Results 81 to 90 of about 39,321 (195)
Research in Molecular Medicine, 2017 Background: Beta thalassemia is a common health problem in Iran especially in Northern provinces. Premarital screening for thalassemia is compulsory in Iran and identification of the carriers is based on primary CBC (Cell Blood Count) and hemoglobin ...
Hossein Karami +3 more
doaj
Novel deletions and unusual genetic mechanisms underlying alpha-thalassemia [PDF]
, 2016 Hemoglobin (Hb) is a protein responsible for oxygen transportation from lungs to the entire body. It is composed by four globular subunits - the globins - each with a central core containing a heme molecule.
Batalha-Reis, Ana +16 more
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Quality of life among patients with beta-thalassemia major in Shahrekord city, Iran [PDF]
, 2016 Background and aims: Nowadays introduction of regular blood transfusion therapy has obviously improved the life expectancy of patients with thalassemia. However, these patients face with newer challenges which influence their quality of life (QoL).
Emadi Dehaghi, B. +2 more
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Studies of bone mineral density in children affected by dietary intolerances [PDF]
, 2014 The Pediatric Department of the University of Ferrara has developed a special expertise in the field of hemoglobinopathies and has also an interest in gastrointestinal diseases.
Baldan, Alessandro +3 more
core +1 more source
HbA1c levels in hemoglobin H disease
Biochemistry and Biophysics ReportsBackground: 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
شيوع هموگلوبينوپاتی با توجه به ميزان انواع هموگلوبين و ارتباط آنها با حجم متوسط گلبول قرمز در بين دانش آموزان پيشدانشگاهی شهر بوشهر؛ 1386 [PDF]
, 2009 زمينه: هموگلوبينوپاتی ها از جمله تالاسمی و کمخونی داسی شکل از فراوان ترين اختلالات ژنتيکی در انسان می باشند. اين بيماری ها در حالت هتروزيگوت بدون علائم بالينی بوده ولی در حالت هموزيگوت نياز به خون و مراقبت های بيمارستانی دارند.
خمیسی پور, غلامرضا +2 more
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Effect of booklet and combined method on parents' awareness of children with β-thalassemia major disorder [PDF]
, 2008 OBJECTIVE: To assess the effects of booklet and combining methods (lecture, video, etc.) on parents' awareness of children with beta-thalassemia major disorder.
Hasanpour-Dehkordi, A. +1 more
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Le Basi biochimiche e molecolari delle talassemie e la diagnosi dell'Alfa-talassemia eterozigote [PDF]
, 1982 Recent aspects of molecular and biochemical basis of thalassemic syndromes are described together with laboratory methods suitable for diagnosis and screening of heterozygous α ...
Masala, Bruno Lucio
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Prevalence of common point mutations of alpha globin gene in Babol, Iran (2005-09)
مجله 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