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Leber's hereditary optic neuropathy: the ophthalmologist point of view

Acta ophthalmologica (Oxford, England), 2017-09, Vol.95 (S259), p.n/a

Barboni, P.

2017

Volltextzugriff (PDF)

Primary mitochondrial optic neuropathies

Acta ophthalmologica (Oxford, England), 2017-09, Vol.95 (S259), p.n/a

Barboni, P.

2017

Volltextzugriff (PDF)

Vascular supply in mitochondrial optic neuropathy and glaucoma

Acta ophthalmologica (Oxford, England), 2015-10, Vol.93 (S255), p.n/a

Barboni, P.

2015

Volltextzugriff (PDF)

Idebenone Treatment In Leber's Hereditary Optic Neuropathy

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

2011

Volltextzugriff (PDF)

OCT angiography in mitochondrial optic neuropathies

Acta ophthalmologica (Oxford, England), 2016-10, Vol.94 (S256), p.n/a

2016

Volltextzugriff (PDF)

Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?

European journal of neurology, 2013-01, Vol.20 (1), p.198-201

2013

Volltextzugriff (PDF)

Correlation between retinal nerve fibre layer thickness and optic nerve head size: an optical coherence tomography study

British journal of ophthalmology, 2005-04, Vol.89 (4), p.489-492

2005

Volltextzugriff (PDF)

Neurological involvement in mitochondrial eye diseases

Acta ophthalmologica (Oxford, England), 2017-09, Vol.95 (S259), p.n/a

2017

Volltextzugriff (PDF)

Effect of pupil dilation on retinal nerve fibre layer thickness measurements and their repeatability with Cirrus HD-OCT

Eye (London), 2010-09, Vol.24 (9), p.1503-1508

2010

Volltextzugriff (PDF)

Optical coherence tomography in the differential diagnosis of true edema versus pseudoedema of the optic disc

Acta ophthalmologica (Oxford, England), 2017-09, Vol.95 (S259), p.n/a

2017

Volltextzugriff (PDF)

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus

Neurology, 2008-03, Vol.70 (10), p.762

2008

Volltextzugriff (PDF)

International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy

Journal of neuro-ophthalmology, 2017-12, Vol.37 (4), p.371-381

2017

Volltextzugriff (PDF)

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

The Journal of clinical investigation, 2020-01, Vol.130 (1), p.108-125

2020

Volltextzugriff (PDF)

The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype

Journal of medical genetics, 2006-07, Vol.43 (7), p.e38-e38

2006

Volltextzugriff (PDF)

Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy

Journal of neurology, neurosurgery and psychiatry, 2002-06, Vol.72 (6), p.805-807

2002

Volltextzugriff (PDF)

Idebenone treatment in patients with OPA1-mutant dominant optic atrophy

Brain (London, England : 1878), 2013-02, Vol.136 (Pt 2), p.e231-e231

2013

Volltextzugriff (PDF)

Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy

Ophthalmology (Rochester, Minn.), 2005, Vol.112 (1), p.120-126

2005

Volltextzugriff (PDF)

Medical management of hereditary optic neuropathies

Frontiers in neurology, 2014-01, Vol.5, p.141-141

2014

Volltextzugriff (PDF)

Tear meniscus evaluation by optical coherence tomography

Ophthalmic surgery, lasers & imaging, 2006-03, Vol.37 (2), p.112

2006

Volltextzugriff (PDF)

Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy

Annals of neurology, 2004-11, Vol.56 (5), p.719-723

2004

Volltextzugriff (PDF)

Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations

Ophthalmology (Rochester, Minn.), 2005, Vol.112 (1), p.127-131

2005

Volltextzugriff (PDF)

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient

Journal of the neurological sciences, 1998-10, Vol.160 (2), p.183-188

1998

Volltextzugriff (PDF)

G.P.18.05 Myopathy and retinopathy are novel features in a patient with Mohr-Tranebjaerg syndrome

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.891-891

2007

Volltextzugriff (PDF)

The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy

Annals of neurology, 2004-11, Vol.56 (5), p.631-641

2004

Volltextzugriff (PDF)

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Leber's hereditary optic neuropathy: the ophthalmologist point of view

Primary mitochondrial optic neuropathies

Vascular supply in mitochondrial optic neuropathy and glaucoma

Idebenone Treatment In Leber's Hereditary Optic Neuropathy

OCT angiography in mitochondrial optic neuropathies

Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?

Correlation between retinal nerve fibre layer thickness and optic nerve head size: an optical coherence tomography study

Neurological involvement in mitochondrial eye diseases

Effect of pupil dilation on retinal nerve fibre layer thickness measurements and their repeatability with Cirrus HD-OCT

Optical coherence tomography in the differential diagnosis of true edema versus pseudoedema of the optic disc

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus

International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype

Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy

Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy

Idebenone treatment in patients with OPA1-mutant dominant optic atrophy

Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy

Medical management of hereditary optic neuropathies

Tear meniscus evaluation by optical coherence tomography

Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy

Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient

G.P.18.05 Myopathy and retinopathy are novel features in a patient with Mohr-Tranebjaerg syndrome

The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy

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