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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Agathe Roubertie »
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Aeyal Raz < Agathe Roubertie < Agid  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 6.
Ident.Authors (with country if any)Title
000112 (2012) Alfonso Fasano [Italie] ; Lucia Ricciardi [Italie] ; Anna Rita Bentivoglio [Italie] ; Carlotta Canavese [Italie] ; Giovanna Zorzi [Italie] ; Igor Petrovic [Serbie] ; Nikola Kresojevic [Serbie] ; Vladimir S. Kostic [Serbie] ; Marina Svetel [Serbie] ; Norbert Kovacs [Hongrie] ; Istvan Balas [Hongrie] ; Agathe Roubertie [France] ; Devendra Mishra [Inde] ; Paolo Mariotti [Italie] ; Teresa Temudo [Portugal] ; Nardo Nardocci [Italie]Status Dystonicus: Predictors of Outcome and Progression Patterns of Underlying Disease
000150 (2011) Arnaud Blanchard [France] ; Agathe Roubertie [France] ; Marion Simonetta-Moreau [France] ; Vuthy Ea [France] ; Coline Coquart [France] ; Melissa Y. Frederic [France] ; Gael Gallouedec [France] ; Jean-Paul Adenis [France] ; Isabelle Benatru [France] ; Michel Borg [France] ; Pierre Burbaud [France] ; Patrick Calvas [France] ; Laura Cif [France] ; Philippe Damier [France] ; Alain Destée [France] ; Laurence Faivre [France] ; Lucie Guyant-Marechal [France] ; Piotr Janik [Pologne] ; Samer Janoura [France] ; Alexandre Kreisler [France] ; Anna Lusakowska [Pologne] ; Sylvie Odent [France] ; Anna Potulska-Chromik [Pologne] ; Monika Rudzi Ska [Pologne] ; Stephane Thobois [France] ; Isabelle Vuillaume [France] ; Christine Tranchant [France] ; Sylvie Tuffery-Giraud [France] ; Philippe Coubes [France] ; Bernard Sablonnière [France] ; Mireille Claustres [France] ; Gwenaelle Collod-Béroud [France]Singular DYT6 phenotypes in association with new THAP1 frameshift mutations
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
000220 (2010) Cecilia Bonnet [France] ; Agathe Roubertie [France] ; Diane Doummar [France] ; Nadia Bahi-Buisson [France] ; Valérie Cochen De Cock [France] ; Emmanuel Roze [France]Developmental and benign movement disorders in childhood
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
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
5Nervous system diseases
4Dystonia
4Humans
3Adult
3Child
3Female
3Male
2Adolescent
2Child, Preschool
2Human
2Infant
2Movement Disorders (complications)
2Young Adult
2dystonia
1Aciduria
1Age Factors
1Apoptosis Regulatory Proteins (genetics)
1Behavior
1Brain Diseases, Metabolic (complications)
1Chorea
1Chorea (complications)
1Chorea (etiology)
1DNA-Binding Proteins (genetics)
1Developmental Disabilities (classification)
1Developmental Disabilities (complications)
1Developmental Disabilities (therapy)
1Developmental disorder
1Diagnosis, Differential
1Dystonia (complications)
1Dystonia (etiology)
1Dystonia Musculorum Deformans (genetics)
1Dystonia Musculorum Deformans (physiopathology)
1Electromyography
1Family Health
1Frameshift Mutation (genetics)
1Frameshift mutation
1GM1 gangliosidosis type 3
1Language disorder
1Lesch‐Nyhan disease
1Magnetic Resonance Imaging
1Mental retardation
1Metabolic diseases
1Midazolam
1Middle Aged
1Mirror
1Movement Disorders (classification)
1Movement Disorders (pathology)
1Movement Disorders (physiopathology)
1Movement Disorders (therapy)
1Multiple Acyl Coenzyme A Dehydrogenase Deficiency (complications)
1Myoclonus
1Neonatal
1Neurologic Examination (methods)
1Newborn
1Nuclear Proteins (genetics)
1Nystagmus
1Pantothenate kinase
1Phenotype
1Prognosis
1Prospective Studies
1Retrospective Studies
1Rhythmic movement
1Sleep
1Sleep disorder
1Speech
1Speech Disorders (etiology)
1Stereotypic Movement Disorder (epidemiology)
1Stereotypic Movement Disorder (physiopathology)
1Stereotypy
1Torticollis
1Transients
1benign jitteriness of newborns
1benign myoclonus of early infancy
1benign neonatal sleep myoclonus
1benign paroxysmal torticollis
1development
1glutaric aciduria type 1
1gratification behavior in early childhood
1hyperkinetic dysarthria
1metabolic disease
1mirror movements, Sandifer's syndrome
1paroxysmal tonic upgaze
1shuddering attacks
1sleep‐related rhythmic movement disorders
1spasmus nutans
1speech apraxia
1speech disorder
1stereotypies
1striatum
1transient dystonia of infancy

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