d'Alva CB - Search Results

1

A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty.

d'Alva CB, Brito VN, Palhares HM, Carvalho FM, Arnhold IJ, Mendonca BB, Latronico AC. d'Alva CB, et al. Clin Endocrinol (Oxf). 2006 Sep;65(3):408-10. doi: 10.1111/j.1365-2265.2006.02596.x. Clin Endocrinol (Oxf). 2006. PMID: 16918965 No abstract available.

2

Letter re: FSH receptor polymorphisms and iatrogenic ovarian hyperstimulation.

d'Alva CB, Serafini P, Motta E, Latronico AC, Mendonca BB. d'Alva CB, et al. J Clin Endocrinol Metab. 2005 Aug;90(8):4978; author reply 4978-9. doi: 10.1210/jc.2005-0863. J Clin Endocrinol Metab. 2005. PMID: 16087961 No abstract available.

3

Absence of mutation in the follicle-stimulating hormone receptor gene in severe primary hypothyroidism associated with gonadal hyperstimulation.

Suarez EA, d'Alva CB, Campbell A, Miller-Horn J, Dever M, Faerber E, Medonca BB, Latronico AC, De Luca F. Suarez EA, et al. J Pediatr Endocrinol Metab. 2007 Aug;20(8):923-31. doi: 10.1515/jpem.2007.20.8.923. J Pediatr Endocrinol Metab. 2007. PMID: 17937064

4

Evaluating the roles of follicle-stimulating hormone receptor polymorphisms in gonadal hyperstimulation associated with severe juvenile primary hypothyroidism.

Ryan GL, Feng X, d'Alva CB, Zhang M, Van Voorhis BJ, Pinto EM, Kubias AE, Antonini SR, Latronico AC, Segaloff DL. Ryan GL, et al. J Clin Endocrinol Metab. 2007 Jun;92(6):2312-7. doi: 10.1210/jc.2006-2086. Epub 2007 Mar 13. J Clin Endocrinol Metab. 2007. PMID: 17356048

5

Absence of follicle-stimulating hormone receptor activating mutations in women with iatrogenic ovarian hyperstimulation syndrome.

d'Alva CB, Serafini P, Motta E, Kohek MB, Latronico AC, Mendonca BB. d'Alva CB, et al. Fertil Steril. 2005 Jun;83(6):1695-9. doi: 10.1016/j.fertnstert.2004.12.044. Fertil Steril. 2005. PMID: 15950638 Free article.

6

Clinical and hormonal features of selective follicle-stimulating hormone (FSH) deficiency due to FSH beta-subunit gene mutations in both sexes.

Berger K, Souza H, Brito VN, d'Alva CB, Mendonca BB, Latronico AC. Berger K, et al. Fertil Steril. 2005 Feb;83(2):466-70. doi: 10.1016/j.fertnstert.2004.06.069. Fertil Steril. 2005. PMID: 15705395 Free article.

7

Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age.

Coletta RR, Jorge AA, D'Alva CB, Pinto EM, Billerbeck AE, Pachi PR, Longui CA, Garcia RM, Boguszewski M, Arnhold IJ, Mendonca BB, Costa EM. Coletta RR, et al. Clinics (Sao Paulo). 2013 Jun;68(6):785-91. doi: 10.6061/clinics/2013(06)10. Clinics (Sao Paulo). 2013. PMID: 23778474 Free PMC article.

8

Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation.

Fontenele EG, Moraes ME, d'Alva CB, Pinheiro DP, Landim SA, Barros FA, Trarbach EB, Mendonca BB, Jorge AA. Fontenele EG, et al. Horm Res Paediatr. 2015;84(4):248-53. doi: 10.1159/000437324. Epub 2015 Aug 18. Horm Res Paediatr. 2015. PMID: 26304632

9

A signal peptide mutation of the arginine vasopressin gene in monozygotic twins.

Boson WL, Sarubi JC, d'Alva CB, Friedman E, Faria D, De Marco L, Wajchenberg B. Boson WL, et al. Clin Endocrinol (Oxf). 2003 Jan;58(1):108-10. doi: 10.1046/j.1365-2265.2003.01667.x. Clin Endocrinol (Oxf). 2003. PMID: 12519420

10

Leu124Serfs*26, a novel AGPAT2 mutation in congenital generalized lipodystrophy with early cardiovascular complications.

Montenegro Junior RM, Lima GEDCP, Fernandes VO, Montenegro APDR, Ponte CMM, Martins LV, Pinheiro DP, de Moraes MEA, de Moraes Filho MO, d'Alva CB. Montenegro Junior RM, et al. Diabetol Metab Syndr. 2020 Apr 6;12:28. doi: 10.1186/s13098-020-00538-y. eCollection 2020. Diabetol Metab Syndr. 2020. PMID: 32280377 Free PMC article.

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