Biomaterial Database

Renal transplantation in Fabry's disease. 1972

P C Peters, and D Leeber, and A R Hull, and M Philippart

UI	MeSH Term	Description	Entries
D007642	Keratosis	Any horny growth such as a wart or callus.	Keratoderma Blennorrhagicum,Keratoma,Keratosis Blennorrhagica,Blennorrhagica, Keratosis,Blennorrhagicas, Keratosis,Blennorrhagicum, Keratoderma,Blennorrhagicums, Keratoderma,Keratoderma Blennorrhagicums,Keratomas,Keratoses,Keratosis Blennorrhagicas
D007668	Kidney	Body organ that filters blood for the secretion of URINE and that regulates ion concentrations.	Kidneys
D007676	Kidney Failure, Chronic	The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION.	ESRD,End-Stage Renal Disease,Renal Disease, End-Stage,Renal Failure, Chronic,Renal Failure, End-Stage,Chronic Kidney Failure,End-Stage Kidney Disease,Chronic Renal Failure,Disease, End-Stage Kidney,Disease, End-Stage Renal,End Stage Kidney Disease,End Stage Renal Disease,End-Stage Renal Failure,Kidney Disease, End-Stage,Renal Disease, End Stage,Renal Failure, End Stage
D008052	Lipid Metabolism, Inborn Errors	Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable.	Lipid Metabolism, Inborn Error
D008297	Male		Males
D002102	Cadaver	A dead body, usually a human body.	Corpse,Cadavers,Corpses
D002554	Cerebrosides	Neutral glycosphingolipids that contain a monosaccharide, normally glucose or galactose, in 1-ortho-beta-glycosidic linkage with the primary alcohol of an N-acyl sphingoid (ceramide). In plants the monosaccharide is normally glucose and the sphingoid usually phytosphingosine. In animals, the monosaccharide is usually galactose, though this may vary with the tissue and the sphingoid is usually sphingosine or dihydrosphingosine. (From Oxford Dictionary of Biochemistry and Molecular Biology, 1st ed)
D005696	Galactosidases	A family of galactoside hydrolases that hydrolyze compounds with an O-galactosyl linkage. EC 3.2.1.-.	Galactosidase
D006017	Glycolipids	Any compound containing one or more monosaccharide residues bound by a glycosidic linkage to a hydrophobic moiety such as an acylglycerol (see GLYCERIDES), a sphingoid, a ceramide (CERAMIDES) (N-acylsphingoid) or a prenyl phosphate. (From IUPAC's webpage)	Glycolipid
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

P C Peters, and D Leeber, and A R Hull, and M Philippart

Renal transplantation in Fabry's disease.

January 1989, Nephron,

P C Peters, and D Leeber, and A R Hull, and M Philippart

Enzyme therapy in Fabry's disease by renal transplantation.

January 1972, Proceedings of the Clinical Dialysis and Transplant Forum,

P C Peters, and D Leeber, and A R Hull, and M Philippart

Immune function and renal transplantation in Fabry's disease.

January 1985, Proceedings of the European Dialysis and Transplant Association - European Renal Association. European Dialysis and Transplant Association - European Renal Association. Congress,

P C Peters, and D Leeber, and A R Hull, and M Philippart

Ten-year experience in renal transplantation for Fabry's disease.

March 1981, Transplantation proceedings,

P C Peters, and D Leeber, and A R Hull, and M Philippart

Renal biopsy in Fabry's disease eight years after successful renal transplantation.

April 1987, Clinical nephrology,

P C Peters, and D Leeber, and A R Hull, and M Philippart

[Renal transplantation in patients suffering from Fabry's disease. Kidney transplantation from an heterozygote subject to a subject without Fabry's disease].

September 1975, La Nouvelle presse medicale,

P C Peters, and D Leeber, and A R Hull, and M Philippart

Correction of enzymatic deficiencies by renal transplantation: Fabry's disease.

August 1972, Surgery,