Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Hans H. Jung »
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List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000175 (2011) Andreas R. Gantenbein [Suisse] ; Nathalie Damon-Perrière [France] ; Jörg E. Bohlender [Suisse] ; Marie Chauveau [France] ; Chrystelle Latxague [France] ; Marcelo Miranda [Chili] ; Hans H. Jung [Suisse] ; François Tison [France]Feeding dystonia in McLeod Syndrome
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
3MacLeod syndrome
3McLeod syndrome
3Nervous system diseases
3Sex linked character
3neuroacanthocytosis
2Chorea
2Chorea (genetics)
2Chorea (pathology)
2Male
2chorea
1Acanthocytosis
1Adult
1Age Factors
1Aged
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)
1Disease Models, Animal
1Dystonia
1Dystonia (etiology)
1Feeding Behavior (physiology)
1Genetic Variation (genetics)
1Genotype
1History, 20th Century
1History, 21st Century
1Lung, Hyperlucent (genetics)
1Lung, Hyperlucent (pathology)
1Lung, Hyperlucent (physiopathology)
1Lung, Hyperlucent (therapy)
1Magnetic Resonance Imaging
1Magnetic Resonance Imaging (methods)
1Middle Aged
1Muscle Weakness (physiopathology)
1Muscle, Skeletal (pathology)
1Muscle, Skeletal (physiopathology)
1Myocardium (pathology)
1Nervous System Diseases (complications)
1Nervous System Diseases (genetics)
1Neuroacanthocytosis (complications)
1Neuroacanthocytosis (genetics)
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
1Vesicular Transport Proteins (genetics)
1acanthocytosis
1chorea‐acanthocytosis
1feeding dystonia

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