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Christopher Zalewski

Showing results (21-30 of 32) with videos related to

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Human Mutation|May 11, 2013
Chimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyXiaohui Tan, Sarah L Anzick, Sikandar G Khan, et al.
JBMR Plus|January 20, 2025
Jansen metaphyseal chondrodysplasia: analysis of craniofacial manifestationsFiona Obiezu, Konstantinia Almpani, Hung Jeffrey Kim, et al.
Brain : a Journal of Neurology|February 1, 2013
Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degenerationMariam B Totonchy, Deborah Tamura, Matthew S Pantell, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 16, 2016
Efficacy and Biomarker Study of Bevacizumab for Hearing Loss Resulting From Neurofibromatosis Type 2-Associated Vestibular SchwannomasJaishri O Blakeley, Xiaobu Ye, Dan G Duda, et al.
Frontiers in Neurology|January 4, 2021
Hearing Loss and Irritability Reporting Without Vestibular Differences in Explosive Breaching ProfessionalsClaire M Modica, Brian R Johnson, Christopher Zalewski, et al.
Annals of the Rheumatic Diseases|June 8, 2014
A 24-month open-label study of canakinumab in neonatal-onset multisystem inflammatory diseaseCailin H Sibley, Andrea Chioato, Sandra Felix, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literatureEmily S Doherty, Felicitas Lacbawan, Donald W Hadley, et al.
Arthritis and Rheumatism|February 2, 2012
Sustained response and prevention of damage progression in patients with neonatal-onset multisystem inflammatory disease treated with anakinra: a cohort study to determine three- and five-year outcomesCailin H Sibley, Nikki Plass, Joseph Snow, et al.
The New England Journal of Medicine|February 8, 2008
Phenotype and course of Hutchinson-Gilford progeria syndromeMelissa A Merideth, Leslie B Gordon, Sarah Clauss, et al.
Human Genetics|October 15, 2021
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Human Mutation|May 11, 2013
Chimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyXiaohui Tan, Sarah L Anzick, Sikandar G Khan, et al.
JBMR Plus|January 20, 2025
Jansen metaphyseal chondrodysplasia: analysis of craniofacial manifestationsFiona Obiezu, Konstantinia Almpani, Hung Jeffrey Kim, et al.
Brain : a Journal of Neurology|February 1, 2013
Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degenerationMariam B Totonchy, Deborah Tamura, Matthew S Pantell, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 16, 2016
Efficacy and Biomarker Study of Bevacizumab for Hearing Loss Resulting From Neurofibromatosis Type 2-Associated Vestibular SchwannomasJaishri O Blakeley, Xiaobu Ye, Dan G Duda, et al.
Frontiers in Neurology|January 4, 2021
Hearing Loss and Irritability Reporting Without Vestibular Differences in Explosive Breaching ProfessionalsClaire M Modica, Brian R Johnson, Christopher Zalewski, et al.
Annals of the Rheumatic Diseases|June 8, 2014
A 24-month open-label study of canakinumab in neonatal-onset multisystem inflammatory diseaseCailin H Sibley, Andrea Chioato, Sandra Felix, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literatureEmily S Doherty, Felicitas Lacbawan, Donald W Hadley, et al.
Arthritis and Rheumatism|February 2, 2012
Sustained response and prevention of damage progression in patients with neonatal-onset multisystem inflammatory disease treated with anakinra: a cohort study to determine three- and five-year outcomesCailin H Sibley, Nikki Plass, Joseph Snow, et al.
The New England Journal of Medicine|February 8, 2008
Phenotype and course of Hutchinson-Gilford progeria syndromeMelissa A Merideth, Leslie B Gordon, Sarah Clauss, et al.
Human Genetics|October 15, 2021
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.
Pageof 4