Brain and muscle energy metabolism studied in vivo by 31P-magnetic resonance spectroscopy in NARP syndrome - Wikidata - wikimedia - TriplyDB

Brain and muscle energy metabolism studied in vivo by 31P-magnetic resonance spectroscopy in NARP syndrome

Brain and muscle energy metabolism studied in vivo by 31P-magnetic resonance spectroscopy in NARP syndrome

http://www.wikidata.org/entity/Q33733427

about

Diagnosis of inherited metabolic disorders affecting the nervous system Brain and skeletal muscle bioenergetic failure in familial hypobetalipoproteinaemia Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993 Neuroimaging of mitochondrial disease.Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck Magnetic resonance imaging biomarkers in patients with progressive ataxia: current status and future direction.Phosphorus and proton magnetic resonance spectroscopy demonstrates mitochondrial dysfunction in early and advanced Parkinson's disease.

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P2860

Brain and muscle energy metabolism studied in vivo by 31P-magnetic resonance spectroscopy in NARP syndrome

http://www.wikidata.org/entity/Q33733427

description

1994 nî lūn-bûn

@nan

1994 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1994 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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1994年の論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年论文

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name

Brain and muscle energy metabo ...... spectroscopy in NARP syndrome

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Brain and muscle energy metabo ...... spectroscopy in NARP syndrome

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Brain and muscle energy metabo ...... spectroscopy in NARP syndrome

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Brain and muscle energy metabo ...... spectroscopy in NARP syndrome

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Journal of Neurology, Neurosurgery and Psychiatry

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Brain and muscle energy metabo ...... spectroscopy in NARP syndrome

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P2860

Cytosolic phosphorylation potential

Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

Prenatal diagnosis of mitochondrial DNA8993 T----G disease.

Retinitis pigmentosa, ataxia, and mental retardation associated with mitochondrial DNA mutation in an Italian family.

Multiple controls of oxidative metabolism in living tissues as studied by phosphorus magnetic resonance.

Control of oxidative metabolism and oxygen delivery in human skeletal muscle: a steady-state analysis of the work/energy cost transfer function.

Phosphorus magnetic resonance spectroscopy of patients with mitochondrial cytopathies demonstrates decreased levels of brain phosphocreatine.

The mitochondrial DNA mutation at 8993 associated with NARP slows the rate of ATP synthesis in isolated lymphoblast mitochondria.

Metabolic recovery after exercise and the assessment of mitochondrial function in vivo in human skeletal muscle by means of 31P NMR.

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