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G Rault

Showing results (21-30 of 41) with videos related to

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Human Genetics|January 1, 1987
Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndromeC Turleau, P Niaudet, C Sultan, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1991
Cystic fibrosis: production of high levels of uromodulin-like protein by HLA-DR blood monocytes differentiating towards a fibroblastic phenotypeM L Labat, A F Bringuier, C Seebold-Choqueux, et al.
The British Journal of Dermatology|March 23, 2010
Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?N Garçon-Michel, A-M Roguedas-Contios, G Rault, et al.
European Child & Adolescent Psychiatry|October 1, 1995
Eating and emotional disorders in adolescent obese girls with insulin-dependent diabetes mellitusG Vila, J J Robert, C Nollet-Clemencon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 8, 2000
[Does neonatal screening of cystic fibrosis affect outcome? Comparative study of two cohorts in Britanny and Loire-Atlantique with follow-up after ten years]D Siret, B Branger, V Storni, et al.
Journal of Medical Genetics|February 1, 1994
Association of 1078 del T cystic fibrosis mutation with severe diseaseP Moullier, M Jéhanne, M P Audrézet, et al.
Human Genetics|November 1, 1995
Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analysesC Férec, C Verlingue, P Parent, et al.
Pediatric Pulmonology|April 11, 2003
Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany)D Siret, G Bretaudeau, B Branger, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations]M Roussey, A Le Bihannic, M P Audrezet, et al.
Journal of Inherited Metabolic Disease|July 17, 2007
Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutationsM Roussey, A Le Bihannic, V Scotet, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Human Genetics|January 1, 1987
Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndromeC Turleau, P Niaudet, C Sultan, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1991
Cystic fibrosis: production of high levels of uromodulin-like protein by HLA-DR blood monocytes differentiating towards a fibroblastic phenotypeM L Labat, A F Bringuier, C Seebold-Choqueux, et al.
The British Journal of Dermatology|March 23, 2010
Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?N Garçon-Michel, A-M Roguedas-Contios, G Rault, et al.
European Child & Adolescent Psychiatry|October 1, 1995
Eating and emotional disorders in adolescent obese girls with insulin-dependent diabetes mellitusG Vila, J J Robert, C Nollet-Clemencon, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 8, 2000
[Does neonatal screening of cystic fibrosis affect outcome? Comparative study of two cohorts in Britanny and Loire-Atlantique with follow-up after ten years]D Siret, B Branger, V Storni, et al.
Journal of Medical Genetics|February 1, 1994
Association of 1078 del T cystic fibrosis mutation with severe diseaseP Moullier, M Jéhanne, M P Audrézet, et al.
Human Genetics|November 1, 1995
Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analysesC Férec, C Verlingue, P Parent, et al.
Pediatric Pulmonology|April 11, 2003
Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany)D Siret, G Bretaudeau, B Branger, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations]M Roussey, A Le Bihannic, M P Audrezet, et al.
Journal of Inherited Metabolic Disease|July 17, 2007
Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutationsM Roussey, A Le Bihannic, V Scotet, et al.
Pageof 5