Some digenetic trematodes found in a loggerhead sea turtle (Caretta caretta) from Brazil by Cavaco B., Madeira De Carvalho L. M., Werneck M. R.

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Utilisation of a cryptic non-canonical donor splice site of the gene encoding PARAFIBROMIN is associated with familial isolated primary hyperparathyroidism. by Bradley, K, Cavaco, B, Bowl, MR, Harding, B, Young, A, Thakker, R

Helminth Fauna of Juvenile Green Sea Turtles (Chelonia mydas) from Rio de Janeiro State, Brazil by Cavaco B., Madeira de Carvalho L. M., Shimoda E., Santoro M., Werneck M. R.

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Expression and function of the chemokine receptor CCR7 in thyroid carcinomas. by Sancho, M, Vieira, J, Casalou, C, Mesquita, M, Pereira, T, Cavaco, B, Dias, S, Leite, V

Expression of vascular endothelial growth factor (VEGF) and its receptors in thyroid carcinomas of follicular origin: a potential autocrine loop. by Vieira, J, Santos, S, Espadinha, C, Correia, I, Vag, T, Casalou, C, Cavaco, B, Catarino, A, Dias, S, Leite, V

Clinical and genetic studies of the hyperparathyroidism-jaw tumor syndrome (HPT-JT) in a kindred from Portugal. by Cavaco, B, Pannett, A, Barros, J, Ruas, L, Ruas, M, Leite, V, Sobrinho, L, Santos, M, Thakker, R

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene. by Cavaco, B, Guerra, L, Bradley, K, Carvalho, D, Harding, B, Oliveira, A, Santos, M, Sobrinho, L, Thakker, R, Leite, V

The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred. by Cavaco, B, Barros, L, Pannett, A, Ruas, L, Carvalheiro, M, Ruas, M, Krausz, T, Santos, M, Sobrinho, L, Leite, V, Thakker, R

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome. by Bradley, K, Hobbs, MR, Buley, I, Carpten, J, Cavaco, B, Fares, J, Laidler, P, Manek, S, Robbins, C, Salti, I, Thompson, N, Jackson, C, Thakker, R

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. by Pannett, A, Kennedy, A, Turner, J, Forbes, SA, Cavaco, B, Bassett, J, Cianferotti, L, Harding, B, Shine, B, Flinter, F, Maidment, C, Trembath, R, Thakker, R

Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions. by Cavaco, B, Domingues, R, Bacelar, M, Cardoso, H, Barros, L, Gomes, L, Ruas, M, Agapito, A, Garrão, A, Pannett, A, Silva, J, Sobrinho, L, Thakker, R, Leite, V

Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999) by Williamson, C, Cavaco, B, Jauch, A, Dixon, P, Forbes, S, Harding, B, Holtgreve-Grez, H, Schoell, B, Pereira, M, Font, A, Loureiro, M, Sobrinho, L, Santos, M, Thakker, R

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. by Bradley, K, Cavaco, B, Bowl, MR, Harding, B, Cranston, T, Fratter, C, Besser, G, Conceição Pereira, M, Davie, M, Dudley, N, Leite, V, Sadler, G, Seller, A, Thakker, R

Erratum: Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (Journal of Bone and Mineral Research (February 1999) 14 (23... by Williamson, C, Cavaco, B, Jauch, A, Dixon, P, Forbes, S, Harding, B, Holtgreve-Grez, H, Schoell, B, Pereira, M, Font, A, Loureiro, M, Sobrinho, L, Santos, M, Thakker, R

Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31. by Williamson, C, Cavaco, B, Jauch, A, Dixon, P, Forbes, S, Harding, B, Holtgreve-Grez, H, Schoell, B, Pereira, M, Font, A, Loureiro, M, Sobrinho, L, Santos, M, Thakker, R, Jausch, A

Genomic profiling reveals mutational landscape in parathyroid carcinomas. by Pandya, C, Uzilov, A, Bellizzi, J, Lau, C, Moe, A, Strahl, M, Hamou, W, Newman, L, Fink, M, Antipin, Y, Yu, W, Stevenson, M, Cavaco, B, Teh, B, Thakker, R, Morreau, H, Schadt, E, Sebra, R, Li, S, Arnold, A, Chen, R