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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Anne Roubergue »
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Anne Pavy-Le Traon < Anne Roubergue < Anne Seychelles  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
000057 (2013) Anne Roubergue [France] ; Emmanuel Roze ; Sandrine Vuillaumier-Barrot ; Marie-Joséphine Fontenille ; Aurélie Méneret ; Marie Vidailhet ; Bertrand Fontaine ; Diane Doummar ; Bertrand Philibert ; Florence Riant ; Sophie NicoleThe multiple faces of the ATP1A3-related dystonic movement disorder.
000319 (2007) Emmanuel Roze [France] ; Valérie Cochen [France] ; Sophie Sangla [France] ; Thierry Bienvenu [France] ; Anne Roubergue [France] ; Smaranda Leu-Semenescu [France] ; Marie Vidaihet [France]Rett syndrome: An overlooked diagnosis in women with stereotypic hand movements, psychomotor retardation, Parkinsonism, and dystonia?
000360 (2006) Emmanuel Roze [France] ; Marie Vidailhet [France] ; Nenad Blau [Suisse] ; Lisbeth Birk Moller [Danemark] ; Diane Doummar [France] ; Thierry Billette De Villemeur [France] ; Anne Roubergue [France]Long‐term follow‐up and adult outcome of 6‐pyruvoyl‐tetrahydropterin synthase deficiency
000408 (2005) Emmanuel Roze [France] ; Eduard Paschke [Autriche] ; Nathalie Lopez [France] ; Thomas Eck [Autriche] ; Kunihiro Yoshida [Japon] ; Annie Maurel-Ollivier [France] ; Diane Doummar [France] ; Catherine Caillaud [France] ; Damien Galanaud [France] ; Thierry Billette De Villemeur [France] ; Marie Vidailhet [France] ; Anne Roubergue [France]Dystonia and parkinsonism in GM1 type 3 gangliosidosis
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
5Female
5Humans
4Adult
4Nervous system diseases
3Adolescent
3Dystonia
2Child, Preschool
2Deficiency
2Dystonia (diagnosis)
2Dystonia (etiology)
2Middle Aged
2Parkinsonism
2Point Mutation (genetics)
2symptomatic dystonia
16‐pyruvoyl‐tetrahydropterin synthase deficiency
1Adrenal Gland Diseases (complications)
1Adrenal Gland Diseases (genetics)
1Age of Onset
1Alleles
1Antiparkinson Agents (therapeutic use)
1Athetosis (diagnosis)
1Athetosis (drug therapy)
1Athetosis (enzymology)
1Body Height
1Bone Diseases, Developmental (radiography)
1Child
1Chorea (diagnosis)
1Chorea (drug therapy)
1Chorea (enzymology)
1Choreoathetosis
1Diagnosis
1Digestive system
1Dose-Response Relationship, Drug
1Dystonia (drug therapy)
1Dystonia (enzymology)
1Dystonic Disorders (genetics)
1Dystonic Disorders (physiopathology)
1Electromyography
1Esophageal Achalasia (complications)
1Esophageal Achalasia (genetics)
1Esophageal Achalasia (physiopathology)
1Exons (genetics)
1Family
1Follow-Up Studies
1GM1 gangliosidosis
1Galactosidase
1Gangliosidosis, GM1 (complications)
1Gangliosidosis, GM1 (diagnosis)
1Gangliosidosis, GM1 (genetics)
1Gastrointestinal Diseases (complications)
1Gastrointestinal Diseases (genetics)
1Gastrointestinal Diseases (physiopathology)
1Gastrointestinal Motility (physiology)
1Hand
1Hemiplegia (genetics)
1Hemiplegia (physiopathology)
1Human
1Hyperphenylalaninemia
1Infant
1Infant, Newborn
1Lacrimal Apparatus Diseases (complications)
1Lacrimal Apparatus Diseases (genetics)
1Levodopa (therapeutic use)
1Lipids
1Long term
1Long-Term Care
1Lysosomal storage disease
1Male
1Malignant tumor
1Motor Skills Disorders (etiology)
1Movement (physiology)
1Muscle Hypotonia (diagnosis)
1Muscle Hypotonia (drug therapy)
1Muscle Hypotonia (enzymology)
1Mutation
1Mutation (genetics)
1Myoclonus
1Myoclonus (complications)
1Nerve Tissue Proteins
1Neurologic Examination
1Nuclear Pore Complex Proteins
1Parkinson Disease (etiology)
1Parkinson Disease (genetics)
1Parkinson Disease (physiopathology)
1Parkinsonian Disorders (etiology)
1Phenylketonurias (diagnosis)
1Phenylketonurias (drug therapy)
1Phenylketonurias (enzymology)
1Phosphorus-Oxygen Lyases (deficiency)
1Polymerase Chain Reaction
1Prognosis
1Proteins (genetics)
1Psychomotor retardation
1Pterins (metabolism)
1Rett Syndrome (diagnosis)
1Rett Syndrome (physiopathology)
1Rett syndrome
1Sodium-Potassium-Exchanging ATPase (genetics)
1Stereotypy
1Syndrome

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