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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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V Sulmont

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The Journal of Clinical Endocrinology and Metabolism|January 19, 2010

Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrierV Tardy, R Menassa, V Sulmont, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1996

[Latex allergy in 16 children]D Sabouraud-Leclerc, J F Fontaine, F Lavaud, et al.

Journal of Medical Genetics|June 14, 2001

SHOX point mutations in dyschondrosteosisC Huber, V Cusin, M Le Merrer, et al.

Diabetes & Metabolism|December 15, 2010

Access of children and adolescents with type 1 diabetes to insulin pump therapy has greatly increased in France since 2001V Sulmont, V Lassmann-Vague, B Guerci, et al.

Journal of Medical Genetics|November 6, 2001

Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritanceL Faivre, M Le Merrer, C Baumann, et al.

Diabetes & Metabolism|September 18, 2012

Real-time continuous glucose monitoring (CGM) integrated into the treatment of type 1 diabetes: consensus of experts from SFD, EVADIAC and SFEP-Y Benhamou, B Catargi, B Delenne, et al.

Pageof 2

Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

The Journal of Clinical Endocrinology and Metabolism|January 19, 2010

Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrierV Tardy, R Menassa, V Sulmont, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1996

[Latex allergy in 16 children]D Sabouraud-Leclerc, J F Fontaine, F Lavaud, et al.

Journal of Medical Genetics|June 14, 2001

SHOX point mutations in dyschondrosteosisC Huber, V Cusin, M Le Merrer, et al.

Diabetes & Metabolism|December 15, 2010

Access of children and adolescents with type 1 diabetes to insulin pump therapy has greatly increased in France since 2001V Sulmont, V Lassmann-Vague, B Guerci, et al.

Journal of Medical Genetics|November 6, 2001

Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritanceL Faivre, M Le Merrer, C Baumann, et al.

Diabetes & Metabolism|September 18, 2012

Real-time continuous glucose monitoring (CGM) integrated into the treatment of type 1 diabetes: consensus of experts from SFD, EVADIAC and SFEP-Y Benhamou, B Catargi, B Delenne, et al.

Pageof 2