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Revue Neurologique
|
May 6, 2014
An overview of neurological and neuromuscular signs in mitochondrial diseases
A Chaussenot, V Paquis-Flucklinger
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 28, 2020
Molecular diagnosis and genetic counseling for spinal muscular atrophy (SMA)
C Rouzier, A Chaussenot, V Paquis-Flucklinger
Revue Neurologique
|
September 24, 2008
[Late cerebellar ataxia associated with fragile X premutation]
A Chaussenot, M Borg, C Bayreuther, et al.
Revue Neurologique
|
June 6, 2009
[Chorea-acanthocytosis without acanthocytes]
C Bayreuther, M Borg, C Ferrero-Vacher, et al.
Revue Neurologique
|
April 25, 2007
[Neurosarcoidosis treated with mycophenolate mofetil: two cases]
A Chaussenot, V Bourg, S Chanalet, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie
|
June 4, 2013
[Bladder-sphincter disorders associated with Wolfram syndrome]
C Ribière, F A Kaboré, A Chaussenot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 14, 2012
[Epilepsy and mitochondrial diseases: retrospective study on 53 epileptic children]
E Caietta, A Cano, C Halbert, et al.
Clinical Genetics
|
June 4, 2014
Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders
A Chaussenot, C Rouzier, M Quere, et al.
Journal of Medical Genetics
|
August 10, 2010
The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein
C Rouzier, S Le Guédard-Méreuze, K Fragaki, et al.
Scientific Reports
|
July 6, 2022
Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach
C Liautard-Haag, G Durif, C VanGoethem, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Revue Neurologique
|
May 6, 2014
An overview of neurological and neuromuscular signs in mitochondrial diseases
A Chaussenot, V Paquis-Flucklinger
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 28, 2020
Molecular diagnosis and genetic counseling for spinal muscular atrophy (SMA)
C Rouzier, A Chaussenot, V Paquis-Flucklinger
Revue Neurologique
|
September 24, 2008
[Late cerebellar ataxia associated with fragile X premutation]
A Chaussenot, M Borg, C Bayreuther, et al.
Revue Neurologique
|
June 6, 2009
[Chorea-acanthocytosis without acanthocytes]
C Bayreuther, M Borg, C Ferrero-Vacher, et al.
Revue Neurologique
|
April 25, 2007
[Neurosarcoidosis treated with mycophenolate mofetil: two cases]
A Chaussenot, V Bourg, S Chanalet, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie
|
June 4, 2013
[Bladder-sphincter disorders associated with Wolfram syndrome]
C Ribière, F A Kaboré, A Chaussenot, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
July 14, 2012
[Epilepsy and mitochondrial diseases: retrospective study on 53 epileptic children]
E Caietta, A Cano, C Halbert, et al.
Clinical Genetics
|
June 4, 2014
Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1-related disorders
A Chaussenot, C Rouzier, M Quere, et al.
Journal of Medical Genetics
|
August 10, 2010
The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein
C Rouzier, S Le Guédard-Méreuze, K Fragaki, et al.
Scientific Reports
|
July 6, 2022
Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach
C Liautard-Haag, G Durif, C VanGoethem, et al.
Page
of 1