Zobrazeno 1 - 10
of 73
pro vyhledávání: '"S.A. Cuevas-Covarrubias"'
Publikováno v:
Revista Médica del Hospital General de México, Vol 80, Iss 2, Pp 97-100 (2017)
Mucopolysaccharidosis type II (MPS II) or Hunter syndrome is an inborn error of metabolism due to lysosomal accumulation, with a recessive inheritance pattern linked to the X chromosome. It is caused by a deficiency in the activity of the lysosomal e
Externí odkaz:
https://doaj.org/article/ce78799117154b0aaf2da182f0f6743b
Publikováno v:
Revista Médica del Hospital General de México, Vol 80, Iss 2, Pp 73-76 (2017)
Non-invasive procedures for prenatal diagnosis are the most frequently used methods in the first trimester of pregnancy in pregnant women under 35 years of age because they do not involve risk of pregnancy loss; however, they are not considered to be
Externí odkaz:
https://doaj.org/article/e1ce72ff50a743bbad21fa2fc96d9a20
Autor:
M. Martín-De Saro, O. Amancio-Chassin, H. Urueta-Cuéllar, L. González-Huerta, S.A. Cuevas-Covarrubias
Publikováno v:
Revista Médica del Hospital General de México, Vol 80, Iss 2, Pp 92-96 (2017)
Background: Cytochrome P450 2C9 (CYP2C9) is an important enzyme in the metabolism of many drugs, including NSAIDs, antidepressants and anticoagulants. In vitro and in vivo studies have demonstrated that CYP2C9 polymorphisms modify the activity of the
Externí odkaz:
https://doaj.org/article/efcbb44ef3a14b45bf62f2ca40cffc42
Autor:
R.M. Arana Trejo, A. del Castillo Moreno, L.G. Alcalá Carmona, V. Madrid Cedillo, J.J. Kassack Ipiña, M. Gutiérrez Romero, A.B. Cervantes Peredo, E. Rozen Fuller, E. Aguilar Martínez, A. Pérez Cabrera, E. Gálvez Galicia, J. Collazo Jaloma, S.A. Cuevas-Covarrubias
Publikováno v:
Revista Médica del Hospital General de México, Vol 80, Iss 2, Pp 87-91 (2017)
Background: Haematologic malignancies are generated by alterations in haematopoietic stem cells. Chromosomal rearrangements are present in >50% of patients and are useful as diagnostic and prognostic factors. Objective: In this study we describe the
Externí odkaz:
https://doaj.org/article/6b2e64d06430481fa030ebaa62438458
Autor:
M. Martínez-Saucedo, M.R. Rivera-Vega, L.M. Gonzalez-Huerta, H. Urueta-Cuéllar, S.A. Cuevas-Covarrubias
Publikováno v:
Revista Médica del Hospital General de México, Vol 80, Iss 2, Pp 77-80 (2017)
Background: Sensorineural hearing loss (SNHL) is a clinically and genetically heterogeneous disease. In some populations, c.365delG mutation in the GJB2 gene represents the most frequent cause of hereditary SNHL. The great diversity of mutations in t
Externí odkaz:
https://doaj.org/article/55fc955ea6fe42679a404ba6655054e2
Autor:
S.A. Cuevas-Covarrubias
Publikováno v:
Revista Médica del Hospital General de México, Vol 80, Iss 2, Pp 71-72 (2017)
Externí odkaz:
https://doaj.org/article/8716368e6c944d35bf99c4c7fc240083
Autor:
S. Díaz Zambrano, L.M. González Huerta, A. Bravo Oro, Carmen Esmer, M. A. Santos Díaz, S.A. Cuevas Covarrubias
Publikováno v:
Anales de Pediatría, Vol 80, Iss 4, Pp 254-258 (2014)
Resumen: Las neuropatías sensitivas autonómicas son parte de las neuropatías periféricas y se deben a disfunción de genes involucrados en el funcionamiento de las neuronas sensoriales y autonómicas. Se conocen 6 variantes clínicas con subtipos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::918386abfb7c21ab79f489f268648924
https://doi.org/10.1016/j.anpedi.2013.05.023
https://doi.org/10.1016/j.anpedi.2013.05.023
Akademický článek
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Publikováno v:
Acta Dermato-Venereologica. 81:54-55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c82b7c3e45b56a91ef0257584cbb16a
https://doi.org/10.1080/000155501750208227
https://doi.org/10.1080/000155501750208227
Akademický článek
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