Search Results - "García-Ribes, Ainhoa"

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  1. 1

    Suspected Herpes Encephalitis and Opercular Syndrome in Childhood

    Authors: García-Ribes, Ainhoa Martínez-González, María Jesús Prats-Viñas, Jose María

    Source: Pediatric Neurology. Mar2007, Vol. 36 Issue 3, p202-206. 5p.

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  2. 2

    Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.

    Authors: Martínez-Rubio, Dolores Hinarejos, Isabel Sancho, Paula et al.

    Source: International Journal of Molecular Sciences. Oct2022, Vol. 23 Issue 19, p11847. 26p.

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  3. 3

    Facial Hypomimia, Oculomotor Paralysis, and Ataxia Associated With GAD65 and Glycine Receptor Antibodies in a Child.

    Authors: Ortiz de Zarate Caballero Z Elosegi Castellanos A García Ribes A et al.

    Source: Neurology [Neurology] 2024 Dec 10; Vol. 103 (11), pp. e210065. Date of Electronic Publication: 2024 Nov 12.

    Publication Type: Journal Article

    Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1526-632X (Electronic) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE; In Process

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  4. 4

    CDKL5 gene status in female patients with epilepsy and Rett-like features: two new mutations in the catalytic domain.

    Authors: Maortua H Martínez-Bouzas C Calvo MT et al.

    Source: BMC medical genetics [BMC Med Genet] 2012 Aug 06; Vol. 13, pp. 68. Date of Electronic Publication: 2012 Aug 06.

    Publication Type: Journal Article; Research Support, Non-U.S. Gov't

    Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350 (Electronic) Linking ISSN: 14712350 NLM ISO Abbreviation: BMC Med Genet Subsets: MEDLINE

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  5. 5

    MECP2 gene study in a large cohort: testing of 240 female patients and 861 healthy controls (519 females and 342 males).

    Authors: Maortua H Martínez-Bouzas C García-Ribes A et al.

    Source: The Journal of molecular diagnostics : JMD [J Mol Diagn] 2013 Sep; Vol. 15 (5), pp. 723-9. Date of Electronic Publication: 2013 Jun 26.

    Publication Type: Journal Article; Research Support, Non-U.S. Gov't

    Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 100893612 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1943-7811 (Electronic) Linking ISSN: 15251578 NLM ISO Abbreviation: J Mol Diagn Subsets: MEDLINE

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  6. 6

    A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3.

    Authors: Tejada MI Martínez-Bouzas C García-Ribes A et al.

    Source: Pediatrics [Pediatrics] 2011 Oct; Vol. 128 (4), pp. e1029-33. Date of Electronic Publication: 2011 Sep 19.

    Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

    Journal Info: Publisher: American Academy of Pediatrics Country of Publication: United States NLM ID: 0376422 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-4275 (Electronic) Linking ISSN: 00314005 NLM ISO Abbreviation: Pediatrics Subsets: MEDLINE

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