Results 81 to 90 of about 1,534,143 (162)

Primary Hyperoxaluria Type 1 with Thrombophilia in Pregnancy: A Case Report

Case Reports in Nephrology and Dialysis, 2018
Background: Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease caused by a mutation in the AGXT gene, resulting in deficiency of the alanineglyoxylate:aminotransferase enzyme.
Asma Hasan, Sharon Maynard, Dominick Santoriello, Henry Schairer   +3 more
doaj   +1 more source

Accelerated Oxalosis Contributing to Delayed Graft Function after Renal Transplantation

Case Reports in Transplantation, 2019
Hyperoxaluria is an important and underrecognized cause for allograft dysfunction and loss after transplantation. It is potentially treatable if recognized in a timely fashion.
Yvelynne P. Kelly, Astrid Weins, Melissa Y. Yeung   +2 more
doaj   +1 more source

A rare case of hyperoxaluria presenting with acute liver injury and stone-free kidney injury

Kidney Research and Clinical Practice, 2015
A 49-year-old woman visited the clinic because of acute hepatitis and acute kidney injury with decreased urine output presenting microscopic hematuria and proteinuria.
Si-eun Kim, Seon-Jae Kim, Seong Taek Chu, Seung Hee Yang, Yon Su Kim, Ran-hui Cha   +5 more
doaj   +1 more source

The characterisation of barley and wheat oxalate oxidases expressed in transgenic plants [PDF]

, 1998
Oxalate oxidase is a water soluble, thermolabile, homo-oligomeric glycoprotein the synthesis of which marks the onset of germination In wheat and barley embryos. The protein Is also highly abundant In barley roots.
Ilett, C.J., Ilett, Colin John
core  

Relationship of Oxalate Nephropathy and Digestive Pathology in Children

, 2021
Study of the structure, combined pathology of the kidneys and the digestive system of nonmicrobial etiology are researched in this article. A survey of 120 children with oxalate nephropathy was conducted.
Bakhodirovna, T. Z. (Tajieva), Atanazarovich, M. S. (Masharipov)   +1 more
core   +1 more source

Oxalate Nephropathy Secondary to Chronic Pancreatitis: Case Report

Turkish Journal of Nephrology, 2019
Chronic pancreatitis is a rare cause of oxalate nephropathy. The aim of this case report was to present a patient hospitalized with acute kidney injury who was diagnosed with oxalate nephropathy and concurrent chronic pancreatitis on further ...
Nergiz BAYRAKCI, Nihal ÖZKAYAR, Aysel ÇOLAK, Müge EREK ERSÖZEN, Ebru GÖK OĞUZ, Fatih DEDE   +5 more
doaj  

The Long Pentraxin PTX3 Is an Endogenous Inhibitor of Hyperoxaluria-Related Nephrocalcinosis and Chronic Kidney Disease

Frontiers in Immunology, 2018
The long pentraxin 3 (PTX3) exerts a variety of regulatory functions in acute and chronic tissue inflammation. In particular, PTX3 acts as an opsonin for a variety of pathogens and endogenous particles.
Julian A. Marschner, Shrikant R. Mulay, Stefanie Steiger, Lidia Anguiano, Zhibo Zhao, Peter Boor, Khosrow Rahimi, Antonio Inforzato, Antonio Inforzato, Cecilia Garlanda, Cecilia Garlanda, Alberto Mantovani, Alberto Mantovani, Hans-Joachim Anders   +13 more
doaj   +1 more source

Combined Liver and Kidney Transplant for Primary Hyperoxaluria Type 2

Indian Journal of Transplantation
Primary hyperoxaluria type 2 (PH2) is a rare autosomal recessive disorder of oxalate overproduction that frequently leads to end-stage renal disease (ESRD). While isolated kidney transplantation is often performed, it carries a high risk of graft failure
Anjana Raina Misri, Madhav Hande, Mahesha Vankalakunti   +2 more
doaj   +1 more source

Evaluating oxalate-degrading Lactobacillus spp. for their ability to be used as probiotics in the treatment of kidney stone disease [PDF]

, 2010
Includes abstract.Includes bibliographical references (leaves 73-95).Although the direct cause of kidney stone formation is not known, reports have suggested it is probably a multifactorial disease.
Kabanda, Siti M
core   +1 more source

Iatrogenic acute oxalate nephropathy [PDF]

Nephrology Dialysis Transplantation, 1996
openaire   +2 more sources