About: Partial ornithine transcarbamylase deficiency simulating Reye syndrome

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scientific article published on 01 December 1981

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1981 (uk) article scientifique publié en 1981 (fr) artículu científicu espublizáu n'avientu de 1981 (ast) im Dezember 1981 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 December 1981 (en)
publication date	wds:Q71008498-F10F708A-E49A-4166-9733-CB712382C0D9
publication date	1981-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71008498-BB42F3B7-5304-48C6-BF09-91B0A26B7051
language of work or name	English
cites work	wds:Q71008498-0C63AC08-F97F-4732-BEE2-09591C690E66 wds:Q71008498-0D257941-CF7F-4ED0-83FF-EA8793CFC2A2 wds:Q71008498-18AEBB1C-F999-45E6-8A61-3730331B92D5 wds:Q71008498-3357E275-1D7A-4737-A77C-AE1085A27060 wds:Q71008498-5D5C1239-3859-49BC-831E-0D575BC34790 wds:Q71008498-7D452708-F0A9-4E16-8D93-A9472069F0BA wds:Q71008498-9766A42C-497A-4F53-ABD3-3FCE6BC33B44 wds:Q71008498-A1CF68E9-2FEA-4C87-9864-1727DF299CE6 wds:Q71008498-FDDE8EAF-BDC7-4D12-8A1F-B525141B1866
cites work	Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency. A direct method for the estimation of ornithine carbamoyltransferase activity in serum Atypical Clinical Course of Ornithine Transcarbamyiase Deficiency Due to a New Mutant (Comparison with Reye's Disease) A COLORIMETRIC DETERMINATION OF OROTIC ACID Role of argininosuccinate synthetase in the regulation of urea synthesis in the rat and argininosuccinate synthetase-associated metabolic disorder in man Some kinetic properties of liver ornithine carbamoyl transferase (oct) in a patient with oct deficiency Hereditary ornithine transcarbamylase deficiency. Report of two male cases with residual enzymatic activity Ornithine transcarbamylase deficiency in a boy with normal development
author name string	wds:Q71008498-4B0933BE-CCC4-413A-A79B-95040C3F8329 wds:Q71008498-4F906CCD-D3F7-46E6-A354-8B09C4B63C6F wds:Q71008498-6CD753A3-23B4-4A0B-9B9E-16AE687FD6A3 wds:Q71008498-6E77AAA1-8624-4543-95E8-821FCF876030 wds:Q71008498-7C8D45E5-F396-4DCA-9011-B4F75F6353D8 wds:Q71008498-849FD769-BCE9-45F5-A841-4AF70BB3EC75 wds:Q71008498-DD7C290F-DA98-44EF-9819-A9156607ADCF wds:Q71008498-F5B68A65-D7DA-4E70-980F-B3F7B6786948
author name string	M Hosoya Y Suzuki R Hayashi N Taniguchi T Saheki T Yokoi T Funabashi K Honke
rdfs:label	Partial ornithine transcarbamylase deficiency simulating Reye syndrome (en) Partial ornithine transcarbamylase deficiency simulating Reye syndrome (nl)
skos:prefLabel	Partial ornithine transcarbamylase deficiency simulating Reye syndrome (en) Partial ornithine transcarbamylase deficiency simulating Reye syndrome (nl)
name	Partial ornithine transcarbamylase deficiency simulating Reye syndrome (en) Partial ornithine transcarbamylase deficiency simulating Reye syndrome (nl)
title	wds:Q71008498-45305158-8987-4F9C-9DF7-7F456C612CB0
title	Partial ornithine transcarbamylase deficiency simulating Reye syndrome (en)
page(s)	wds:Q71008498-46F880AB-BC04-40E9-9833-334CB2D3EADF
page(s)	929-931
instance of	wds:Q71008498-3B7F00BA-129B-4C64-B4EA-E97A6B660CC6
instance of	scholarly article
main subject	wds:Q71008498-C81526A1-4DC0-498D-885E-0084122B74E0
main subject	Reye syndrome
PubMed ID	wds:Q71008498-AF280139-A783-4244-962F-09764E7D187F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7310587
PubMed ID	7310587
published in	wds:Q71008498-B747C170-4AD7-4D03-94E3-AEB3954E1E8A
published in	The Journal of Pediatrics
issue	wds:Q71008498-F06B9CBD-4855-4216-BCE0-D49CC43AB8A2
volume	wds:Q71008498-9A34B16F-7BA2-4807-AB04-885A9F96D10F
issue	6
volume	99
DOI	wds:Q71008498-8B3DD05F-FD47-4333-A748-2412DB300C6A
DOI	http://dx.doi.org/10.1016/S0022-3476(81)80025-X
DOI	10.1016/S0022-3476(81)80025-X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71008498
is cites work of	A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiency X-linked dominant inherited diseases with lethality in hemizygous males Significant hepatic involvement in patients with ornithine transcarbamylase deficiency Late onset ornithine carbamoyl transferase deficiency in males Ammonia metabolism in the CNS Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency Structural organization of the human ornithine transcarbamylase gene Molecular basis of ornithine transcarbamylase deficiency lacking enzyme protein Reye's syndrome in Olmsted County, Minnesota: did it exist before 1963? Ornithine transcarbamylase deficiency: a case with a truncated enzyme precursor and a case with undetectable mRNA activity
is cites work of	wds:Q33804620-3399C93A-161F-42B9-B13F-DA3DDBB2059D wds:Q35528677-8C952742-F579-423C-AB57-E400DB7A0ACD wds:Q30412871-0BCBE45E-59DF-440E-937E-F1AC689581D7 wds:Q42112096-64593337-5B04-4215-9C54-6034B82297C4 wds:Q68276775-DE6B12ED-9BD1-4DF9-8532-9DE3CC0176EA wds:Q39109681-91018945-8210-4589-8AA9-3ED522381444 wds:Q67240665-319050D7-D9CC-41AE-ACE6-1D7323ED79EB wds:Q34108827-783326C4-9AAC-4AAF-8BB0-B14C892AD42A wds:Q48853933-013D37A5-6026-4AC1-9A7E-9F1EC04EEED1 wds:Q70303097-C0F1025D-0F7C-4458-A4E5-EEA8F651162B

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