Adriana Lasa - Dissemin

Papers authored by Adriana Lasa

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2002 Nomdedéu Jf, Josep F. Nomdedéu, Adriana Lasa

, Josep Ubeda, Giuseppe Saglio, Mar Bellido, Sílvia Casas, Maria J. Carnicer, Carnicer Mj, Anna Aventín, Anna Sureda, Jorge Sierra, Montserrat Baiget

Interstitial deletions at the long arm of chromosome 13 may be as common as monosomies in multiple myeloma. A genotypic study

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Mj J. Carnicer, Jf F. Nomdedéu

, A. Lasa

, M. Bellido, A. Aventín, M. Baiget, J. Sierra

AML-1 mutations outside the RUNT domain: Description of two cases in myeloid malignancies

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J. Eirís Puñal, E. Pintos Martínez, A. Lasa

, P. Gallano, M. Castro Gago

[Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation]

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2001 Isabel Illa, Carme Serrano‐Munuera, Eduard Gallardo, Adriana Lasa

, Ricardo Rojas‐García, Jaume Palmer, Pia Gallano, Montserrat Baiget, Chie Matsuda, Robert H. Brown, Brown Rh

Distal anterior compartment myopathy: A dysferlin mutation causing a new muscular dystrophy phenotype

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1999 C. de Diego, J. Gámez, E. Plassart Schiess, A. Lasa

, E. Del Río, C. Cervera, M. Baiget, P. Gallano, B. Fontaine

Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish families

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I. Richard, C. Roudaut, A. Saenz, R. Pogue, J. E. M. A. Grimbergen, L. V. B. Anderson, C. Beley, A.-M. Cobo, C. de Diego, B. Eymard, P. Gallano, H. B. Ginjaar, A. Lasa

, C. Pollitt, H. Topaloglu and 8 other authors

Calpainopathy-a survey of mutations and polymorphisms.

Download from www.ncbi.nlm.nih.gov

A. López de Munain, A. Urtasun, Poza Jj, J. Ruiz, A. Sáenz, Cobo Am, A. Lasa

, P. Gallano, M. Baiget, Martí Massó Jf

[Alterations in functional proteins. Calpaine-3 deficiency].

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1998 Louise V. B. Anderson, Keith Davison, Jennifer A. Moss, Isabelle Richard, Michel Fardeau, Fernando M. S. Tomé, Christoph Hübner, Adriana Lasa

, Jaume Colomer, Jacques S. Beckmann

Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A

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Adriana Lasa

, Federica Piccolo, Carles de Diego, Marc Jeanpierre, Jaume Colomer, Maria José Rodríguez, Jon Andoni Urtizberea, Montserrat Baiget, Jean Claude Kaplan, Pia Gallano

Severe limb girdle muscular dystrophy in Spanish gypsies: Further evidence for a founder mutation in the γ-sarcoglycan gene

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M. Urtasun, Poza Jj, P. Gallano, A. Lasa

, A. Sáenz, Cobo Am, F. Leturcq, A. López de Munain, F. García Bragado

[Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex]

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Nomdedéu Jf, Josep F. Nomdedéu

, Montserrat Baiget, Gianluca Gaidano, Camino Estivill, Adriana Lasa

, Enriqueta Rubiol, Roser Mateu, Ramón Bordes, Salut Brunet, Giuseppe Saglio, Jesüs Soler

p53 Mutation in a Case of Blastic Transformation of Follicular Lymphoma with Double bcl-2 Rearrangement (MBR and VCR)

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1997 Nomdedéu Jf, J. F. Nomdedéu, I. Lete, M. Baiget, A. Lasa

, C. Estivill, E. Rubiol, I. Badell, N. Pardo, J. Cubells, R. Mateu, S. Brunet, R. Bordes, J. Soler

Mutational analysis of p53 in 16 cases of acute lymphoblastic leukemia and Burkitt's lymphoma

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Adriana Lasa

, Pia Gallano, Montserrat Baiget

Three novel point mutations in the dystrophin gene in DMD patients

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1996 J. Nomdedéu

, A. Lasa

, R. Seminago, R. Mateu, E. Rubiol, M. Baiget, J. Soler

Mutational analysis of RAG-1 in lymphoid malignancies.

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Nomdedéu Jf, J. F. Nomdedéu, A. Lasa

, R. Seminago, E. Rubiol, M. Baiget, J. Soler

Two new variants of RAG-1 protein predicted by SSCP

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1995 P. Gallano, A. Lasa

, M. Baiget

[Dystrophinopathies]

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A. Lasa

, P. Gallano, J. Colomer, M. Baiget

A novel insertional mutation of a single base on exon 12 of the dystrophin gene.

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Nomdedéu Jf, A. Lasa

, R. Seminago, M. Baiget, J. Soler

Polymorphism in the RAG-1 gene identified by SSCP.

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Papers authored by Adriana Lasa