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Multiple Sclerosis (Houndmills, Basingstoke, England)|November 7, 2012
Acute disseminated encephalomyelitis followed by recurrent or monophasic optic neuritis in pediatric patientsPeter Huppke, Kevin Rostasy, Michael Karenfort, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 11, 2024
CSF and venous blood flow from childhood to adulthood studied by real-time phase-contrast MRIPrativa Sahoo, Jost M Kollmeier, Nora Wenkel, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|July 30, 2014
JC virus antibody status in a pediatric multiple sclerosis cohort: prevalence, conversion rate and influence on disease severityPeter Huppke, Hanna Hummel, David Ellenberger, et al.
Journal of Magnetic Resonance Imaging : JMRI|August 23, 2012
Assessment of myelination in hypomyelinating disorders by quantitative MRISteffi F Dreha-Kulaczewski, Knut Brockmann, Marco Henneke, et al.
Orphanet Journal of Rare Diseases|September 22, 2012
Leukoencephalopathy with accumulated succinate is indicative of SDHAF1 related complex II deficiencyAndreas Ohlenbusch, Simon Edvardson, Johannes Skorpen, et al.
The Journal of Biological Chemistry|July 5, 2007
Live cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3)Merle Hillebrand, Sophie E Verrier, Andreas Ohlenbusch, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|June 2, 2018
Relapse Rate and MRI Activity in Young Adult Patients With Multiple Sclerosis: A Post Hoc Analysis of Phase 3 Fingolimod TrialsJutta Gärtner, Tanuja Chitnis, Angelo Ghezzi, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Typical cMRI pattern as diagnostic clue for D-bifunctional protein deficiency without apparent biochemical abnormalities in plasmaSabine Grønborg, Ralph Krätzner, Juliane Spiegler, et al.
Pediatric Research|March 22, 2008
Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS studySteffi F Dreha-Kulaczewski, Peter Dechent, Jürgen Finsterbusch, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
A new CUL4B variant associated with a mild phenotype and an exceptional pattern of leukoencephalopathySusann Weissbach, Marie-Christine Reinert, Janine Altmüller, et al.
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