Search Results - "Suarez Cuervo, A"

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    Familial episodic ataxia type 2. Clinical and genetic study of one family by Suárez-Cuervo, A, Salas-Puig, J, Alvarez, V, Coto, E, Fernández, J M, Lahoz, C H

    Published in Neurología (Barcelona, Spain) (01-10-1998)
    “…Episodic familial ataxia type 2 is caused by mutations in the gene CACNA1A, in chromosome 19p, that codifies part of a calcium channel. We report a family…”
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    Intercritical SPECT in drug-resistant partial epilepsy with normal MRI: a study of 33 cases by Vidal, J A, Salas-Puig, J, Fernández-Raigoso, P, Roiz, C, Fernández, J M, Suárez-Cuervo, A, Lahoz, C H

    Published in Revista de neurologiá (01-01-1997)
    “…We made a prospective study of the intercritical changes in cerebral perfusion using SPECT with 99mTc-HMPAO in 33 adult patients with focal epilepsy which was…”
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    Journal Article