نتایج جستجو برای: sickle cell heart function tests

تعداد نتایج: 3238778  

2017
Sarah Feray Pierre Mora Maxens Decavele Tài Pham El Mahdi Hafiani Muriel Fartoukh

Plastic bronchitis is used to designate endobronchial plugs of rubber-like consistency that form into bronchial trees. It has been described in several diseases like asthma, cystic fibrosis, pulmonary infection, cyanotic congenital heart disease and in few young children with homozygous sickle cell disease. We report the first sickle cell adult case of plastic bronchitis during acute chest synd...

Journal: :The Journal of clinical investigation 1985
C T Noguchi G J Dover G P Rodgers G R Serjeant S E Antonarakis N P Anagnou D R Higgs D J Weatherall A N Schechter

Homozygous alpha-thalassemia has the beneficial effect in sickle cell anemia of reducing the hemolytic severity while changing several other hematological parameters. We examined in detail the cellular basis of some of these hematologic alterations. We find that the broad distribution in erythrocyte density and the large proportion of dense cells associated with sickle cell anemia are both redu...

2013
Caroline Barakat-Haddad

This study examined the prevalence of high blood pressure, heart disease, and medical diagnoses in relation to blood disorders, among 6,329 adolescent students (age 15 to 18 years) who reside in the United Arab Emirates (UAE). Findings indicated that the overall prevalence of high blood pressure and heart disease was 1.8% and 1.3%, respectively. Overall, the prevalence for thalassemia, sickle-c...

2011
Husain H. Jabbad

Patients with sickle cell trait or a disease who require cardiac surgery are at risk of a potentially fatal sickling crisis, which may be induced by hypothermia, hypoxia, acidosis, or low-flow states. Literature on the evaluation and specific management of these patients remains limited, and further studies are strongly recommended. This presents 3 years experience in King Abdulaziz University ...

Journal: :Blood 2000
M C Walters R Storb M Patience W Leisenring T Taylor J E Sanders G E Buchanan Z R Rogers P Dinndorf S C Davies I A Roberts R Dickerhoff A M Yeager L Hsu J Kurtzberg K Ohene-Frempong N Bunin F Bernaudin W Y Wong J P Scott D Margolis E Vichinsky D A Wall A S Wayne C Pegelow R Redding-Lallinger J Wiley M Klemperer W C Mentzer F O Smith K M Sullivan

Fifty children who had symptomatic sickle cell disease received matched sibling marrow allografts between September 1991 and March 1999, with Kaplan-Meier probabilities of survival and event-free survival of 94% and 84%, respectively. Twenty-six patients (16 male, 10 female) had at least 2 years of follow-up after transplantation and were evaluated for late effects of transplantation and for it...

Journal: :Caspian journal of internal medicine 2013
Adedoyin O Dosunmu Rachael A Akinola Josephine A Onakoya Taiwo M Balogunt Olufunke O Adeyeye Akinsegun A Akinbami Olanrewaju M Arogundade Ayodeji T Brodie-Mends

BACKGROUND The vascular response to recurrent tissue hypoxia and reperfusion following red blood cell sickling causes acute chest syndrome and chronic lung disease. The purpose of this study was to determine the pattern of chronic lung lesions and possible risk factors in sickle cell patients in lagos, Nigeria. METHODS From July 2012 to April 2013, Pulmonary function test (PFT) and chest-x-ra...

2015
ALVAN R. FEINSTEIN

The label of rheumatic fever is now given to a population of patients more distinct and diagnostically "pure" than ever before. The Jones criteria, described in 1944 and modified in 1956 (American Heart Association, 1956), circumscribe the diagnostic boundaries of the disease, and exclude many minor illnesses that formerly were designated inappropriately as rheumatic fever. Other major illnesse...

Journal: :Emerging science journal 2021

A molecule called hemoglobin is found in red blood cells that holds oxygen all over the body. Hemoglobin elastic, round, and stable a healthy human. This makes it possible to float across cells. But composition of unhealthy if you have sickle cell disease. It refers compact bent The odd obstruct flow blood. dangerous can result severe discomfort, organ damage, heart strokes, other symptoms. hum...

Journal: :jundishapur journal of microbiology 0
mehri ghafourian-boroujerdnia department of immunology, hemoglobinopathy and thalassemia research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; department of immunology, hemoglobinopathy and thalassemia research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran. tel: +98-6113738225, fax: +98-6113332036 mohammad ali assarehzadegan department of immunology, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran khodamorad zandian hemoglobinopathy and thalassemia research center, shafa hospital, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

background although it is life-saving, blood transfusion therapy has resulted in risk for transfusion-transmitted infections (ttis) in the majority of sickle cell anemia being patients. objectives the current study aimed to determine the prevalence of hbv, hcv and different genotypes of hcv among sickle cell anemia (sca) patients in ahvaz city, south-western iran. materials and methods a cross-...

2016
Narcisse Elenga Aurélie Adeline John Balcaen Tania Vaz Mélanie Calvez Anne Terraz Laetitia Accrombessi Gabriel Carles

Sickle cell disease is a serious genetic disorder affecting 1/235 births in French Guiana. This study aimed to describe the follow-up of pregnancies among sickle cell disease patients in Cayenne Hospital, in order to highlight the most reported complications. 62 records of pregnancies were analyzed among 44 females with sickle cell disease, between 2007 and 2013. Our results were compared to th...

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