Results 161 to 170 of about 7,435 (215)
Probiotic and Synbiotic Interventions Targeting Oxalate-Degrading Gut Bacteria for the Prevention of Kidney Stones: A Systematic Review. [PDF]
CureusBhardwaj M +3 more
europepmc +1 more source
Pathophysiology and Management of Hyperoxaluria and Oxalate Nephropathy: A Review
American Journal of Kidney Diseases, 2022 Hyperoxaluria results from either inherited disorders of glyoxylate metabolism leading to hepatic oxalate overproduction (primary hyperoxaluria), or increased intestinal oxalate absorption (secondary hyperoxaluria).
Michel Jadoul +2 more
exaly +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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
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
Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I [PDF]
FEBS Letters, 1986 Activities of alanine:glyoxylate aminotransferase in the livers of two patients with primary hyperoxaluria type I were substantially lower than those found in five control human livers.
P R Jennings, C J Danpure
exaly +2 more sources
Oral Manifestations of Hyperoxaluria
Journal of Craniofacial Surgery, 2011Primary 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 +4 more
openaire +2 more sources
Primary Hyperoxaluria in Infancy
Australasian Radiology, 1986ABSTRACTPrimary 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
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
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
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 2017
Oxalate (Ox) is an end-product of metabolism, important for poor solubility of its calcium salt in biological fluids. Ox can therefore be found in about 70% of urinary calculi. Hyperoxaluria (HOx) defined as Ox exceeding 0.5 mmol)/day, may cause nephrolithiasis/nephrocalcinosis and may be classified as dietary (DH), enteric (EH) or primary (PH ...
Martino, Marangella +4 more
openaire +1 more source
Oxalate (Ox) is an end-product of metabolism, important for poor solubility of its calcium salt in biological fluids. Ox can therefore be found in about 70% of urinary calculi. Hyperoxaluria (HOx) defined as Ox exceeding 0.5 mmol)/day, may cause nephrolithiasis/nephrocalcinosis and may be classified as dietary (DH), enteric (EH) or primary (PH ...
Martino, Marangella +4 more
openaire +1 more source