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Results: 1-25 | 26-37 |
Results: 26-37/37
Multiple endocrine neoplasia type 1
Authors: Pannett, AAJ Thakker, RV
Citation: Aaj. Pannett et Rv. Thakker, Multiple endocrine neoplasia type 1, ENDOCR-R CA, 6(4), 1999, pp. 449-473
Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease
Authors: Devuyst, O Christie, PT Courtoy, PJ Beauwens, R Thakker, RV
Citation: O. Devuyst et al., Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease, HUM MOL GEN, 8(2), 1999, pp. 247-257
A familial syndrome due to Arg648Stop mutation in the X-linked renal chloride channel gene
Authors: Bosio, M Bianchi, ML Lloyd, SE Thakker, RV
Citation: M. Bosio et al., A familial syndrome due to Arg648Stop mutation in the X-linked renal chloride channel gene, PED NEPHROL, 13(4), 1999, pp. 278-283
Renal chloride channel, CLCN5, mutations in Dent's disease
Authors: Cox, JPD Yamamoto, K Christie, PT Wooding, C Feest, T Flinter, FA Goodyer, PR Leumann, E Neuhaus, T Reid, C Williams, PF Wrong, O Thakker, RV
Citation: Jpd. Cox et al., Renal chloride channel, CLCN5, mutations in Dent's disease, J BONE MIN, 14(9), 1999, pp. 1536-1542
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
Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1
Authors: Bassett, JHD Rashbass, P Harding, B Forbes, SA Pannett, AAJ Thakker, RV
Citation: Jhd. Bassett et al., Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1, J BONE MIN, 14(1), 1999, pp. 3-10
Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism
Authors: Bassett, JHD O'Halloran, DJ Williams, GR Beardwell, CG Shale, SM Thakker, RV
Citation: Jhd. Bassett et al., Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism, CLIN ENDOCR, 50(1), 1999, pp. 69-75
Mechanisms of disease - Genetic disorders of renal electrolyte transport
Authors: Scheinman, SJ Guay-Woodford, LM Thakker, RV Warnock, DG
Citation: Sj. Scheinman et al., Mechanisms of disease - Genetic disorders of renal electrolyte transport, N ENG J MED, 340(15), 1999, pp. 1177-1187
Sequence analysis and transcript expression of the MEN1 gene in sporadic pituitary tumours
Authors: Farrell, WE Simpson, DJ Bicknell, J Magnay, JL Kyrodimou, E Thakker, RV Clayton, RN
Citation: We. Farrell et al., Sequence analysis and transcript expression of the MEN1 gene in sporadic pituitary tumours, BR J CANC, 80(1-2), 1999, pp. 44-50
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13
Authors: Lloyd, SE Pannett, AAJ Dixon, PH Whyte, MP Thakker, RV
Citation: Se. Lloyd et al., Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13, AM J HU GEN, 64(1), 1999, pp. 189-195
Disorders of the calcium-sensing receptor
Authors: Thakker, RV
Citation: Rv. Thakker, Disorders of the calcium-sensing receptor, BBA-MOL CEL, 1448(2), 1998, pp. 166-170
Risultati: 1-25 | 26-37 |