Results 71 to 80 of about 722,667 (218)

Examination and Sampling of Chorionic Villi for the Diagnosis of Beta-Thalassemia Major in the First Trimester of Pregnancy in Southwestern Iran [PDF]

open access: yesArmaghane Danesh Bimonthly Journal, 2023
Background & aim: Beta thalassemia is one of the most common hereditary diseases in Iran. The birth of a child with thalassemia causes many social and economic problems for parents and the health care system.
E Shams   +3 more
doaj  

Optimising Haematopoietic Stem Cell Transplantation: Enhancing Myeloablation Sensitivity and Alleviating Anaemia Using Roxadustat (FG‐4592)

open access: yesCell Proliferation, EarlyView.
The use of FG‐4592 in the process of myeloablation can promote haematopoietic cell apoptosis for more effective myeloablation, maintain the number of RBC and may create a pluripotent microenvironment suitable for donor cells, so as to enable more effective haematopoietic reconstruction of donor cells in vivo.
Guanheng Yang   +8 more
wiley   +1 more source

THALASSEMIA MINOR SCREENING APPLICATION USING THE C4.5 METHOD BASED ON LARAVEL [PDF]

open access: yes
Thalassemia is an inherited blood disorder that causes anaemia and weak red blood cells. Thalassemia minor is a type of thalassemia where the patient is a carrier of thalassemia and only experiences mild anaemia.
Wijayanto, Bangun   +2 more
core   +1 more source

Gene Editing for Haemophilia—The Next Frontier

open access: yesHaemophilia, EarlyView.
ABSTRACT The recently approved haemophilia A and B gene therapies via adeno‐associated virus (AAV) showed a promising therapeutic response after a single injection, but there are still limitations, including the potential loss of transgene expression and restriction in adults.
Mirko Pinotti   +3 more
wiley   +1 more source

Bone minerals in beta-thalassemia minor

open access: yes, 1995
Homozygous beta-thalassemia is a severe hereditary disorder associated with osteopenia. Recently it was suggested that thalassemia minor may be a risk factor for osteoporosis. The purpose of the present study was to investigate this suggestion.
Glaros, D.   +7 more
core  

Is there an association of giardiasis with beta-thalassemia minor? [PDF]

open access: yes, 2010
Beta–thalassemia minor is a symptomless carrier state of a hemoglobinopathy which predisposes to bacterial infections. We report three cases presenting with giardiasis, a parasitic infection of gastrointestinal tract caused by Giardia lamblia.
Yakoob, Javed   +2 more
core  

Smartphone‐Based Teledentistry to Support Clinical Triage and Risk‐Informed Dental Care in Patients With Inherited Bleeding and Haemoglobin Disorders: A Cross‐Sectional Diagnostic Agreement Study

open access: yesHaemophilia, EarlyView.
ABSTRACT Introduction Patients with inherited bleeding and haemoglobin disorders face barriers to accessing timely dental care, increasing the risk of untreated oral disease and complications related to invasive procedures. Aim To evaluate the agreement between smartphone‐based asynchronous teledentistry and face‐to‐face examination for oral conditions,
Victor Cordeiro da Silva   +7 more
wiley   +1 more source

Prevalence of minor Thalassemia in first and second degree relatives of patients with major Thalassemia in Kashan in 1377-78

open access: yes, 2000
History and Objectives: Minor thalassemia is one of hereditary diseases, due to different prevalence of this disease in first and second degree relatives of patients with major Thalassemia and in order to determine the prevalence of minor thalassemia in ...
Sadr, S.F.   +3 more
core  

Anemia in Pregnancy: Think beyond Iron Deficiency

open access: yesIndian Journal of Medical Specialities, 2019
We hereby describe a rare case of delta beta (δβ)-thalassemia as a cause of anemia in a 2-month pregnant female who was diagnosed as homozygous δβ-thalassemia after gene mutation studies.
Faisal A. Memon   +2 more
doaj   +1 more source

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