نتایج جستجو برای: aspartoacylase deficiency

تعداد نتایج: 137211  

Journal: :iranian red crescent medical journal 0
niloofar khodabandehloo department of internal medicine, tehran university of medical sciences, tehran, ir iran masoud vakili department of hematology and oncology, tehran university of medical sciences, tehran, ir iran zahra hashemian department of pediatrics, hematology, oncology and genetics research center, shahid sadoughi university of medical sciences, yazd, ir iran; department of pediatrics, hematology, oncology and genetics research center, shahid sadoughi university of medical sciences, yazd, ir iran, tel: +98-3518224000, fax: +98-3518224100 hadi zare zardini department of pediatrics, hematology, oncology and genetics research center, shahid sadoughi university of medical sciences, yazd, ir iran; young researchers and elite club, yazd branch, islamic azad university, yazd, ir iran

objectives we assessed functional vitamin b12 deficiency in tehranian elderly admitted to elderly research center, university of social welfare and rehabilitation sciences. conclusions the prevalence of b12 deficiency was higher in this study compared to other studies, so more attention and massive efficacious policy should be designed to reduce the deficiency of this vitamin. results cut-off o...

Journal: :gene, cell and tissue 0
ebrahim miri-moghaddam genetics of non-communicable disease research center, zahedan university of medical sciences, zahedan, ir iran; department of genetics, zahedan university of medical sciences, zahedan, ir iran yasaman garmie department of biology, faculty of science, sistan and balouchestan university, zahedan, ir iran majid naderi genetics of non-communicable disease research center, zahedan university of medical sciences, zahedan, ir iran; genetics of non-communicable disease research center, ali-asghar hospital, azadi ave., zahedan, ir iran. tel: +98-5413414567, fax: +98-5413218998

background congenital factor xiii (fxiii) deficiency is a rare severs autosomal recessive bleeding disorder. objectives the aim of the study was to determine the c559t > c fxiiia genotype frequency in patients with fxiii hemophilia who lived in sistan and balouchestan province in southeast of iran. patients and methods we determined the genotype of 180 patients with factor xiii hemophilia by te...

ژورنال: :iranian red crescent medical journal 0
bita geramizadeh department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran; transplant research center, shiraz university of medical sciences, shiraz, ir iran; department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran. tel: +98-7116474331, fax: +98-7116474331 zahra jowkar department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran leila karami department of pathology, transplant research center, shiraz university of medical sciences, shiraz, ir iran masoum masoumpour department of internal medicine, shiraz university of medical sciences, shiraz, ir iran samrad mehrabi department of internal medicine, shiraz university of medical sciences, shiraz, ir iran mohammad-ali ghayoumi department of internal medicine, shiraz university of medical sciences, shiraz, ir iran

background alpha-1 antitrypsin deficiency is a genetic disease which affects both lung and liver. this disease is a recognized factor for chronic obstructive pulmonary disease (copd). however its importance as the cause of copd in a country such as iran is unclear. objectives this study was conducted to find out the role of α-1 antitrypsin deficiency as a cause of copd in iranian patients. mate...

Introduction: Vitamin D deficiency (VDD) causes same diseases such as osteoporosis, osteomalacia, and fractures, and also it is shown that Vitamin D deficiency could lead to some cardiovascular disease, diabetes and many types of cancer. Therefore, this study aimed to determine the frequency of vitamin D deficiency among referring to laboratories in Eyvan city during 2015 and 2016. Methods: ...

Journal: :acta medica iranica 0
s. behjati-ardakani a. nikkhah m. sedaghat

glucose-6-phosphate dehydrogenase (g6pd) deficiency is the most important disease of the hexose monophosphate pathway. deficiency of this enzym can lead to hemolysis of red blood cells. our aim was to study the prevalence of g6pd deficiency in relation to neonatal jaundice. we studied 456 clinically icteric neonates laboratory investigations included determination of direct and indirect serum b...

Journal: :international journal of reproductive biomedicine 0
fatemeh mirzaei tayebeh amiri moghadam peyman arasteh

background: vitamin d deficiency during pregnancy is associated with some adverse pregnancy outcomes but its relationship with fetal growth is unknown. objective: we compared the 25-hydroxy vitamin d levels between mothers and their small for gestational age (sga) newborns with mothers and their appropriate for gestational age (aga) newborns. materials and methods: the study population included...

ژورنال: Hormozgan Medical Journal 2004
Farshidfar, GH.R, Khademi, Z, Shahi, A, Vaziri, F, Zare, SH,

Introduction: Iron deficiency anemia is the most known form of nutritional deficiency in the world. It particularly occurs in women during their fertility age. The current researches indicate that maternal iron deficiency anemia is associated with preterm delivery and low birth weight. This study was conducted to estimate the prevalence of iron deficiency anemia in pregnant women who referred...

F Farnaghi, H Hassanian Moghadam, H Owliaey, N Momtazmanesh, S Shadnia,

Aluminium Phosphide poisoning and glucose‐6‐phosphate dehydrogenase deficiency are two commonly seen clinical presentations in Iran. However, hemolysis associated with Aluminium Phosphide poisoning is very rare. We report a case of concurrent Aluminium Phosphide poisoning and glucose‐6‐phosphate dehydrogenase deficiency in a 24 year old man presenting with intravascular hemolysis. Key words...

Journal: :گوارش 0
hosein ali abbasi abbas esmaeeilzadeh homan mosanan mosannen mozaffari ali bahari kambiz akhavan rezayat omid ghanaei

background vitamin d deficiency is believed to cause variety of abnormalities such as liver stiffness and fibrosis. it is also shown that vitamin d deficiency may result in chronic liver disease or liver cirrhosis. in this study, we aimed to systematically review the literature wherein the relationship between vitamin d deficiency and the severity of chronic liver disease or liver cirrhosis had...

Journal: :caspian journal of neurological sciences 0
maryam mohammadi majid ghasemi associate professor of neurology, department of neurology, isfahan neuroscience research center, alzahra hospital, isfahan university of medical sciences, isfahan, iran; [email protected] fariborz khorvash parisa maddahian

background: menstrual migraine (mm) is a subgroup of migraine headache that affect the quality of life of patients in menstrual age. iron deficiency anemia (ida) is the most common cause of anemia, especially in women of reproductive age. objectives: to determine the association of iron deficiency anemia with menstrual migraine. materials and methods: this descriptive-analytic study was conduct...

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