(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2. - Wikidata - awgldk - TriplyDB

(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

http://www.wikidata.org/entity/Q34172946

about

Longitudinal 1H MRS of rat forebrain from infancy to adulthood reveals adolescence as a distinctive phase of neurometabolite development.Quantitative in vivo neurochemical profiling in humans: where are we now?Consensus paper: radiological biomarkers of cerebellar diseases Degenerative Ataxias: challenges in clinical research.Magnetic resonance imaging biomarkers in patients with progressive ataxia: current status and future direction.The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician.Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency.Ultra-High Field Proton MR Spectroscopy in Early-Stage Amyotrophic Lateral Sclerosis.Combined Cerebellar Proton MR Spectroscopy and DWI Study of Patients with Friedreich's Ataxia.

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(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

http://www.wikidata.org/entity/Q34172946

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

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(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

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type

label

(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

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(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

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(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

@ast

(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2.

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J.BRAINRES.2010.08.030

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(1)H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2

@en

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Christopher M Gomez

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Diane Hutter

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H Brent Clark

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Isabelle Iltis

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Khalaf O Bushara

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Myron Gross

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P2860

Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage

Functional role for senataxin, defective in ataxia oculomotor apraxia type 2, in transcriptional regulation

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

Intercellular metabolic compartmentation in the brain: past, present and future.

Autosomal recessive cerebellar ataxias.

N-acetyl aspartate: a marker for neuronal loss or mitochondrial dysfunction.

A novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia.

Assessment of brain white matter fiber bundle atrophy in patients with Friedreich ataxia.

In vivo 1H NMR spectroscopy of the human brain at high magnetic fields: metabolite quantification at 4T vs. 7T.

Noninvasive detection of presymptomatic and progressive neurodegeneration in a mouse model of spinocerebellar ataxia type 1.

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200-210

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scholarly article

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10.1016/J.BRAINRES.2010.08.030

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1358

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2010-08-14T00:00:00Z

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45659338

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20713024

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2949538

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