Results 141 to 150 of about 1,145,402 (246)

Red blood cell indices and\ud Prevalence of Hemoglobinopathies and Glucose 6 Phosphate Dehydrogenase Deficiencies in Male Tanzanian Residents of Dar es Salaam [PDF]

Hemoglobinopathies, disorders of hemoglobin structure and production, are one of the most common monogenic disorders in humans. Glucose 6 phosphate dehydrogenase deficiency (G6PD) is an inherited enzymopathy resulting in increased oxygen stress ...
Athuman, Thabit, Daubenberge, Claudia A, Hamad, Ali, Jongo, Said, Joseph, Selina, Kamaka, Kasimu, Lweno, Omar, Mohammed, Mgeni, Moreno, Elena, Mwakasungula, Solomon, Rashid, Ramla, Schindler, Tobias, Shekalaghe, Seif, Tanner, Marcel, Tumbo, Anneth Mwasi   +14 more
core  

Molecular patterns of alpha-thalassemia in the kingdom of Saudi Arabia: identification of prevalent genotypes and regions with high incidence. [PDF]

Thromb J, 2023
Alhuthali HM, Ataya EF, Alsalmi A, Elmissbah TE, Alsharif KF, Alzahrani HA, Alsaiari AA, Allahyani M, Gharib AF, Qanash H, Elmasry HM, Hassanein DE.   +11 more
europepmc   +1 more source

Prevalence of hemoglobinopathies in premarriage individuals referred to Babolsar, Iran (2006-09)

مجله دانشگاه علوم پزشکی گرگان, 2012
Background and Objective: According to world health organization statistics, at least 5.2% of world population is carrier for a main hemoglobin disorder. Previous reports showed that more than 10% of people are carrier for beta-thalassemia Northern Iran.
Valizadeh F (MD), Mousavi A (BSc), Hashemi-Soteh MB (PhD)   +2 more
doaj  

Hematological Indices of Parents in Non-Immune Hydrops Fetalis Pregnancie

Journal of Family and Reproductive Health, 2008
Objective:To investigate the hematologic indices of mothers in non-immune hydrops fetalis pregnancies and identify the possible causative role of Alpha-Thalassemia among them.
Saeed Reza Ghaffari, Farzaneh Larti, Tayebeh Sabokbar, Maryam Rafati, Jila Dastan, Laleh Eslamian, Fatemeh Rahimi, Sedighe Borna   +7 more
doaj  

The burden and consequences of inherited blood disorders among young children in western Kenya [PDF]

, 2014
Earley, M, Macharia, A, Ruth, LJ, Suchdev, PS, Williams, TN   +4 more
core   +1 more source

The impact of in utero transfusions on perinatal outcomes in patients with alpha thalassemia major: the UCSF registry. [PDF]

Blood Adv, 2023
Schwab ME, Lianoglou BR, Gano D, Gonzalez Velez J, Allen IE, Arvon R, Baschat A, Bianchi DW, Bitanga M, Bourguignon A, Brown RN, Chen B, Chien M, Davis-Nelson S, de Laat MWM, Ekwattanakit S, Gollin Y, Hirata G, Jelin A, Jolley J, Meyer P, Miller J, Norton ME, Ogasawara KK, Panchalee T, Schindewolf E, Shaw SW, Stumbaugh T, Thompson AA, Towner D, Tsai PS, Viprakasit V, Volanakis E, Zhang L, Vichinsky E, MacKenzie TC.   +35 more
europepmc   +1 more source

A retinopathy in young patient with co-inheritance of heterozygous alpha + −thalassemia and sickle trait: a case report [PDF]

, 2017
Abdellah Dami, Aissam El Maataoui, Asmae Biaz, Fatiha Benchrifa, Nezha Messaoudi, Samira El Machtani, Sanae Bouhsain, Zeinab Traore, Zohra Ouzzif   +8 more
core   +1 more source

Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster. [PDF]

Int J Mol Sci, 2023
Cardiero G, Musollino G, Prezioso R, Nigro V, Lacerra G.   +4 more
europepmc   +1 more source

Machine learning improves detection of alpha thalassemia carriers compared to clinical features. [PDF]

Sci Rep
Mohammadi E, Rastegar M, Jamshidnezhad A, Azizi A.   +3 more
europepmc   +1 more source

Alpha-Thalassemia Unmasked in a Patient With Sickle Cell Trait: A Case Report. [PDF]

Cureus
Chuquimarca B, Carrión C, Matosas V, Riva E.   +3 more
europepmc   +1 more source