? 2024 Elsevier B.V.Thalassemia is one of the most common and damaging monogenic diseases in the world. It is caused by pathogenic variants of α- and/or ... J Long,C Yu,L Sun,... - 《Clinica Chimica Acta International Journal of Clinical Chemistry & Applied Molecular Biology》 被引量...
Which of the following statements is not true regarding this diagnosis? a) The cause of beta-thalassemia is genetic. b) Beta-thalassemia major is a grave condition and has a high mortali Which is a disorder of the nervous ...
Background and purpose: Beta thalassemia is the most common genetic disease in the world. It has a high prevalence in and in Mazandaran province in particu... M Kosaryan,Ôkhvatian, A,F Babamahmoodi - 《Helsingin Yliopisto》 被引量: 2发表: 2004年 Hitler'sEffectonWildlifeinNebraska:World...
Genetic diseases such as Huntingdon's disease, Duchenne's myopathy, phenylketonuria and b-thalassemia can be diagnosed by analysing the DNA from individuals. Furthermore, the diagnosis or the identification of viruses, viroids, bacteria, fungi, protozoa or some other form of plant or animal life ...
Sickle cell disease and β-thalassemia are among the most common monogenic disorders globally, causing significant morbidity and early mortality. The only curative option available is allogeneic hematopoietic stem cell transplantation, which is limited by a lack of matched donors and risks, including ...
ALT values of thalassemia patients after one year of treatment with Compound I at different dosages (separate trial as compared to the results in Table 1). Compound I Number of patients Mean of ALT (Units/liter) 5 mg/kg/day 2 35.25 10 mg/kg/day 8 26.62 20 mg/kg/day 21 3.17 ...
Class 12 BIOLOGY The inborn error of metabolism which lig... A Albinism B Alkaptonuria C Gaucher's disease D Phenylketonuria Video Solution | Answer Step by step video, text & image solution for The inborn error of metabolism which lightens the skin colour is by Biology experts to help you...
Background: Reduced bone density is a well-known complication of thalassemia major. This problem has been manifested more commonly due to longer life of affected individuals. The present study was conducted to determine the prevalence of... M Tabatabaeifar,A. Shamshirsaz,MR Bakhirnia,... 被引...
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2024. "Genotype–Phenotype Correlation in a Couple in Which the Wife Is a Carrier of the Beta-Thalassemia Trait and the Husband Is a Carrier of a Mutation in the ALAS2 Gene: Both Gene Defects Are Associated with Non-Iron-Deficiency Microcytic Anemia" Thalassemia Reports 14, no. 4: 118-...