نتایج جستجو برای: disease diagnosis

تعداد نتایج: 1804944  

Journal: :Australian Veterinary Journal 2002

Journal: :Journal of Fetal Medicine 2014

Journal: :Indian Journal of Clinical Biochemistry 1999

Journal: :Indian Journal of Hematology and Blood Transfusion 2015

Journal: :Medical Journal Armed Forces India 2010

Journal: :iranian journal of allergy, asthma and immunology 0
yavuz köker m immunology division, diskapi children’s research hospital, ankara, turkey metin ayşe immunology division, hacettepe university children’s hospital, ankara, turkey özgür tuba t immunology division, hacettepe university children’s hospital, ankara, turkey de boer martin sanquin research, and landsteiner laboratory, academic medical centre, university of amsterdam, roos dirk sanquin research, and landsteiner laboratory, academic medical centre, university of amsterdam,

mutations in any of four known nadph-oxidase components lead to cgd. x-linked cgd (x-cgd) is caused by defects in cybb, the gene that encodes gp91-phox. autosomal recessive (ar) cgd is caused by defects in the genes for p47 phox, p22-phox or p67-phox. the aim of this study was to screen the molecular defect in the fetus of an x-cgd carrier mother and postnatal confirmation of the results. in a ...

Multiple myeloma is a monoclonal malignant proliferation of plasma cells. The disease is more frequent in men, and the average age of patients at the time of diagnosis of the disease is about 60 years. Solitary myeloma may be the first manifestation of the disseminated form of multiple myeloma, which is characterized by multiple skeletal lesions, general metabolic alterations, impairment of ren...

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