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Items: 5

1.

Familial Turner syndrome: the importance of information.

Periquito I, Carrusca C, Morgado J, Robalo B, Pereira C, de Lurdes Sampaio M.

J Pediatr Endocrinol Metab. 2016 May 1;29(5):617-20. doi: 10.1515/jpem-2015-0277.

PMID:
26824976
2.

Adrenal Hypoplasia Congenita: A Rare Cause of Primary Adrenal Insufficiency and Hypogonadotropic Hypogonadism.

Loureiro M, Reis F, Robalo B, Pereira C, Sampaio L.

Pediatr Rep. 2015 Sep 28;7(3):5936. doi: 10.4081/pr.2015.5936. eCollection 2015 Sep 28.

3.

[Growth and puberty in type 1 diabetes mellitus - experience from a pediatric endocrinology unit].

Timóteo C, Castanhinha S, Constant C, Robalo B, Pereira C, Sampaio L.

Acta Med Port. 2012 Jul-Aug;25(4):213-8. Epub 2012 Aug 31. Portuguese.

4.

The multiple meanings of "wheezing": a questionnaire survey in Portuguese for parents and health professionals.

Fernandes RM, Robalo B, Calado C, Medeiros S, Saianda A, Figueira J, Rodrigues R, Bastardo C, Bandeira T.

BMC Pediatr. 2011 Dec 12;11:112. doi: 10.1186/1471-2431-11-112.

5.

An unusual case of renal medullary hyperechogenicity and hypertension. Autosomal recessive polycystic kidney disease (ARPKD).

Robalo B, Stone R, Saldanha J, Lobo L, Almeida M.

Pediatr Nephrol. 2009 Aug;24(8):1473-6. doi: 10.1007/s00467-008-1071-z. Epub 2008 Dec 13. No abstract available.

PMID:
19083020

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