tien Nguyen, Camille Cotteret, Clarisse Gins, et al.
Bulletin De L'Academie Nationale De Medecine
|
January 26, 2006
[Spinal muscular atrophy. A 4-year prospective, multicenter, longitudinal study (168 cases)]
Annie Barois, Michèle Mayer, Isabelle Desguerre, et al.
Human Mutation
|
April 23, 2008
Clinical, cellular, and neuropathological consequences of AP1S2 mutations: further delineation of a recognizable X-linked mental retardation syndrome
Guntram Borck, Anahi Mollà-Herman, Nathalie Boddaert, et al.
Stroke
|
May 27, 2017
Regional Pediatric Acute Stroke Protocol: Initial Experience During 3 Years and 13 Recanalization Treatments in Children
Laurence Tabone, Nicolas Mediamolle, Celine Bellesme, et al.
Cells
|
June 25, 2025
Muscle Spatial Transcriptomic Reveals Heterogeneous Profiles in Juvenile Dermatomyositis and Persistence of Abnormal Signature After Remission
Margot Tragin, Séverine A Degrelle, Baptiste Periou, et al.
Muscle & Nerve
|
May 15, 2012
A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophy
Isabelle Desguerre, Ludovic Arnold, Alban Vignaud, et al.
Journal of Neuromuscular Diseases
|
August 20, 2025
Association between exon-skipping therapy with eteplirsen and cardiac outcomes in Duchenne muscular dystrophy
Joel Iff, Isabelle Desguerre, Yunjuan Liu, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2008
Misleading behavioural phenotype with adenylosuccinate lyase deficiency
Cyril Gitiaux, Irène Ceballos-Picot, Sandrine Marie, et al.
Page
of 24
Search research articles
Search
Showing results (71-80 of 235) with videos related to
Sort By:
Page
of 24
Brain & Development
|
February 5, 2008
Unusual magnetic resonance imaging features in Menkes disease
Christine Barnerias, Nathalie Boddaert, Pascale Guiraud, et al.
Epilepsia Open
|
March 15, 2019
Autism spectrum disorder and cognitive profile in children with Dravet syndrome: Delineation of a specific phenotype
Lisa Ouss, Dorothee Leunen, Jacques Laschet, et al.
Pediatric Neurology
|
May 11, 2024
Safety of Obinutuzumab in Children With Autoimmune Encephalitis and Early B-Cell Repopulation on Rituximab
Ai-Tien Nguyen, Camille Cotteret, Clarisse Gins, et al.
Bulletin De L'Academie Nationale De Medecine
|
January 26, 2006
[Spinal muscular atrophy. A 4-year prospective, multicenter, longitudinal study (168 cases)]
Annie Barois, Michèle Mayer, Isabelle Desguerre, et al.
Human Mutation
|
April 23, 2008
Clinical, cellular, and neuropathological consequences of AP1S2 mutations: further delineation of a recognizable X-linked mental retardation syndrome
Guntram Borck, Anahi Mollà-Herman, Nathalie Boddaert, et al.
Stroke
|
May 27, 2017
Regional Pediatric Acute Stroke Protocol: Initial Experience During 3 Years and 13 Recanalization Treatments in Children
Laurence Tabone, Nicolas Mediamolle, Celine Bellesme, et al.
Cells
|
June 25, 2025
Muscle Spatial Transcriptomic Reveals Heterogeneous Profiles in Juvenile Dermatomyositis and Persistence of Abnormal Signature After Remission
Margot Tragin, Séverine A Degrelle, Baptiste Periou, et al.
Muscle & Nerve
|
May 15, 2012
A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophy
Isabelle Desguerre, Ludovic Arnold, Alban Vignaud, et al.
Journal of Neuromuscular Diseases
|
August 20, 2025
Association between exon-skipping therapy with eteplirsen and cardiac outcomes in Duchenne muscular dystrophy
Joel Iff, Isabelle Desguerre, Yunjuan Liu, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2008
Misleading behavioural phenotype with adenylosuccinate lyase deficiency
Cyril Gitiaux, Irène Ceballos-Picot, Sandrine Marie, et al.
Page
of 24