Alexander U. Brandt researcher
Brandt, Alexander Ulrich 1975-
VIAF ID: 311733404 (Personal)
Permalink: http://viaf.org/viaf/311733404
Preferred Forms
4xx's: Alternate Name Forms (2)
5xx's: Related Names (1)
Works
Title | Sources |
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APOSTEL 2.0 recommendations for reporting quantitative optical coherence tomography studies | |
Considerations for Mean Upper Cervical Cord Area Implementation in a Longitudinal MRI Setting: Methods, Interrater Reliability, and MRI Quality Control | |
Cortical topological network changes following optic neuritis | |
Effect of vitamin D supplementation on N-glycan branching and cellular immunophenotypes in MS | |
Epigallocatechin Gallate in Relapsing-Remitting Multiple Sclerosis | |
Evaluation of the 'ring sign' and the 'core sign' as a magnetic resonance imaging marker of disease activity and progression in clinically isolated syndrome and early multiple sclerosis | |
High-dose vitamin D supplementation in multiple sclerosis - results from the randomized EVIDIMS (efficacy of vitamin D supplementation in multiple sclerosis) trial | |
Intrathecal IgM production is a strong risk factor for early conversion to multiple sclerosis | |
Longitudinal optic neuritis-unrelated visual evoked potential changes in NMO spectrum disorders | |
A novel investigation method for axonal damage in neuromyelitis optica spectrum disorder: In vivo corneal confocal microscopy | |
Optic nerve head volumetry by optical coherence tomography in papilledema related to idiopathic intracranial hypertension | |
Optical coherence tomography in myelin-oligodendrocyte-glycoprotein antibody-seropositive patients: a longitudinal study | |
Optimal intereye difference thresholds by optical coherence tomography in multiple sclerosis: An international study | |
Pain in AQP4-IgG-positive and MOG-IgG-positive neuromyelitis optica spectrum disorders. | |
Retinal inner nuclear layer volume reflects inflammatory disease activity in multiple sclerosis; a longitudinal OCT study | |
Spinal cord lesions and atrophy in NMOSD with AQP4-IgG and MOG-IgG associated autoimmunity | |
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder |