 |
|
|
 |
|
Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism
Coutinho AM, Oliveira G, Morgadinho T, Fesel C, Macedo TR, Bento C, Marques C, Ataide A, Miguel T, Borges L, Vicente AM
Mol Psychiatry 9(3):264-71
|
|
|
|
A band 3-based macrocomplex of integral and peripheral proteins in the red cell membrane
Bruce LJ, Beckmann R, Ribeiro ML, Peters LL, Chasis JA, Delaunay J, Mohandas N, Anstee DJ, Tanner MJA
(Prepublished online as a Blood First Edition Paper)
|
|
|
|
Trastornos congénitos de la membrana eritrocitária
Ribeiro ML, Tamagnini G
Libro de Hematología, Parte 2 – Alteraciones de los eritrocitos, Ediciones Aran SA
|
|
|
|
A splicing alteration of 4.1R pre-mRNA generates two protein isoforms with distinct assembly to spindle poles in mitotic cells
Delhommeau F, Vasseur-Godbillon C, Leclerc P, Schischmanoff PO, Croisille L, Rince P, Moriniere M, Benz, Jr EJ, Tchernia G, Tamagnini G, Ribeiro ML, Delaunay J, Baklouti F
Blood 100(7):2629-36
|
|
|
|
Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin- and band 3-deficient hereditary spherocytosis
Reliene R, Mariani M, Zanella A, Reinhart WH, Ribeiro ML, del Giudice EM, Perrotta S, Iolascon A, Eber S, Lutz HU
Blood 100(6):2208-15
|
|
|
|
Consequences at mRNA level of the PKLR gene splicing mutations IVS10(+1) G-C and IVS8(+2) T-C causing pyruvate kinase deficiency
Manco L, Bento C, Ribeiro ML, Tamagnini G
Br J Haematol 118(3):927-8
|
|
|
|
Abnormal NK cell lymphocytosis detected after splenectomy: association with repeated infections, relapsing neutropenia, and persistent polyclonal B-cell proliferation
Granjo E, Lima M, Fraga M, Santos F, Magalhaes C, Queiros ML, Moreira I, Rocha S, Silva AS, Rebelo I, Quintanilha A, Ribeiro ML, Candeias J, Orfao A.,
Int J Hematol 75(5):484-8
|
|
|
|
Síndroma de Beckwith-Wiedmann – casos clínicos e caracterização molecular
J Saraiva, L Ramos, E Cunha
Acta Pediatr Port 33(4):287-92
|
|
|
|
Pancreatite aguda e hemofilia B – caso clínico
F Rodrigues, A Rocha, A Nogueira Brandão, P Coelho, J Gil, L Maricato, A Mendes António
Acta Pediatr Port 32(5): 307-9
|
|
|
|
Síndroma de Gilbert-Frequência do genótipo UGT1(TA)7/(TA)7 numa amostra da população portuguesa
E Gonçalves, MC Bento, L Relvas, ML Ribeiro, GP Tamagnini
Jornal Português de Gastrenterologia 8:250-3
|
|
|
|
< anterior 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 seguinte >
|
|
|
|
|
|
|
|
|
