نتایج جستجو برای: 12rβ1 deficiency

تعداد نتایج: 137176  

اخوان‌کرباسی, صدیقه, فلاح, راضیه, گلستان, مطهره, اسلامی, ضیاء, صدربافقی, مهدخت, ملکی, غضنفر , موسوی, سید عبدالحمید, میرناصری, فهیمه السادات,

Introduction: Zinc deficiency is a health problem in many communities, especially among children because of growth spurt. Zinc deficiency can causegrowth limitation, delay in sexuel maturity, behavior disorders and abnormalities of immune system,susceptibility to respiratory and gasterointestinal infections and impairment of taste and smell perception. Material and Method: One of the methods ...

Journal: :iranian journal of public health 0
hafzan yusoff nutrition programme, school of health sciences, universiti sains malaysia, kelantan, malaysia. wan nudri wan daud zulkifli ahmad

this study was carried out to compare the effect between nutrition education intervention and non-nutrition education intervention on awareness regarding iron deficiency among schooling adolescents in tanah merah, one of rural district in kelantan, malaysia.this study which was started in year 2010 involved 280 respondents (223 girls, 57 boys, age: 16 yr) from schools in tanah merah. the select...

Journal: :فیض 0
یوسف مرتضوی yousef mortazavi department of pathology, zanjan university of medical scinces, zanjan, iranزنجان، دانشگاه علوم پزشکی زنجان، گروه آسیب شناسی عبدالرضا اسماعیل زاده abdoreza esmaeilzadeh صدرالدین کلانتری sadroddein kalantari

background: glucose-6-phosphate dehydrogenase (g6pd) is an x-linked enzymopathy affecting about 400 million people worldwide. neonatal jaundice, drug induced haemolysis and infection-induced haemolysis may happen in some deficient individuals and lead to considerable mortality. the distribution of g6pd deficiency and the molecular genetics of this enzyme vary widely among different ethnic group...

Journal: :iranian journal of allergy, asthma and immunology 0
saghafi shiva pourpak zahra aghamohammadi asghar pourfathollah ali akbar samadian azam farghadan maryam

selective deficiency of immunoglobulin a (iga) is the most frequent primary hypogammaglobulinemia. as some iga-deficient patients have iga antibodies in their plasma which may cause anaphylactic reactions, blood centers usually maintain a list of iga-deficient blood donors to prepare compatible blood components. in this study we determined the incidence of selective iga deficiency (sigad) in no...

Journal: :international journal of hematology-oncology and stem cell research 0
soheila zareifar pediatric hematology and oncology department, shiraz university of medical sciences, shiraz, iran. seyed mohsen dehghani gasteroenterology department, shiraz university of medical sciences, shiraz, iran. najmeh rahanjam pediatric hematology and oncology department, shiraz university of medical sciences, shiraz, iran. mohammad reza farahmand far pediatric hematology and oncology department, shiraz university of medical sciences, shiraz, iran.

background: among the many complications reported for cirrhosis, iron deficiency anemia (ida) has attracted much attention. this type of anemia, in contrast to other types of anemia, is easy to treat prophylactically, but if left untreated can lead to a poor quality of life. the aim of this study was to estimate the hemoglobin and serum iron levels among patients with liver cirrhosis for the ea...

Journal: :acta medica iranica 0
h. r. sadeghipour roudsari m. farahani a. mogharabi

we studied the prevalence of iron-deficiency anaemia in women of reproductive age, between 15 to 49, with a mean age of 31-56±1.34 years, attending mirzakoochak khan hospital ob. gyn. center for routine gynecological and obstetrical examination. we compa'tred mean values for the serum tests and haematological data and investigated etiological factors such as age, marital status, education, spou...

Journal: :caspian journal of internal medicine 0
behzad heidari mobility impairment research center yahya javadian mobility impairment research center mahmoud monadi department of internal medicine, rouhani hospital, babol university of medical sciences, babol, iran. yahya dankoub department of internal medicine, rouhani hospital, babol university of medical sciences, babol, iran. alireza firouzjahi department of laboratory medicine, ayatollah rouhani hospital, babol university of medical sciences, babol, iran

background: vitamin d has a potential to modulate inflammatory response against noxious particles in patients with chronic obstructive pulmonary disease (copd). the present study was conducted to determine the status of serum vitamin d in copd versus healthy group. methods: the patients presented to the outpatient pulmonary clinic of ayatollah rouhani hospital, babol iran. diagnosis of copd was...

Journal: :iranian journal of pediatric hematology and oncology 0
sar azarpeikan shahid sadoughi university of medical sciences and health services, yazd, iran azam sadat hashemi department of pediatrics, hematology, oncology and genetics research center, shahid sadoughi university of medical scienسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences) atef atefi hematology, oncology and genetics research center, shahid sadoughi university of medical sciences and health services, yسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences)

abstract arterial ischemic stroke defines as a new focal neurologic deficit that lasted 24 hours or longer. stroke is relatively rare in children and incidence of cerebrovascular disease is 1 per 4000 in neonates and 1 per 7000 to 1 per 70000 in older children (1 month to 18 years). protein s deficiency is one of the causes of the stroke in children. major manifestations of protein s deficiency...

Journal: :international journal of molecular and cellular medicine 0
yadollah zahedpasha non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) mousa ahmadpour kachouri non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) haleh akhavan niaki cellular and molecular biology research center (cmbrc), babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) roya farhadi non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences)

background and aim: jaundice is a common disorder in neonates and one of the provable causes of glucose-6-phosphate dehydrogenase (g6pd) deficiency, some mutation types of which may be associated with severe neonatal icter. in this line, the present study has been conducted to compare g6pd mutations in incteric and non icteric neonates. materials and methods: this case-control study was impleme...

Journal: :iranian red crescent medical journal 0
sepideh mohammadi central medical laboratory, ayatollah taleghani hospital, tehran, iran zahra torab hematology and oncology research center, tabriz university of medical sciences, tabriz, iran soheila aghakhani faculty of biological science, islamic azad university, north-tehran branch, tehran, iran mina ghalandari emergency medicine specialist, department of emergency medicine, ayatollah taleghani hospital, shahid beheshti university of medical sciences, tehran, iran; emergency medicine specialist, department of emergency medicine, ayatollah taleghani hospital, shahid beheshti university of medical sciences,tehran, iran reyhaneh mohammadimanesh department of chemical engineering, biotechnology faculty of engineering, payame noor university, tehran, iran; emergency medicine specialist, department of emergency medicine, ayatollah taleghani hospital, shahid beheshti university of medical sciences,tehran, iran vahid asgary department of immunology, school of medicine, tehran university of medical sciences, tehran, iran

discussions as one ich patient whose pt and aptt suggest a coagulation disorder secondary to vitamin k deficiency or coagulation factor deficiency, unresponsiveness to vitamin k therapy should be useful to take fx deficiency into consideration. background inborn factor x deficiency (fxd) is a very rare (1: 500,000) hereditary coagulation disorder, which is characterized by clinical manifestatio...

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