Sage Journals: Discover world-class research

Retricted access

Research article

First published 2012-7

The time course and phenotype of Uhthoff phenomenon following optic neuritis

Clare L Fraser, Indran Davagnanam, Mark Radon [...]

Multiple Sclerosis Journal

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Case report

First published 2023-7

Diabetic papillopathy in patients with optic disc drusen: Description of two different phenotypes

Daniel Becker, Michael Larsen, Henrik Lund-Andersen [...]

European Journal of Ophthalmology

Open access

Research article

First published 2016

Relapsing optic neuritis and isolated transverse myelitis are the predominant clinical phenotypes for patients with antibodies to myelin oligodendrocyte glycoprotein in India

Lekha Pandit, Douglas Kazutoshi Sato, Sharik Mustafa [...]

Multiple Sclerosis Journal – Experimental,Translational and Clinical

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Research article

First published 2018-07

Phenotyping the Microvasculature in Critical-Sized Calvarial Defects via Multimodal Optical Imaging

Adam Mendez, Alexandra N. Rindone, Namrata Batra [...]

Tissue Engineering Part C: Methods

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Case report

First published 2023-12

Dominant Optic Atrophy With Varied Phenotype in a Family of Eastern India: A Case Report of a Rare Mutation

Camelia Porey, Binaya Kumar Jaiswal

Indian Journal of Clinical Medicine

Open access

Research article

First published 2025

A multimodal approach to distinguish multiple sclerosis phenotypes at diagnosis using biomarker profiles

Aurora Zanghì, Paola Sofia Di Filippo, Annamaria Greco [...]

Therapeutic Advances in Neurological Disorders

Open access

Research article

First published 2019-05

Single-Cell RNA-Sequencing and Optical Electrophysiology of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Reveal Discordance Between Cardiac Subtype-Associated Gene Expression Patterns and Electrophysiological Phenotypes

Sherri M. Biendarra-Tiegs, Xing Li, Dan Ye [...]

Stem Cells and Development

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Research article

First published 2005-10

Apo E in multiple sclerosis and optic neuritis: the Apo E-o4 allele is associated with progression of multiple sclerosis

M Pinholt, J L Frederiksen, P S Andersen [...]

Multiple Sclerosis Journal

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Research article

First published 2014-8

Uncommon Leber “Plus” Disease Associated With Mitochondrial Mutation m.11778G>A in a Premature Child

Stéphanie Paquay, Valérie Benoit, Catherine Wetzburger [...]

Journal of Child Neurology

Open access

Case report

First published 2018-5

Wolff-Parkinson-White syndrome and noncompaction in Leber’s hereditary optic neuropathy due to the variant m.3460G>A

Josef Finsterer, Claudia Stollberger, Edmund Gatterer

Journal of International Medical Research

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