Results 121 to 130 of about 5,140 (180)

Kidney Stone Events and ESKD Incidence in Patients with Enteric Hyperoxaluria from Diverse Enteric Etiologies. [PDF]

Kidney360
Tatton RW, O'Neill SR, Jordan D, Vaughan LE, Lieske JC, Keddis MT.   +5 more
europepmc   +1 more source

Real-world burden of primary hyperoxaluria with chronic kidney disease in the United States: a retrospective administrative claims analysis. [PDF]

BMC Nephrol
Goldfarb DS, Modersitzki F, Skaar JR, Li O, Salem S, Chen JV.   +5 more
europepmc   +1 more source

Re: Pierre Letourneau, Lara Cabezas, Aurélie De Mul, et al. Optimizing Screening Performance for the Risk of Hyperoxaluria and Urolithiasis Using the Urinary Oxalate/Creatinine Ratio: A Retrospective Analysis. Eur Urol Open Sci 2025;75:20-8. [PDF]

Eur Urol Open Sci
Liu D, Guan Z, Du Y.
europepmc   +1 more source

Lumasiran at birth changes the trajectory of primary hyperoxaluria type 1: same disease, different outcomes in two affected siblings. [PDF]

J Nephrol
Peruzzi L, Leporati M, Pediatric Oxal Turin Working Group.   +2 more
europepmc   +1 more source

First retrospective study on pediatric nephrocalcinosis in Syria: clinical symptoms and causes. [PDF]

Front Pediatr
Ghanem H, Hassan M, Swideah S, Wannous H.   +3 more
europepmc   +1 more source

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The Primary Hyperoxalurias

Seminars in Nephrology, 2008
The primary hyperoxalurias (PHs) are rare autosomal-recessive inborn errors of metabolism. In the most severe form (type 1), recurrent kidney stones and progressive nephrocalcinosis lead to the loss of kidney function, accompanied by systemic oxalosis, and often requires dialysis and/or transplantation.
Amy E, Bobrowski, Craig B, Langman
openaire   +2 more sources

Oral Manifestations of Hyperoxaluria

Journal of Craniofacial Surgery, 2011
Primary hyperoxaluria is a rare, inherited autosomal recessive disease caused by defects in the metabolism of glyoxylate. Oral manifestations of hyperoxaluria are rare. However, bone and tooth resorption may be the result of chronic inflammation and the presence of osteoclastic cells surrounding the oxalate crystal deposit. A deposit of calcium oxalate
Eliete Neves da Silva, Guerra, Leonora, Vianna, Maria Nazareth, Sobreira, Flavio Nader Gross, de Araújo, Nilce Santos, de Melo   +4 more
openaire   +2 more sources

Primary Hyperoxaluria in Infancy

Australasian Radiology, 1986
ABSTRACTPrimary Hyperoxaluria is a rare autosomal recessive disorder causing progressive renal failure and death before adulthood in most cases1. Acute renal failure due to Primary Hyperoxaluria with renal oxalosis is rare in infancy2‐ 3 and we report such a case emphasizing the importance of ultrasonographic examination in the diagnosis of this ...
H N, Srinivas, C, Ramkumar
openaire   +2 more sources

Hyperoxaluria.

Mineral and electrolyte metabolism, 1987
Urinary oxalate is considered to play a crucial role in the formation of renal stones. In this respect hyperoxaluria constitutes a special problem, mainly because of the specific physicochemical properties of oxalate. The appropriate management of patients with this disorder must be based on a thorough understanding of the absorption, metabolism and ...
L, Larsson, H G, Tiselius
openaire   +1 more source