Personas / Equipo Humano

Daniel Raúl Grinberg Vaisman

Buscador de publicaciones

Publicaciones

  • Pintó X, Vilaseca MA, Balcells S, Artuch-Iriberri R, Corbella E, Meco JF, Vila R, Pujol R and Grinberg-Vaisman DR.

    A folate-rich diet is as effective as folic acid from supplements in decreasing plasma homocysteine concentrations.

    INTERNATIONAL JOURNAL OF MEDICAL SCIENCES . 2(2): 58-63. Nº de citas: 21

    [doi:10.7150/ijms.2.58]

  • Mainou Cid C, García Giralt N, Vilaseca MA, Ferrer I, Meco López JF, Mainou Pintó A, Pintó Sala X, Grinberg-Vaisman DR and Balcells S.

    Hiperhomocistinemia y polimorfismo 677C T de la 5,10-metilenotetrahidrofolato reductasa en hijos de pacientes con enfermedad coronaria prematura.

    Anales espanoles de pediatria . 56(5): 402-408.

  • Bayés M, Goldaracena B, Martínez-Mir A, Iragui-Madoz MI, Solans T, Chivelet P, Bussaglia E, Ramos-Arroyo MA, Baiget M, Vilageliu L, Balcells S, Gonzalez R and Grinberg-Vaisman DR.

    A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

    JOURNAL OF MEDICAL GENETICS . 35(2): 141-145. Nº de citas: 29

    [doi:10.1136/jmg.35.2.141]

  • Martínez-Mir A, Vilela C, Bayés M, Valverde D, Dain L, Beneyto M, Marco M, Baiget M, Grinberg-Vaisman DR, Balcells S, Gonzalez R and Vilageliu L.

    Putative association of a mutant ROM1 allele with retinitis pigmentosa.

    HUMAN GENETICS . 99(6): 827-830. Nº de citas: 9

    [doi:10.1007/s004390050456]

  • Martínez-Mir A, Bayés M, Vilageliu L, Grinberg-Vaisman DR, Ayuso C, del Río T, García-Sandoval B, Bussaglia E, Baiget M, Gonzalez R and Balcells S.

    A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21.

    Genomics . 40(1): 142-146. Nº de citas: 41

    [doi:10.1006/geno.1996.4528]

  • Bayés M, Martínez-Mir A, Valverde D, del Río E, Vilageliu L, Grinberg-Vaisman DR, Balcells S, Ayuso C, Baiget M and Gonzalez R.

    Autosomal recessive retinitis pigmentosa in Spain: evaluation of four genes and two loci involved in the disease.

    CLINICAL GENETICS . 50(5): 380-387. Nº de citas: 14

  • Chabás A, Cormand B, Balcells S, Gonzalez R, Casanova C, Colomer J, Vilageliu L and Grinberg-Vaisman DR.

    Neuronopathic and non-neuronopathic presentation of Gaucher disease in patients with the third most common mutation (D409H) in Spain.

    JOURNAL OF INHERITED METABOLIC DISEASE . 19(6): 798-800. Nº de citas: 15

    [doi:10.1007/BF01799179]

  • Cormand B, Vilageliu L, Balcells S, Gonzalez R, Chabás A and Grinberg-Vaisman DR.

    Two novel (1098insA and Y313H) and one rare (R359Q) mutations detected in exon 8 of the beta-glucocerebrosidase gene in Gaucher's disease patients.

    HUMAN MUTATION . 7(3): 272-274.

    [doi:10.1002/(SICI)1098-1004(1996)7:3272::AID-HUMU143.0.CO;2-#]

  • Valverde D, Solans T, Grinberg-Vaisman DR, Balcells S, Vilageliu L, Bayés M, Chivelet P, Besmond C, Goossens M, Gonzalez R and Baiget M.

    A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family.

    HUMAN GENETICS . 97(1): 35-38. Nº de citas: 22

  • Chabás A, Cormand B, Grinberg-Vaisman DR, Burguera JM, Balcells S, Merino JL, Mate I, Sobrino JA, Gonzalez R and Vilageliu L.

    Unusual expression of Gaucher's disease: cardiovascular calcifications in three sibs homozygous for the D409H mutation.

    JOURNAL OF MEDICAL GENETICS . 32(9): 740-742. Nº de citas: 95

    [doi:10.1136/jmg.32.9.740]