Pages that link to "Q56446942"
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The following pages link to Chiara La Morgia (Q56446942):
Displaying 50 items.
- Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions (Q21093316) (← links)
- OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes (Q24304868) (← links)
- Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background (Q24678122) (← links)
- Melanopsin-expressing retinal ganglion cells: implications for human diseases (Q27687754) (← links)
- A neurodegenerative perspective on mitochondrial optic neuropathies (Q28072026) (← links)
- Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder (Q28117097) (← links)
- OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation (Q28255026) (← links)
- Syndromic parkinsonism and dementia associated with OPA1 missense mutations (Q28259640) (← links)
- Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy (Q31081831) (← links)
- Medical management of hereditary optic neuropathies (Q33980183) (← links)
- Strio-pallido-dentate calcinosis: a diagnostic approach in adult patients. (Q34177183) (← links)
- The optic nerve: a "mito-window" on mitochondrial neurodegeneration (Q34298350) (← links)
- Secondary post-geniculate involvement in Leber's hereditary optic neuropathy (Q34500034) (← links)
- Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders (Q34958336) (← links)
- The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cells (Q35067031) (← links)
- Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies (Q35116526) (← links)
- Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy? (Q35636297) (← links)
- Macular Microcysts in Mitochondrial Optic Neuropathies: Prevalence and Retinal Layer Thickness Measurements. (Q35654658) (← links)
- Mitochondrial optic neuropathies: how two genomes may kill the same cell type? (Q36811238) (← links)
- Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions (Q37187580) (← links)
- Mitochondrial dysfunction in optic neuropathies: animal models and therapeutic options (Q38072808) (← links)
- Mitochondrial optic neuropathies: our travels from bench to bedside and back again. (Q38083877) (← links)
- Macular nerve fibre and ganglion cell layer changes in acute Leber's hereditary optic neuropathy (Q38937826) (← links)
- P027. Idiopathic intracranial hypertension without papilledema in refractory chronic daily headache (Q42075104) (← links)
- 'Behr syndrome' with OPA1 compound heterozygote mutations (Q42538852) (← links)
- Retinal function and neural conduction along the visual pathways in affected and unaffected carriers with Leber's hereditary optic neuropathy. (Q44043383) (← links)
- Microcystic macular degeneration from optic neuropathy: not inflammatory, not trans-synaptic degeneration. (Q45818795) (← links)
- Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlation (Q46722740) (← links)
- Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. (Q46793891) (← links)
- Narcolepsy is a common phenotype in HSAN IE and ADCA-DN. (Q48113682) (← links)
- Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1. (Q48114747) (← links)
- Idebenone treatment in patients with OPA1-mutant dominant optic atrophy (Q48173657) (← links)
- Diffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies (Q48270984) (← links)
- Multifocal VEP provide electrophysiological evidence of predominant dysfunction of the optic nerve fibers derived from the central retina in Leber's hereditary optic neuropathy (Q48279017) (← links)
- Sleep-related periodic respiration with central sleep apnea in Leber Hereditary Optic Neuropathy (LHON). (Q48377717) (← links)
- 'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2. (Q48412586) (← links)
- International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy (Q48577544) (← links)
- Idebenone treatment in Leber's hereditary optic neuropathy. (Q48968245) (← links)
- A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intolerance (Q50355104) (← links)
- Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations (Q51752193) (← links)
- Nocturnal melatonin regulation in post-traumatic vegetative state: a possible role for melatonin supplementation? (Q52648927) (← links)
- Optical coherence tomography angiography of the peripapillary retina and optic nerve head in dominant optic atrophy. (Q53516001) (← links)
- High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families. (Q54418514) (← links)
- Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern? (Q54522196) (← links)
- Idiopathic Intracranial Hypertension Without Papilledema (IIHWOP) in Chronic Refractory Headache (Q56378366) (← links)
- Epilepsy in coeliac disease: not just a matter of calcifications (Q56983781) (← links)
- Retinal nerve fiber layer thickness in dominant optic atrophy measurements by optical coherence tomography and correlation with age (Q56984401) (← links)
- Augmentation of restless legs syndrome with long-term tramadol treatment (Q56995821) (← links)
- Leber's hereditary optic neuropathy with childhood onset (Q56996756) (← links)
- Leber’s Hereditary Optic Neuropathy (Q57721071) (← links)