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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
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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
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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
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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
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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
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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
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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
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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
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THE RETINOPATHY OF PRIMARY HYPEROXALURIA
Retina, 1985The ophthalmoscopic and fluorescein angiographic findings in a seven-year-old boy with primary hyperoxaluria presented. The retinal findings in this condition have been reported previously in only ten patients. The fluorescein pattern which is considered to be very suggestive was reported previously in only one patient.
E I, Traboulsi +3 more
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