Authors:
Rodriguez-Soriano, J
Vallo, A
Quintela, MJ
de Nanclares, GP
Bilbao, JR
Castano, L
Citation: J. Rodriguez-soriano et al., Familial hypercalcemia and hypercalciuria: no mutations in the Ca2+-sensing receptor gene, PED NEPHROL, 16(9), 2001, pp. 748-751
Authors:
Rodriguez-Soriano, J
Vallo, A
Bilbao, JR
Castano, L
Citation: J. Rodriguez-soriano et al., Branchio-oto-renal syndrome: identification of a novel mutation in the EYA1 gene, PED NEPHROL, 16(7), 2001, pp. 550-553
Authors:
Soria, JM
Baiget, M
Castano, L
Tejada, MI
Perez-Nanclares, G
Fontcuberta, J
Citation: Jm. Soria et al., Genetic risk factors for thrombosis in a Basque population and their possible contribution to the analysis of a complex disease such as thrombophilia, HAEMATOLOG, 86(8), 2001, pp. 889-890
Authors:
de Nanclares, GP
Castano, L
Martul, P
Rica, I
Vela, A
Sanjurjo, P
Aldamiz-Echevarria, K
Martinez, R
Sarrionandia, MJ
Citation: Gp. De Nanclares et al., Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family, J PED END M, 14(3), 2001, pp. 295-300
Authors:
Bilbao, JR
Rica, I
Vazquez, JA
Busturia, MA
Castano, L
Citation: Jr. Bilbao et al., Influence of sex and age at onset on autoantibodies against insulin, GAD(65) and IA2 in recent onset type 1 diabetic patients, HORMONE RES, 54(4), 2000, pp. 181-185
Authors:
Calvo, B
Castano, L
Marcus-Bagley, D
Fici, DA
Awdeh, Z
Alper, CA
Citation: B. Calvo et al., The [HLA-B18, F1C30, DR3] conserved extended haplotype carries a susceptibility gene for IgD deficiency, J CLIN IMM, 20(3), 2000, pp. 216-220
Authors:
de Nanclares, GP
Castano, L
Gaztambide, S
Bilbao, JR
Pi, J
Gonzalez, ML
Vazquez, JA
Citation: Gp. De Nanclares et al., Excess iron storage in patients with type 2 diabetes unrelated to primary hemochromatosis, N ENG J MED, 343(12), 2000, pp. 891-891
Authors:
Valdes, N
de Nanclares, GP
Alvarez, V
Castano, L
Diaz-Cadorniga, F
Aller, J
Coto, E
Citation: N. Valdes et al., Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop), CLIN ENDOCR, 50(3), 1999, pp. 309-313
Authors:
Calvo, B
Bilbao, JR
Rodriguez, A
Rodriguez-Arnao, MD
Castano, L
Citation: B. Calvo et al., Molecular analysis in familial neurohypophyseal diabetes insipidus: Early diagnosis of an asymptomatic carrier, J CLIN END, 84(9), 1999, pp. 3351-3354
Authors:
de Nanclares, GP
Bilbao, JR
Nistico, L
Buzzetti, R
Larsen, ZM
Pociot, F
Castano, L
Citation: Gp. De Nanclares et al., No evidence of association of chromosome 2q with Type I diabetes in the Basque population, DIABETOLOG, 42(1), 1999, pp. 119-120