Leite V - 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: leite v. 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

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. Among authors: leite v. J Clin Endocrinol Metab. 1995 Aug;80(8):2342-6. doi: 10.1210/jcem.80.8.7629227. J Clin Endocrinol Metab. 1995. PMID: 7629227

3

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. Among authors: leite v. J Endocrinol Invest. 1999 Mar;22(3):203-8. doi: 10.1007/BF03343542. J Endocrinol Invest. 1999. PMID: 10219888

4

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. Among authors: leite v. QJM. 2001 Apr;94(4):213-22. doi: 10.1093/qjmed/94.4.213. QJM. 2001. PMID: 11294964

5

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. Among authors: leite v. Eur J Endocrinol. 2001 Sep;145(3):311-6. doi: 10.1530/eje.0.1450311. Eur J Endocrinol. 2001. PMID: 11517012

6

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. Among authors: leite v. Eur J Endocrinol. 2002 Jan;146(1):27-33. doi: 10.1530/eje.0.1460027. Eur J Endocrinol. 2002. PMID: 11751063

7

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. Among authors: leite v. Clin Endocrinol (Oxf). 2002 Apr;56(4):465-73. doi: 10.1046/j.1365-2265.2002.01505.x. Clin Endocrinol (Oxf). 2002. PMID: 11966739

8

Medullary carcinomas of the thyroid: a monoclonal origin.

Marques AR, Catarino AL, Moniz S, Cavaco B, Roque L, Sobrinho L, Leite V. Marques AR, et al. Among authors: leite v. Thyroid. 2001 Dec;11(12):1109-13. doi: 10.1089/10507250152740948. Thyroid. 2001. PMID: 12186497

9

Preoperative diagnosis of suspicious parathyroid adenomas by RT-PCR using mRNA extracted from leftover cells in a needle used for ultrasonically guided fine needle aspiration cytology.

Cavaco BM, Torrinha F, Mendonça E, Pratas S, Boavida J, Sobrinho LG, Leite V. Cavaco BM, et al. Among authors: leite v. Acta Cytol. 2003 Jan-Feb;47(1):5-12. doi: 10.1159/000326468. Acta Cytol. 2003. PMID: 12585024

10

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene.

Cavaco BM, Guerra L, Bradley KJ, Carvalho D, Harding B, Oliveira A, Santos MA, Sobrinho LG, Thakker RV, Leite V. Cavaco BM, et al. Among authors: leite v. J Clin Endocrinol Metab. 2004 Apr;89(4):1747-52. doi: 10.1210/jc.2003-031016. J Clin Endocrinol Metab. 2004. PMID: 15070940

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