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Nature Genetics|July 16, 2002
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeKirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.Cell Reports|June 1, 2026
Mutational signatures of environmental carcinogens in human tissue organoids revealed by duplex sequencingJill E Kucab, Shuvro P Nandi, Halh Al-Serori, et al.Brain Communications|October 24, 2024
The use of 7T MRI in multiple sclerosis: review and consensus statement from the North American Imaging in Multiple Sclerosis CooperativeDaniel M Harrison, Pascal Sati, Eric C Klawiter, et al.Medrxiv : the Preprint Server for Health Sciences|October 27, 2023
Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosisErin S Beck, W Andrew Mullins, Jonadab Dos Santos Silva, et al.Brain Communications|May 31, 2024
Contribution of new and chronic cortical lesions to disability accrual in multiple sclerosisErin S Beck, W Andrew Mullins, Jonadab Dos Santos Silva, et al.The Lancet. Neurology|July 24, 2021
BK virus-specific T cells for immunotherapy of progressive multifocal leukoencephalopathy: an open-label, single-cohort pilot studyIrene Cortese, Erin S Beck, Omar Al-Louzi, et al.Radiology|February 7, 2023
Multicenter Evaluation of AI-generated DIR and PSIR for Cortical and Juxtacortical Multiple Sclerosis Lesion DetectionPiet M Bouman, Samantha Noteboom, Fernando A Nobrega Santos, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|June 1, 2026
Spinal cord imaging for multiple sclerosis: Advances, priorities, and opportunitiesCornelia Laule, Julien Cohen-Adad, Atlee A Witt, et al.Nature Communications|December 18, 2025
Pre- and postsynaptic upregulation of FasII synergistically underlies neuropathological and behavioral phenotypes in a Drosophila model of myotonic dystrophyAlex Chun Koon, Ka Yee Winnie Yeung, Yitao Wu, et al.Molecular Psychiatry|November 21, 2012
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorderI Jarick, A-L Volckmar, C Pütter, et al.Pageof 67