نتایج جستجو برای: Nephropathic

تعداد نتایج: 729  

Journal: :Diabetes research and clinical practice 2010
Mohammad Kazemi Arababadi Reza Nosratabadi Gholamhossein Hassanshahi Narges Yaghini Vahid Pooladvand Ali Shamsizadeh Hamid Hakimi Reza Derakhshan

The impact of several environmental and genetic factors on diabetes and its complications is well documented. The present study was aimed to examine the serum levels of IL-17A and IFN-gamma as antagonistic cytokines in nephropathic and non-nephropathic type-2 diabetic patients. In this experimental study, serum samples were obtained from 180 type-2 diabetic patients, 100 nephropathic type-2 dia...

Animesh Kumar Chakraborty Bakul Kumar Datta, Jeevan Ranjan Dash Moloy Kumar Bhar Pabitra Hridoy Patra Tapan Kumar Mandal Tapas Kumar Sar

Fifteen broiler chickens (COBB 400) of 42 days of age weighing 1.8 to 2.0 kg were equally divided into 3 groups, each consisting of 5 birds. Hepatopathy was induced by oral administration of paracetamol while nephropathy was induced by intravenous administration of uranyl nitrate. Kinetic study was investigated in healthy, hepatopathic and nephropathic birds following single oral administration...

Journal: :Journal of the American Society of Nephrology : JASN 2015
Poonam Sansanwal Li Li Minnie M Sarwal

Nephropathic cystinosis, characterized by accumulation of cystine in the lysosomes, is caused by mutations in CTNS. The molecular and cellular mechanisms underlying proximal tubular dysfunction and progressive renal failure in nephropathic cystinosis are largely unclear, and increasing evidence supports the notion that cystine accumulation alone is not responsible for the end organ injury in cy...

Journal: :Journal of the American Society of Nephrology : JASN 2002
Margaret Park Amanda Helip-Wooley Jess Thoene

Nephropathic cystinosis is a lethal disorder of lysosomal cystine storage due to defective lysosomal cystine transport. How lysosomal cystine causes this multisystemic disorder culminating in end-stage renal disease is not known, because the cystine is isolated from cellular metabolism by the lysosomal membrane. It is here reported that in both normal and nephropathic cystinotic fibroblasts and...

2017
Mariam Azeem Adil Iqbal Nasir Farooq Butt Fawad Ahmad Randhawa Uzma Malik

Objective The objective of this study was to determine the frequency of Type 2 diabetes mellitus (T2DM) in patients with nephropathy (i.e. Chronic Kidney Disease Stage 1 to 3) and to compare the mean magnesium levels in diabetic nephropathic patients and non-diabetic nephropathic patients. Methods This cross-sectional study was conducted in department of Medicine, Mayo Hospital Lahore from Au...

Journal: :veterinary research forum 2012
moloy kumar bhar bakul kumar datta pabitra hridoy patra jeevan ranjan dash tapas kumar sar

fifteen broiler chickens (cobb 400) of 42 days of age weighing 1.8 to 2.0 kg were equally divided into 3 groups, each consisting of 5 birds. hepatopathy was induced by oral administration of paracetamol while nephropathy was induced by intravenous administration of uranyl nitrate. kinetic study was investigated in healthy, hepatopathic and nephropathic birds following single oral administration...

Journal: :Kidney International 2008

Journal: :Bioorganic & medicinal chemistry letters 2008
Bridgeen McCaughan Graeme Kay Rachel M Knott Donald Cairns

Nephropathic cystinosis is a rare autosomal recessive disease characterised by raised lysosomal levels of cystine in the cells of most organs. The disorder is treated by regular administration of the aminothiol, cysteamine, an odiferous and unpleasant tasting compound that along with its metabolites is excreted in breath and sweat, leading to poor patient compliance. In an attempt to improve pa...

2018
Sören Bäumner Lutz T. Weber

Cystinosis is a rare autosomal recessive lysosomal storage disorder caused by mutations in the CTNS gene. Main dysfunction is a defective clearance of cystine from lysosomes that leads to accumulation of cystine crystals in every tissue of the body. There are three different forms: infantile nephropathic cystinosis, which is the most common form, juvenile nephropatic, and non-nephropathic cysti...

Journal: :The Journal of pediatrics 2017
Craig B Langman

Cystinosis is recognized as a systemic disease because of mutations in the gene encoding cystinosin, the lysosomal cystine exporter. In the nephropathic form that affects infants and young children, the kidney Fanconi syndrome leads to metabolic acidosis, hypophosphatemia attributable to phosphaturia, and reduced synthesis of the active metabolite of vitamin D, 1,25-dihydroxyvitamin D3, also kn...

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