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Movement Disorders (revue) - Analysis (France)

Index « Auteurs » - entrée « Claire-Marie Dhaenens »
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Claire-Lise Gervason < Claire-Marie Dhaenens < Clare Fowler  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
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
000359 (2006) David Devos [France] ; Isabelle Vuillaume [France] ; Alix De Becdelievre [France] ; Berengère De Martinville [France] ; Claire-Marie Dhaenens [France] ; Jean-Christophe Cuvellier [France] ; Jean-Marie Cuisset [France] ; Louis Vallée [France] ; Marie-Pierre Lemaitre [France] ; Hélène Bourteel [France] ; Eric Hachulla [France] ; Benoit Wallaert [France] ; Alain Destée [France] ; Luc Defebvre [France] ; Bernard Sablonnière [France]New syndromic form of benign hereditary chorea is associated with a deletion of TITF‐1 and PAX‐9 contiguous genes
000410 (2005) Claire-Marie Dhaenens [France] ; Pierre Krystkowiak [France] ; Xavier Douay [France] ; Pierre Charpentier [France] ; Sylvain Bele [France] ; Alain Destée [France] ; Bernard Sablonnière [France]Clinical and genetic evaluation in a French population presenting with primary focal dystonia

List of associated KwdEn.i

Nombre de
documents		Descripteur
3Humans
3Nervous system diseases
2DNA Mutational Analysis
2Dystonia
2Dystonic Disorders (genetics)
2Female
2France (epidemiology)
2French
2Male
2movement disorders
1Adult
1Age Factors
1Age of Onset
1Aged
1Alleles
1Aspartic Acid (genetics)
1Blepharospasm (genetics)
1Carrier Proteins (genetics)
1Child
1Child, Preschool
1Chorea
1Chorea (genetics)
1Chorea (physiopathology)
1Chromosome Mapping
1Chromosomes, Human, Pair 14
1Chromosomes, Human, Pair 9
1DYT1
1Deletion
1Dystonic Disorders (classification)
1Dystonic Disorders (epidemiology)
1Evaluation
1Family Health
1France (ethnology)
1Gene Deletion
1Gene Frequency
1Histidine (genetics)
1In Situ Hybridization, Fluorescence (methods)
1Linkage Disequilibrium
1Lung
1Lung Diseases (etiology)
1Microsatellite Repeats (genetics)
1Middle Aged
1Molecular Chaperones (genetics)
1Nuclear Proteins (genetics)
1PAX gene
1PAX9 Transcription Factor (genetics)
1Polymorphism, Single Nucleotide (genetics)
1Retrospective Studies
1TITF‐1 gene
1TOR1A
1Thyroid Diseases (etiology)
1Thyroid gland
1Tooth Diseases (etiology)
1Transcription Factors (genetics)
1Trinucleotide Repeats
1benign hereditary chorea
1brain–thyroid–lung syndrome
1dystonia
1genetic modifiers
1population studies

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