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Publications by Serena Giannelli
Whole Brain Delivery of an Instability-Prone Mecp2 Transgene Improves Behavioral and Molecular Pathological Defects in Mouse Models of Rett Syndrome
Related publications
Systemic Delivery of MeCP2 Rescues Behavioral and Cellular Deficits in Female Mouse Models of Rett Syndrome
Journal of Neuroscience
Neuroscience
Rett Syndrome and MeCP2
NeuroMolecular Medicine
Molecular Neuroscience
Neurology
Molecular Medicine
Cellular
MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches
Journal of Neonatal Biology
Loss of Mecp2 Causes Atypical Synaptic and Molecular Plasticity of Parvalbumin-Expressing Interneurons Reflecting Rett Syndrome-Like Sensorimotor Defects
eNeuro
Medicine
Neuroscience
Rett Syndrome Without MECP2 Mutation in a Pakistani Girl
Life and Science
MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome
Neurology
Neurology
The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders
Pediatric Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
Structure of the MeCP2–TBLR1 Complex Reveals a Molecular Basis for Rett Syndrome and Related Disorders
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Bisphosphonates and MeCP2 Deficiency: Cellular Studies and Clinical Application in Rett Syndrome
Journal of Musculoskeletal Disorders and Treatment
