(Q57911781)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Evidence for retrochiasmatic tissue loss in Leber's hereditary optic neuropathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

hereditary optic neuropathy

13 February 2020

main subject

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Andrea Falini

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Massimo Filippi

8

1 reference

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13 February 2020

Stefania Bianchi Marzoli

3

object named as

Stefania Bianchi-Marzoli

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

4

Jacopo Milesi

1 reference

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13 February 2020

1

Valeria Barcella

1 reference

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13 February 2020

author name string

Lisa Melzi

5

1 reference

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13 February 2020

Luisa Pierro

7

1 reference

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13 February 2020

publication date

13 May 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

number of pages

7

0 references

published in

Human Brain Mapping

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

volume

31

1 reference

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13 February 2020

issue

12

1 reference

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13 February 2020

page(s)

1900-1906

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

Leber's hereditary optic neuropathy: Genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family

13 February 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FHBM.20985

White matter fiber tracts of the human brain: three-dimensional mapping at microscopic resolution, topography and intersubject variability

21 January 2018

1 reference

12 December 2020

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

12 December 2020

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations

1 reference

12 December 2020

Magnetic resonance imaging in Leber's optic neuropathy

1 reference

12 December 2020

Selective magnetization transfer ratio decrease in the visual cortex following optic neuritis.

1 reference

12 December 2020

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

Quantifying axonal loss after optic neuritis with optical coherence tomography.

1 reference

12 December 2020

Voxel-based morphometry–the methods

1 reference

12 December 2020

Regional lobar atrophy predicts memory impairment in multiple sclerosis.

1 reference

12 December 2020

Leber hereditary optic neuropathy: respiratory chain dysfunction and degeneration of the optic nerve

1 reference

12 December 2020

Brain volumetrics to investigate aging and the principal forms of degenerative cognitive decline: a brief review

1 reference

12 December 2020

Focal thinning of the cerebral cortex in multiple sclerosis

1 reference

12 December 2020

Semi-automatic brain region extraction (SABRE) reveals superior cortical and deep gray matter atrophy in MS

1 reference

12 December 2020

Leber's hereditary optic atrophy: some clinical and aetiological considerations.

1 reference

12 December 2020

Assessing atrophy of the major white matter fiber bundles of the brain from diffusion tensor MRI data

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets

1 reference

12 December 2020

Retinal nerve fiber layer is associated with brain atrophy in multiple sclerosis

1 reference

12 December 2020

A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

1 reference

12 December 2020

Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation

1 reference

12 December 2020

Magnetization transfer and diffusion tensor MR imaging of the optic radiations and calcarine cortex from patients with Leber's hereditary optic neuropathy

1 reference

12 December 2020

Magnetic resonance imaging, magnetisation transfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damage in Leber's hereditary optic neuropathy.

1 reference

12 December 2020

Leber's hereditary optic neuropathy differentially affects smaller axons in the optic nerve.

1 reference

12 December 2020

Optic nerve atrophy and retinal nerve fibre layer thinning following optic neuritis: evidence that axonal loss is a substrate of MRI-detected atrophy

1 reference

12 December 2020

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

1 reference

12 December 2020

The neuropathology of hereditary optic atrophy (Leber's disease); the first complete anatomic study.

1 reference

12 December 2020

Optical coherence tomography in multiple sclerosis

1 reference

12 December 2020

The measurement and clinical relevance of brain atrophy in multiple sclerosis

1 reference

12 December 2020

Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutation

1 reference

12 December 2020

A fast diffeomorphic image registration algorithm

1 reference

12 December 2020

Retinal abnormalities in human albinism translate into a reduction of grey matter in the occipital cortex

1 reference

12 December 2020

Changes in cortical grey matter density associated with long-standing retinal visual field defects

1 reference

12 December 2020

Mitochondrial dysfunction as a cause of optic neuropathies

1 reference

12 December 2020

Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studies

1 reference

12 December 2020

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

Analysis of fMRI Time-Series Revisited

1 reference

12 December 2020

Effects of retinal ganglion cell loss on magno-, parvo-, koniocellular pathways in the lateral geniculate nucleus and visual cortex in glaucoma

1 reference

12 December 2020

Identifiers

DOI

10.1002/HBM.20985

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20827728%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference