Publicacions
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Pineda L, Cabana-Domínguez J, Roncero C, Cozar M, Grau-López L, Abad AC, Martínez-Luna N, Robles-Martínez M, Sánchez-Mora C, Ramos-Quiroga JA, Casas M, Ribasés M, Fernandez-Castillo N and Cormand B.
Evaluation of previous substance dependence genome-wide significant findings in a Spanish sample.
DRUG AND ALCOHOL DEPENDENCE . 187: 358-362. Nº de cites: 3
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Cammarata-Scalisi F, Stock F, Avendaño A, Cozar M, Balcells S and Grinberg-Vaisman DR.
Estudio clínico y molecular en una familia con osteocondromatosis mltiple.
Acta ortopédica mexicana . 32(2): 108-111.
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Canals I, Beneto N, Cozar M, Vilageliu L and Grinberg-Vaisman DR.
EXTL2 and EXTL3 inhibition with siRNAs as a promising substrate reduction therapy for Sanfilippo C syndrome.
SCIENTIFIC REPORTS . 5: 13654-13654. Nº de cites: 22
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Gómez-Grau M, Garrido E, Cozar M, Rodriguez-Sureda V, Domínguez C, Arenas C, Gatti RA, Cormand B, Grinberg-Vaisman DR and Vilageliu L.
Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage Diseases.
PLoS One . 10(8): . Nº de cites: 28
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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. Nº de cites: 3
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Cozar M, Urreizti R, Vilarinho L, Grosso C, Dodelson de Kremer R, Asteggiano CG, Dalmau J, García AM, Vilaseca MA, Grinberg-Vaisman DR and Balcells S.
Identification and functional analyses of CBS alleles in Spanish and Argentinian homocystinuric patients.
HUMAN MUTATION . 32(7): 835-842. Nº de cites: 13
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Cozar M, Bembi B, Dominissini S, Zampieri S, Vilageliu L, Grinberg-Vaisman DR and Dardis A.
Molecular characterization of a new deletion of the GBA1 gene due to an inter Alu recombination event.
MOLECULAR GENETICS AND METABOLISM . 102(2): 226-228. Nº de cites: 10