Neuropathology of mitochondrial diseases. - Wikidata - awgldk - TriplyDB

Neuropathology of mitochondrial diseases.

Neuropathology of mitochondrial diseases.

http://www.wikidata.org/entity/Q34633350

about

Neuropathological diagnosis of vascular cognitive impairment and vascular dementia with implications for Alzheimer's disease Electron Transport Disturbances and Neurodegeneration: From Albert Szent-Györgyi's Concept (Szeged) till Novel Approaches to Boost Mitochondrial Bioenergetics A rapid and accurate approach to identify single nucleotide polymorphisms of mitochondrial DNA using MALDI-TOF mass spectrometry.Young-onset dementia Mitochondrial dysfunction in the striatum of aged chronic mouse model of Parkinson's disease.The neurodegenerative mitochondriopathies.Leukoencephalopathies in mitochondrial disorders: clinical and MRI findings.Region-Specific Defects of Respiratory Capacities in the Ndufs4(KO) Mouse Brain Loss of myelin-associated glycoprotein in kearns-sayre syndrome Clinical and Brain Magnetic Resonance Imaging Features in a Cohort of Chinese Patients with Kearns-Sayre Syndrome.Spectrum of mitochondrial DNA deletions within the common deletion region induced by low levels of UVB irradiation of human keratinocytes in vitro.Abnormal regulation of TSG101 in mice with spongiform neurodegeneration.Mitochondrial DNA variant interactions modify breast cancer risk.Bioenergetic medicine.The possible involvement of mitochondrial dysfunctions in Lewy body dementia: a systematic review.Leigh syndrome: One disorder, more than 75 monogenic causes.Revisiting mitochondrial ocular myopathies: a study from the Italian Network.Redefining phenotypes associated with mitochondrial DNA single deletion.Myopathology of Adult and Paediatric Mitochondrial Diseases.Advances in molecular diagnostics for mitochondrial diseases.Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNA(Trp) gene.Complex I inhibition in the visual pathway induces disorganization of the node of Ranvier.NEWS and VIEWS: mitochondrial encephalomyopathies.Clinical, pathological and functional characterization of riboflavin-responsive neuropathy.A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder."Myo-cardiomyopathy" is commonly associated with the A8344G "MERRF" mutation.Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis.Is deltoid muscle biopsy useful in isolated camptocormia? A prospective study.The role of the cerebellum in the pathogenesis of cortical myoclonus

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P2860

Neuropathology of mitochondrial diseases.

http://www.wikidata.org/entity/Q34633350

description

2007 nî lūn-bûn

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2007 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հունիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年學術文章

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name

Neuropathology of mitochondrial diseases.

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Neuropathology of mitochondrial diseases.

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Neuropathology of mitochondrial diseases.

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type

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Neuropathology of mitochondrial diseases.

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Neuropathology of mitochondrial diseases.

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Neuropathology of mitochondrial diseases.

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Neuropathology of mitochondrial diseases.

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Neuropathology of mitochondrial diseases.

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Neuropathology of mitochondrial diseases.

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S10540-007-9034-3

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Bioscience Reports

P1476

Neuropathology of mitochondrial diseases.

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P2093

Alessandro Padovani

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Alessandro Simonati

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Gaetano Vattemi

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Giuliano Tomelleri

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Massimiliano Filosto

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Mauro Scarpelli

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Nicolò Rizzuto

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Paola Tonin

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P2860

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation.

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia.

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s10540-007-9034-3

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23-30

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10.1007/S10540-007-9034-3

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1-3

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27

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