Rett Syndrome Latest Advances

Efficacy and Safety of Cannabinoid-Based Products in Children and Adolescents with Autism Spectrum Disorder, Fragile X Syndrome and Rett Syndrome: A Systematic Review.

Journal: Journal of child and adolescent psychopharmacology

Published: June 24, 2026

Early postnatal DNA methylation dynamics define neuronal subtypes and are disrupted by MECP2 loss.

Journal: bioRxiv : the preprint server for biology

Published: June 22, 2026

Inhibition of protein tyrosine phosphatase PTP1B function ameliorates pathophysiological deficits in Rett Syndrome.

Journal: bioRxiv : the preprint server for biology

Published: June 22, 2026

Rett syndrome and real-world treatment patterns of trofinetide in the United States.

Journal: Journal of medical economics

Published: June 13, 2026

Single-nucleus profiling reveals a core disease signature and cell type-specific vulnerabilities in early Rett syndrome.

Journal: Science advances

Published: June 10, 2026

MeCP2 is Necessary in Cerebellar Purkinje Cells for Precise Network Dynamics During Associative Motor Learning.

Journal: bioRxiv : the preprint server for biology

Published: June 05, 2026

Publisher Correction: Presymptomatic training mitigates functional deficits in a mouse model of Rett syndrome.

Journal: Nature

Published: May 11, 2026

Genetic analysis of a boy with congenital variant Rett syndrome due to a novel variant of FOXG1 gene and literature review

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 06, 2026

Loss of enteric BDNF-TrkB signaling and VIPergic dysfunction underlie gastrointestinal dysmotility in a Mecp2-null mouse model of Rett syndrome.

Journal: bioRxiv : the preprint server for biology

Published: April 27, 2026

Increased Osteoclast Activity Contributes to Bone Resorption and Osteopenia in a Rett Syndrome Mouse Model.

Journal: Cells

Published: April 24, 2026

Real-World Treatment Landscape of Individuals with Rett Syndrome Treated and Untreated with Trofinetide in the United States.

Journal: Journal of health economics and outcomes research

Published: April 23, 2026

A functional MeCP2-LBX1 axis regulates neuronal gene expression in neuronal cells.

Journal: Biochemical and biophysical research communications

Published: April 22, 2026

Rett Syndrome Latest Advances

Find the Latest Research About Rett Syndrome

Efficacy and Safety of Cannabinoid-Based Products in Children and Adolescents with Autism Spectrum Disorder, Fragile X Syndrome and Rett Syndrome: A Systematic Review.

Efficacy and Safety of Cannabinoid-Based Products in Children and Adolescents with Autism Spectrum Disorder, Fragile X Syndrome and Rett Syndrome: A Systematic Review.

Early postnatal DNA methylation dynamics define neuronal subtypes and are disrupted by MECP2 loss.

Early postnatal DNA methylation dynamics define neuronal subtypes and are disrupted by MECP2 loss.

Inhibition of protein tyrosine phosphatase PTP1B function ameliorates pathophysiological deficits in Rett Syndrome.

Inhibition of protein tyrosine phosphatase PTP1B function ameliorates pathophysiological deficits in Rett Syndrome.

Rett syndrome and real-world treatment patterns of trofinetide in the United States.

Rett syndrome and real-world treatment patterns of trofinetide in the United States.

Single-nucleus profiling reveals a core disease signature and cell type-specific vulnerabilities in early Rett syndrome.

Single-nucleus profiling reveals a core disease signature and cell type-specific vulnerabilities in early Rett syndrome.

MeCP2 is Necessary in Cerebellar Purkinje Cells for Precise Network Dynamics During Associative Motor Learning.

MeCP2 is Necessary in Cerebellar Purkinje Cells for Precise Network Dynamics During Associative Motor Learning.

Publisher Correction: Presymptomatic training mitigates functional deficits in a mouse model of Rett syndrome.

Publisher Correction: Presymptomatic training mitigates functional deficits in a mouse model of Rett syndrome.

Genetic analysis of a boy with congenital variant Rett syndrome due to a novel variant of FOXG1 gene and literature review

Genetic analysis of a boy with congenital variant Rett syndrome due to a novel variant of FOXG1 gene and literature review

Loss of enteric BDNF-TrkB signaling and VIPergic dysfunction underlie gastrointestinal dysmotility in a Mecp2-null mouse model of Rett syndrome.

Loss of enteric BDNF-TrkB signaling and VIPergic dysfunction underlie gastrointestinal dysmotility in a Mecp2-null mouse model of Rett syndrome.

Increased Osteoclast Activity Contributes to Bone Resorption and Osteopenia in a Rett Syndrome Mouse Model.

Increased Osteoclast Activity Contributes to Bone Resorption and Osteopenia in a Rett Syndrome Mouse Model.

Real-World Treatment Landscape of Individuals with Rett Syndrome Treated and Untreated with Trofinetide in the United States.

Real-World Treatment Landscape of Individuals with Rett Syndrome Treated and Untreated with Trofinetide in the United States.

A functional MeCP2-LBX1 axis regulates neuronal gene expression in neuronal cells.

A functional MeCP2-LBX1 axis regulates neuronal gene expression in neuronal cells.