Zobrazeno 1 - 3
of 3
pro vyhledávání: '"María Sánchez Villalobos"'
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
Autor:
Asunción Beltrán, María Sánchez-Villalobos, Eduardo Salido, Carmen Algueró, Eulalia Campos, Ana Belén Pérez-Oliva, Miguel Blanquer, José M. Moraleda
Publikováno v:
Biomedicines, Vol 12, Iss 7, p 1607 (2024)
Hereditary spherocytosis (HS) is a membranopathy that impacts the vertical junctions between the cytoskeleton and the plasma membrane of erythrocytes. The gold standard method for diagnosing it is osmotic gradient ektacytometry (OGE). However, access
Externí odkaz:
https://doaj.org/article/02a23b33cbf84477aff34ea6ccf1c1d3
Autor:
María Sánchez-Villalobos, Eulalia Campos Baños, María Jesús Juan Fita, José María Egea Mellado, Inmaculada Gonzalez Gallego, Asunción Beltrán Videla, Mercedes Berenguer Piqueras, Mar Bermúdez Cortés, José María Moraleda Jiménez, Encarna Guillen Navarro, Eduardo Salido Fierrez, Ana B. Pérez-Oliva
Publikováno v:
International Journal of Neonatal Screening, Vol 9, Iss 4, p 55 (2023)
Sickle cell disease (SCD) is an inherited autosomal recessive hemoglobin disorder caused by the presence of hemoglobin S, a mutant abnormal hemoglobin caused by a nucleotide change in codon 6 of the β-globin chain gene. SCD involves a chronic inflam
Externí odkaz:
https://doaj.org/article/9546bdae6acb46e69273e85dad40b1a2