Detalhe da pesquisa
1.
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.
Nat Genet
; 28(4): 365-70, 2001 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-11479539
2.
Genetic exclusion of 14 candidate genes in lipoatropic diabetes using linkage analysis in 10 consanguineous families.
J Clin Endocrinol Metab
; 82(10): 3438-44, 1997 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-9329383
3.
Extremely low values of serum leptin in children with congenital generalized lipoatrophy.
Eur J Endocrinol
; 140(1): 107-9, 1999 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-10037260
4.
[Early hypomagnesemia, hypercalciuria and nephrocalcinosis: two cases in a family]. / Hypomagnésémie, hypercalciurie et néphrocalcinose de révélation précoce: deux observations familiales.
Arch Pediatr
; 6(7): 748-51, 1999 Jul.
Artigo
em Francês
| MEDLINE | ID: mdl-10429815
5.
Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes.
Diabetes
; 47(3): 490-2, 1998 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-9519760
6.
[Autoimmunity and insulin-dependent diabetes mellitus. Experimental data and therapeutic prospects]. / Auto-immunité et diabète insulinodépendant. Données expérimentales et perspectives thérapeutiques.
Pediatrie
; 44(4): 247-57, 1989.
Artigo
em Francês
| MEDLINE | ID: mdl-2677968
7.
Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylase.
Horm Res
; 53(2): 77-82, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-10971093