Costa C - Search Results

1

The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17β-hydroxysteroid-dehydrogenase type 3 enzyme deficiency.

Costa C, Castro-Correia C, Mira-Coelho A, Monteiro B, Monteiro J, Hughes I, Fontoura M. Costa C, et al. Endocrinol Diabetes Metab Case Rep. 2014;2014:140064. doi: 10.1530/EDM-14-0064. Epub 2014 Sep 1. Endocrinol Diabetes Metab Case Rep. 2014. PMID: 25298885 Free PMC article.

2

The acute abdomen in the newborn.

Rocha G, Costa C, Correia-Pinto J, Monteiro J, Guimarães H. Rocha G, et al. Among authors: costa c. Acta Med Port. 2009 Sep-Oct;22(5):559-66. Epub 2009 Oct 22. Acta Med Port. 2009. PMID: 19944039 Free article.

3

[Neonatal tumors].

Costa C, Rocha G, Grilo M, Bianchi R, Sotto Mayor T, Monteiro J, Guimarães H. Costa C, et al. Acta Med Port. 2010 May-Jun;23(3):405-12. Epub 2010 Jun 14. Acta Med Port. 2010. PMID: 20654259 Free article. Portuguese.

4

Thyroid carcinoma in children and adolescents: a retrospective review.

Neiva F, Mesquita J, Paco Lima S, Matos MJ, Costa C, Castro-Correia C, Fontoura M, Martins S. Neiva F, et al. Among authors: costa c. Endocrinol Nutr. 2012 Feb;59(2):105-8. doi: 10.1016/j.endonu.2011.11.003. Epub 2012 Jan 3. Endocrinol Nutr. 2012. PMID: 22222852 English, Spanish.

5

[Growth hormone treatment in childhood cancer survivors].

Sampaio M, Oliveira A, Soro I, Costa C, Castro-Correia C, Fontoura M. Sampaio M, et al. Among authors: costa c. Acta Med Port. 2011 Dec;24 Suppl 2:393-8. Epub 2011 Dec 31. Acta Med Port. 2011. PMID: 22849927 Free article. Portuguese.

6

Permanent neonatal diabetes by a new mutation in KCNJ11: unsuccessful switch to sulfonylurea.

Lau E, Correia C, Freitas P, Nogueira C, Costa M, Saavedra A, Costa C, Carvalho D, Fontoura M. Lau E, et al. Among authors: costa c, costa m. Arch Endocrinol Metab. 2015 Dec;59(6):559-61. doi: 10.1590/2359-3997000000076. Epub 2015 Aug 28. Arch Endocrinol Metab. 2015. PMID: 26331221

7

Metabolic risk factors in adolescent girls with type 1 diabetes.

Castro-Correia C, Santos-Silva R, Pinheiro M, Costa C, Fontoura M. Castro-Correia C, et al. Among authors: costa c. J Pediatr Endocrinol Metab. 2018 Jun 27;31(6):631-635. doi: 10.1515/jpem-2018-0053. J Pediatr Endocrinol Metab. 2018. PMID: 29750655

8

Pituitary incidentalomas in paediatric age are different from those described in adulthood.

Souteiro P, Maia R, Santos-Silva R, Figueiredo R, Costa C, Belo S, Castro-Correia C, Carvalho D, Fontoura M. Souteiro P, et al. Among authors: costa c. Pituitary. 2019 Apr;22(2):124-128. doi: 10.1007/s11102-019-00940-4. Pituitary. 2019. PMID: 30684167

9

Carney complex due to a novel pathogenic variant in the PRKAR1A gene - a case report.

Ferreira SH, Costa MM, Rios E, Santos Silva R, Costa C, Castro-Correia C, Fontoura M. Ferreira SH, et al. Among authors: costa mm, costa c. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):197-202. doi: 10.1515/jpem-2018-0199. J Pediatr Endocrinol Metab. 2019. PMID: 30699069

10

Genetic analyses in a cohort of Portuguese pediatric patients with congenital hypothyroidism.

Santos-Silva R, Rosário M, Grangeia A, Costa C, Castro-Correia C, Alonso I, Leão M, Fontoura M. Santos-Silva R, et al. Among authors: costa c. J Pediatr Endocrinol Metab. 2019 Nov 26;32(11):1265-1273. doi: 10.1515/jpem-2019-0047. J Pediatr Endocrinol Metab. 2019. PMID: 31430255

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