People / Staff

Daniel Raúl Grinberg Vaisman

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Publications

  • Rodríguez-Sanz M, García-Giralt N, Prieto-Alhambra D, Servitja S, Balcells S, Pecorelli R, Díez-Pérez A, Grinberg-Vaisman DR, Tusquets I and Nogués X.

    CYP11A1 expression in bone is associated with aromatase inhibitor-related bone loss.

    J MOL ENDOCRINOL . 55(1): 69-79. Number of citations: 22

    [doi:10.1530/JME-15-0079]

  • Dimitriou E, Cozar M, Mavridou I, Grinberg-Vaisman DR, Vilageliu L and Michelakakis H.

    The Spectrum of Krabbe Disease in Greece: Biochemical and Molecular Findings.

    JIMD Reports . 25: 57-64. Number of citations: 3

    [doi:10.1007/8904_2015_457]

  • Carcavilla A, García-Miñaúr S, Pérez-Aytés A, Vendrell T, Pinto I, Guillén-Navarro E, González-Meneses A, Aoki Y, Grinberg-Vaisman DR and Ezquieta B.

    Síndrome cardiofaciocutáneo, un trastorno relacionado con el síndrome de Noonan: hallazgos clínicos y moleculares en 11 pacientes.

    MEDICINA CLINICA . 144(2): 67-72. Number of citations: 2

    [doi:10.1016/j.medcli.2014.06.009]

  • Matos L, Canals I, Dridi L, Choi Y, Prata MJ, Jordan P, Desviat LR, Pérez-Dueñas B, Pshezhetsky AV, Grinberg-Vaisman DR, Alves S and Vilageliu L.

    Therapeutic strategies based on modified U1 snRNAs and chaperones for Sanfilippo C splicing mutations

    ORPHANET JOURNAL OF RARE DISEASES . 9: 180-180. Number of citations: 35

    [doi:10.1186/s13023-014-0180-y]

  • Delgado MA, Martinez-Domenech G, Sarrión P, Urreizti R, Zecchini L, Robledo HH, Segura F, de Kremer RD, Balcells S, Grinberg-Vaisman DR and Asteggiano CG.

    A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG.

    SCIENTIFIC REPORTS . 4: 6407-6407. Number of citations: 14

    [doi:10.1038/srep06407]

  • Serra-Vinardell J, Díaz L, Guitiérrez-de Terán H, Sánchez-Ollé G, Bujons J, Michelakakis H, Mavridou I, Aerts JM, Delgado A, Grinberg-Vaisman DR, Vilageliu L and Casas J.

    Selective chaperone effect of aminocyclitol derivatives on G202R and other mutant glucocerebrosidases causing Gaucher disease.

    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY . 54: 245-254. Number of citations: 8

    [doi:10.1016/j.biocel.2014.07.017]

  • Serra-Vinardell J, Díaz L, Casas J, Grinberg-Vaisman DR, Vilageliu L, Michelakakis H, Mavridou I, Aerts JM, Decroocq C, Compain P and Delgado A.

    Glucocerebrosidase enhancers for selected Gaucher disease genotypes by modification of a-1-C-substituted imino-D-xylitols (DIXs) by click chemistry.

    Chemmedchem . 9(8): 1744-1754. Number of citations: 15

    [doi:10.1002/cmdc.201402023]

  • Reverter M, Rentero C, Garcia-Melero A, Hoque M, Vilà de Muga S, Alvarez-Guaita A, Conway JR, Wood P, Cairns R, Lykopoulou L, Grinberg-Vaisman DR, Vilageliu L, Bosch M, Heeren J, Blasi J, Timpson P, Pol A, Tebar F, Murray RZ, Grewal T and Enrich C.

    Cholesterol regulates Syntaxin 6 trafficking at trans-Golgi network endosomal boundaries.

    CELL REPORTS . 7(3): 883-897. Number of citations: 83

    [doi:10.1016/j.celrep.2014.03.043]

  • Sarrión P, Mellibovsky L, Urreizti R, Civit S, Cols N, García-Giralt N, Yoskovitz G, Aranguren A, Malouf J, Di Gregorio S, Río LD, Güerri R, Nogués X, Díez-Pérez A, Grinberg-Vaisman DR and Balcells S.

    Genetic analysis of high bone mass cases from the BARCOS cohort of Spanish postmenopausal women.

    PLoS One . 9(4): . Number of citations: 15

    [doi:10.1371/journal.pone.0094607]

  • Carreño O, Corominas R, Serra SA, Sintas C, Fernández-Castillo N, Vila-Pueyo M, Toma C, Gené GG, Pons R, Llaneza M, Sobrido MJ, Grinberg-Vaisman DR, Valverde MÁ, Fernández-Fernández JM, Macaya A and Cormand B.

    Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.

    Molecular genetics & genomic medicine . 1(4): 206-222.

    [doi:10.1002/mgg3.24]