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A Lienhardt

Showing results (11-20 of 27) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Radiological quiz of the month]A Lienhardt, C Laroche, M P Boncoeur, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 10, 1998
Double maternal seroconversion to cytomegalovirus and Toxoplasma gondiiY Aubard, S Rogez, M L Darde, et al.
Diabete & Metabolisme|January 1, 1993
Insulin resistance and excess weight in adolescent insulin-dependent diabetic girlsS Souissi, B Rakotoambinina, V Foussier, et al.
Fetal Diagnosis and Therapy|October 26, 1999
A rare cause of fetal ascites: A case report of Günther's diseaseA Lienhardt, Y Aubard, C Laroche, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|November 26, 1998
Insulin secretion and sensitivity in children on cyclic total parenteral nutritionA Lienhardt, B Rakotoambinina, V Colomb, et al.
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.
Prenatal Diagnosis|September 5, 2002
Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counsellingB Gilbert, C Yardin, S Briault, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Activating mutations of the calcium-sensing receptor: management of hypocalcemiaA Lienhardt, M Bai, J P Lagarde, et al.
Hormone Research|January 12, 2002
Growth abnormalities associated with adrenal disorders and their managementM O Savage, M C Lebrethon, J C Blair, et al.
The Journal of Clinical Endocrinology and Metabolism|April 19, 2000
A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemiaA Lienhardt, M Garabédian, M Bai, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Radiological quiz of the month]A Lienhardt, C Laroche, M P Boncoeur, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 10, 1998
Double maternal seroconversion to cytomegalovirus and Toxoplasma gondiiY Aubard, S Rogez, M L Darde, et al.
Diabete & Metabolisme|January 1, 1993
Insulin resistance and excess weight in adolescent insulin-dependent diabetic girlsS Souissi, B Rakotoambinina, V Foussier, et al.
Fetal Diagnosis and Therapy|October 26, 1999
A rare cause of fetal ascites: A case report of Günther's diseaseA Lienhardt, Y Aubard, C Laroche, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|November 26, 1998
Insulin secretion and sensitivity in children on cyclic total parenteral nutritionA Lienhardt, B Rakotoambinina, V Colomb, et al.
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.
Prenatal Diagnosis|September 5, 2002
Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counsellingB Gilbert, C Yardin, S Briault, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2001
Activating mutations of the calcium-sensing receptor: management of hypocalcemiaA Lienhardt, M Bai, J P Lagarde, et al.
Hormone Research|January 12, 2002
Growth abnormalities associated with adrenal disorders and their managementM O Savage, M C Lebrethon, J C Blair, et al.
The Journal of Clinical Endocrinology and Metabolism|April 19, 2000
A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemiaA Lienhardt, M Garabédian, M Bai, et al.
Pageof 3