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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Fabienne Clot »
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Fabienne Calvas < Fabienne Clot < Fabienne Marquant  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 4.
Ident.Authors (with country if any)Title
000232 (2009) Mélissa Yana Frédéric [France] ; Fabienne Clot [France] ; Arnaud Blanchard [France] ; Claire-Marie Dhaenens [France] ; Gaëtan Lesca [France] ; Laura Cif [France] ; Alexandra Dürr [France] ; Marie Vidailhet [France] ; Bernard Sablonniere [France] ; Alain Calender [France] ; Maria Martinez [France] ; Nicolas Molinari [France] ; Alexis Brice [France] ; Mireille Claustres [France] ; Sylvie Tuffery-Giraud [France] ; Gwenaëlle Collod-Beroud [France]The p.Asp216His TOR1A allele effect is not found in the French population
000244 (2009) Kiyoka Kinugawa [France] ; Marie Vidailhet [France] ; Fabienne Clot [France] ; Emmanuelle Apartis [France] ; David Grabli [France] ; Emmanuel Roze [France]Myoclonus‐dystonia: An update
000251 (2009) Diane Doummar [France] ; Fabienne Clot [France] ; Marie Vidailhet [France] ; Alexandra Afenjar [France] ; Alexandra Durr [France] ; Alexis Brice [France] ; Cyril Mignot [France] ; Agnès Guet [France] ; Thierry Billette De Villemeur [France] ; Diana Rodriguez [France]Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene
000269 (2009) Mélissa Yana Frederic [France] ; Fabienne Clot [France] ; Amaud Blanchard [France] ; Claire-Marie Dhaenens [France] ; Gaëtan Lesca [France] ; Laura Cif [France] ; Alexandra Dürr [France] ; Marie Vidailhet [France] ; Bernard Sablonniere [France] ; Alain Calender [France] ; Maria Martinez [France] ; Nicolas Molinari [France] ; Alexis Brice [France] ; Mireille Claustres [France] ; Sylvie Tuffery-Giraud [France] ; Gwenaëlle Collod-Beroud [France]The p.Asp216His TOR1A Allele Effect Is Not Found in the French Population

List of associated KwdEn.i

Nombre de
documents		Descripteur
3Humans
2DNA Mutational Analysis
2Dystonia
2Mutation (genetics)
2Nervous system diseases
1Alleles
1Aspartic Acid (genetics)
1DYT1
1Diagnosis, Differential
1Dystonia (complications)
1Dystonia (diagnosis)
1Dystonia (genetics)
1Dystonia (therapy)
1Dystonic Disorders (genetics)
1Female
1France (epidemiology)
1France (ethnology)
1French
1Gene Frequency
1Histidine (genetics)
1Homovanillic Acid (metabolism)
1Hydroxyindoleacetic Acid (metabolism)
1Infant
1Magnetic Resonance Imaging (methods)
1Molecular Chaperones (genetics)
1Movement Disorders (genetics)
1Movement Disorders (physiopathology)
1Movement Disorders (therapy)
1Muscle Hypotonia (genetics)
1Muscle Hypotonia (metabolism)
1Muscle Hypotonia (physiopathology)
1Myoclonus
1Myoclonus (complications)
1Myoclonus (diagnosis)
1Myoclonus (genetics)
1Myoclonus (therapy)
1Neurology
1Pathophysiology
1Polymorphism, Single Nucleotide (genetics)
1Sarcoglycans (genetics)
1TOR1A
1Tyrosine 3-Monooxygenase (genetics)
1clinical neurology
1dystonia
1epsilon‐sarcoglycan
1genetic modifiers
1genetics
1movement disorders
1myoclonus‐dystonia
1pathophysiology
1population studies
1primary dystonia

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