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 (111-120 of 166) with videos related to

Pageof 17
Sort By:
Spine Deformity|August 21, 2018
Predictive Value and Interrater Reliability of Radiographic Factors in Neurofibromatosis Patients With Dystrophic ScoliosisA Noelle Larson, Charles Gerald T Ledonio, Ann M Brearley, et al.
American Journal of Medical Genetics. Part A|May 1, 2012
Candidate locus analysis for PHACE syndromeSheri Mitchell, Dawn H Siegel, Joseph T C Shieh, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 9, 2011
Pediatric 25-hydroxyvitamin D concentrations in neurofibromatosis type 1David A Stevenson, David H Viskochil, John C Carey, et al.
Plos One|March 19, 2015
Dystrophic spinal deformities in a neurofibromatosis type 1 murine modelSteven D Rhodes, Wei Zhang, Dalong Yang, et al.
Nature Communications|September 22, 2015
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasiaViktor Lukacs, Jayanti Mathur, Rong Mao, et al.
Muscle & Nerve|August 22, 2012
Peripheral muscle weakness in RASopathiesDavid A Stevenson, Shawn Allen, William E Tidyman, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequencesKaren W Gripp, Katia Sol-Church, Patroula Smpokou, et al.
American Journal of Medical Genetics. Part A|November 13, 2007
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genesSteven B Bleyl, Janice L B Byrne, Sarah T South, et al.
Human Molecular Genetics|July 19, 2013
Hyperactive Ras/MAPK signaling is critical for tibial nonunion fracture in neurofibromin-deficient miceRicha Sharma, Xiaohua Wu, Steven D Rhodes, et al.
Nature Medicine|July 7, 2014
Asfotase-α improves bone growth, mineralization and strength in mouse models of neurofibromatosis type-1Jean de la Croix Ndong, Alexander J Makowski, Sasidhar Uppuganti, et al.
Pageof 17

Showing results (111-120 of 166) with videos related to

Sort By:
Pageof 17
Spine Deformity|August 21, 2018
Predictive Value and Interrater Reliability of Radiographic Factors in Neurofibromatosis Patients With Dystrophic ScoliosisA Noelle Larson, Charles Gerald T Ledonio, Ann M Brearley, et al.
American Journal of Medical Genetics. Part A|May 1, 2012
Candidate locus analysis for PHACE syndromeSheri Mitchell, Dawn H Siegel, Joseph T C Shieh, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 9, 2011
Pediatric 25-hydroxyvitamin D concentrations in neurofibromatosis type 1David A Stevenson, David H Viskochil, John C Carey, et al.
Plos One|March 19, 2015
Dystrophic spinal deformities in a neurofibromatosis type 1 murine modelSteven D Rhodes, Wei Zhang, Dalong Yang, et al.
Nature Communications|September 22, 2015
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasiaViktor Lukacs, Jayanti Mathur, Rong Mao, et al.
Muscle & Nerve|August 22, 2012
Peripheral muscle weakness in RASopathiesDavid A Stevenson, Shawn Allen, William E Tidyman, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequencesKaren W Gripp, Katia Sol-Church, Patroula Smpokou, et al.
American Journal of Medical Genetics. Part A|November 13, 2007
Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genesSteven B Bleyl, Janice L B Byrne, Sarah T South, et al.
Human Molecular Genetics|July 19, 2013
Hyperactive Ras/MAPK signaling is critical for tibial nonunion fracture in neurofibromin-deficient miceRicha Sharma, Xiaohua Wu, Steven D Rhodes, et al.
Nature Medicine|July 7, 2014
Asfotase-α improves bone growth, mineralization and strength in mouse models of neurofibromatosis type-1Jean de la Croix Ndong, Alexander J Makowski, Sasidhar Uppuganti, et al.
Pageof 17