Results 71 to 80 of about 4,438 (134)

Primary Hyperoxaluria Diagnosed Based on Bone Marrow Biopsy in Pancytopenic Adult with End Stage Renal Disease

Case Reports in Hematology, 2015
Inborn errors of metabolism cause increase of metabolites in serum and their deposition in various organs including bone marrow. Primary hyperoxaluria (PH) is a rare inborn error in the pathway of glyoxylate metabolism which causes excessive oxalate ...
Pardis Nematollahi, Fereshteh Mohammadizadeh   +1 more
doaj   +1 more source

Multiomics Assessment of the Gut Microbiome in Rare Hyperoxaluric Conditions

Kidney International Reports
Introduction: Hyperoxaluria is a risk factor for kidney stone formation and chronic kidney disease progression. The microbiome is an important protective factor against oxalate accumulation through the activity of its oxalate-degrading enzymes (ODEs). In
Nadim Zaidan, Chan Wang, Ze Chen, John C. Lieske, Dawn Milliner, Barbara Seide, Melody Ho, Huilin Li, Kelly V. Ruggles, Frank Modersitzki, David S. Goldfarb, Martin Blaser, Lama Nazzal   +12 more
doaj   +1 more source

Primary hiperoxaluria diagnosed after kidney transplantation: report of 2 cases and literature review

Brazilian Journal of Nephrology
Primary hyperoxaluria (PH) is a very rare genetic disorder; it is characterized by total or partial deficiency of the enzymes related to the metabolism of glyoxylate, with an overproduction of calcium oxalate that is deposited in different organs, mainly
John Fredy Nieto Rios, Monica Zuluaga, Lina Maria Serna Higuita, Adriana Florez, Diana Carolina Bello-Marquez, Arbey Aristizábal, Catalina Ocampo Kohn, Gustavo Adolfo Zuluaga   +7 more
doaj   +1 more source

Navigating the Evolving Landscape of Primary Hyperoxaluria: Traditional Management Defied by the Rise of Novel Molecular Drugs

Biomolecules
Primary hyperoxalurias (PHs) are inherited metabolic disorders marked by enzymatic cascade disruption, leading to excessive oxalate production that is subsequently excreted in the urine.
Yueqi Huang, Wei Zhu, Jia Zhou, Qiulin Huang, Guohua Zeng   +4 more
doaj   +1 more source

CHRONIC RENAL FAILURE DUE TO HYPER OXALURIA IN PEDIATRIC PATIENTS

Turkish Journal of Nephrology, 2019
Primary hyperoxaluria is a rarely encountered disease characterised by recurrent urolithiasis, nephrocalcinosis, and oxalate deposition in almost all tissues, generally inherited in autosomal recessive fashion and the important complications of which can
Ali DELİBAŞ, Özlem ERDOĞAN, Mehmet BÜLBÜL, Kenan BEK, Gülay DEMİRCİN, Ayşe ÖNER   +5 more
doaj  

Primary hyperoxaluria and systemic oxalosis

Indian Journal of Urology, 2007
K Sriram, Nitin S Kekre, Ganesh Gopalakrishnan   +2 more
doaj   +1 more source

A case of oxalate nephropathy presenting with acute kidney injury [PDF]

Journal of Krishna Institute of Medical Sciences University
Oxalate Nephropathy (ON) represents a serious condition characterized by a decline in renal function associated with calcium oxalate crystal deposition within renal tubules. It can arise from Primary Hyperoxaluria (PH) due to genetic defects or secondary
Pradnya Mukund Diggikar, Mayank Mundada, Raju Hansini Reddy, Tushar Pancholi   +3 more
doaj  

Mutational Landscape of Primary Hyperoxaluria in Morocco: Update and Implications for Diagnosis. [PDF]

Genes (Basel)
Batta O, Rahmuni Y, Lyahyai J, Rchiad Z, Doubaj Y, Sefiani A, Jaouad IC.   +6 more
europepmc   +1 more source

Primary Hyperoxaluria Type 1 Diagnosed After Kidney Transplantation in the Absence of Classical Features. [PDF]

Case Rep Nephrol
Sultan R, Alsayed-Ahmad ZA, Shheibar AR, Shawwa R, Albitar K, Albitar S.   +5 more
europepmc   +1 more source

Dental implant rehabilitation in a patient with primary hyperoxaluria type 1: a 14-month case report. [PDF]

BMC Oral Health
Sulaiman AR, Bassit GE.
europepmc   +1 more source