نتایج جستجو برای: thalassaemia

تعداد نتایج: 1772  

Journal: :Journal of Clinical Pathology 1963

Journal: :Archives of Disease in Childhood 1968

Journal: :Thalassemia Reports 2013

Journal: :Sri Lanka Journal of Child Health 2018

Journal: :international journal of hematology-oncology and stem cell research 0
fatemeh shirani mahin lashkari ali shahriari-ahmadi mohsen arabi nastaran asefi

introduction: thalassemia is the most common genetic disorder, affecting around 200 million people worldwide. the etiology of this bone disease is multifactorial. seemingly, in the setting of increased bone turnover which manifests by increased bone resorption and remodeling; bone density decreases. in this research, thalassaemia patients with osteoporosis were placed on oral alendronate therap...

Journal: :Journal of clinical pathology 1997
N Jackson M Zaki A R Rahman M Nazim M N Win S Osman

A 35 year old man with a fatal Campylobacter jejuni infection is described. He had HbE/beta zero thalassaemia and had undergone splenectomy nine months previously for hypersplenism; he also had chronic hepatitis C infection. He presented with high grade fever but no gastrointestinal symptoms and rapidly progressed to septicaemic shock and hepatic encephalopathy despite treatment with penicillin...

Journal: :Molecular biotechnology 2008
V Konstantinos Kakavas Panagiotis Plageras T Antonios Vlachos Agelos Papaioannou V Argiris Noulas

Single strand conformation polymorphism (SSCP) is a reproducible, rapid and quite simple method for the detection of deletions/insertions/rearrangements in polymerase chain reaction amplified DNA. All the details for the use of PCR-SSCP are presented in the direction of genetic diseases (beta-thalassaemia, cystic fibrosis), optimum gel conditions, sensitivity and the latest modifications of the...

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