Results 101 to 110 of about 1,319,935 (211)

HbA1c levels in hemoglobin H disease

open access: yesBiochemistry and Biophysics Reports
Background: Patients with beta-thalassemia have been shown to exhibit lower HbA1c levels, often correlating with reduced hemoglobin (Hb) concentrations.
Pasiri Kerdsinchai   +14 more
doaj   +1 more source

[alpha-thalassemia accompanied with Gilbert's syndrome].

open access: yes[Rinsho ketsueki] The Japanese journal of clinical hematology, 1998
A 15-year-old boy was admitted to our hospital because of microcytic hypochromic erythrocytosis and hyperbilirubinemia in October 1996. The laboratory findings were RBC: 597 x 10(4)/microliter, Hb: 13.1 g/dl, Ht: 40.8%, MCV: 70fl, MCH: 22pg, total bilirubin: 3.2 mg/dl (indirect: 2.2 mg/dl), s-Fe: 99 micrograms/dl, and ferritin: 25 ng/ml.
KOISO, Hiromi   +9 more
openaire   +2 more sources

Prevalence of common point mutations of alpha globin gene in Babol, Iran (2005-09)

open access: yesمجله دانشگاه علوم پزشکی گرگان, 2012
Background and Objective: Alpha thalassemia is one of the most common hemoglobin disorders. Some combination of alpha globin gene mutations may cause HbH disease with severe anemia or intermediate thalassemia.
Akhavan-Niaki H (PhD)   +4 more
doaj  

An Immunological and Molecular Study to Investigate the Genes (β-globin and HBA1F) in Patients with Thalassemia in Najaf Governorate

open access: yesJournal of Preventive, Diagnostic and Treatment Strategies in Medicine
BACKGROUND: Thalassemia, a hereditary blood disorder, poses a significant health challenge globally. This study delves into the prevalence and characteristics of thalassemia, emphasizing the need for enhanced awareness and diagnostic measures ...
Hussein Fadi Ibrahim   +4 more
doaj   +1 more source

Preimplantation Genetic Diagnosis for Alpha Thalassemia: Experience in Siriraj Hospital

open access: yesSiriraj Medical Journal, 2008
Objective: Detection of fetal thalassemia using preimplantation genetic diagnosis (PGD) can make a diagnosis before pregnancy so termination of pregnancy in that patient is eliminated.
Japarath Prechapanich   +5 more
doaj  

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

open access: yesمجله 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)   +2 more
doaj  

alpha-Thalassemia trait in the region of Ferrara.

open access: yesHaematologica, 1981
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DEL SENNO, Laura   +13 more
openaire   +3 more sources

Hematological Indices of Parents in Non-Immune Hydrops Fetalis Pregnancie

open access: yesJournal 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   +7 more
doaj  

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