LONG-TERM STUDY OF STEROID SENSITIVE NEPHROSIS (SSN)
نویسندگان
چکیده
منابع مشابه
Long-term dwarfing effects of corticosteroid treatment for childhood nephrosis.
Children with the idiopathic nephrotic syndrome have been treated with intensive steroid therapy at various centres since prednisolone became available in 1955. Five years after onset, 65-70% of such children are free from significant proteinuria, and the death rate has been reduced to 10-15% by such therapy (Arneil and Lam, 1966; Cornfeld and Schwartz, 1966). Serious untoward effects, such as ...
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از گذشته تا کنون، تحقیقات بسیاری صورت گرفته است که همگی به گونه ای بر مثمر ثمر بودن استفاده از استراتژی های یادگیری لغت در یک زبان بیگانه اذعان داشته اند. این تحقیق به بررسی تاثیر دو روش مختلف آموزش واژگان انگلیسی (کلیدی و بافتی) بر تلفظ و دانش لغوی فراگیران ایرانی زیر متوسط زبان انگلیسی و بر ماندگاری آن در حافظه می پردازد. به این منظور، تعداد شصت نفر از زبان آموزان ایرانی هشت تا چهارده ساله با...
15 صفحه اولLong-term outcome of children with steroid-sensitive idiopathic nephrotic syndrome.
I n children, the most frequent glomerular disease is idiopathic nephrotic syndrome, which is defined by the combination of a nephrotic syndrome and nonspecific histologic abnormalities of the kidney including minimal changes, FSGS, and diffuse mesangial proliferation. The term minimalchange disease has become synonymous with steroid-sensitive idiopathic nephrotic syndrome, although renal biops...
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An 18-year-old Malay lady was treated with high dose steroids for three and a half years for idiopathic thrombocytopaenic purpura. At 21 years, after a series of relapses, a splenectomy was carried out. In addition, two nodules at the hilum of the spleen were also removed. Histological examination of these nodules revealed features of Kaposi's sarcoma. Kaposi's sarcoma resulting from immunosupp...
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Studies of Mendelian forms of focal segmental glomerulosclerosis (FSGS) and nephrotic syndrome have provided new insights into the mechanism of these diseases. Congenital nephrotic syndrome and familial forms of FSGS form a spectrum of podocyte diseases of varying severity and age of onset. Mutations in both nephrin gene (NPHS1) alleles lead to congenital nephrosis, podocyte foot process efacem...
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ژورنال
عنوان ژورنال: Pediatric Research
سال: 1980
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-198008000-00163