نتایج جستجو برای: homozygous sickle cell disease

تعداد نتایج: 2943221  

Journal: :jundishapur journal of chronic disease care 0
mehrnaz ahmadi department of nursing, school of nursing and midwifery, ahvaz jundishapur university of medical sciences, ahvaz, ir iran abdolali shariati department of nursing, school of nursing and midwifery, ahvaz jundishapur university of medical sciences, ahvaz, ir iran simin jahani department of nursing, school of nursing and midwifery, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; department of nursing, school of nursing and midwifery, ahvaz jundishapur university of medical sciences, ahvaz, ir iran hamed tabesh department of biostatistics and epidemiology, ahvaz jundishapur university of medical sciences, ahvaz, ir iran bijan keikhaei health research institute, research center of thalassemia and hemoglobinopathy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

conclusions the results of this study showed that self-management interventions are effective in promoting self-efficacy in patients with sickle cell disease. thus, the use of self-management programs is advisable to change behaviors and promote self-efficacy in such patients. background patients with sickle cell disease suffer from various complications during their lifetime. in order to cope ...

Journal: :journal of herbal drugs 0
anand dilip firodiya human genetic lab, centre for scientific research and development, peoples university, bhopal-462037, madhya pradesh, india abin mani human genetic lab, centre for scientific research and development, peoples university, bhopal-462037, madhya pradesh, india vijay thawani human genetic lab, centre for scientific research and development, peoples university, bhopal-462037, madhya pradesh, india

background & aim:combretaceae family is   known for efficacy in the management of sickle cell disorder (scd). based on   the earlier reports of anti-sickling property of terminalia genus the study investigates in vitro antisickling properties of terminalia arjuna and terminalia   bellirica. experimental: anti-sickling   assay of methanolic and aqueous extract of t. arjuna and t. bellirica   on ...

Journal: :Journal of the American College of Cardiology 1987

2015
J. H. Gillis S. K. Satapathy L. Parsa P. B. Sylvestre N. Dbouk

Acute sickle hepatic crisis (ASHC) has been observed in approximately 10% of patients with sickle cell disease. It occurs predominantly in patients with homozygous (Hb SS) sickle cell anemia and to a lesser degree in patients with Hb SC disease, sickle cell trait, and Hb S beta thalassemia. Patients commonly present with jaundice, right upper quadrant pain, nausea, low-grade fever, tender hepat...

Afshin Fathi, Bijan Keikhaei, Firoozeh Dehyouri, Mohammad Pedram,

Background: Sickle cell disease occurs due to a mutation in β chains and the substitution of valine instead of glutamate in the sixth position of the ß-chain that causes polymerization and vascular blockage. The aim of this study was to compare the serum C, S proteins and factor V Leiden between sickle cell patients and the control group. Materials and Methods: In this case-control study, perf...

Journal: :The West Indian medical journal 2006
N D Duncan I Tennant A Crawford-Sykes A Barnett M Scarlett S E Dundas G Badal B Chin

A total of 110 patients with sickle cell disease who had open splenectomy at the University Hospital of the West Indies over a 10-year period are reviewed Patients with homozygous sickle cell disease numbered 94, S beta0 and S beta+ thalassaemias (11 and 4 respectively) and one patient with SC disease. Postoperative acute chest syndrome was the most common complication (9 of 110). There were no...

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