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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Cyril Mignot »
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Cyril Goizet < Cyril Mignot < Cyril Pernet  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000025 (2015) Diane Doummar [France] ; Cyril Mignot [France] ; Emmanuelle Apartis [France] ; Laurent Villard [France] ; Diana Rodriguez [France] ; Sandra Chantot-Bastauraud [France] ; Lydie Burglen [France]A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.
000123 (2012) Aurélie Meneret [France] ; Cyril Mignot [France] ; Isabelle An [France] ; Marie-Odile Habert [France] ; Aurélia Jacquette [France] ; Marie Vidailhet [France] ; Thierry Bienvenu [France] ; Emmanuel Roze [France]Generalized Dystonia, Athetosis, and Parkinsonism Associated with FOXG1 Mutation
000251 (2009) Diane Doummar [France] ; Fabienne Clot [France] ; Marie Vidailhet [France] ; Alexandra Afenjar [France] ; Alexandra Durr [France] ; Alexis Brice [France] ; Cyril Mignot [France] ; Agnès Guet [France] ; Thierry Billette De Villemeur [France] ; Diana Rodriguez [France]Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene
000430 (2004) Anne Roubergue [France] ; Emmanuelle Apartis [France] ; Marie Vidailhet [France] ; Cyril Mignot [France] ; Anna Tullio-Pelet [France] ; Stanislas Lyonnet [France] ; Thierry Billette De Villemeur [France]Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutation

List of associated KwdEn.i

Nombre de
documents		Descripteur
2Female
2Humans
2Mutation
2Nervous system diseases
1Adrenal Gland Diseases (complications)
1Adrenal Gland Diseases (genetics)
1Adult
1Athetosis
1DNA Mutational Analysis
1Digestive system
1Dystonia
1Electromyography
1Esophageal Achalasia (complications)
1Esophageal Achalasia (genetics)
1Esophageal Achalasia (physiopathology)
1Gastrointestinal Diseases (complications)
1Gastrointestinal Diseases (genetics)
1Gastrointestinal Diseases (physiopathology)
1Gastrointestinal Motility (physiology)
1Homovanillic Acid (metabolism)
1Hydroxyindoleacetic Acid (metabolism)
1Infant
1Lacrimal Apparatus Diseases (complications)
1Lacrimal Apparatus Diseases (genetics)
1Muscle Hypotonia (genetics)
1Muscle Hypotonia (metabolism)
1Muscle Hypotonia (physiopathology)
1Mutation (genetics)
1Myoclonus
1Myoclonus (complications)
1Nerve Tissue Proteins
1Nuclear Pore Complex Proteins
1Parkinsonism
1Point Mutation (genetics)
1Proteins (genetics)
1Syndrome
1Tyrosine 3-Monooxygenase (genetics)
1digestive dysmotility
1myoclonus
1triple A syndrome

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