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Results: 1-9 |
Results: 9
The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred
Authors: Cavaco, BM Barros, L Pannett, AAJ Ruas, L Carvalheiro, M Ruas, MMA Krausz, T Santos, MA Sobrinho, LG Leite, V Thakker, RV
Citation: Bm. Cavaco et al., The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred, QJM-MON J A, 94(4), 2001, pp. 213-222
Presence of a Gs alpha mutation in an adrenal tumor expressing LH/hCG receptors and clinically associated with Cushing's syndrome
Authors: Bugalho, MJM Li, X Rao, CV Soares, J Sobrinho, LG
Citation: Mjm. Bugalho et al., Presence of a Gs alpha mutation in an adrenal tumor expressing LH/hCG receptors and clinically associated with Cushing's syndrome, GYNECOL END, 14(1), 2000, pp. 50-54
Medullary thyroid carcinoma: an accurate pre-operative diagnosis by reverse transcription-PCR
Authors: Bugalho, MJGB Mendonca, E Sobrinho, LG
Citation: Mjgb. Bugalho et al., Medullary thyroid carcinoma: an accurate pre-operative diagnosis by reverse transcription-PCR, EUR J ENDOC, 143(3), 2000, pp. 335-338
Somatic trinucleotide change encompassing codons 882 and 883 of the RET proto-oncogene in a patient with sporadic medullary thyroid carcinoma
Authors: Bugalho, MJ Coelho, I Sobrinho, LG
Citation: Mj. Bugalho et al., Somatic trinucleotide change encompassing codons 882 and 883 of the RET proto-oncogene in a patient with sporadic medullary thyroid carcinoma, EUR J ENDOC, 142(6), 2000, pp. 573-575
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999)
Authors: 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
Citation: C. Williamson et al., Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31 (vol 14, pg 230, 1999), J BONE MIN, 14(8), 1999, pp. 1472-1472
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31
Authors: Williamson, C Cavaco, BM Jausch, A Dixon, P Forbes, S Harding, B Holtgreve-Grez, H Schoell, B Pereira, MC Font, AP Loureiro, MM Sobrinho, LG Santos, MA Thakker, RV
Citation: C. Williamson et al., Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31, J BONE MIN, 14(2), 1999, pp. 230-239
Hyperprolactinemia due to big big prolactin is differently detected by commercially available immunoassays
Authors: Cavaco, B Prazeres, S Santos, MA Sobrinho, LG Leite, V
Citation: B. Cavaco et al., Hyperprolactinemia due to big big prolactin is differently detected by commercially available immunoassays, J ENDOC INV, 22(3), 1999, pp. 203-208
Spontaneously occurring anti-PTH autoantibodies must be considered in the differential diagnosis of patients with elevated serum PTH levels
Authors: Cavaco, B Leite, V Loureiro, MM Ferreira, MF Pereira, MC Santos, MA Sobrinho, LG
Citation: B. Cavaco et al., Spontaneously occurring anti-PTH autoantibodies must be considered in the differential diagnosis of patients with elevated serum PTH levels, J ENDOC INV, 22(11), 1999, pp. 829-834
Rapid weight gain, at least in some women, is an expression of a neuroendocrine state characterized by reduced hypothalamic dopaminergic tone
Authors: Ferreira, MF Sobrinho, LG Santos, MA Sousa, MFF Uvnas-Moberg, K
Citation: Mf. Ferreira et al., Rapid weight gain, at least in some women, is an expression of a neuroendocrine state characterized by reduced hypothalamic dopaminergic tone, PSYCHONEURO, 23(8), 1998, pp. 1005-1013
Risultati: 1-9 |