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Archives Francaises De Pediatrie
|
March 1, 1985
[Somatocrinin and children in 1984. Application to the etiological diagnosis of somatotropin deficiencies]
P Chatelain, J Bertrand, M David, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 30, 2000
Bilateral laparoscopic adrenalectomy for congenital adrenal hyperplasia with severe hypertension, resulting from two novel mutations in splice donor sites of CYP11B1
O Chabre, S Portrat-Doyen, P Chaffanjon, et al.
Medicine
|
January 1, 1995
Diagnostic criteria for cystic fibrosis in men with congenital absence of the vas deferens
I Durieu, F Bey-Omar, J Rollet, et al.
Human Genetics
|
January 1, 1989
Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population
M Vidaud, A Kitzis, C Ferec, et al.
American Journal of Human Genetics
|
July 1, 1988
Assignment of the functional gene for human adrenodoxin to chromosome 11q13----qter and of adrenodoxin pseudogenes to chromosome 20cen----q13.1
Y Morel, J Picado-Leonard, D A Wu, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial
|
August 24, 2002
[Atypical neurosyphilis: 28 cases observed at the University Hospital Center of Conakry]
A Cisse, I S Souare, S Larkhis, et al.
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-HSD
E Rhéaume, R Sanchez, F Mébarki, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 3, 2014
[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome]
O Delmas, C Marrec, E Caietta, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1986
Long term treatment of male and female precocious puberty by periodic administration of a long-acting preparation of D-Trp6-luteinizing hormone-releasing hormone microcapsules
M Roger, J L Chaussain, P Berlier, et al.
Hormone Research
|
November 25, 2006
Cosegregation of a novel homozygous CYP11B1 mutation with the phenotype of non-classical congenital adrenal hyperplasia in a consanguineous family
C J Peters, T Nugent, L A Perry, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 138) with videos related to
Sort By:
Page
of 14
Archives Francaises De Pediatrie
|
March 1, 1985
[Somatocrinin and children in 1984. Application to the etiological diagnosis of somatotropin deficiencies]
P Chatelain, J Bertrand, M David, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 30, 2000
Bilateral laparoscopic adrenalectomy for congenital adrenal hyperplasia with severe hypertension, resulting from two novel mutations in splice donor sites of CYP11B1
O Chabre, S Portrat-Doyen, P Chaffanjon, et al.
Medicine
|
January 1, 1995
Diagnostic criteria for cystic fibrosis in men with congenital absence of the vas deferens
I Durieu, F Bey-Omar, J Rollet, et al.
Human Genetics
|
January 1, 1989
Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population
M Vidaud, A Kitzis, C Ferec, et al.
American Journal of Human Genetics
|
July 1, 1988
Assignment of the functional gene for human adrenodoxin to chromosome 11q13----qter and of adrenodoxin pseudogenes to chromosome 20cen----q13.1
Y Morel, J Picado-Leonard, D A Wu, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial
|
August 24, 2002
[Atypical neurosyphilis: 28 cases observed at the University Hospital Center of Conakry]
A Cisse, I S Souare, S Larkhis, et al.
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-HSD
E Rhéaume, R Sanchez, F Mébarki, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 3, 2014
[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome]
O Delmas, C Marrec, E Caietta, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1986
Long term treatment of male and female precocious puberty by periodic administration of a long-acting preparation of D-Trp6-luteinizing hormone-releasing hormone microcapsules
M Roger, J L Chaussain, P Berlier, et al.
Hormone Research
|
November 25, 2006
Cosegregation of a novel homozygous CYP11B1 mutation with the phenotype of non-classical congenital adrenal hyperplasia in a consanguineous family
C J Peters, T Nugent, L A Perry, et al.
Page
of 14