Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « G. Chazot »
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Fénelon < G. Chazot < G. Dellatolas  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 3.
Ident.Authors (with country if any)Title
000529 (2000) G. Demarquay [France] ; A. Setiey [France] ; Y. Morel [France] ; C. Trepo [France] ; G. Chazot [France] ; E. Broussolle [France]Clinical report of three patients with hereditary hemochromatosis and movement disorders
000638 (1993) Broussolle [France] ; L. Cinotti [France] ; Pierre Pollak [France] ; P. Landais [France] ; D. Le Bars [France] ; G. Galy [France] ; F. Lavenne [France] ; Y. Khalfallah [France] ; G. Chazot [France] ; F. Mauguière [France]Relief of akinesia by apomorphine and cerebral metabolic changes in parkinson's disease
000648 (1993) E. Broussolle [France] ; L. Cinotti [France] ; Pierre Pollak [France] ; P. Landais [France] ; D. Le Bars [France] ; G. Galy [France] ; F. Lavenne [France] ; Y. Khalfallah ; G. Chazot [France] ; F. Mauguiere [France]Relief of akinesia by apomorphine and cerebral metabolic changes in Parkinson's disease

List of associated KwdEn.i

Nombre de
documents
Descripteur
2Aged
2Akinesia
2Female
2Humans
2Male
1Adult
1Apomorphine (pharmacology)
1Apomorphine (therapeutic use)
1Brain (blood supply)
1Brain (drug effects)
1Brain (metabolism)
1Case study
1Cerebellar syndrome
1Cerebral Cortex (metabolism)
1Cerebrovascular Circulation (drug effects)
1Chronic acquired hepatocerebral degeneration
1Complication
1Corpus Striatum (drug effects)
1Corpus Striatum (metabolism)
1Dystonia
1Exploration
1Glucose (metabolism)
1Hemochromatosis
1Hemochromatosis (blood)
1Hemochromatosis (complications)
1Hemochromatosis (diagnosis)
1Hemochromatosis (genetics)
1Hepatolenticular Degeneration (blood)
1Hepatolenticular Degeneration (genetics)
1Hereditary hemochromatosis
1Human
1Iron
1Iron (adverse effects)
1Iron (blood)
1Metabolism
1Motor fluctuations
1Motor system disorder
1Movement Disorders (blood)
1Movement Disorders (diagnosis)
1Movement Disorders (genetics)
1Movement disorders
1Parkinson Disease (drug therapy)
1Parkinson Disease (metabolism)
1Parkinson Disease (physiopathology)
1Parkinson disease
1Parkinson's disease
1Parkinsonism
1Pathogenesis
1Positron emission tomography
1Receptors, Dopamine (drug effects)
1Regional cerebral metabolism
1Tomography, Emission-Computed
1Tremor
1[18F]Fluorodeoxyglucose

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