Batteries not included: diagnosis and management of mitochondrial disease.
about
Leber hereditary optic neuropathy: current perspectivesMitochondrial disorders: challenges in diagnosis & treatmentA computational screen for regulators of oxidative phosphorylation implicates SLIRP in mitochondrial RNA homeostasis.Control of mitochondrial integrity in ageing and diseaseInherited mitochondrial DNA variants can affect complement, inflammation and apoptosis pathways: insights into mitochondrial-nuclear interactions.Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor.The neuro-ophthalmology of mitochondrial diseaseMitochondrial DNA variants mediate energy production and expression levels for CFH, C3 and EFEMP1 genes: implications for age-related macular degeneration.Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.Causes of Death in Adults with Mitochondrial DiseaseThe ageing neuromuscular system and sarcopenia: a mitochondrial perspective.Mitochondrial disease in pregnancy: a systematic review.The Neuro-Immune Pathophysiology of Central and Peripheral Fatigue in Systemic Immune-Inflammatory and Neuro-Immune Diseases.Chemotherapy-Induced Neuropathy in Cancer Survivors.Increased expression of ApoE and protection from amyloid-beta toxicity in transmitochondrial cybrids with haplogroup K mtDNA.Myopathology of Adult and Paediatric Mitochondrial Diseases.Truth is a daughter of time: a case of MELAS diagnosed 25 years after initial manifestation.A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephaly.Pontocerebellar hypoplasia type 6 caused by mutations in RARS2: definition of the clinical spectrum and molecular findings in five patients.Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans.Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency.Quantification of changes in muscle from individuals with and without mitochondrial disease.The Role of Mitochondria in AMD: Current Knowledge and Future Applications.Hearing loss and tinnitus in survivors with chemotherapy-induced neuropathy.Human diseases associated with defects in assembly of OXPHOS complexesNeurobiology, pathophysiology, and treatment of melatonin deficiency and dysfunction
P2860
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P2860
Batteries not included: diagnosis and management of mitochondrial disease.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Batteries not included: diagnosis and management of mitochondrial disease.
@en
Batteries not included: diagnosis and management of mitochondrial disease.
@nl
type
label
Batteries not included: diagnosis and management of mitochondrial disease.
@en
Batteries not included: diagnosis and management of mitochondrial disease.
@nl
prefLabel
Batteries not included: diagnosis and management of mitochondrial disease.
@en
Batteries not included: diagnosis and management of mitochondrial disease.
@nl
P2860
P1476
Batteries not included: diagnosis and management of mitochondrial disease
@en
P2093
D M Turnbull
P2860
P304
P356
10.1111/J.1365-2796.2008.02066.X
P407
P577
2009-02-01T00:00:00Z