Menin Deficiency Induces Autism-Like Behaviors by Regulating Foxg1 Transcription and Participates in Foxg1-Related Encephalopathy
Source: Advanced Science
Automatic Classification and Visualization of Text Data on Rare Diseases
Source: Journal of Personalized Medicine
Drug repurposing in Rett and Rett-like syndromes: a promising yet underrated opportunity?
Source: Frontiers in Medicine
Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders
Source: Cytogenetic and Genome Research
Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study
Source: Journal of Neurodevelopmental Disorders
For Patient Families
To support patients and caregivers, Elsevier Health is making the latest research on these rare disorders available upon request at no cost.
Learn More
Note:
User acknowledges that these materials are provided for use at no charge as part of Elsevier’s efforts to support healthcare providers and patients. The information contained within the website is intended as a supplement to, and not a substitute for, the knowledge, expertise, skill and judgment of healthcare professionals involved in patient care. The content within this page may not be re-used, modified or re-distributed without prior written permission.
Cookies are used by this site. To decline or learn more, visit our cookie notice.
Copyright © 2024 Elsevier, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
