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David A Stevenson

Showing results (81-90 of 166) with videos related to

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The Laryngoscope|November 25, 2017
Epistaxis in children and adolescents with hereditary hemorrhagic telangiectasiaCristian D Gonzalez, Jamie Mcdonald, David A Stevenson, et al.
Journal of Neuro-Oncology|April 18, 2018
Racial/ethnic disparities and incidence of malignant peripheral nerve sheath tumors: results from the Surveillance, Epidemiology, and End Results Program, 2000-2014Erin C Peckham-Gregory, Roberto E Montenegro, David A Stevenson, et al.
American Journal of Human Genetics|June 15, 2006
Double inactivation of NF1 in tibial pseudarthrosisDavid A Stevenson, Holly Zhou, Shadi Ashrafi, et al.
Cancer Epidemiology|April 24, 2018
Evaluation of racial disparities in pediatric optic pathway glioma incidence: Results from the Surveillance, Epidemiology, and End Results Program, 2000-2014Erin C Peckham-Gregory, Roberto E Montenegro, David A Stevenson, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|April 9, 2013
Low bone mineral content and challenges in interpretation of dual-energy X-ray absorptiometry in children with mucopolysaccharidosis types I, II, and VILynda E Polgreen, William Thomas, Ellen Fung, et al.
Journal of the American Academy of Dermatology|March 2, 2019
Localization and age distribution of telangiectases in children and adolescents with hereditary hemorrhagic telangiectasia: A retrospective cohort studyCristian D Gonzalez, Sarah D Cipriano, Christina A Topham, et al.
Journal of Molecular Neuroscience : MN|February 20, 2019
NF1 Somatic Mutation in Dystrophic ScoliosisRebecca L Margraf, Chad VanSant-Webb, Rong Mao, et al.
Journal of Pediatric Orthopedics|February 24, 2015
The Occurrence of Occult Acetabular Dysplasia in Relatives of Individuals With Developmental Dysplasia of the HipKristen L Carroll, Alison N Schiffern, Kathleen A Murray, et al.
Orphanet Journal of Rare Diseases|December 24, 2011
5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasiaKristy Damjanovich, Carmen Langa, Francisco J Blanco, et al.
Journal of Pediatric Orthopedics|May 23, 2009
Analysis of radiographic characteristics of anterolateral bowing of the leg before fracture in neurofibromatosis type 1David A Stevenson, John C Carey, David H Viskochil, et al.
Pageof 17

Showing results (81-90 of 166) with videos related to

Sort By:
Pageof 17
The Laryngoscope|November 25, 2017
Epistaxis in children and adolescents with hereditary hemorrhagic telangiectasiaCristian D Gonzalez, Jamie Mcdonald, David A Stevenson, et al.
Journal of Neuro-Oncology|April 18, 2018
Racial/ethnic disparities and incidence of malignant peripheral nerve sheath tumors: results from the Surveillance, Epidemiology, and End Results Program, 2000-2014Erin C Peckham-Gregory, Roberto E Montenegro, David A Stevenson, et al.
American Journal of Human Genetics|June 15, 2006
Double inactivation of NF1 in tibial pseudarthrosisDavid A Stevenson, Holly Zhou, Shadi Ashrafi, et al.
Cancer Epidemiology|April 24, 2018
Evaluation of racial disparities in pediatric optic pathway glioma incidence: Results from the Surveillance, Epidemiology, and End Results Program, 2000-2014Erin C Peckham-Gregory, Roberto E Montenegro, David A Stevenson, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry|April 9, 2013
Low bone mineral content and challenges in interpretation of dual-energy X-ray absorptiometry in children with mucopolysaccharidosis types I, II, and VILynda E Polgreen, William Thomas, Ellen Fung, et al.
Journal of the American Academy of Dermatology|March 2, 2019
Localization and age distribution of telangiectases in children and adolescents with hereditary hemorrhagic telangiectasia: A retrospective cohort studyCristian D Gonzalez, Sarah D Cipriano, Christina A Topham, et al.
Journal of Molecular Neuroscience : MN|February 20, 2019
NF1 Somatic Mutation in Dystrophic ScoliosisRebecca L Margraf, Chad VanSant-Webb, Rong Mao, et al.
Journal of Pediatric Orthopedics|February 24, 2015
The Occurrence of Occult Acetabular Dysplasia in Relatives of Individuals With Developmental Dysplasia of the HipKristen L Carroll, Alison N Schiffern, Kathleen A Murray, et al.
Orphanet Journal of Rare Diseases|December 24, 2011
5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasiaKristy Damjanovich, Carmen Langa, Francisco J Blanco, et al.
Journal of Pediatric Orthopedics|May 23, 2009
Analysis of radiographic characteristics of anterolateral bowing of the leg before fracture in neurofibromatosis type 1David A Stevenson, John C Carey, David H Viskochil, et al.
Pageof 17