Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David A Stevenson

Showing results (91-100 of 166) with videos related to

Pageof 17
Sort By:
American Journal of Medical Genetics. Part A|November 19, 2016
Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1Emily R Sites, Teresa A Smolarek, Lisa J Martin, et al.
Journal of Pediatric Rehabilitation Medicine|August 7, 2014
Biomarkers of bone remodeling in children with mucopolysaccharidosis types I, II, and VIDavid A Stevenson, Kyle Rudser, Alicia Kunin-Batson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1David A Stevenson, David H Viskochil, Elizabeth K Schorry, et al.
Bone|January 3, 2009
Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomographyDavid A Stevenson, David H Viskochil, John C Carey, et al.
Journal of Autism and Developmental Disorders|July 29, 2016
Brief Report: The Prevalence of Neurofibromatosis Type 1 among Children with Autism Spectrum Disorder Identified by the Autism and Developmental Disabilities Monitoring NetworkDeborah A Bilder, Amanda V Bakian, David A Stevenson, et al.
Journal of Neurosurgery. Pediatrics|June 5, 2012
Spinal arteriovenous fistulas in children with hereditary hemorrhagic telangiectasiaAmy R U L Calhoun, Robert J Bollo, Sarah T Garber, et al.
Human Molecular Genetics|April 12, 2011
Neurofibromin (Nf1) is required for skeletal muscle developmentNadine Kossler, Sigmar Stricker, Christian Rödelsperger, et al.
Pediatric Research|March 5, 2008
Evidence of increased bone resorption in neurofibromatosis type 1 using urinary pyridinium crosslink analysisDavid A Stevenson, Elisabeth L Schwarz, David H Viskochil, et al.
American Journal of Medical Genetics. Part A|May 29, 2013
The generalized bone phenotype in children with neurofibromatosis 1: a sibling matched case-control studyLinlea Armstrong, Kimberly Jett, Patricia Birch, et al.
Lymphatic Research and Biology|January 23, 2026
Molecular Characterization of Vascular Anomalies Tissues Guides Clinical DiagnosisScott B Henslee, Whitney L Wooderchak-Donahue, J Fred Grimmer, et al.
Pageof 17

Showing results (91-100 of 166) with videos related to

Sort By:
Pageof 17
American Journal of Medical Genetics. Part A|November 19, 2016
Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1Emily R Sites, Teresa A Smolarek, Lisa J Martin, et al.
Journal of Pediatric Rehabilitation Medicine|August 7, 2014
Biomarkers of bone remodeling in children with mucopolysaccharidosis types I, II, and VIDavid A Stevenson, Kyle Rudser, Alicia Kunin-Batson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007
The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1David A Stevenson, David H Viskochil, Elizabeth K Schorry, et al.
Bone|January 3, 2009
Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomographyDavid A Stevenson, David H Viskochil, John C Carey, et al.
Journal of Autism and Developmental Disorders|July 29, 2016
Brief Report: The Prevalence of Neurofibromatosis Type 1 among Children with Autism Spectrum Disorder Identified by the Autism and Developmental Disabilities Monitoring NetworkDeborah A Bilder, Amanda V Bakian, David A Stevenson, et al.
Journal of Neurosurgery. Pediatrics|June 5, 2012
Spinal arteriovenous fistulas in children with hereditary hemorrhagic telangiectasiaAmy R U L Calhoun, Robert J Bollo, Sarah T Garber, et al.
Human Molecular Genetics|April 12, 2011
Neurofibromin (Nf1) is required for skeletal muscle developmentNadine Kossler, Sigmar Stricker, Christian Rödelsperger, et al.
Pediatric Research|March 5, 2008
Evidence of increased bone resorption in neurofibromatosis type 1 using urinary pyridinium crosslink analysisDavid A Stevenson, Elisabeth L Schwarz, David H Viskochil, et al.
American Journal of Medical Genetics. Part A|May 29, 2013
The generalized bone phenotype in children with neurofibromatosis 1: a sibling matched case-control studyLinlea Armstrong, Kimberly Jett, Patricia Birch, et al.
Lymphatic Research and Biology|January 23, 2026
Molecular Characterization of Vascular Anomalies Tissues Guides Clinical DiagnosisScott B Henslee, Whitney L Wooderchak-Donahue, J Fred Grimmer, et al.
Pageof 17