Results 111 to 120 of about 5,205 (214)

Combined liver-kidney transplantation in primary hyperoxaluria type 1. Bone histopathology and oxalate body content.

, 1995
In three patients with end-stage renal failure due to primary hyperoxaluria type 1, successful combined liver-kidney transplantation enabled us to assess the insoluble oxalate pool, which was compared with the histopathological changes observed in iliac ...
Vienne, Anne, Janssen, Françoise, Pasteels, Jean Lambert, De Pauw, Luc, Toussaint, Charles, Gelin, Michel, Hall, Michelle, Schurmans, Thierry   +7 more
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Biochemical insights into Primary hyperoxaluria type III

, 2016
Primary hyperoxaluria 3 (PH3) is a rare, autosomal-recessive inherited disorder characterized by increased oxalate production. It is caused by mutations in the HOGA1 gene encoding the enzyme 4-hydroxy-2-oxoglutarate aldolase (HOGA).
Loomes, Kerry
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Extreme intrafamilial variability of Saudi brothers with primary hyperoxaluria type 1

, 2012
Majid Alfadhel,1 Khalid A Alhasan,2 Mohammed Alotaibi,3 Khalid Al Fakeeh41Division of Genetics, Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia; 2Division of Nephrology ...
Al Fakeeh K, Alfadhel M, Alotaibi M, Alhasan KA   +3 more
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Renal graft failure due to type 1 primary hyperoxaluria.

, 2002
Primary hyperoxaluria type 1 (PH1) usually presents with recurrent urolithiasis, nephrocalcinosis and progressive renal failure at a relatively young age.
Huysmans, F.T.M., Assmann, K.J.M., Timmers, H.J.L.M., Riksen, N.P.   +3 more
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Comparison of Risk Profiles, Nutrient Intake, and Kidney Function of Calcium Oxalate Stone Formers with and without Enteric Hyperoxaluria. A Matched Case-Control Study. [PDF]

Nutrients
Ernsten C, Spuck N, Hesse A, Siener R.
europepmc   +1 more source

Metabolic origins of hyperoxaluria: the critical role of precursors and vitamin B6 status in rats. [PDF]

Urolithiasis
Ogawa Y.
europepmc   +1 more source

Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics. [PDF]

Metabolites
Kuhara T, Ohse M, Fukasawa T, Maruyama K, Pitt J.   +4 more
europepmc   +1 more source

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine. [PDF]

Int J Mol Sci
Popa S, Grădinaru AC, Braha EE, Grămescu M, Babici R, Ailenei C, Butnariu LI.   +6 more
europepmc   +1 more source

Domino hepatic transplantation using the liver from a patient with primary hyperoxaluria

, 2001
We report a case of domino liver transplantation using the liver harvested from a patient who underwent a combined liver and kidney transplantation for primary hyperoxaluria (PH).SCOPUS: ar.jinfo:eu-repo/semantics ...
Bourgeois, Nadine, Louis, Hubert, El Nakadi, Issam, Adler, Michael, Le Moine, Olivier, Closset, Jean, Gelin, Michel, Donckier De Donceel, Vincent, Ickx, Brigitte   +8 more
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Urinary biomarkers of urolithiasis risk in Crohn's disease: hyperoxaluria, hypocitraturia, and hypomagnesuria in patients with and without ileocolic resection. [PDF]

Crohns Colitis 360
Navratil V, Pipek B, Falt P, Zapletalova J, Krivinka J, Solitano V, Kunovsky L.   +6 more
europepmc   +1 more source