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C Carel

Showing results (101-110 of 129) with videos related to

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Biochemistry|March 7, 1995
Identification and characterization of the G15D mutation found in a male patient with 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency: alteration of the putative NAD-binding domain of type II 3 beta-HSDE Rhéaume, R Sanchez, F Mébarki, et al.
Diabetes & Metabolism|December 5, 2012
Continuous subcutaneous insulin infusion allows tolerance induction and diabetes treatment in a type 1 diabetic child with insulin allergyC Hasselmann, C Pecquet, E Bismuth, et al.
Genes and Immunity|June 11, 2010
Risk of autoimmune diabetes in APECED: association with short alleles of the 5'insulin VNTRJ Paquette, D S E Varin, C E Hamelin, et al.
European Journal of Endocrinology|March 15, 2011
Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndromeA Linglart, S Cabrol, P Berlier, et al.
Diabetologia|March 1, 1989
Hypoglycaemia induced by antibodies to insulin receptor following a bone marrow transplantation in an immunodeficient childN Rochet, S Blanche, J C Carel, et al.
Diabetologia|October 1, 1998
Low dose linomide in Type I juvenile diabetes of recent onset: a randomised placebo-controlled double blind trialR Coutant, P Landais, M Rosilio, et al.
Journal of Medical Genetics|September 1, 1996
A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalitiesL Telvi, A Ion, J C Carel, et al.
Molecular Psychiatry|April 24, 2001
Association of anorexia nervosa with the high activity allele of the COMT gene: a family-based study in Israeli patientsA Frisch, N Laufer, Y Danziger, et al.
Brain : a Journal of Neurology|January 29, 2000
Cortical motor reorganization in akinetic patients with Parkinson's disease: a functional MRI studyU Sabatini, K Boulanouar, N Fabre, et al.
Human Molecular Genetics|February 1, 1995
Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyS Kosugi, C Van Dop, M E Geffner, et al.
Pageof 13

Showing results (101-110 of 129) with videos related to

Sort By:
Pageof 13
Biochemistry|March 7, 1995
Identification and characterization of the G15D mutation found in a male patient with 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) deficiency: alteration of the putative NAD-binding domain of type II 3 beta-HSDE Rhéaume, R Sanchez, F Mébarki, et al.
Diabetes & Metabolism|December 5, 2012
Continuous subcutaneous insulin infusion allows tolerance induction and diabetes treatment in a type 1 diabetic child with insulin allergyC Hasselmann, C Pecquet, E Bismuth, et al.
Genes and Immunity|June 11, 2010
Risk of autoimmune diabetes in APECED: association with short alleles of the 5'insulin VNTRJ Paquette, D S E Varin, C E Hamelin, et al.
European Journal of Endocrinology|March 15, 2011
Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndromeA Linglart, S Cabrol, P Berlier, et al.
Diabetologia|March 1, 1989
Hypoglycaemia induced by antibodies to insulin receptor following a bone marrow transplantation in an immunodeficient childN Rochet, S Blanche, J C Carel, et al.
Diabetologia|October 1, 1998
Low dose linomide in Type I juvenile diabetes of recent onset: a randomised placebo-controlled double blind trialR Coutant, P Landais, M Rosilio, et al.
Journal of Medical Genetics|September 1, 1996
A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalitiesL Telvi, A Ion, J C Carel, et al.
Molecular Psychiatry|April 24, 2001
Association of anorexia nervosa with the high activity allele of the COMT gene: a family-based study in Israeli patientsA Frisch, N Laufer, Y Danziger, et al.
Brain : a Journal of Neurology|January 29, 2000
Cortical motor reorganization in akinetic patients with Parkinson's disease: a functional MRI studyU Sabatini, K Boulanouar, N Fabre, et al.
Human Molecular Genetics|February 1, 1995
Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyS Kosugi, C Van Dop, M E Geffner, et al.
Pageof 13