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1.
Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients.
Clin Endocrinol (Oxf)
; 69(3): 426-31, 2008 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-18331608
2.
[Tolerance of the oral clonidine test in 180 patients: efficacy of the volemic expantion in controlling arterial hypotension]. / Tolerância ao teste da clonidina em 180 pacientes: estudo da eficácia da expansão volêmica para o controle de hipotensão arterial.
Arq Bras Endocrinol Metabol
; 49(4): 510-5, 2005 Aug.
Artículo
en Portugués
| MEDLINE | ID: mdl-16358078
3.
Usefulness of MLPA in the detection of SHOX deletions.
Eur J Med Genet
; 53(5): 234-8, 2010.
Artículo
en Inglés
| MEDLINE | ID: mdl-20538086
4.
The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administration.
Clin Endocrinol (Oxf)
; 60(1): 36-40, 2004 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-14678285
5.
Tolerância ao teste da clonidina em 180 pacientes: estudo da eficácia da expansão volêmica para o controle de hipotensão arterial / Tolerance of the oral clonidine test in 180 patients: efficacy of saline resuscitation in controlling arterial hypotension
Arq. bras. endocrinol. metab
; 49(4): 510-515, ago. 2005. tab
Artículo
en Portugués
| LILACS | ID: lil-414768
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