Detalhe da pesquisa
1.
Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review.
BMC Pediatr
; 20(1): 120, 2020 03 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32164589
2.
Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche.
J Pediatr Endocrinol Metab
; 25(11-12): 1059-64, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23329749
3.
Cushing's Syndrome in a 6-month-old Boy: A Rare Side-effect due to Inadequate use of Topical Corticosteroids.
Acta Derm Venereol
; 96(1): 138-9, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26038976
4.
Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experience.
Ital J Pediatr
; 42(1): 73, 2016 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27485500
5.
Partially reversible hypopituitarism in an adolescent with a rathke cleft cyst.
Clin Pediatr Endocrinol
; 21(4): 75-80, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23926414