Eduardo Gutiérrez‐Rivas

Hospital Universitario 12 De Octubre — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index1.2kcitations45works0.02yr avg
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Research Topics

Mitochondrial Function and Pathology(9), Genetic Neurodegenerative Diseases(9), Muscle Physiology and Disorders(6), Glycogen Storage Diseases and Myoclonus(6), Lysosomal Storage Disorders Research(5)

Publications45 total

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease
Neurología (English Edition)·2020· 26 citedOpen Access
Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia
Journal of Medical Genetics·2020· 31 cited
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease
Medicina Clínica (English Edition)·2019· 16 cited
Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert
Neurología·2019· 30 citedOpen Access
Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert
Medicina Clínica·2019· 8 cited
Propedéutica médica y neurología
Revista de Neurología·2017· 1 cited
[How we, as neurologists, write. Reply].
PubMed·2016
[How we, as neurologists, write].
PubMed·2016
Targeted screening for the detection of Pompe disease in patients with unclassified limb-girdle muscular dystrophy or asymptomatic hyperCKemia using dried blood: A Spanish cohort
Neuromuscular Disorders·2015· 59 cited
Dried Blood Spot for Screening for Late-Onset Pompe Disease: A Spanish Cohort
Journal of Neuromuscular Diseases·2015· 3 citedOpen Access
Guía para el seguimiento de la enfermedad de Pompe de inicio tardío
Revista de Neurología·2015· 5 cited
The alpha-galactosidase A p.Arg118Cys variant does not cause a Fabry disease phenotype: Data from individual patients and family studies
Molecular Genetics and Metabolism·2014· 88 citedOpen Access
Long‐term outcome in chronic inflammatory demyelinating polyneuropathy patients treated with intravenous immunoglobulin: A retrospective study
Muscle & Nerve·2013· 47 citedOpen Access
Genotype and phenotype study of 34 Spanish patients diagnosed with oculopharyngeal muscular dystrophy
Journal of Neurology·2012· 21 cited
Guía clínica de la enfermedad de Pompe de inicio tardío
Revista de Neurología·2012· 46 citedOpen Access
Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 gene
Neuromuscular Disorders·2011· 36 citedOpen Access
P2.34 Mutational spectrum of sarcoglycanopathies in Spain
Neuromuscular Disorders·2011Open Access
Chemotherapy-induced peripheral neuropathy: clinical features, diagnosis, prevention and treatment strategies
Clinical & Translational Oncology·2010· 180 citedOpen Access
Characterization of novel CAPN3 isoforms in white blood cells: an alternative approach for limb-girdle muscular dystrophy 2A diagnosis
Neurogenetics·2008· 37 cited
G.P.7.01 Facioscapulohumeral muscular dystrophy: A review of 76 patients
Neuromuscular Disorders·2007
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Frequent Co-authors

Adolfo López de Munaín(8), Samuel Ignacio Pascual Pascual(8), Gerardo Gutiérrez‐Gutiérrez(6), Juan J. Vílchez(6), Joaquı́n Arenas(6), Jordi Díaz‐Manera(6), Isabel Illa(6), Roberto Fernández‐Torrón(6), Yolanda Campos(5), José Luís Muñoz-Blanco(5), Loreto Martorell(5), J. Bautista(4), Ana María Cobo(4), Míriam Almendrote(4), Sharona Azriel(4), José Eulalio Bárcena(4), Pablo Cabezudo‐García(4), Ana Camacho(4), Carlos Casanova Rodríguez(4), Patricia Díaz Guardiola(4)