OpenURL Connection Search

Select item for more details and to access through your institution.

Mutation in JPH2 cause dilated cardiomyopathy.
Published in:
Clinical Genetics, 2016, v. 90, n. 5, p. 468, doi. 10.1111/cge.12825
By:
- Sabater‐Molina, M.;
- Navarro, M.;
- García‐Molina Sáez, E.;
- Garrido, I.;
- Pascual‐Figal, D.;
- González Carrillo, J.;
- Gimeno Blanes, J.R.
Publication type:
Article
Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.
Published in:
Clinical Genetics, 2016, v. 90, n. 2, p. 171, doi. 10.1111/cge.12760
By:
- San Román, I.;
- Navarro, M.;
- Martínez, F.;
- Albert, L.;
- Polo, L.;
- Guardiola, J.;
- García‐Molina, E.;
- Muñoz‐Esparza, C.;
- López‐Ayala, J. M.;
- Sabater‐Molina, M.;
- Gimeno, J. R.
Publication type:
Article
A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.
Published in:
Clinical Genetics, 2013, v. 83, n. 6, p. 530, doi. 10.1111/cge.12017
By:
- García‐Molina, E;
- Lacunza, J;
- Ruiz‐Espejo, F;
- Sabater, M;
- García‐Alberola, A;
- Gimeno, JR;
- Cañizares, F;
- García, A;
- Martínez, P;
- Valdés, M;
- Tovar, I
Publication type:
Article
Diagnostic delay and outcome in immunocompetent patients with primary central nervous system lymphoma in Spain: a multicentric study.
Published in:
Journal of Neuro-Oncology, 2020, v. 148, n. 3, p. 545, doi. 10.1007/s11060-020-03547-z
By:
- Velasco, R.;
- Mercadal, S.;
- Vidal, N.;
- Alañá, M.;
- Barceló, M. I.;
- Ibáñez-Juliá, M. J.;
- Bobillo, S.;
- Caldú Agud, R.;
- García Molina, E.;
- Martínez, P.;
- Cacabelos, P.;
- Muntañola, A.;
- García-Catalán, G.;
- Sancho, J. M.;
- Camro, I.;
- Lado, T.;
- Erro, M. E.;
- Gómez-Vicente, L.;
- Salar, A.;
- Caballero, A. C.
Publication type:
Article

Found: 4

Mutation in JPH2 cause dilated cardiomyopathy.

Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.

A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.

Diagnostic delay and outcome in immunocompetent patients with primary central nervous system lymphoma in Spain: a multicentric study.