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Publications by Maurizio Giustetto
Loss of Mecp2 Causes Atypical Synaptic and Molecular Plasticity of Parvalbumin-Expressing Interneurons Reflecting Rett Syndrome-Like Sensorimotor Defects
eNeuro
Medicine
Neuroscience
Related publications
Rett Syndrome and MeCP2
NeuroMolecular Medicine
Molecular Neuroscience
Neurology
Molecular Medicine
Cellular
MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches
Journal of Neonatal Biology
Atypical Rett Syndrome
State-Dependent Subnetworks of Parvalbumin-Expressing Interneurons in Neocortex
Cell Reports
Biochemistry
Genetics
Molecular Biology
Gross Rearrangements of the MECP2 Gene Are Found in Both Classical and Atypical Rett Syndrome Patients
Journal of Medical Genetics
Genetics
Impaired Excitability of Somatostatin- And Parvalbumin-Expressing Cortical Interneurons in a Mouse Model of Dravet Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Whole Brain Delivery of an Instability-Prone Mecp2 Transgene Improves Behavioral and Molecular Pathological Defects in Mouse Models of Rett Syndrome
Association of Atypical Rett Syndrome and Autism
Sakarya Medical Journal
Tau Pathology Induces Loss of GABAergic Interneurons Leading to Altered Synaptic Plasticity and Behavioral Impairments
Acta neuropathologica communications
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
