Results 221 to 230 of about 1,145,402 (246)

Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort

Annals of Hematology, 2021
B. L. Hatzlhofer, D. Pereira-Martins, Igor de Farias Domingos, G. S. Arcanjo, I. Weinhäuser, D. A. Falcão, Isabela Cristina Cordeiro Farias, Jéssica Vitória Gadelha de Freitas Batista, L. Prado, Jéssica M F Oliveira, Thais H C Batista, Marcondes J. Sobreira, Rodrigo Marcionilo de Santana, A. S. Araujo, Manuela A de Melo, Bruna Vasconcelos de Ancântara, J. Coelho-Silva, Ana Beatriz Lucas de Moura Rafael, Danízia Menezes de Lima Silva, F. P. Albuquerque, M. N. Santos, A. C. D. dos Anjos, F. Costa, Aderson da Silva Araujo, A. Lucena-Araújo, M. Bezerra   +25 more
semanticscholar   +1 more source

Alpha-thalassemia in Thailand.

Hemoglobin, 1989
The alpha-thalassemia syndromes are remarkable both for their phenotypic diversity and for their different clinical severity. They are associated with variable degrees of alpha-chain deficits; the clinical manifestations range from asymptomatic cases with normal hematologic findings to the totally lethal Hb Bart's hydrops fetalis syndrome.
P, Winichagoon, V, Thonglairuam, S, Fucharoen, V S, Tanphaichito, P, Wasi   +4 more
openaire   +1 more source

Co-Inheritance of alpha-thalassemia and sickle cell disease in a cohort of Angolan pediatric patients

Molecular Biology Reports, 2020
Brígida Santos, M. Delgadinho, J. Ferreira, I. Germano, Armandina Miranda, A. P. Arez, P. Faustino, M. Brito   +7 more
semanticscholar   +1 more source

[Clinical practice guidelines for alpha-thalassemia].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2020
Writing Group For Practice Guidelines For Diagnosi, X. Shang, Xin-hua Zhang, Fang Yang, Xiangmin Xu   +4 more
semanticscholar   +1 more source

Alpha‐Thalassemia

2004
Renzo Galanello, Antonio Cao
openaire   +2 more sources

[alpha-thalassemia among Danish immigrants].

Ugeskrift for laeger, 2002
alpha-thalassaemia is the most common hereditary anaemia in the world. The majority of Danish immigrants come from countries, where the prevalence of alpha-thalassaemia is high. The aim of this study was to evaluate its frequency in Danish immigrants.Over a year, all samples sent for haemoglobin analysis to our institution from patients with an MCV ...
Henrik S, Birgens, Hans, Karle, Pia, Taaning   +2 more
openaire   +1 more source

Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlation

Pediatric Blood & Cancer, 2018
Sharon A. Singh, Susmita N Sarangi, Abena Appiah-Kubi, P. Hsu, W. Byron Smith, Patrick G Gallagher, B. Glader, David H. K. Chui   +7 more
semanticscholar   +1 more source

Genetics of Iranian Alpha-Thalassemia Patients: A Comprehensive Original Study

Biochemical Genetics, 2018
B. Keikhaei, Pejman Slehi-fard, G. Shariati, A. Khosravi   +3 more
semanticscholar   +1 more source

Favorable outcomes after in utero transfusion in fetuses with alpha thalassemia major: a case series and review of the literature

Prenatal Diagnosis, 2016
Emily M Kreger, S. Singer, Russell G. Witt, Nancy Sweeters, B. Lianoglou, A. Lal, T. Mackenzie, E. Vichinsky   +7 more
semanticscholar   +1 more source

Alpha-thalassemia.

Current topics in hematology, 1983
D R, Higgs, D J, Weatherall
openaire   +1 more source