Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Luis Hernández Echebarría"'
Autor:
Luis Hernández Echebarría
Publikováno v:
BULERIA. Repositorio Institucional de la Universidad de León
instname
instname
189 p. En este estudio realizamos un ensayo clínico para evaluar la asociación levodopa/carbidopa-cáscaras de semillas de Plantago ovata en pacientes con enfermedad de Parkinson de diagnóstico reciente y que están siendo tratados con levodopa/ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07404391b7d86541cdcbc45e23b42d06
https://doi.org/10.18002/10612/858
https://doi.org/10.18002/10612/858
Autor:
Luis Hernández-Echebarría, Begoña Gómez, Albert Saiz, Domingo Escudero, Nuria Sola-Valls, Manuel Baron, Maria Sepúlveda, Josep Dalmau, Francesc Graus, Bojan Rojc
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Background: In a minority of patients with neuromyelitis optica spectrum disorder (NMOSD) and aquaporin-4 antibodies (AQP4-IgG), the disease has a paraneoplastic origin. It is unknown whether these patients have distinctive clinical features. Objecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7ac0d87dd2c207d338ec5fe193c96be
https://saludmadrid.ibai.com/handle/20.500.12530/38956
https://saludmadrid.ibai.com/handle/20.500.12530/38956
Publikováno v:
Europe PubMed Central
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disease characterized by chronic intravascular hemolysis, cytopenia and increased tendency to thrombosis. Arterial thrombosis has been observed in patients with PNH but is uncommon compa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c698cbc4c0c0b73d37296df2c744aec7
https://pubmed.ncbi.nlm.nih.gov/17853967
https://pubmed.ncbi.nlm.nih.gov/17853967
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fbca4336f1c68ea19c97d5ee5579623e
https://pubmed.ncbi.nlm.nih.gov/10320964
https://pubmed.ncbi.nlm.nih.gov/10320964
Publikováno v:
Europe PubMed Central
Friedreich's ataxia is an autosomal recessive disease generally characterized by the presence of microsatellite expansion in a GAA triplet. The patients inherit a pathologic allele from each one of their parents, that may sometimes show GAA triplet e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b70a6a398c7adbf38c3580674a28b14e
http://europepmc.org/abstract/med/14505249
http://europepmc.org/abstract/med/14505249