Výsledky vyhledávání - "B. Sánchez-Marín"

[Application of a clinical pathway for the treatment of transient ischaemic attacks: implementation strategies and appraisal at two years]

Autor: J I, López-Gastón, B, Sánchez-Marín, J, Marta, R, Alarcia-Alejos, J A, Oliván-Usieto, J, Artal-Roy, M J, García-Gomara

Publikováno v: Revista de neurologia. 44(12)

Management of cerebral vascular pathologies by means of clinical pathways allows us to make cost effective use of resources, to enhance health care quality and to obtain a greater degree of satisfaction in patients.To assess the efficiency of applyin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2ec6af2385edb48ffa8ebe9a54285e83
https://pubmed.ncbi.nlm.nih.gov/17583863

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[Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism in ischemic vascular disease]

Autor: B, Sánchez-Marín, J M, Grasa

Publikováno v: Revista de neurologia. 43(10)

Genetic and metabolism of C677T methylenetetrahydrofolate reductase (MTHFR) mutation and its relationship with ischemic vascular disease are revised.Homocygotes for C677T MTHFR mutation, 10-15% of general population, develop a thermolabil variant of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b54ef8021a3fbb28eca7343094421451
https://pubmed.ncbi.nlm.nih.gov/17099857

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[Prevalence of methylenetetrahydrofolate reductase C677T mutation among patients with acute ischemic cerebrovascular disease in Aragon]

Autor: B, Sánchez-Marín, J M, Grasa, M, Torres, M T, Calvo, B, Martínez-Jarreta, J A, García-Erce, M, Giralt

Publikováno v: Anales de medicina interna (Madrid, Spain : 1984). 23(4)

Mutation C677T of the methylenetetrahydrofolate reductase (MTHFR) is the main cause of mild hyperhomocysteinemia. Hyperhomocysteinemia is a recognized risk factor for aterothrombosis. MTHFR C677T patients have higher levels of homocysteine in absence

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e08db34d6fd26b0a0c7c482634a52fd7
https://pubmed.ncbi.nlm.nih.gov/16796406

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Prevalencia de la mutación C677T del gen de la metilentetrahidrofolato reductasa en pacientes con patología isquémica cerebrovascular aguda en la Comunidad Autónoma Aragonesa

Autor: J M Grasa, B Martínez-Jarreta, M T Calvo, M Torres, J A García-Erce, B. Sánchez-Marín, M Giralt

Publikováno v: Anales de Medicina Interna v.23 n.4 2006
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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Fundamentos: La mutación C677T de la metilentetrahidrofolato reductasa (MTHFR) es la principal causa de hiperhomocisteinemia moderada en nuestro medio. La hiperhomocisteinemia es un factor reconocido de riesgo para aterotrombosis. Los pacientes con

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51ab744c0f7048094f1d3d4292ffb853
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0212-71992006000400002

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