Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults. - Wikidata - wikimedia - TriplyDB

Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.

Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.

http://www.wikidata.org/entity/Q33476720

about

Brain imaging in urea cycle disorders Hyperpolarized MR imaging: neurologic applications of hyperpolarized metabolism.13C MRS studies of neuroenergetics and neurotransmitter cycling in humans Glial dysfunction in abstinent methamphetamine abusers.Swift Acetate Glial Assay (SAGA): an accelerated human ¹³C MRS brain exam for clinical diagnostic use.13C MRS of occipital and frontal lobes at 3 T using a volume coil for stochastic proton decoupling.Impact of fasting on human brain acid-base homeostasis using natural abundance (13) C and (31) P MRS Ornithine transcarbamylase deficiency presenting with acute reversible cortical blindness.

P2860

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P2860

Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.

http://www.wikidata.org/entity/Q33476720

description

2009 nî lūn-bûn

@nan

2009 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Ornithine transcarbamylase def ...... lutamate metabolism in adults.

@ast

Ornithine transcarbamylase def ...... lutamate metabolism in adults.

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type

label

Ornithine transcarbamylase def ...... lutamate metabolism in adults.

@ast

Ornithine transcarbamylase def ...... lutamate metabolism in adults.

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prefLabel

Ornithine transcarbamylase def ...... lutamate metabolism in adults.

@ast

Ornithine transcarbamylase def ...... lutamate metabolism in adults.

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RADIOL.2523081878

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Ornithine transcarbamylase def ...... lutamate metabolism in adults.

@en

P2093

Andrea L Gropman

http://www.w3.org/2001/XMLSchema#string

Brian D Ross

http://www.w3.org/2001/XMLSchema#string

Kent C Harris

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Napapon Sailasuta

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Osama Abulseoud

http://www.w3.org/2001/XMLSchema#string

P2860

Automated data processing of [1H-decoupled] 13C MR spectra acquired from human brain in vivo.

Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis.

Incidence of inborn errors of metabolism in British Columbia, 1969-1996.

Mutations and polymorphisms in the human ornithine transcarbamylase gene.

Measurements of the anaplerotic rate in the human cerebral cortex using 13C magnetic resonance spectroscopy and [1-13C] and [2-13C] glucose.

1H MRS allows brain phenotype differentiation in sisters with late onset ornithine transcarbamylase deficiency (OTCD) and discordant clinical presentations.

Clinical NOE 13C MRS for neuropsychiatric disorders of the frontal lobe.

1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.

Cognitive development in children with inborn errors of urea synthesis.

Urea cycle disorders: diagnosis, pathophysiology, and therapy.

P304

833-841

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scholarly article

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10.1148/RADIOL.2523081878

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3

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19567648

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2734894

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