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Brain Research. Molecular Brain Research|December 8, 2004
Human blood genomics: distinct profiles for gender, age and neurofibromatosis type 1Yang Tang, Aigang Lu, Ruiqiong Ran, et al.Journal of Pediatric Orthopedics|March 14, 2013
Approaches to treating NF1 tibial pseudarthrosis: consensus from the Children's Tumor Foundation NF1 Bone Abnormalities ConsortiumDavid A Stevenson, David Little, Linlea Armstrong, et al.American Journal of Medical Genetics. Part A|September 19, 2009
Skeletal abnormalities in neurofibromatosis type 1: approaches to therapeutic optionsFlorent Elefteriou, Mateusz Kolanczyk, Aaron Schindeler, et al.Journal of Attention Disorders|December 17, 2019
Cognition, ADHD Symptoms, and Functional Impairment in Children and Adolescents With Neurofibromatosis Type 1Jonathan M Payne, Kristina M Haebich, Rachel MacKenzie, et al.American Journal of Medical Genetics. Part A|January 29, 2011
Back to the future: proceedings from the 2010 NF ConferenceSusan M Huson, Maria T Acosta, Allan J Belzberg, et al.Annals of Clinical and Translational Neurology|December 5, 2019
Reproducibility of cognitive endpoints in clinical trials: lessons from neurofibromatosis type 1Jonathan M Payne, Stephen J C Hearps, Karin S Walsh, et al.Journal of Pediatric Orthopedics|May 30, 2023
Consensus-Based Best Practice Guidelines for the Management of Spinal Deformity and Associated Tumors in Pediatric Neurofibromatosis Type 1: Screening and Surveillance, Surgical Intervention, and Medical TherapyAmy L Xu, Krishna V Suresh, Jaime A Gomez, et al.Neuro-Oncology|July 5, 2022
MEK inhibitors for neurofibromatosis type 1 manifestations: Clinical evidence and consensusPeter M K de Blank, Andrea M Gross, Srivandana Akshintala, et al.Nature Genetics|July 14, 2015
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorderAlexander J Abrams, Robert B Hufnagel, Adriana Rebelo, et al.American Journal of Human Genetics|April 15, 2014
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5Margaret J McMillin, Anita E Beck, Jessica X Chong, et al.Pageof 5