Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndrome - Wikidata - awgldk - TriplyDB

Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndrome

Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndrome

http://www.wikidata.org/entity/Q34165551

about

New Pathogenic Concepts and Therapeutic Approaches to Oxidative Stress in Chronic Kidney Disease Diabetic Kidney Disease: A Syndrome Rather Than a Single Disease.Renal manifestations of primary mitochondrial disorders.Mitochondrial dysfunction and risk of cancer Mitochondrial tRNA(Phe) mutation as a cause of end-stage renal disease in childhood.Isolating glomeruli from mice: A practical approach for beginners.Mitochondrial dysfunction in the pathophysiology of renal diseases.Renal manifestations of genetic mitochondrial disease.

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P2860

Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndrome

http://www.wikidata.org/entity/Q34165551

description

2012 nî lūn-bûn

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2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի փետրվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Chronic kidney disease, severe ...... involvement in MELAS syndrome

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Federica Fassio

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Federica Neve Vigotti

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Francesco Porpiglia

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Giorgina Barbara Piccoli

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Isabelle Brocheriou

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Laura Davico Bonino

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Martina Ferraresi

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Paola Campisi

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P2860

Omega-3 fatty acid supplementation attenuates oxidative stress, inflammation, and tubulointerstitial fibrosis in the remnant kidney

Diagnosis and management of MELAS.

Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness

Mechanisms of progression and regression of renal lesions of chronic nephropathies and diabetes.

Renal complications in a patient with A-to-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.

Friedrich Nietzsche (1844-1900): a classical case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome?

Misapplications of commonly used kidney equations: renal physiology in practice

Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.

Implications of mitochondrial DNA mutations and mitochondrial dysfunction in tumorigenesis.

MELAS with recurrent complex partial seizures, nonconvulsive status epilepticus, psychosis, and behavioral disturbances: case analysis with literature review.

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9

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10.1186/1471-2369-13-9

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Gabriella Restagno

Isabelle Brocheriou

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