About: Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation

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About: Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation Goto Sponge NotDistinct Permalink

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scientific article published on 01 March 1987

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1987 (uk) article scientifique publié en 1987 (fr) im März 1987 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 1987 (ast) scientific article published on 01 March 1987 (en)
publication date	wds:Q68936935-DBFC82EF-0923-40BE-91F5-C73ACD7F4476
publication date	1987-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q68936935-9FC28D03-BDBA-4A59-A954-9CB7CF0C5A3B
language of work or name	English
cites work	wds:Q68936935-0D621964-A2B9-4CB2-A886-661BEB64E14B wds:Q68936935-29819F8C-F455-482F-9B71-9F7C5BA9C206 wds:Q68936935-36552DED-226D-4624-80A0-383159813F33 wds:Q68936935-3743DE7C-02B5-40C1-931D-E84A80789A05 wds:Q68936935-38502FB2-CF62-4B46-96DA-FA99002591F9 wds:Q68936935-599363D8-8C05-4275-AE26-46ECB9C87C5F wds:Q68936935-832FAC6B-2C9D-4FF5-A29E-DC4ABEB9B430 wds:Q68936935-AF8E698B-93E5-43E1-A2FA-96136FE46E7E wds:Q68936935-BDD3A967-0D43-41A7-BA36-AD8D714E9434 wds:Q68936935-DDF72B24-1BE3-4117-AC1F-F99E1272766F wds:Q68936935-E207BB42-5C60-44F2-AA03-278C04695478 wds:Q68936935-F30ACC53-90A8-439E-B454-977FF1E0FF67
cites work	The occurrence of hepatoma in the chronic form of hereditary tyrosinemia Studies in lead poisoning. II. Correlation between the ratio of activated to inactivated delta-aminolevulinic acid dehydratase of whole blood and the blood lead level Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetone Persistent succinylacetone excretion after liver transplantation in a patient with hereditary tyrosinaemia type I STUDIES ON TYROSINOSIS: 1, EFFECT OF LOW-TYROSINE AND LOW-PHENYLALANINE DIET Hyperkalaemia in cyclosporin-treated renal allograft recipients Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemia Tyrosinosis. A study of 6 cases Tyrosinemia with acute intermittent porphyria: aminolevulinic acid dehydratase deficiency related to elevated urinary aminolevulinic acid levels Excretion of δ-aminolevulinic acid in hereditary tyrosinemia Determination of urinary succinylacetone by capillary gas chromatography Enzyme Defect in a Case of Tyrosinemia Type I, Acute Form
author name string	wds:Q68936935-64D75745-A741-448B-82AB-40C8A35E35F1 wds:Q68936935-A8B6B20E-4C78-4676-B64C-9C3CCD6F6E3F wds:Q68936935-E13A0A29-5A0E-4169-80FF-CB13B91447CF
author name string	M Tuchman J R Bloomer M L Ramnaraine
rdfs:label	Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (en) Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (nl)
skos:prefLabel	Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (en) Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (nl)
name	Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (en) Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (nl)
author	wds:Q68936935-039AC7B3-A5CA-4A36-B1C1-ACE449FA7E1F wds:Q68936935-6E14186E-A135-4255-8603-B61FA5FC77DB wds:Q68936935-BA0C29AD-9A5D-4A09-9F4F-159268444961
author	Nancy Ascher Deborah K. Freese Harvey L. Sharp
title	wds:Q68936935-CBDA52BA-BEB4-4D1D-AF45-D5F6511DF982
title	Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (en)
page(s)	wds:Q68936935-C8D56746-5DD8-4164-93BC-E2EC805F0AE3
page(s)	399-403
instance of	wds:Q68936935-D53308D4-B375-4CFB-A0A0-8F32E4F2F65D
instance of	scholarly article
main subject	wds:Q68936935-817A0AEF-61E9-46C7-BFE9-CE773ACC0069
main subject	tyrosinemia type I
PubMed ID	wds:Q68936935-EBBB170A-44D6-485A-8E85-72ED09ACD744
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3546650
PubMed ID	3546650
published in	wds:Q68936935-956FA834-A03C-4704-8CFD-F52B4E2F58E5
published in	The Journal of Pediatrics
issue	wds:Q68936935-669E9095-C22C-4E5C-9568-BFEEFCF97DBF
volume	wds:Q68936935-53564D32-6E49-4B5A-891B-2795A6E510C5
issue	3
volume	110
DOI	wds:Q68936935-57DCD223-F299-436F-BB3F-926274BD185D
DOI	http://dx.doi.org/10.1016/S0022-3476(87)80501-2
DOI	10.1016/S0022-3476(87)80501-2
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q68936935
is cites work of	Plasma succinylacetone is persistently raised after liver transplantation in tyrosinaemia type 1. Liver transplantation for tyrosinemia. A review of 10 cases from the University of Pittsburgh Renal function in tyrosinaemia type I after liver transplantation: a long-term follow-up. Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15 Visceral pathology of hereditary tyrosinemia type I. Current strategies for the treatment of hereditary tyrosinemia type I. Liver transplantation for hereditary tyrosinemia: the Quebec experience Early nitisinone treatment reduces the need for liver transplantation in children with tyrosinaemia type 1 and improves post-transplant renal function Treatment of inherited metabolic disorders by liver transplantation Treatment of two children with hereditary tyrosinaemia type I and long-standing renal disease with a 4-hydroxyphenylpyruvate dioxygenase inhibitor (NTBC) Tyrosinaemia type I — an update Liver transplantation in nine Spanish patients with tyrosinaemia type I A pediatric perspective on liver transplantation. Liver transplantation and the Najarian footprint Hematin therapy for the neurologic crisis of tyrosinemia Biochemical and Clinical Aspects of Hereditary Tyrosinemia Type 1. NTBC and Correction of Renal Dysfunction. Liver Transplantation for Hereditary Tyrosinaemia Type 1 in the United Kingdom.
is cites work of	wds:Q35198085-900D9AA6-20EA-4A9B-AAFE-F15EF685C04C wds:Q46910574-1B002B29-70D4-4605-B89D-10D68907D5B3 wds:Q24679398-4E51E7B2-9DDA-4494-BC20-47ABB41D8857 wds:Q46826393-4E4B36DE-7AC2-410A-AD6A-E85493A85699 wds:Q45238007-488C72A9-0EF0-49D6-B604-8BD19A2AEFFD wds:Q40584024-6F5135D6-C0DD-4531-8B28-7449C2D6272C wds:Q71754946-F20C7DCA-5B5F-499D-856F-743305AEBF3D wds:Q87269621-5E9C8AAC-C9F1-4420-BFE3-F31C800980A5

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