Results 101 to 110 of about 4,024 (132)
4-hydroxy-2-oxoglutarate metabolism in a mouse model of Primary Hyperoxaluria Type 3. [PDF]
Biochem Biophys RepLi X +5 more
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Spinal Cord Compression as the First Presentation of Primary Hyperoxaluria in a Patient With Kidney Failure: A Case Report and Literature Review. [PDF]
Kidney MedKliea M +5 more
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Mutation Characteristics of Primary Hyperoxaluria in the Chinese Population and Current International Diagnosis and Treatment Status. [PDF]
Kidney Dis (Basel)Zhu X, Cheung WW, Zhang A, Ding G.
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Second transplantation after kidney graft loss in primary hyperoxaluria type 2: a pedigree study and mutation analysis. [PDF]
Ren FailPeng Y +12 more
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Urinary Oxalate Excretion During Pregnancy in Primary Hyperoxaluria Type 1: A Report of 4 Cases. [PDF]
Kidney MedMiao J +5 more
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How We Treat Primary Hyperoxaluria Type 1.
Clin J Am Soc NephrolBreeggemann MC +4 more
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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
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
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.
Antonio Capone, Travis A. Meredith
openaire +3 more sources
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.
Antonio Capone, Travis A. Meredith
openaire +3 more sources