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Strategies for fighting mitochondrial diseases

Journal of internal medicine, 2020-06, Vol.287 (6), p.665-684

2020

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AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome

Gene therapy, 2017-10, Vol.24 (10), p.661-667

2017

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Mitochondrial disorders

Brain (London, England : 1878), 2004-10, Vol.127 (10), p.2153-2172

2004

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Loss of apoptosis-inducing factor critically affects MIA40 function

Cell death & disease, 2015-07, Vol.6 (7), p.e1814-e1814

2015

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Idebenone Treatment In Leber's Hereditary Optic Neuropathy

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.e188-e188

2011

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Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk

Journal of internal medicine, 2009-02, Vol.265 (2), p.174-192

2009

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Reduced mitochondrial Ca2+ transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase

Cell death and differentiation, 2016-02, Vol.23 (2), p.231-241

2016

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Clinical and molecular features of mitochondrial DNA depletion syndromes

Journal of inherited metabolic disease, 2009-04, Vol.32 (2), p.143-158

2009

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Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cells

Mitochondrion, 2012-03, Vol.12 (2), p.328-335

2012

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SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype

Biochimica et biophysica acta. Molecular basis of disease, 2018-06, Vol.1864 (6), p.2131-2142

2018

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Revisiting mitochondrial ocular myopathies: a study from the Italian Network

Journal of neurology, 2017-08, Vol.264 (8), p.1777-1784

2017

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Clinical and molecular findings in children with complex I deficiency

Biochimica et biophysica acta, 2004-12, Vol.1659 (2), p.136-147

2004

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Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

Science (American Association for the Advancement of Science), 2000-08, Vol.289 (5480), p.782-785

2000

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Properties of a sandy clay loam Haplic Ferralsol and soybean grain yield in a five-year field trial as affected by biochar amendment

Geoderma, 2017-11, Vol.305, p.100-112

2017

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Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations

Neurology, 2005-04, Vol.64 (7), p.1204-1208

2005

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Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease

Journal of medical genetics, 2011-10, Vol.48 (10), p.660-668

2011

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Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases

Neuromuscular disorders : NMD, 2012-12, Vol.22 (3-3), p.S226-S229

2012

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Local and systemic control of powdery mildew in eucalyptus using essential oils and decoctions from traditional Brazilian medicinal plants

Forest pathology = Journal de pathologie forestière = Zeitschrift für Forstpathologie, 2014-04, Vol.44 (2), p.145-153

2014

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GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy

Neurology, 2006-07, Vol.67 (2), p.273-279

2006

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M.I.3 Nuclear genes involved in mitochondrial syndromes

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.764-765

Zeviani, M

2007

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Mitochondrial Diseases in Childhood

Current molecular medicine, 2014-01, Vol.14 (8), p.1069-1078

2014

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Crushed crambe from biodiesel production as replacement for soybean meal in the supplement of steers grazing

Italian journal of animal science, 2019-01, Vol.18 (1), p.316-327

2019

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Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

Neurology, 2003-04, Vol.60 (8), p.1354-1356

2003

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EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias

European journal of neurology, 2009-07, Vol.16 (7), p.777-785

2009

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EFNS guidelines on the molecular diagnosis of mitochondrial disorders

European journal of neurology, 2009-12, Vol.16 (12), p.1255-1264

2009

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Strategies for fighting mitochondrial diseases

AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome

Mitochondrial disorders

Loss of apoptosis-inducing factor critically affects MIA40 function

Idebenone Treatment In Leber's Hereditary Optic Neuropathy

Disorders from perturbations of nuclear‐mitochondrial intergenomic cross‐talk

Reduced mitochondrial Ca2+ transients stimulate autophagy in human fibroblasts carrying the 13514A>G mutation of the ND5 subunit of NADH dehydrogenase

Clinical and molecular features of mitochondrial DNA depletion syndromes

Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cells

SURF1 knockout cloned pigs: Early onset of a severe lethal phenotype

Revisiting mitochondrial ocular myopathies: a study from the Italian Network

Clinical and molecular findings in children with complex I deficiency

Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance

Properties of a sandy clay loam Haplic Ferralsol and soybean grain yield in a five-year field trial as affected by biochar amendment

Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations

Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease

Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases

Local and systemic control of powdery mildew in eucalyptus using essential oils and decoctions from traditional Brazilian medicinal plants

GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy

M.I.3 Nuclear genes involved in mitochondrial syndromes

Mitochondrial Diseases in Childhood

Crushed crambe from biodiesel production as replacement for soybean meal in the supplement of steers grazing

Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias

EFNS guidelines on the molecular diagnosis of mitochondrial disorders

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