Maria A Ramos-Arroyo

Maria A Ramos-Arroyo

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Maria A Ramos-Arroyo

Maria A Ramos-Arroyo

Publications by authors named "Maria A Ramos-Arroyo"

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15Publications

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Clinical manifestations of homozygote allele carriers in Huntington disease.

Neurology 2019 04 13;92(18):e2101-e2108. Epub 2019 Mar 13.

From the Neurology Department (E.C., C.G.-P., I.M., K.L., N.M., D.D., A.G., L.A.) and Research Unit (S.C.), Hospital Universitario Burgos; Movement Disorders Unit, Neurology Department (S.-I.M.-H., F.S.S.), Hospital de La Santa Creu I Sant Pau, Barcelona; Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED) (S.-I.M.-H., F.S.S.), Madrid; Neurology Department (A.M.D.), Fundación Jiménez Diez, Madrid; and Genetic Department (M.A.R.-A.), Complejo Hospitalario de Navarra, Pamplona, Spain.

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http://dx.doi.org/10.1212/WNL.0000000000007147DOI Listing
April 2019

[Implementing a population-based rare diseases registry in Spain: the Navarre´s experience].

Rev Esp Salud Publica 2018 Nov 19;92. Epub 2018 Nov 19.

Sección del Observatorio de la Salud Comunitaria. Servicio de Promoción de la Salud Comunitaria. Instituto de Salud Pública y Laboral de Navarra. Pamplona. España.

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November 2018

The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease Patients.

Mol Neurobiol 2017 07 6;54(5):3906-3910. Epub 2016 Dec 6.

Dermatology Department, Melanoma Unit, Hospital Clinic & IDIBAPS (Institut d'Investigacions Biomèdiques August Pi i Sunyer), Barcelona, Spain.

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http://dx.doi.org/10.1007/s12035-016-0305-5DOI Listing
July 2017

Clinical manifestations of intermediate allele carriers in Huntington disease.

Neurology 2016 Aug 8;87(6):571-8. Epub 2016 Jul 8.

From the Neurology Department (E.C., C.G.-P.) and Research Unit (S.C.), Hospital Universitario Burgos; Genetic Department (M.A.R.-A.), Complejo Hospitalario de Navarra, Pamplona; Movement Disorders Unit, Neurology Department (S.M.-H.), Hospital de la Santa Creu i Sant Pau, Barcelona; and Neurology Department (A.M.-D.), Fundación Jimenez Diez, Madrid, Spain.

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http://dx.doi.org/10.1212/WNL.0000000000002944DOI Listing
August 2016

Two novel SCN1A mutations identified in families with familial hemiplegic migraine.

Cephalalgia 2014 Nov 4;34(13):1062-9. Epub 2014 Apr 4.

Department of Human Genetics, Leiden University Medical Center, the Netherlands Department of Neurology, Leiden University Medical Center, the Netherlands.

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http://dx.doi.org/10.1177/0333102414529195DOI Listing
November 2014

Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.

Mol Vis 2012 29;18:3070-8. Epub 2012 Dec 29.

Grupo de Investigación en Enfermedades Neurosensoriales, Instituto de Investigación Sanitaria IIS - La Fe, Valencia, Spain.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538041PMC
May 2013