Cavaco BM - Search Results

1

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

Bradley KJ, Cavaco BM, Bowl MR, Harding B, Cranston T, Fratter C, Besser GM, Conceição Pereira M, Davie MW, Dudley N, Leite V, Sadler GP, Seller A, Thakker RV. Bradley KJ, et al. Among authors: cavaco bm. Clin Endocrinol (Oxf). 2006 Mar;64(3):299-306. doi: 10.1111/j.1365-2265.2006.02460.x. Clin Endocrinol (Oxf). 2006. PMID: 16487440

2

[Iodine intake in Portuguese school children].

Limbert E, Prazeres S, São Pedro M, Madureira D, Miranda A, Ribeiro M, Carrilho F, Jácome de Castro J, Lopes MS, Cardoso J, Carvalho A, Oliveira MJ, Reguengo H, Borges F; Grupo de Estudos da Tiroide da Sociedade Portuguesa de Endocrinologia Diabetes e Metabolismo. Limbert E, et al. Acta Med Port. 2012 Jan-Feb;25(1):29-36. Epub 2012 May 25. Acta Med Port. 2012. PMID: 22883246 Free article. Portuguese.

3

Some forms of big big prolactin behave as a complex of monomeric prolactin with an immunoglobulin G in patients with macroprolactinemia or prolactinoma.

Cavaco B, Leite V, Santos MA, Arranhado E, Sobrinho LG. Cavaco B, et al. J Clin Endocrinol Metab. 1995 Aug;80(8):2342-6. doi: 10.1210/jcem.80.8.7629227. J Clin Endocrinol Metab. 1995. PMID: 7629227

4

Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31.

Williamson C, Cavaco BM, Jauch A, Dixon PH, Forbes S, Harding B, Holtgreve-Grez H, Schoell B, Pereira MC, Font AP, Loureiro MM, Sobrinho LG, Santos MA, Thakker RV. Williamson C, et al. Among authors: cavaco bm. J Bone Miner Res. 1999 Feb;14(2):230-9. doi: 10.1359/jbmr.1999.14.2.230. J Bone Miner Res. 1999. PMID: 9933477 Free article.

5

Hyperprolactinemia due to big big prolactin is differently detected by commercially available immunoassays.

Cavaco B, Prazeres S, Santos MA, Sobrinho LG, Leite V. Cavaco B, et al. J Endocrinol Invest. 1999 Mar;22(3):203-8. doi: 10.1007/BF03343542. J Endocrinol Invest. 1999. PMID: 10219888

6

The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred.

Cavaco BM, Barros L, Pannett AA, Ruas L, Carvalheiro M, Ruas MM, Krausz T, Santos MA, Sobrinho LG, Leite V, Thakker RV. Cavaco BM, et al. QJM. 2001 Apr;94(4):213-22. doi: 10.1093/qjmed/94.4.213. QJM. 2001. PMID: 11294964

7

Hypoglycaemia due to insulin autoimmune syndrome: report of two cases with characterisation of HLA alleles and insulin autoantibodies.

Cavaco B, Uchigata Y, Porto T, Amparo-Santos M, Sobrinho L, Leite V. Cavaco B, et al. Eur J Endocrinol. 2001 Sep;145(3):311-6. doi: 10.1530/eje.0.1450311. Eur J Endocrinol. 2001. PMID: 11517012

8

Clonal origin of non-medullary thyroid tumours assessed by non-random X-chromosome inactivation.

Moniz S, Catarino AL, Marques AR, Cavaco B, Sobrinho L, Leite V. Moniz S, et al. Eur J Endocrinol. 2002 Jan;146(1):27-33. doi: 10.1530/eje.0.1460027. Eur J Endocrinol. 2002. PMID: 11751063

9

Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions.

Cavaco BM, Domingues R, Bacelar MC, Cardoso H, Barros L, Gomes L, Ruas MM, Agapito A, Garrão A, Pannett AA, Silva JL, Sobrinho LG, Thakker RV, Leite V. Cavaco BM, et al. Clin Endocrinol (Oxf). 2002 Apr;56(4):465-73. doi: 10.1046/j.1365-2265.2002.01505.x. Clin Endocrinol (Oxf). 2002. PMID: 11966739

10

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome.

Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, Simonds WF, Gillanders EM, Kennedy AM, Chen JD, Agarwal SK, Sood R, Jones MP, Moses TY, Haven C, Petillo D, Leotlela PD, Harding B, Cameron D, Pannett AA, Höög A, Heath H 3rd, James-Newton LA, Robinson B, Zarbo RJ, Cavaco BM, Wassif W, Perrier ND, Rosen IB, Kristoffersson U, Turnpenny PD, Farnebo LO, Besser GM, Jackson CE, Morreau H, Trent JM, Thakker RV, Marx SJ, Teh BT, Larsson C, Hobbs MR. Carpten JD, et al. Among authors: cavaco bm. Nat Genet. 2002 Dec;32(4):676-80. doi: 10.1038/ng1048. Epub 2002 Nov 18. Nat Genet. 2002. PMID: 12434154

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