Results 11 to 20 of about 3,873 (265)
Recent advances in β-thalassemias
Pediatric Reports, 2011 β-thalassemias, a group of autosomal recessive disorders resulting from reduced or absent production of β-globin chains from the β-globin locus, are very heterogeneous at the molecular level (for review see Weatherall & Clegg, 2001 and Cao & Galanello).1-
Antonio Cao, Paolo Moi, Renzo Galanello
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Indian Journal of Pathology and Microbiology, 2014 Background: The hereditary hemoglobin (Hb) disorders are the most commonly encountered single gene disorders in India. Data pertaining to the pattern of hemoglobinopathies and thalassemias is scarce in North East India, and hence it was considered ...
Mrinal Kumar Baruah +2 more
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PRENATAL DIAGNOSIS OF β-THALASSEMIAS AND HEMOGLOBINOPATHIES
Mediterranean Journal of Hematology and Infectious Diseases, 2009 <p class="MsoNormal" style="text-align: justify; line-height: 200%; margin: 0cm 0cm 0pt;"><span style="font-family: " lang="EN-US"><span style="font-size: small;"> </span></span></p><p class="MsoNormal" style ...
Luisella Saba, Maria Cristina Rosatelli
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CONCISE REVIEW ON THE FREQUENCY, MAJOR RISK FACTORS AND SURVEILLANCE OF HEPATOCELLULAR CARCINOMA (HCC) IN Β-THALASSEMIAS: PAST, PRESENT AND FUTURE PERSPECTIVES [PDF]
Mediterranean Journal of Hematology and Infectious Diseases, 2020 Due to the recent alarming increase in the incidence of hepatocellular carcinoma (HCC) in thalassemias, the aim of the present report is to review briefly the frequency, the major risk factors and the surveillance of HCC in β-thalassemias.
Vincenzo De Sanctis
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Thalassemias. From gene to therapy
, 2021 Thalassemias (α, β, γ, δ, δβ, and εγδβ) are the most common genetic disorders worldwide and constitute a heterogeneous group of hereditary diseases characterized by the deficient synthesis of one or more hemoglobin (Hb) chain(s).
Nervi C. +5 more
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Thalassemia (Beta-Thalassemia)
International Journal For Multidisciplinary Research, 2023 Thalassemia is an inherited blood disorder characterized by less oxygen carrying protein (Haemoglobin) and fever red blood cells in the body than normal. There are mainly two types of thalassemia i.e. Alpha and Beta thalassemia about 1-5% of the global population 80-90 million people are the carrier of ß thalassemia which is major concern.
Tathe Pratiksha Annasaheb - +2 more
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Hemoglobin genes; Sickle-cell anemia - Thalassemias [PDF]
, 2009 Educational Items on Hemoglobin genes; Sickle-cell anemia ...
Huret, JL, Troussard, X
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Thalassemia ENDOCRINOPATHIES IN THALASSEMIA PATIENTS
PAFMJ, 2021 Objective: To determine the common endocrine complications found in children having thalassemia major. Study Design: Cross-sectional study. Place and Duration of Study: Department of Pediatric Medicine, Combined Military Hospital Multan, from May to Nov 2019. Methodology: A total of 160 Children with thalassemia were taken in this ...
Umer Touheed +5 more
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Oro-dental clinical aspects in children with thalassemia [PDF]
Archives of the Balkan Medical Union, 2019 Introduction. Thalassemias are the most common monogenic diseases. They are divided in two major categories: alpha – thalassemias (minor thalassemia), that do not have a special symptomatology and beta-thalassemias, which are a form of hereditary disease
Andrei KOZMA +4 more
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Journal of Applied Hematology, 2017 Background: Beta thalassemias are a group of hereditary blood disorders that are characterized by reduction or complete absence of the β-globin chain synthesis due to mutations, affecting critical areas of the β-globin gene on the chromosome 11.
Ayman Mashi +4 more
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