Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Ruth H. Walker »
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Ruth Djaldetti < Ruth H. Walker < Ruth Ottman  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
000289 (2008) Guilherme G. Riccioppo Rodrigues ; Ruth H. Walker [États-Unis] ; Alexis Brice [France] ; Cécile Cazeneuve [France] ; Odile Russaouen [France] ; Helio A. G. Teive [Brésil] ; Renato Puppi Munhoz [Brésil] ; Nilson Becker [Brésil] ; Salmo Raskin [Brésil] ; Lineu Cesar Werneck [Brésil] ; Wilson Marques Junior ; Vitor TumasHuntington's disease‐like 2 in Brazil—Report of 4 patients
000309 (2008) Guilherme G. Riccioppo Rodrigues [Brésil] ; Ruth H. Walker [États-Unis] ; Alexis Brice [France] ; Cécile Cazeneuve [France] ; Odile Russaouen [France] ; Helio A. G. Teive [Brésil] ; Renato Puppi Munhoz [Brésil] ; Nilson Becker [Brésil] ; Salmo Raskin [Brésil] ; Lineu Cesar Wemeck [Brésil] ; Wilson Marques Junior [Brésil] ; Vitor Tumas [Brésil]Huntington's Disease-Like 2 in Brazil-Report of 4 Patients
000324 (2007) Ruth H. Walker [États-Unis] ; Hans H. Jung [Suisse] ; François Tison [France] ; Soohee Lee [États-Unis] ; Adrian Danek [Allemagne]Phenotypic variation among brothers with the McLeod neuroacanthocytosis syndrome
000370 (2006) Ruth H. Walker [États-Unis] ; Adrian Danek [Allemagne] ; Carol Dobson-Stone [Australie] ; Renzo Guerrini [Italie] ; Hans H. Jung [Suisse] ; Anne-Louise Lafontaine [Canada] ; Luca Rampoldi [Italie] ; François Tison [France] ; Eva Andermann [Canada]Developments in neuroacanthocytosis: Expanding the spectrum of choreatic syndromes
000394 (2005) Eva Andermann [Canada] ; Adrian Danek [Allemagne] ; Glenn Irvine [Royaume-Uni] ; Hans H. Jung [Suisse] ; Luca Rampoldi [Italie] ; François Tison [France] ; Ruth H. Walker [États-Unis]Second International Neuroacanthocytosis Symposium: Expanding the spectrum of choreatic syndromes: Montreal Neurological Hospital and Institute, April 17–19

List of associated KwdEn.i

Nombre de
documents
Descripteur
3Humans
3Nervous system diseases
2Adult
2Brazil
2Chorea
2Chorea (genetics)
2Chorea (pathology)
2MacLeod syndrome
2Magnetic Resonance Imaging
2Male
2McLeod syndrome
2Sex linked character
2chorea
2neuroacanthocytosis
1Acanthocytosis
1Age Factors
1Amino Acid Transport Systems, Neutral (genetics)
1Animals
1Atrial Fibrillation (complications)
1Atrial Fibrillation (pathology)
1Atrial Fibrillation (physiopathology)
1Brain (pathology)
1Central Nervous System Diseases (complications)
1Central Nervous System Diseases (genetics)
1Central Nervous System Diseases (pathology)
1Chorea (history)
1Chorea (physiopathology)
1Chorea (therapy)
1Chromosomes, Human, X (genetics)
1DNA Mutational Analysis
1Disease Models, Animal
1Exons (genetics)
1Female
1Genetic Variation (genetics)
1Genotype
1History, 20th Century
1History, 21st Century
1Human
1Huntington Disease (genetics)
1Huntington Disease (pathology)
1Huntington disease
1Huntington's disease
1Huntington's disease like
1Lung, Hyperlucent (genetics)
1Lung, Hyperlucent (pathology)
1Lung, Hyperlucent (physiopathology)
1Lung, Hyperlucent (therapy)
1Magnetic Resonance Imaging (methods)
1Membrane Proteins (genetics)
1Middle Aged
1Muscle Weakness (physiopathology)
1Muscle, Skeletal (pathology)
1Muscle, Skeletal (physiopathology)
1Myocardium (pathology)
1Neurodegenerative Diseases (genetics)
1Neurodegenerative Diseases (history)
1Neurodegenerative Diseases (physiopathology)
1Neurodegenerative Diseases (therapy)
1Peripheral Nervous System Diseases (complications)
1Peripheral Nervous System Diseases (genetics)
1Peripheral Nervous System Diseases (pathology)
1Phenotype
1Siblings
1Syndrome
1Trinucleotide Repeat Expansion (genetics)
1Vesicular Transport Proteins (genetics)
1Young Adult
1acanthocytosis
1chorea‐acanthocytosis
1junctophilin 3

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