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BMC Medical Genetics|February 24, 2010
Study of the serotonin transporter (SLC6A4) and BDNF genes in French patients with non syndromic mental deficiencyRefaat Tabagh, Christian R Andres, Sylviane Védrine, et al.
Neuroscience Letters|January 18, 2011
A functional tetranucleotide (AAAT) polymorphism in an Alu element in the NF1 gene is associated with mental retardationSylviane Marouillat Védrine, Patrick Vourc'h, Refaat Tabagh, et al.
Contemporary Clinical Trials|June 12, 2022
A novel 'social contract' - An attempt to harmonize a sponsor's exploratory research with a clinical study participant's data rightsLaurence Mignon, Kim Doan, Michael Murphy, et al.
Annals of Clinical and Translational Neurology|January 22, 2025
Comprehensive assessment reveals numerous clinical and neurophysiological differences between MECP2-allelic disordersDavut Pehlivan, Chengjun Huang, Holly K Harris, et al.
Nature Communications|November 12, 2024
A framework for N-of-1 trials of individualized gene-targeted therapies for genetic diseasesOlivia Kim-McManus, Joseph G Gleeson, Laurence Mignon, et al.
Nature Medicine|August 9, 2024
Antisense oligonucleotide therapy in an individual with KIF1A-associated neurological disorderAlban Ziegler, Joanne Carroll, Jennifer M Bain, et al.
JAMA Neurology|October 30, 2023
Exploratory Tau Biomarker Results From a Multiple Ascending-Dose Study of BIIB080 in Alzheimer Disease: A Randomized Clinical TrialAmanda L Edwards, Jessica A Collins, Candice Junge, et al.
Nature Medicine|July 21, 2026
Individualized antisense oligonucleotides for SCN2A-related developmental epileptic encephalopathyOlivia Kim-McManus, Laurence Mignon, Julie Douville, et al.
Neurology|April 26, 2019
Nusinersen in later-onset spinal muscular atrophy: Long-term results from the phase 1/2 studiesBasil T Darras, Claudia A Chiriboga, Susan T Iannaccone, et al.
Nucleic Acids Research|June 2, 2026
Addressing the needs of nano-rare patients: the n-Lorem experienceStanley T Crooke, Sarah Glass, Joseph G Gleeson, et al.
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