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Primary and secondary hyperoxaluria: Understanding the enigma

Primary and secondary hyperoxaluria: Understanding the enigma

http://www.wikidata.org/entity/Q35567868

about

Experimental models of renal calcium stones in rodents Assessing the iron delivery efficacy of transferrin in clinical samples by native electrospray ionization mass spectrometry Malabsorption syndrome as a rare cause of nephrocalcinosis.Effect of endoplasmic reticulum stress inhibition on hyperoxaluria-induced oxidative stress: influence on cellular ROS sources.Pathogenesis of calcium oxalate urinary stone disease: species comparison of humans, dogs, and cats.Of Inflammasomes and Alarmins: IL-1β and IL-1α in Kidney Disease.Hyperoxaluria Requires TNF Receptors to Initiate Crystal Adhesion and Kidney Stone Disease.Pathology and Epidemiology of Oxalate Nephrosis in Cheetahs.Bone Marrow Oxalosis in a Patient With Pancytopenia Following Bilateral Nephrectomy.Folding Defects Leading to Primary Hyperoxaluria.Bilateral native nephrectomy to reduce oxalate stores in children at the time of combined liver-kidney transplantation for primary hyperoxaluria type 1.Bilateral native nephrectomy reduces systemic oxalate level after combined liver-kidney transplant: A case report.Another atypical case of acute kidney injury-or not? Answers.Oxalate nephropathy from cashew nut intake.Efficacy of Hydroxy-L-proline (HYP) analogs in the treatment of primary hyperoxaluria in Drosophila Melanogaster.The Long Pentraxin PTX3 Is an Endogenous Inhibitor of Hyperoxaluria-Related Nephrocalcinosis and Chronic Kidney Disease

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Primary and secondary hyperoxaluria: Understanding the enigma

http://www.wikidata.org/entity/Q35567868

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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Primary and secondary hyperoxaluria: Understanding the enigma

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Primary and secondary hyperoxaluria: Understanding the enigma

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Primary and secondary hyperoxaluria: Understanding the enigma

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Primary and secondary hyperoxaluria: Understanding the enigma

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Primary and secondary hyperoxaluria: Understanding the enigma

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World journal of nephrology

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Primary and secondary hyperoxaluria: Understanding the enigma

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Bhavna Bhasin

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Hatice Melda Ürekli

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Mohamed G Atta

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P2860

The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type II

Mutations in DHDPSL are responsible for primary hyperoxaluria type III

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1

Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis

Hyperoxaluria: a gut-kidney axis?

The SLC26 gene family of multifunctional anion exchangers

Plasma and urine glycolate assays for differentiating the hyperoxaluria syndromes

Calcium oxalate urolithiasis in mice lacking anion transporter Slc26a6

Endourologic treatment of nephrocalcinosis.

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235-244

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scholarly article

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10.5527/WJN.V4.I2.235

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2

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2015-05-01T00:00:00Z

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276068729

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25949937

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4419133

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