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Shedding New Light

Published:2023-10 Issue:5 Volume:70 Page:937-950
ISSN:0031-3955
Container-title:Pediatric Clinics of North America
language:en
Short-container-title:Pediatric Clinics of North America

Author:

Pillay-Smiley Natasha,Fletcher Jonathan S.,de Blank Peter,Ratner Nancy

Funder

National Institutes of Health

U.S. Department of Defense

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference71 articles.

1. Prevalence of neurofibromatosis type 1 in the Finnish population;Kallionpaa;Genet Med,2018

2. Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variants;Kehrer-Sawatzki;Hum Genet,2022

3. Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation;Legius;Genet Med,2021

4. Cognitive function and academic performance in neurofibromatosis. 1: consensus statement from the NF1 Cognitive Disorders Task Force;North;Neurology,1997

5. Genetic and cellular evidence of vascular inflammation in neurofibromin-deficient mice and humans;Lasater;J Clin Invest,2010

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Reduced PTPRS expression promotes epithelial-mesenchymal transition of Schwann cells in NF1-related plexiform neurofibromas;Cancer Letters;2024-09

2. Visual Deficits and Diagnostic and Therapeutic Strategies for Neurofibromatosis Type 1: Bridging Science and Patient-Centered Care;Vision;2024-05-09

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