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Frontiers in Cellular Neuroscience|December 6, 2021
Rett Syndrome and Fragile X Syndrome: Different Etiology With Common Molecular DysfunctionsSnow Bach, Stephen Shovlin, Michael Moriarty, et al.
Orphanet Journal of Rare Diseases|July 13, 2018
Transcriptome level analysis in Rett syndrome using human samples from different tissuesStephen Shovlin, Daniela Tropea
Frontiers in Neuroscience|June 17, 2022
Molecular Signatures of Response to Mecasermin in Children With Rett SyndromeStephen Shovlin, Chloe Delepine, Lindsay Swanson, et al.
Orphanet Journal of Rare Diseases|January 30, 2024
Rett syndrome in Ireland: a demographic studyKomal Zade, Ciara Campbell, Snow Bach, et al.
Scientific Reports|December 18, 2020
Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disordersSnow Bach, Niamh M Ryan, Paolo Guasoni, et al.
Med (New York, N.Y.)|October 12, 2024
Trofinetide treatment for Rett syndrome: Lessons to learnDaniela Tropea
Molecular Psychiatry|January 8, 2021
Role of phosphodiesterases in the pathophysiology of neurodevelopmental disordersSébastien Delhaye, Barbara Bardoni
Biochimie|June 24, 2010
The role of G-quadruplex in RNA metabolism: involvement of FMRP and FMR2PMireille Melko, Barbara Bardoni
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