Browsing by Author Volpini Bertrán, Víctor
Showing results 1 to 9 of 9
| Issue Date | Title | Author(s) |
|---|---|---|
| 1-Jun-2007 | Allelic and genotypic associations of DRD2 Taq I A polymorphism with heroin dependence in Spanish subjects: a case control study | Pérez de los Cobos Peris, José C.; Baiget Bastús, Montserrat; Trujols i Albet, Joan; Sinol, Nuria; Volpini Bertrán, Víctor; Banuls, Enrique; Calafell, Francesc; Luquero, Elena; Rio, Elisabeth del; Alvarez, Enric |
| 1995 | Bases moleculars de la cistinúria | Palacín Prieto, Manuel; Mora, Conchi; Chillarón Chaves, José Julio; Calonge, María Julia; Estévez Povedano, Raúl; Torrents, D.; Testar, Xavier; Zorzano Olarte, Antonio; Nunes Martínez, Virginia; Purroy, J.; Nadal, M.; Volpini Bertrán, Víctor; Estivill, Xavier, 1955-; Rousaud, F.; Barceló, P. |
| 1-Jan-1995 | Clinical, neuropathologic and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred: (CAG)n expansion and early premonitory signs and symptoms | Genís, David; Matilla-Dueñas, Antoni; Volpini Bertrán, Víctor; Rosell, J.; Dávalos, Antoni; Ferrer, Isidro (Ferrer Abizanda); Molins, Albert; Estivill, Xavier, 1955- |
| Oct-2009 | Diagnosis of Charcot-Marie-Tooth disease | Banchs, Isabel; Casasnovas Pons, Carlos; Albertí, María A.; Jorge, Laura de; Povedano, Mònica; Montero, Jordi; Martínez Matos, Juan Antonio; Volpini Bertrán, Víctor |
| 13-Apr-2010 | Enfermedad de Charcot-Marie-Tooth: Estudio clínico y molecular de los genes GJB-1 y MFN2 en la población española. | Casasnovas Pons, Carlos |
| 1-May-2014 | Mosaicism of alpha-synuclein gene rearrangements: Report of two unrelated cases of early-onset parkinsonism | Perandones, C.; Giugni, J. C.; Calvo, D. S.; Raina, G. B.; Jorge López, L. de; Volpini Bertrán, Víctor; Zabetian, C. P.; Mata, Ignacio F.; Caputo, M.; Corach, D.; Radrizzani, M.; Micheli, F. E. |
| 31-May-2017 | Mutation spectrum in the CACNA1A gene in 49 patients with episodic ataxia | Sintas Vives, Cèlia; Carreño, Oriel; Fernàndez Castillo, Noèlia; Corominas Castiñeira, Roser; Vila Pueyo, Marta; Toma, Claudio; Cuenca León, Ester; Barroeta, Isabel; Roig i Arnall, Carles; Volpini Bertrán, Víctor; Macaya Ruiz, Alfons; Cormand Rifà, Bru |
| 1996 | A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. | Barrientos Rubio, Antoni; Volpini Bertrán, Víctor; Casademont i Pou, Jordi; Genís, David; Manzanares, Josep-Maria; Ferrer, Isidro (Ferrer Abizanda); Corral, Jordi; Cardellach, Francesc; Urbano Márquez, A. (Álvaro); Estivill, Xavier, 1955-; Nunes Martínez, Virginia |
| 26-Apr-2011 | Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT | Cassereau, Julien; Casasnovas Pons, Carlos; Gueguen, Naïg; Malinge, Marie Claire; Guillet, Virginie; Reynier, Pascal; Bonneau, Dominique; Amati-Bonneau, Patrizia; Banchs, Isabel; Volpini Bertrán, Víctor; Procaccio, Vincent; Chevrollier, Arnaud |