Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maria Sanchez Villalobos"'
Autor:
Maria Sanchez-Villalobos, Miguel Blanquer, Jose M. Moraleda, Eduardo J. Salido, Ana B. Perez-Oliva
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
β-thalassemia is a disease caused by genetic mutations including a nucleotide change, small insertions or deletions in the β-globin gene, or in rare cases, gross deletions into the β-globin gene. These mutations affect globin-chain subunits within
Externí odkaz:
https://doaj.org/article/25eaabd7b6114881868f6478aeec0445
Autor:
Julia Manzanares Lopez, Maria del Pilar Marin Sanchez, Joaquin Gomez Espuch, Isabel Ntildeiguez Sevilla, Maria Sanchez Villalobos, Elena Gurrea Almela
Publikováno v:
SURGERIES. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f16ded07274b455478d001559257cf3d
https://doi.org/10.35702/surg.10005
https://doi.org/10.35702/surg.10005
Autor:
María Sánchez Villalobos, Eduardo Salido Fiérrez, Jorge Martínez Nieto, Mª Carmen García Garay, Asunción Beltrán Videla, Ana Belen Pérez Oliva, Miguel Blanquer Blanquer, José María Moraleda Jiménez
Publikováno v:
Hematology Reports, Vol 14, Iss 4, Pp 300-304 (2022)
Hereditary pyropoikilocytosis (HPP) is characterised by severe hemolytic anemia due to membrane instability. We report the case of a 13-day-old boy with neonatal jaundice and severe hemolytic anemia. A peripheral smear examination showed severe aniso
Externí odkaz:
https://doaj.org/article/0a1b763d9cd44a2f82caace5345ab164