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Mitochondrial Diseases
Mitochondrial diseases
Overview
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Mitochondrial genetics
Human mitochondrial DNA
Mitochondrial dna
Mitochondrial eve
Cambridge Reference Sequence
CoRR Hypothesis
Eurasian Adam
Genes on chromosome MT
Genetic disorders
(14)
Hereditary diseases
Ragged red fibers
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
Carnitine deficiency
Methylmalonic aciduria
Methylmalonic aciduria
MNGIE
Metachromatic leukodystrophy
Friedreich ataxia
LHON
Muscular dystrophies
Pearson syndrome
Neuropathy, ataxia, and retinitis pigmentosa
Spinocerebellar ataxia
Homocystinuria
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Diseases and disorders
(28)
Mitochondrial myopathy
Metabolic diseases
Myopathies
Ophthalmoplegia
Mitochondrial myopathy-e- ncephalopa- thy-lactic acidosis
Mitochondrial myopathy-e- ncephalopathy-lactic acidosis
Leigh syndrome
Chronic Progressive External Ophthalmoplegia
Myoclonic epilepsy
Mixed connective tissue disease
Myoclonus epilepsy
Lipid storage myopathy
Endocrine diseases
Acute disseminated encephalomyelitis
Hyperammonemia
Diabetes mellitus and deafness
Demyelinating disease
Metabolic disorders
Glycogen storage disease
Optic atrophy
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
Carnitine deficiency
Methylmalonic aciduria
Metachromatic leukodystrophy
Friedreich ataxia
LHON
Muscular dystrophies
Pearson syndrome
Homocystinuria
more...
Cellular respiration
(57)
Atp synthase
Coenzyme Q
Complex III
Cristae
Cytochrome c oxidase
Cytochrome c oxidase
Mitochondrial
Oxidative phosphorylation
Respiratory chain
ATP hydrolysis
ATP/ADP Translocase
Adenosine diphosphate
Adenosine triphosphate
Adenylate kinase
Aerobic organism
Alternative oxidase
Anaerobic organism
Anaerobic respiration
Anaplerotic reactions
Beta oxidation
Chemiosmosis
Citric acid cycle
Complete glucose breakdown
Cytochrome c
D-amino acid dehydrogenase
Electrochemical gradient
Electron-t- ransferring-flavoprotein dehydrogenase
Ethanol fermentation
Facultative anaerobic organism
Flavin group
Formate dehydrogenase
Glucose metabolism disorders
Glycolysis
Lactic acid fermentation
Maintenance respiration
Malate dehydrogenase
Malate-aspartate shuttle
Malic acid
Methemoglobin
Methylglyoxal pathway
Mitochondrial permeability transition
NAD+ kinase
NADH dehydrogenase
Nanaerobe
Nicotinamide adenine dinucleotide
Phosphate homeostasis
Photosynthesis
Pyruvate decarboxylation
Pyruvate dehydrogenase complex
Pyruvic acid
Q cycle
Quinone-interacting membrane-bound oxidoreductase
Submitochondrial particle
Substrate-level phosphorylation
Thermogenin
Trimethylamine N-oxide reductase
Ubiquinol oxidase
petite mutation
more...
Organelles
Mitochondria
Peroxisomes
Mitochondrial
DNA
Nuclear DNA
Haplogroups
Mitochondrial dna
Mitochondrial eve
Mitochondrial diseases
(16)
Kearns-Sayre syndrome
Diabetes mellitus and deafness
Friedreich ataxia
LHON
Leigh syndrome
Leigh syndrome
MNGIE
Mitochondrial disease
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
Mitochondrial myopathy
Neuropathy, ataxia, and retinitis pigmentosa
Nonsyndromic deafness
Pearson syndrome
Progressive external ophthalmoplegia
Ragged red fibers
Threshold expression
Wolfram syndrome
more...
Muscular disorders
(23)
Arthrogryposis
Central core disease
Centronuclear myopathy
Chronic Progressive External Ophthalmoplegia
Congenital myopathy
Congenital myopathy
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathy
Muscular dystrophies
Myokmia
Myopathies
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
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Genetics
(8)
Maternal inheritance
Mendelian
Mutations
Neurogenetics
Nuclear gene
Nuclear gene
Mitochondrial genetics
Genetic disorders
Hereditary diseases
more...
Muscular system
Muscle biopsy
Muscular diseases
Neuromuscular diseases
Skeletal muscle
See also
(20)
Mitochondrial biogenesis
Metabolism
UMDF
Intermembrane space
Neurodegenerative diseases
Neurodegenerative diseases
Dichloroacetate
Mitochondrial matrix
Complex II
Fatty acid oxidation
Cytochrome b
Lactic acidosis
Hannah Poling
Mitochondrial toxicity
Acyl CoA dehydrogenase
George Chinnery
Heteroplasmy
Friedreich
Dr. David Samuels
Pro-apoptotic
Free radical theory of aging
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