Cauda equina syndrome with beta thalassemia: a case report Ahmed Almoallem Saud Alhamad Shahid Bashir Case Report27 Sept 2024 Squamous cell carcinoma of the urinary bladder in patients with chronic spinal cord injury: A case series Patrick Levien ...
Beta-thalassemia major (β-TM) patients are more likely to experience blood glucose intolerance and to date; the blood markers that could evaluate this are debatable. So, this study aimed to assess the roles of glycated hemoglobin A1c (HbA1c) and fructosamine in evaluating glucose intolerance in...
which rely on barcode sequences, STARR-seq inserts small genomic DNA fragments into the 3’ UTR position of the reporter gene. Following the transfection of vectors into host cells, deep sequencing is then employed to directly assess the reporter gene transcripts. This assay enables the ...
CHMMOTv1 - cardiac and hepatic multi-echo (T2*) MRI images and clinical dataset for Iron overload on thalassemia patients Iraj Abedi, Maryam Zamanian, Hamidreza Bolhasani, Milad Jalilian Article:339 Download PDF (996KB) View Article Data Note Database of twitter influencers in cryptocur...
Al Adham EA, Hassan AI, Hamed SM, Saber AA (2017) Evaluation of iron-chelating activity of Caulerpa racemosa in iron-dextran induced iron overload in an experimental model of thalassemia. Int J Clin Exp Med 10(3):5561–5577 CAS Google Scholar Alam SS, Abd El-Kader HAM, Abd El-Rahim...
HBE BETA-THALASSEMIA IS ASSOCIATED WITH IGA NEPHROPATHY Ayan Thakur, Souvik Bhandari, Md Obaidur Rahman, Srijana Pradhan, Subhabrata Ray and Abhed Biswas GoogleDownload PDFView Abstract No. of Downloads:1|No. of Views:1 AN IDEAL WAY TO OUR EDUCATIONAL SYSTEM ...
Beta-thalassemia Sturge-Weber syndrome DNA/RNA Local identity-related attitude Food taboos PMDD Osteomyelitis Tooth microchip Hip Arthroplasty Phenobarbital Temporomandibular joint Neuroendocrine system Nephrotic syndromeLatest Articles Open accessResearch ArticleArticle ID: ascr-aid1083Views: 10Download: 14 Intell...
STAT Plus:Chinese biotech says it will start first in vivo beta-thalassemia trial The ReadoutMeghana Keshavan STAT Plus:A next-generation form of chemotherapy wins FDA approval HealthElizabeth Cooney STAT Plus:What can’t GLP-1s do? Study maps benefits while warning of uncommon risks ...
For example, mutations in the splice-site sequences of the HBB (hemoglobin, beta) gene lead to abnormal splicing of HBB and defective synthesis of its protein β-globin in human β+-thalassemia [43,44,45]. In human multisystem proteinopathy and amyotrophic lateral sclerosis (ALS), mutations ...
Current results and future research priorities in late effects after hematopoietic stem cell transplantation for children with sickle cell disease and thalassemia: a consensus statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects After Pediatric ...