Eduardo Rivas-Gutierrez
Madrid, MD, Spain
Last Updated: 09/26/2026
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Found 12 publications
Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia.
Journal: Journal of medical genetics
Published: October 22, 2019
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.
Journal: Medicina clinica
Published: September 07, 2018
Guidelines for monitoring late-onset Pompe disease.Sociedad Española de Medicina Interna (SEMI), Sociedad Española de Neurología (SEN) y Sociedad Española de Neumología y CirugíaTorácica (SEPAR)
Journal: Revista de neurologia
Published: March 26, 2015
Dried Blood Spot for Screening for Late-Onset Pompe Disease: A Spanish Cohort.
Journal: Journal of neuromuscular diseases
Published: January 01, 2015
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.
Journal: Neuromuscular disorders : NMD
Published: November 03, 2014
The alpha-galactosidase A p.Arg118Cys variant does not cause a Fabry disease phenotype: data from individual patients and family studies.
Journal: Molecular genetics and metabolism
Published: September 02, 2014
Sympathetic skin response: reference data for 100 normal subjects
Journal: Revista de neurologia
Published: March 14, 2013
Clinical guidelines for late-onset Pompe disease.
Journal: Revista de neurologia
Published: April 12, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026