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[Primary hyperoxaluria and pregnancy].
Minerva urologica e nefrologica = The Italian journal of urology and nephrology, 2005A rare case of pregnancy in a patient with primary hyperoxaluria type 1 is reported offering a clinical contribution for the prognostic study of a natural event such as the pregnancy on these patients. It is underlined how epicriticity of the hepatorenal system is remarkably altered during the last weeks of pregnancy with a great increase of calciuria ...
CIMINO, SEBASTIANO +6 more
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Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2015
Primary hyperoxaluria (PH) occurs due to an autosomal recessive hereditary disorder of the metabolism of glyoxylate, which causes excessive oxalate production. The most frequent and serious disorder is due to enzyme deficit of alanine-glyoxylate aminotransferase (PH type I) specific to hepatic peroxisome.
Víctor, Lorenzo +2 more
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Primary hyperoxaluria (PH) occurs due to an autosomal recessive hereditary disorder of the metabolism of glyoxylate, which causes excessive oxalate production. The most frequent and serious disorder is due to enzyme deficit of alanine-glyoxylate aminotransferase (PH type I) specific to hepatic peroxisome.
Víctor, Lorenzo +2 more
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1998
Abstract Although oxalate has a biological role in plants and fungi-providing a protective calcium oxalate exoskeleton-no useful function has been defined in man. Nonetheless, a normal adult will excrete up to 0.Smmol/24h of oxalate in the urine derived from diet and the endogenous metabolism of glyoxylate and ascorbic acid (vitamin C ...
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Abstract Although oxalate has a biological role in plants and fungi-providing a protective calcium oxalate exoskeleton-no useful function has been defined in man. Nonetheless, a normal adult will excrete up to 0.Smmol/24h of oxalate in the urine derived from diet and the endogenous metabolism of glyoxylate and ascorbic acid (vitamin C ...
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California medicine, 1968
These discussions are selected from the weekly staff conferences in the Department of Medicine, University of California Medical Center, San Francisco. Taken from transcriptions, they are prepared by Drs. Martin J. Cline and Hibbard E. Williams, Assistant Professors of Medicine, under the direction of Dr. Lloyd H.
M J, Cline, H E, Williams, L H, Smith
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These discussions are selected from the weekly staff conferences in the Department of Medicine, University of California Medical Center, San Francisco. Taken from transcriptions, they are prepared by Drs. Martin J. Cline and Hibbard E. Williams, Assistant Professors of Medicine, under the direction of Dr. Lloyd H.
M J, Cline, H E, Williams, L H, Smith
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Ugeskrift for laeger, 1989
Primary hyperoxaluria is a recessive hereditary disturbance of glyoxylate metabolism caused by deficiency of the liver enzyme, alanine glyoxylate transaminase. The main symptoms are recurrent renal stones, nephrocalcinosis and renal failure. In the advanced state, the disease is frequently complicated by osseous disease, vascular insufficiency and ...
S D, Ladefoged, H E, Jørgensen
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Primary hyperoxaluria is a recessive hereditary disturbance of glyoxylate metabolism caused by deficiency of the liver enzyme, alanine glyoxylate transaminase. The main symptoms are recurrent renal stones, nephrocalcinosis and renal failure. In the advanced state, the disease is frequently complicated by osseous disease, vascular insufficiency and ...
S D, Ladefoged, H E, Jørgensen
openaire +1 more source