Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Walter Rodríguez-Romero"'
Publikováno v:
Acta Médica Costarricense, Vol 48, Iss 4, Pp 172-178 (2006)
En tanto que para las hemoglobinas Hbs anormales es posible determinar los lugares de su origen (marcadores antropológicos), en las enfermedades talasémicas se tiene el problema de su amplia distribución en las principales poblaciones ancestrales.
Externí odkaz:
https://doaj.org/article/bea96e672c3a4363abc56dfd17255b6a
Publikováno v:
Clinical Case Reports, Vol 9, Iss 1, Pp 291-293 (2021)
Clinical Case Reports, Clin Case Rep. 2020;00:1-3
Kérwá
Universidad de Costa Rica
instacron:UCR
Clinical Case Reports
Clinical Case Reports, Clin Case Rep. 2020;00:1-3
Kérwá
Universidad de Costa Rica
instacron:UCR
Clinical Case Reports
This case report highlights the importance for health care providers to be aware of the αlpha‐thalassemia syndromes, their relevance to clinical care and family counseling, appropriate diagnostic algorithm for definitive diagnosis.
This case
This case
Autor:
Allan X Pernudy-Ubau, Valeska A Campos-Gómez, Walter Rodríguez-Romero, Lucía L Rojas-Vanegas, Milena L. Ramírez, Gerardo Mejía Baltodano
Publikováno v:
Acta Médica Costarricense, Volume: 60, Issue: 4, Pages: 162-166, Published: DEC 2018
Resumen Justificación y objetivo: Gran parte de los casos descritos de anemias microcíticas-hipocrómicas corresponden a anemias ferropénicas y síndromes talasémicos. El diagnóstico diferencial se complementa con pruebas de laboratorio como el
Autor:
Hong-Yuan Luo, Marianela Ortiz-Lopez, Kenia García-Rosales, Yaneris Requenez, Anaishelle Rodríguez-Estrada, Jaslyn Salinas-Molina, Walter Rodríguez-Romero, Gerardo Mejía-Baltodano, Allan Pernudy-Ubau, David H.K. Chui, Ann-Christin Puller
Publikováno v:
Hemoglobin. 41:50-52
Hemoglobin (Hb) is the protein responsible for oxygen transportation. It is a tetrameric protein comprising two α- and two β-globin subunits. In the literature, a large number of mutations in the α- and β-globin genes have been documented. Among
Autor:
Jorge Chaves-Villalobos, Neil S. Harris, Jonielle Garcia-Quesada, Louis Almero Du Pisani, David H.K. Chui, Heather L. Edward, Walter Rodríguez-Romero, Bernard G. Forget, Martin H. Steinberg, Hong-Yuan Luo
Publikováno v:
Hemoglobin. 38:381-384
Hb Youngstown is a rare hemoglobin (Hb) variant caused by substitution of glutamic acid with alanine at amino acid residue 101 of the β-globin chain as a result of an A > C transversion on the β-globin gene nucleotide sequences [β101(G3)Glu → Al
Publikováno v:
Blood Advances. 2:58-59
Nicaragua is a low-income country located in Central America. The country has a multiethnic population, with Mestizos, American Indian, and black being the most predominant ethnic groups. Nicaragua lacks a national newborn screening program and facil