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Results: 1-15 |
Results: 15
Magnetism of the series UFexAl12-x
Authors: Catarino, I Cardoso, C Goncalves, AP Waerenborgh, JC Cruz, MM Kuznietz, M Almeida, M Bonfait, G Godinho, M
Citation: I. Catarino et al., Magnetism of the series UFexAl12-x, J MAGN MAGN, 226, 2001, pp. 1120-1122
T-cell receptor repertoire in hereditary hemochromatosis: A study of 32 hemochromatosis patients and 274 healthy subjects
Authors: Cardoso, C Porto, G Lacerda, R Resende, D Rodrigues, P Bravo, F Oliveira, JC Justica, B de Sousa, M
Citation: C. Cardoso et al., T-cell receptor repertoire in hereditary hemochromatosis: A study of 32 hemochromatosis patients and 274 healthy subjects, HUMAN IMMUN, 62(5), 2001, pp. 488-499
Clinical determinants of increased QT dispersion in patients with diabetesmellitus
Authors: Cardoso, C Salles, G Bloch, K Deccache, W Siqueira, AG
Citation: C. Cardoso et al., Clinical determinants of increased QT dispersion in patients with diabetesmellitus, INT J CARD, 79(2-3), 2001, pp. 253-262
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ
Authors: Leventer, RJ Cardoso, C Ledbetter, DH Dobyns, WB
Citation: Rj. Leventer et al., LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ, NEUROLOGY, 57(3), 2001, pp. 416-422
The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disorders
Authors: Cardoso, C Mignon, C Hetet, G Grandchamps, B Fontes, M Colleaux, L
Citation: C. Cardoso et al., The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disorders, EUR J HUM G, 8(3), 2000, pp. 174-180
The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene
Authors: Cardoso, C Leventer, RJ Matsumoto, N Kuc, JA Ramocki, MB Mewborn, SK Dudlicek, LL May, LF Mills, PL Das, S Pilz, DT Dobyns, WB Ledbetter, DH
Citation: C. Cardoso et al., The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene, HUM MOL GEN, 9(20), 2000, pp. 3019-3028
Evolution of magnetism in the UFexAl12-x intermetallic series
Authors: Cardoso, C Catarino, I Goncalves, AP Waerenborgh, JC Cruz, MM Bonfait, G Kuznietz, M Almeida, M Godinho, M
Citation: C. Cardoso et al., Evolution of magnetism in the UFexAl12-x intermetallic series, PHYSICA B, 284, 2000, pp. 1339-1340
Influence of thermal treatment and crystal growth on the final compositionand magnetic properties of the YFexAl12-x (4 <= x <= 4.2) Intermetallics
Authors: Waerenborgh, JC Salamakha, P Sologub, O Goncalves, AP Cardoso, C Serio, S Godinho, M Almeida, M
Citation: Jc. Waerenborgh et al., Influence of thermal treatment and crystal growth on the final compositionand magnetic properties of the YFexAl12-x (4 <= x <= 4.2) Intermetallics, CHEM MATER, 12(6), 2000, pp. 1743-1749
Expansions of CD8+CD28-and CD8+TcRV beta 5.2+T cells in peripheral blood of heavy alcohol drinkers
Authors: Arosa, FA Porto, G Cabeda, JM Lacerda, R Resende, D Cruz, E Cardoso, C Fonseca, M Simoes, C Rodrigues, P Bravo, F Oliveira, JC Alves, H Fraga, J Justica, B de Sousa, M
Citation: Fa. Arosa et al., Expansions of CD8+CD28-and CD8+TcRV beta 5.2+T cells in peripheral blood of heavy alcohol drinkers, ALC CLIN EX, 24(4), 2000, pp. 519-527
Two affected boys in a Rett syndrome family - Clinical and molecular findings
Authors: Villard, L Kpebe, A Cardoso, C Chelly, J Tardieu, M Fontes, M
Citation: L. Villard et al., Two affected boys in a Rett syndrome family - Clinical and molecular findings, NEUROLOGY, 55(8), 2000, pp. 1188-1193
ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein
Authors: Cardoso, C Lutz, Y Mignon, C Compe, E Depetris, D Mattei, MG Fontes, M Colleaux, L
Citation: C. Cardoso et al., ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein, J MED GENET, 37(10), 2000, pp. 746-751
T-lymphocyte expression and function in hemochromatosis
Authors: de Sousa, M Porto, G Arosa, FA Cardoso, C Cabeda, JM LaCcerda, R Fraga, J
Citation: M. De Sousa et al., T-lymphocyte expression and function in hemochromatosis, HEMOCHROMATOSIS: GENETICS, PATHOPHYSIOLOGY, DIAGNOSIS AND TREATMENT, 2000, pp. 396-407
Peptide binding inhibits aggregation of soluble MHC class II in solution
Authors: Arimilli, S Astafieva, I Mukku, PV Cardoso, C Deshpande, S Nag, B
Citation: S. Arimilli et al., Peptide binding inhibits aggregation of soluble MHC class II in solution, IUBMB LIFE, 48(5), 1999, pp. 483-491
Bartter's syndrome and pregnancy
Authors: Clode, N Mendonca, E Stone, R Soares, L Cardoso, C Graca, LM Rosa, FC
Citation: N. Clode et al., Bartter's syndrome and pregnancy, EUR J OB GY, 82(1), 1999, pp. 17-18
Mutation of the XNP/ATR-X gene in a family with severe mental retardation,spastic paraplegia and skewed pattern of X inactivation: Demonstration that the mutation is involved in the inactivation bias
Authors: Lossi, AM Millan, JM Villard, L Orellana, C Cardoso, C Prieto, F Fontes, M Martinez, F
Citation: Am. Lossi et al., Mutation of the XNP/ATR-X gene in a family with severe mental retardation,spastic paraplegia and skewed pattern of X inactivation: Demonstration that the mutation is involved in the inactivation bias, AM J HU GEN, 65(2), 1999, pp. 558-562
Risultati: 1-15 |