Results 111 to 120 of about 40,068 (239)
Absence of beta mRNA in beta0-thalassemia in Kurdish Jews [PDF]
, 1978 Francesco Ramirez +5 more
openalex +1 more source
Recent Progress in Gene Delivery Systems Based on Gemini‐Surfactant
MedComm – Future Medicine, Volume 4, Issue 3, September 2025.Gene delivery is a key area in biomedicine, where nucleic acids are delivered into cells to treat diseases by modulating genes. The low micelle concentration, effective nucleic acid complexation, and low immunogenicity make Gemini surfactants promising gene delivery vectors.
Peng Qian +5 more
wiley +1 more source
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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MedComm – Oncology, Volume 4, Issue 3, September 2025.TGF‐β inhibition is emerging as a promising cancer therapy, yet translating laboratory success to bedside implementation has suffered significant setbacks. The associated challenges include adverse drug reactions, inadequate predictive models, and activation of alternative signaling pathways.
Faizah A. Alabi +5 more
wiley +1 more source
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. [PDF]
, 1972 P. K. Sukumaran +4 more
openalex +1 more source
Pregnancy‐ and Disease‐Related Morbidity Among Medicaid Enrollees With Sickle Cell Disease
Pediatric Blood &Cancer, Volume 72, Issue 9, September 2025.ABSTRACT Background Whereas pregnancy in sickle cell disease (SCD) is considered high risk, there is limited understanding of pregnancy‐ and SCD‐related morbidity to inform clinical practice and health policy. Procedure This retrospective cohort study aimed to describe pregnancy‐ and disease‐related morbidity among individuals with SCD for up to 1 year
Mariam Kayle +10 more
wiley +1 more source
Anemia, 2015 Background. Nontransfusion dependent thalassemia (NTDT) is a milder form of thalassemia that does not require regular transfusion. It is associated with many complications, which differ from that found in transfusion-dependent thalassemia (TDT ...
Poramed Winichakoon +7 more
doaj +1 more source
Insulin-like growth factor-1 levels in children with Beta-thalassemia minor [PDF]
, 2008 Objective: Growth retardation in children with b-thalassemia major is multifactorial. Some etiologies described for this condition are hemochromatosis, disturbed growth hormone (GH) / insulin growth factor-1 (IGF-1) axis, undernutrition and ...
Hamdollah Karamifar +2 more
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International Journal of Paediatric Dentistry, Volume 35, Issue 5, Page 945-953, September 2025.ABSTRACT Background Molar incisor hypomineralization (MIH) is associated with enamel's existing qualitative developmental defects. Aim This study aimed to assess the cortical and trabecular mandibular bone morphology in pediatric patients with MIH using fractal analysis (FA) and digital panoramic radiography (DPR) with various radiomorphometric indices.
Asli Soğukpinar Önsüren +1 more
wiley +1 more source
Creating Public Awareness of Thalassemia as a Marketing Communication Strategy at Genetic Clinic Genneka [PDF]
, 2013 Indonesia, with the population of almost 250 millions people, have high number of genetic disorders which should be treated and managed. One of genetic disorders in Indonesia with high number of registered patients is Thalassemia, a red blood cell ...
Inggriantara, A. (Alibasjah) +1 more
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