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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Frédéric Sedel »
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Frédéric Moisan < Frédéric Sedel < Frédéric Tankere  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000094 (2012) Julien Lagarde [France] ; Emmanuel Roze ; Emmanuelle Apartis ; Deepa Pothalil ; Frédéric Sedel ; Philippe Couvert ; Marie Vidailhet ; Bertrand DegosMyoclonus and dystonia in cerebrotendinous xanthomatosis.
000119 (2012) Julien Lagarde [France] ; Emmanuel Roze [France] ; Emmanuelle Apartis [France] ; Deepa Pothalil [France] ; Frédéric Sedel [France] ; Philippe Couvert [France] ; Marie Vidailhet [France] ; Bertrand Degos [France]Myoclonus and Dystonia in Cerebrotendinous Xanthomatosis
000241 (2009) Ichraf Kraoua [France] ; Jérôme Stirnemann [France] ; Maria João Ribeiro [France] ; Tiphaine Rouaud [France] ; Marc Verin [France] ; Agnès Annic [France] ; Christian Rose [France] ; Luc Defebvre [France] ; Liliane Réménieras [France] ; Michaël Schüpbach [France] ; Nadia Belmatoug [France] ; Marie Vidailhet [France] ; Frédéric Sedel [France]Parkinsonism in Gaucher's disease type 1: Ten new cases and a review of the literature
000585 (1997) Alain Créange [France] ; Frédéric Sedel [France] ; Pierre Brugières [France] ; Marie-Christine Voisin [France] ; Jean-Denis Degos [France]Primary Sjögren's syndrome presenting as progressive parkinsonia syndrome

List of associated KwdEn.i

Nombre de
documents		Descripteur
3Humans
2Adult
2Female
2Male
2Nervous system diseases
2Parkinsonism
1Adolescent
1Age of Onset
1Aged
1Bilateral
1Brain (pathology)
1Case study
1Cerebrotendinous xanthomatosis
1Cognition Disorders (complications)
1Cognition Disorders (genetics)
1Dentate nucleus
1Diagnosis, Differential
1Diagnostic Imaging
1Dystonia
1Dystonia (complications)
1Dystonia (genetics)
1Epilepsy (complications)
1Functional Laterality (physiology)
1Gaucher
1Gaucher Disease (classification)
1Gaucher Disease (complications)
1Gaucher Disease (genetics)
1Gaucher Disease (pathology)
1Gaucher disease
1Glucosylceramidase (genetics)
1Glucosylceramidase (metabolism)
1Human
1Inaugural sign
1Lewy body dementia
1Lipids
1Magnetic Resonance Imaging
1Middle Aged
1Myoclonus
1Myoclonus (complications)
1Myoclonus (genetics)
1Neurologic Examination
1Parkinson Disease, Secondary (diagnosis)
1Parkinson disease
1Parkinson's disease
1Parkinsonian Disorders (etiology)
1Parkinsonian Disorders (genetics)
1Parkinsonian Disorders (pathology)
1Parkinsonian Disorders (therapy)
1Sjogren's Syndrome (diagnosis)
1Sjögren syndrome
1Symptomatology
1Xanthomatosis, Cerebrotendinous (etiology)
1Xanthomatosis, Cerebrotendinous (genetics)
1glucocerebrosidase
1parkinsonism

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