Detalhe da pesquisa
1.
Salivary morning androstenedione and 17α-OH progesterone levels in childhood and puberty in patients with classic congenital adrenal hyperplasia.
Clin Chem Lab Med
; 53(3): 461-8, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25283138
2.
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorder.
Am J Med Genet A
; 158A(11): 2733-42, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23023959
3.
Cardiac evaluation in children with Prader-Willi syndrome.
Acta Paediatr
; 101(5): e225-31, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22181352
4.
Pubarche and serum dehydroepiandrosterone sulphate levels in children with Prader-Willi syndrome.
Clin Endocrinol (Oxf)
; 75(1): 83-9, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21521261
5.
The effect of oxandrolone on body proportions and body composition in growth hormone-treated girls with Turner syndrome.
Clin Endocrinol (Oxf)
; 73(2): 212-9, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20105186
6.
The effect of the weak androgen oxandrolone on psychological and behavioral characteristics in growth hormone-treated girls with Turner syndrome.
Horm Behav
; 57(3): 297-305, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20053349
7.
A healthy, female chimera with 46,XX/46,XY karyotype.
J Pediatr Endocrinol Metab
; 22(1): 97-102, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19344081
8.
Long-term follow-up of children with classic congenital adrenal hyperplasia: suggestions for age dependent treatment in childhood and puberty.
J Pediatr Endocrinol Metab
; 32(10): 1055-1063, 2019 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31573958
9.
High prevalence of central adrenal insufficiency in patients with Prader-Willi syndrome.
J Clin Endocrinol Metab
; 93(5): 1649-54, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18303077
10.
Randomized controlled GH trial: effects on anthropometry, body composition and body proportions in a large group of children with Prader-Willi syndrome.
Clin Endocrinol (Oxf)
; 69(3): 443-51, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18363884
11.
Testicular tumors in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency show functional features of adrenocortical tissue.
J Clin Endocrinol Metab
; 92(9): 3674-80, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17595257
12.
Testicular adrenal rest tumors in adult males with congenital adrenal hyperplasia: evaluation of pituitary-gonadal function before and after successful testis-sparing surgery in eight patients.
J Clin Endocrinol Metab
; 92(2): 612-5, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17090637
13.
Prevalence of testicular adrenal rest tumours in male children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Eur J Endocrinol
; 157(3): 339-44, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17766717
14.
Absence of increased height velocity in the first year of life in untreated children with simple virilizing congenital adrenal hyperplasia.
J Clin Endocrinol Metab
; 91(4): 1205-9, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16464952
15.
Cutoff levels of 17-alpha-hydroxyprogesterone in neonatal screening for congenital adrenal hyperplasia should be based on gestational age rather than on birth weight.
J Clin Endocrinol Metab
; 90(7): 3904-7, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15797960
16.
A review of neuropsychological and motor studies in Turner Syndrome.
Neurosci Biobehav Rev
; 27(4): 329-38, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12946685
17.
Growth inhibition by glucocorticoid treatment in salt wasting 21-hydroxylase deficiency: in early infancy and (pre)puberty.
J Clin Endocrinol Metab
; 88(8): 3525-30, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12915631
18.
CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations.
J Clin Endocrinol Metab
; 88(8): 3852-9, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12915679
19.
Normal bone mineral density and lean body mass, but increased fat mass, in young adult patients with congenital adrenal hyperplasia.
J Clin Endocrinol Metab
; 88(3): 1036-42, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12629082
20.
Differential inhibition of 17alpha-hydroxylase and 17,20-lyase activities by three novel missense CYP17 mutations identified in patients with P450c17 deficiency.
J Clin Endocrinol Metab
; 87(12): 5714-21, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12466376