Sarrionandia MJ - Search Results

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Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family.

Pérez de Nanclares G, Castaño L, Martul P, Rica I, Vela A, Sanjurjo P, Aldamiz-Echevarría K, Martínez R, Sarrionandia MJ. Pérez de Nanclares G, et al. Among authors: sarrionandia mj. J Pediatr Endocrinol Metab. 2001 Mar;14(3):295-300. doi: 10.1515/jpem.2001.14.3.295. J Pediatr Endocrinol Metab. 2001. PMID: 11308047

[Surgical treatment of partial anomalous pulmonary venous drainage].

Cabrera A, Idígoras G, Sarrionandía MJ, Martínez P, Rumoroso JR, Alcíbar J. Cabrera A, et al. Among authors: sarrionandia mj. Rev Esp Cardiol. 1996 Feb;49(2):130-5. Rev Esp Cardiol. 1996. PMID: 8948723 Clinical Trial. Spanish.

[The usefulness of two-dimensional echocardiography in the diagnosis of an interventricular aneurysm].

Cabrera A, Idígoras G, Sarrionandia MJ, Peña P, Lizárraga M, Estébanez MS, Peña N, Pastor E, Galdeano JM. Cabrera A, et al. Among authors: sarrionandia mj. Rev Esp Cardiol. 1992 Feb;45(2):111-6. Rev Esp Cardiol. 1992. PMID: 1561467 Spanish.

[Cardiovascular pathology in Marfan syndrome. Study of 11 children using two-dimensional echocardiography].

Modesto C, Cabrera A, Pastor E, Hernáez E, Sarrionandia MJ, Zubeldia J, Galdeano JM, Cabrera JA. Modesto C, et al. Among authors: sarrionandia mj. Rev Esp Cardiol. 1989 May;42(5):318-21. Rev Esp Cardiol. 1989. PMID: 2772367 Spanish.

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