نتایج جستجو برای: primary c3 deficiency

تعداد نتایج: 784306  

2013
Lijun Fu Meirong Huang Shubao Chen

Carnitine is essential for the transfer of long-chain fatty acids from the cytosol into mitochondria for subsequent β-oxidation. A lack of carnitine results in impaired energy production from long-chain fatty acids, especially during periods of fasting or stress. Primary carnitine deficiency (PCD) is an autosomal recessive disorder of mitochondrial β-oxidation resulting from defective carnitine...

Journal: :Archives of disease in childhood 1974
J L van den Brande M V du Caju H K Visser W Schopman W H Hackeng H J Degenhart

Primary somatomedin deficiency: case report. A child presenting with the clinical features of hyposomatotropism but with high immunoreactive plasma growth hormone is described. During short-term administration of human growth hormone (HGH) his response with regard to fasting blood-glucose and free fatty acids, plasma-somatomedin, urinary excretion of calcium, nitrogen, and hydroxyproline was mi...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه پیام نور - دانشگاه پیام نور استان همدان - دانشکده ادبیات و علوم انسانی 1390

abstract this study is an attempt to determine the effect of nano- technology education on science lesson for fifth grade in primary school in the city of kermanshah. this research is experimental and is conducted in the from of pre-test and post- test for the control group. an achievement test was administered to determine the rate of learning in the students. the research is an applied one. ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Jeffrey M Harder Catherine E Braine Pete A Williams Xianjun Zhu Katharine H MacNicoll Gregory L Sousa Rebecca A Buchanan Richard S Smith Richard T Libby Gareth R Howell Simon W M John

Various immune response pathways are altered during early, predegenerative stages of glaucoma; however, whether the early immune responses occur secondarily to or independently of neuronal dysfunction is unclear. To investigate this relationship, we used the Wlds allele, which protects from axon dysfunction. We demonstrate that DBA/2J.Wlds mice develop high intraocular pressure (IOP) but are pr...

Journal: :iranian journal of immunology 0
soheyla alyasin clinical immunology and allergy, allergy research center farhad abolnezhadian department of pediatrics, division of immunology and allergy, namazi hospital, shiraz university of medical sciences, shiraz maryam khoshkhui department of clinical immunology and allergy, mashhad university of medical science , mashhad, iran

major histocompatibility complex (mhc) class ii deficiency is a primary immunodeficiency disease characterized by abnormality of mhc class ii molecules surface expression on peripheral blood lymphocytes and monocytes. clinical manifestations include extreme susceptibility to viral, bacterial, and fungal infections but the immunodeficiency is not as severe as scid (severe combined immunodeficien...

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