Prenatal treatment path for angelman syndrome and other neurodevelopmental disorders-Reference-Cited by-同舟云学术

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Prenatal treatment path for angelman syndrome and other neurodevelopmental disorders

Published:2019-09-06 Issue:1 Volume:13 Page:11-17
ISSN:1939-3792
Container-title:Autism Research
language:en
Short-container-title:Autism Research

Author:

Zylka Mark J.¹^ORCID

Affiliation:

1. UNC Neuroscience CenterThe University of North Carolina at Chapel Hill Chapel Hill North Carolina

Funder

Angelman Syndrome Foundation

National Institute of Environmental Health Sciences

Simons Foundation

Publisher

Wiley

Subject

Genetics(clinical),Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/aur.2203

Reference67 articles.

1. A Randomized Trial of Prenatal versus Postnatal Repair of Myelomeningocele

2. Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome

3. Protein Delivery of an Artificial Transcription Factor Restores Widespread Ube3a Expression in an Angelman Syndrome Mouse Brain

4. Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development

5. Exceptionally mild Angelman syndrome phenotype associated with an incomplete imprinting defect

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1. Importancia de la valoración genética y la asesoría preconcepcional, a propósito de un caso de síndrome de Prader-Willi/Angelman;Revista Peruana de Ginecología y Obstetricia;2024-06-29

2. Integrating reinforcement learning and serious games to support people with rare genetic diseases and neurodevelopmental disorders: outcomes on parents and caregivers;Frontiers in Psychology;2024-04-05

3. Age of diagnosis for children with chromosome 15q syndromes;Journal of Neurodevelopmental Disorders;2023-11-07

4. Hyperexcitability and translational phenotypes in a preclinical model of SYNGAP1 mutations;2023-09-13

5. Hyperexcitability and translational phenotypes in a preclinical model ofSYNGAP1mutations;2023-07-26

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