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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Diana Rodriguez »
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Devendra Mishra < Diana Rodriguez < Diane Doummar  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
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.
000193 (2010) Constance Flamand-Rouvière [France] ; Emilie Guettard [France] ; Caroline Moreau [France] ; Nadia Bahi-Buisson [France] ; Vassili Valayannopoulos [France] ; David Grabli [France] ; Jacques Motte [France] ; Diana Rodriguez [France] ; Agathe Roubertie [France] ; Lisa Maintigneux [France] ; Isabelle Kemlin [France] ; Irène Ceballos-Picot [France] ; David Adams [France] ; Marie Vidailhet [France] ; Emmanuel Roze [France]Speech disturbances in patients with dystonia or chorea due to neurometabolic disorders
000226 (2010) Constance Flamand-Rouviere [France] ; Emilie Guettard [France] ; Caroline Moreau [France] ; Nadia Bahi-Buisson [France] ; Vassili Valayannopoulos [France] ; David Grabli [France] ; Jacques Motte [France] ; Diana Rodriguez [France] ; Agathe Roubertie [France] ; Lisa Maintigneux [France] ; Isabelle Kemlin [France] ; Irène Ceballos-Picot [France] ; David Adams [France] ; Marie Vidailhet [France] ; Emmanuel Roze [France]Speech Disturbances in Patients With Dystonia or Chorea Due to Neurometabolic Disorders
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
000278 (2008) Cyril Gitiaux [France] ; Emmanuel Roze [France] ; Kiyoka Kinugawa [France] ; Constance Flamand-Rouvière [France] ; Nathalie Boddaert [France] ; Emmanuelle Apartis [France] ; Vassili Valayannopoulos [France] ; Guy Touati [France] ; Jacques Motte [France] ; David Devos [France] ; Karine Mention [France] ; Dries Dobbelaere [France] ; Diana Rodriguez [France] ; Agathe Roubertie [France] ; Brigitte Chabrol [France] ; François Feillet [France] ; Marie Vidailhet [France] ; Nadia Bahi-Buisson [France]Spectrum of movement disorders associated with glutaric aciduria type 1: A study of 16 patients

List of associated KwdEn.i

Nombre de
documents		Descripteur
3Female
3Humans
2Adolescent
2Adult
2Child
2Child, Preschool
2Dystonia
2Human
2Infant
2Male
2Nervous system diseases
2Young Adult
2dystonia
1Aciduria
1Age Factors
1Brain Diseases, Metabolic (complications)
1Chorea
1Chorea (complications)
1Chorea (etiology)
1DNA Mutational Analysis
1Dystonia (complications)
1Dystonia (etiology)
1Electromyography
1Family Health
1GM1 gangliosidosis type 3
1Homovanillic Acid (metabolism)
1Hydroxyindoleacetic Acid (metabolism)
1Language disorder
1Lesch‐Nyhan disease
1Magnetic Resonance Imaging
1Metabolic diseases
1Movement Disorders (complications)
1Movement Disorders (pathology)
1Movement Disorders (physiopathology)
1Multiple Acyl Coenzyme A Dehydrogenase Deficiency (complications)
1Muscle Hypotonia (genetics)
1Muscle Hypotonia (metabolism)
1Muscle Hypotonia (physiopathology)
1Mutation (genetics)
1Neurologic Examination (methods)
1Prospective Studies
1Retrospective Studies
1Speech
1Speech Disorders (etiology)
1Tyrosine 3-Monooxygenase (genetics)
1development
1glutaric aciduria type 1
1hyperkinetic dysarthria
1metabolic disease
1speech apraxia
1speech disorder
1striatum

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