نتایج جستجو برای: hyperoxaluria

تعداد نتایج: 893  

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2011
Marguerite Hatch Altin Gjymishka Eduardo C Salido Milton J Allison Robert W Freel

Oxalobacter colonization of rat intestine was previously shown to promote enteric oxalate secretion and elimination, leading to significant reductions in urinary oxalate excretion (Hatch et al. Kidney Int 69: 691-698, 2006). The main goal of the present study, using a mouse model of primary hyperoxaluria type 1 (PH1), was to test the hypothesis that colonization of the mouse gut by Oxalobacter ...

Journal: :Kidney International 1999

Journal: :Journal of the American Society of Nephrology 1999

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2017
Waqar Ahmed Abad Ur Rehman Sumit Acharya

Primary hyperoxaluria is a rare autosomal recessive disorder, characterised by precipitation of insoluble oxalate crystals in the joints, kidneys, heart, eyes, skin, nerves, and bone marrow. The patients of primary oxaluria usually present with renal stone/nephrocalcinosis, and isolated kidney transplantation should not be done in these patients. We present a case report of 31-year lady with ac...

Journal: :Postgraduate medical journal 1994
R G Woolfson M A Mansell

Many Western countries are experiencing an epidemic of renal calculi, causing immediate problems with acute pain and morbidity together with worries for the future because of the likelihood of recurrent stone formation. Renal or ureteric colic is the commonest surgical admission diagnosis in this country and it has been suggested that up to 12 million Americans will suffer a stone episode durin...

Journal: :British medical journal 1975
P J Moorhead D J Cooper W R Timperley

In a patient suffering from primary hyperoxaluria with oxalosis a progressive peripheral neuropathy was associated with intra-axonal deposition of microcrystals of calcium oxalate. Probably his neuropathy was the result of mechanical obstruction of axoplasmic flow.

Journal: :Clinical journal of the American Society of Nephrology : CJASN 2011
Carla G Monico Sandro Rossetti Ruth Belostotsky Andrea G Cogal Regina M Herges Barbara M Seide Julie B Olson Eric J Bergstrahl Hugh J Williams William E Haley Yaacov Frishberg Dawn S Milliner

BACKGROUND AND OBJECTIVES Primary hyperoxaluria types I and II (PHI and PHII) are rare monogenic causes of hyperoxaluria and calcium oxalate urolithiasis. Recently, we described type III, due to mutations in HOGA1 (formerly DHDPSL), hypothesized to cause a gain of mitochondrial 4-hydroxy-2-oxoglutarate aldolase activity, resulting in excess oxalate. DESIGN, SETTING, PARTICIPANTS, & MEASUREMEN...

Journal: :Gut 1977
G B McDonald D L Earnest W H Admirand

The effect of fat malabsorption on the absorption and renal excretion of dietary oxalate was studied in four patients with sprue and in two patients with dermatitis herpetiformis and sprue-like jejunal histology. Hyperoxaluria was present in all patients with sprue when fat malabsorption was severe. Urinary oxalate excretion decreased in two of the three patients with coeliac sprue when their f...

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