نتائج البحث - V. Volpini

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  1. 1
    Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2.

    Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2. حسب Roser Torrá, Célia Bádenas, A Darnell, Carlos Nicolau, V. Volpini, L Revert, Xavier Estivill

    منشور في 1996
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    Artigo
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  2. 2
    Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred

    Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred حسب D. E. Genis, T. Matilla, V. Volpini, Jordi Rosell, Antonio Dávalos, Isidró Ferrer, A. Barnadas Molins, Xavier Estivill

    منشور في 1995
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    Artigo
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  3. 3
    Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes

    Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes حسب Ester Cuenca-León, Roser Corominas, Noèlia Fernàndez‐Castillo, V. Volpini, Mireia del Toro, Manuel G. Roig, Alfons Macaya, Bru Cormand

    منشور في 2008
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    Artigo
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  4. 4
    Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria.

    Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria. حسب Marı́a Julia Calonge, V. Volpini, Luigi Bisceglia, F. Rousaud, Luisa De Sanctis, Ercole Beccia, Leopoldo Zelante, Xavier Testar, António Zorzano, Xavier Estivill

    منشور في 1995
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    Artigo
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  5. 5
    A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

    A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. حسب Antoni Barrientos, V. Volpini, Jordi Casademont, D. E. Genis, José María Manzanares, Isidró Ferrer, Jordi Corral, Francesc Cardellach, Á Urbano-Márquez, Xavier Estivill, Virginia Nunes

    منشور في 1996
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    Artigo
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  6. 6
    Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study

    Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study حسب Cláudia Gaspar, Íscia Lopes‐Cendes, Sean M. Hayes, J. Goto, Karin Arvidsson, Manuel Aureliano, Isabel Silveira, Patrı́cia Maciel, Paula Coutinho, Manuela Lima, Yongxing Zhou, Bing‐Wen Soong, Masao Watanabe, Paola Giunti, Giovanni Stévanin, Olaf Rieß, Hidenao Sasaki, Mingli Hsieh, Garth A. Nicholson, E. R. Brunt, Joe Higgins, Martin Lauritzen, Lisbeth Tranebjærg, V. Volpini, Nicholas Wood, Laura P.W. Ranum, Shoji Tsuji, Alexis Brice, Jorge Sequeiros, Guy A. Rouleau

    منشور في 2001
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