Results 81 to 90 of about 8,777 (197)

Prevalence of thalassemia and hemoglobinopathy in eastern India: A 10-year high-performance liquid chromatography study of 119,336 cases

, 2016
Background: Hereditary hemoglobin (Hb) disorders are the most commonly encountered single gene disorders in India. Proper timely identification of these disorders is of paramount importance to prevent thalassemia major and clinically severe ...
Saikat Mandal, Santosh Kumar Mondal
core   +1 more source

Primer caso de hemoglobina Köln (codon98 GTG>ATG) en Costa Rica First case of hemoglobin Köln (codon98 GTG>ATG) in Costa Rica

Acta Médica Costarricense, 2010
La exposición a ciertos medicamentos puede provocar anemia hemolítica con presencia de cuerpos de Heinz en sangre periférica. Esta anemia puede presentarse por sobredosis de medicamentos, tanto en individuos sanos como en personas con deficiencias ...
Walter Cartín, Carlos Suárez, Luis Mora, Kathia Valverde, Berta Valverde, Evan Jensen, Gabriela Abarca, Rafael Jiménez   +7 more
doaj  

Hemoglobinopathies

Japanese Journal of Transfusion and Cell Therapy, 2022
Taiju Utsugisawa, Hitoshi Kanno
openaire   +2 more sources

Hemoglobinopathies

, 2019
Hereditary hemoglobin disorders with thalassemia and sickle-cell anemia are the most common monogenic diseases in the world. It is estimated that about 1-5% of the global population is the carriers of a genetic thalassemia mutation. Hemoglobinopathies are among the most common hereditary blood diseases also in Turkey and are an important health problem
Arpacı, Abdullah, Elmacıoğlu, Sibel, Ünlü, Bahar   +2 more
openaire   +1 more source

Immune Thrombocytopenic Purpura in Children and Adults: A Comparative Retrospective Study in IRAN

International Journal of Hematology-Oncology and Stem Cell Research, 2014
Background: Immune thrombocytopenic purpura (ITP) is an autoimmune disease that can cause bleeding disorders in patients, and presents in acute and chronic forms. The acute form is frequently seen in children, but the chronic form mainly inflicts adults.
Sajedeh Saeidi, Kaveh Jaseb, Ali Amin Asnafi, Fakher Rahim, Fatemeh Pourmotahari, Samira Mardaniyan, Homayon Yousefi, Arash Alghasi, Mohammad Shahjahani, Najmaldin Saki   +9 more
doaj  

Study of the Prevalence of Cytomegalovirus in Children with Malignancy in Southwestern Iran from 2016-2023 [PDF]

Iranian South Medical Journal
Background: Cytomegalovirus (CMV) infection is one of the most common infections worldwide. This infection is especially dangerous for people with weakened immune systems and patients who have had organ transplants.
Arash Alghasi, Saeed Bitraf, Roya Salehi Kahyesh, Yasin Alidadi, Homayoun Yousefi, Manouchehr Makvandi   +5 more
doaj  

Evaluation of hemoglobinopathy screening results of a six year period in Turkey

, 2012
Background and Objectives: Hemoglobinopathies are autosomal recessive inherited diseases more commonly seen in Mediterranean countries. Hereditary blood diseases including Bthalassemia and sickle cell anemia are important health problems. In our study we
Silfeler, Dbrahim, Silfeler, Dilek Benk, Turhan, Ebru, Ařca, Vefik, ÖZER, CAHİT, Altun, Ayse Betül, Arica, Seçil Gunher   +6 more
core   +1 more source

Validation of Gazelle Microchip Electrophoresis for Premarital Hemoglobinopathy Screening in Türkiye. [PDF]

EJHaem
Canatan D, Delibaş S, Altunsoy E, Gökkaya EG, Aydın S, Tuncel DA, Natu R, Thota P, Gurkan UA.   +8 more
europepmc   +1 more source

Hemoglobinopathy diagnostics: the HELIOS Action survey. [PDF]

Blood Adv
Waye JS, Nfonsam LE.
europepmc   +1 more source

Aging with Thalassemia and Sickle Cell Disease: A Gerontological Model of Accelerated Multimorbidity and Function-Centered Care Beyond Midlife. [PDF]

Mediterr J Hematol Infect Dis
Delicou S, Aggeli C, Mani I, Savvidis C, Palkopoulou M, Aforozis T, Kouroukli I, Giannou P, Mika A, Xydaki A, Moraki M, Papatheodorou E, Kapota A, Ilias I, Koskinas J.   +14 more
europepmc   +1 more source