نتایج جستجو برای: iduronidase enzyme deficiency

تعداد نتایج: 368943  

Journal: :Proceedings of the National Academy of Sciences 1991

Journal: :journal of sciences, islamic republic of iran 2003
m.r. noori-daloii

glucose-6-phosphate dehydrogenase (g6pd) is a cytosolic enzyme which its main function is to produce nadph in the red blood cells by controlling the step from glucose-6-phosphate to 6-phospho gluconate in the pentose phosphate pathway. g6pd deficiency is the most common x-chromosome linked hereditary enzymopathy in the world, that result in reduced enzyme activity and more than 125 different mu...

Journal: :The Southeast Asian journal of tropical medicine and public health 2003
O Ainoon A Alawiyah Y H Yu S K Cheong N H Hamidah N Y Boo M Zaleha

Neonatal screening for G6PD deficiency has long been established in many countries. The aim of the study was to determine whether the routine semiquantitative fluorescent spot test could detect all cases of G6PD deficiency, including those cases with partial deficiency (residual red cell G6PD activity between 20-60% of normal). We compared the results of G6PD screening by the semiquantitative f...

Journal: :The American journal of pathology 1983
M E Haskins G D Aguirre P F Jezyk R J Desnick D F Patterson

Five cats with feline alpha-L-iduronidase-deficient mucopolysaccharidosis were studied. Membrane-bound cytoplasmic inclusions were present in central nervous system neurons, hepatocytes, chondrocytes, vascular and splenic smooth muscle cells, bone marrow leukocytes, and fibroblasts of the skin, eye, and cardiac valves. The lesions in these cats closely resemble those described in human patients...

Mitra Samareh Fekri Mohammad Rahmatian, Nasrin Bazargan Harandi Nasrollah Jamshidi Gohari, Sayed Mehdi Hashemi Bajgani,

Background: One of the genetic risk factors for chronic obstructive pulmonary disease (COPD) is deficiency of Alpha-1 Antitrypsin (A1AT). There is no exact statistics about the prevalence of this disease in different regions of Iran. The present study aimed to determine the prevalence of alpha-1 antitrypsin (A1AT) deficiency in COPD patients in Kerman, Iran. Metho...

B Darbandi, F Mehrabian, M Jafroodi, M Noghbaei,

Background Glucose-6-phosphate dehydrogenase (G6PD) enzyme deficiency is one of the prevalent disorders in Guilan province, northern Iran, causing many patients to suffer from acute hemolysis. This disease has imposed tremendous costs both on patients and Health systems. The aim of this study was to compare the direct costs of favism treatment on patients and health system with G6PD en...

Atefi, Aref , Fallah , Tahereh , Ghanizadeh, Fatemeh , Ghiaspour , Esmat , Hashemi , Azam , Heydari , Safiyehsadat , Sadri , Zahra , Sheikhpour , Elnaz, Zare-Zardini , Hadi ,

Vitamin D deficiency is known as the most common nutritional deficiency. It is created during infancy due to different factors, including decreased dietary intake, decreased dermal synthesis, malabsorption, enzyme-inducing medications, and exclusive breastfeeding. Vitamin D deficiency is associated with poor bone health such as rickets and osteomalacia in children. Despite vitamin D plays an im...

ژورنال: Medical Laboratory Journal 2011
Abasi, Y, , Emadi, A, , Ghods, F, , Habibeh Najar, H, , Khaleghian, A, , Mohammadi, A., , Monem, M, , Nazari, H, , Salehiyan, A, ,

Abstract Background and objectives: Glucose-6-phosphate dehydrogenase (G6PD) is an enzyme in the pentose phosphate pathway. G6PD deficiency (an X-linked recessive hereditary disease) is an inherited condition affecting approximately 3% of the people globally. This deficiency can cause hemolytic anemia and jaundice in neonates. The goal of this study is to detect the prevalence of G6PD deficienc...

Journal: :international journal of hematology-oncology and stem cell research 0
mehrdad payandeh medical biology research center, kermanshah university of medical sciences, kermanshah, iran mohammad erfan zare medical biology research center, kermanshah university of medical sciences, kermanshah, iran; studen atefeh nasir kansestani medical biology research center, kermanshah university of medical sciences, kermanshah, iran; studen kamran mansouri medical biology research center, kermanshah university of medical sciences, kermanshah, iran; departmant zohreh rahimi medical biology research center, kermanshah university of medical sciences, kermanshah, iran; departmant amir hossein hashemian department of biostatistics, faculty of public health, kermanshah university of medical sciences, kermanshah

introduction: normal homeostasis system has several inhibitor mechanisms in front of the amplifier’s natural clotting enzyme to prevent fibrin clots in the vessels. the main inhibitors of coagulation pathway are antithrombin (at), protein c and protein s. patients with hereditary deficiency of coagulation inhibitors are susceptible to venous thromboembolism (vte). one of the major clinical mani...

Journal: :iranian journal of pediatric hematology and oncology 0
b darbandi pediatric hematologist and oncologist,: pediatrics growth disorders research center, 17th sharivar hospital, guilan univ m noghbaei pediatrician, 31thkhordad hospital, manjil, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی گیلان (guilan university of medical sciences) f mehrabian health service management,guilan university of medical sciences. rasht,iran m jafroodi pediatric hematologist and oncologist,: pediatrics growth disorders research center, 17th sharivar hospital, guilan univسازمان اصلی تایید شده: دانشگاه علوم پزشکی گیلان (guilan university of medical sciences)

background glucose-6-phosphate dehydrogenase (g6pd) enzyme deficiency is one of the prevalent disorders in guilan province, northern iran, causing many patients to suffer from acute hemolysis. this disease has imposed tremendous costs both on patients and health systems. the aim of this study was to compare the direct costs of favism treatment on patients and health system with g6pd enzyme scre...

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