نتایج جستجو برای: hemoglobinopathies

تعداد نتایج: 1591  

2014
Mehrdad Payandeh Zohreh Rahimi Mohammad Erfan Zare Atefeh Nasir Kansestani Farzad Gohardehi Amir Hossein Hashemian

Hemoglobinopathies are the most common single gene disorders worldwide with a considerable frequency in certain area particularly Mediterranean and Middle Eastern countries. Hemoglobinopathies include structural variants of hemoglobin (Hb S, Hb C, HbE,…) and thalassaemias which are inherited defects in the globin chains synthesis. The present study was conducted to determine the prevalence of h...

Journal: :American Journal of Clinical Pathology 2017

Journal: :International Journal of Laboratory Hematology 2013

Journal: :Hematology. American Society of Hematology. Education Program 2007
Frans A Kuypers

The red blood cell (RBC) membrane is a complex mixture of lipids and proteins. Hundreds of phospholipid molecular species spontaneously arrange themselves in a lipid bilayer and move rapidly in the plane as well as across the bilayer in a dynamic but highly organized fashion. Areas enriched in certain lipids determine proper protein function. Phospholipids are asymmetrically distributed across ...

2015
Stephanie Phillips Shayla Bergmann

The use of the pulse oximeter to estimate oxygen saturation has revolutionized monitoring capabilities in medicine. However, there can be circumstances in which there is a discordance between oxygen saturation measurements via pulse oximeter (SpO2) and actual arterial oxygen levels (PaO2). In these situations, there is a possibility the patient could have a variant hemoglobin as the etiology of...

2013
Julio Da Luz Amalia Ávila Sandra Icasuriaga María Gongóra Luis Castillo Alejandra Serrón Elza Miyuki Kimura Fernando Ferreira Costa Mónica Sans Maria de Fátima Sonati

Hemoglobinopathies are the most common recessive diseases worldwide but their prevalence in Uruguay has not been investigated. In this study, 397 unrelated outpatient children from the Pereira Rosell Hospital Center (CHPR), as well as 31 selected patients with microcytic anemia and 28 β-thalassemia carriers were analyzed for hemoglobinopathies by using biochemical and molecular biology methods....

2012
Ciro Cesar Alvear Miriam Barboza Maricela Viola Carlos Moneriz Luz Marina Araque

INTRODUCTION The hemoglobinopathies are a heterogeneous group of congenital anemias from Africa, Asia and the Mediterranean. Due to the migration of this population have spread worldwide, especially in Latin America and the Caribbean region, which Cartagena de Indias is included, with a large proportion of people of African descent. The lack of routine programs that include an appropriate metho...

Journal: :The Korean journal of laboratory medicine 2011
Ji-Eun Kim Bo-Ram Kim Kwang-Sook Woo Jeong-Man Kim Joo-In Park Jin-Yeong Han

BACKGROUND β-thalassemia is primarily found in individuals of Mediterranean and Southeast Asian ancestry. With rapid growth in the Southeast Asian segments of the Korean population, the geographic distribution of hemoglobinopathies is expected to become significantly different from what it is today. In this study, Hb fractions were measured in patients with hypochromic microcytosis to detect th...

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