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Carmen Brewer

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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.
American Journal of Human Genetics|June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutationsJennifer J Johnston, Katie L Lewis, David Ng, et al.
The Journal of Clinical Investigation|August 10, 2023
A phase III randomized crossover trial of plerixafor versus G-CSF for treatment of WHIM syndromeDavid H McDermott, Daniel Velez, Elena Cho, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2016
Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylationChristina Lam, Carlos Ferreira, Donna Krasnewich, et al.
Medrxiv : the Preprint Server for Health Sciences|February 5, 2024
GM1 Gangliosidosis Type II: Results of a 10-Year Prospective StudyPrecilla D'Souza, Cristan Farmer, Jean Johnston, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2024
GM1 gangliosidosis type II: Results of a 10-year prospective studyPrecilla D'Souza, Cristan Farmer, Jean M Johnston, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 27, 2020
Safety and recommendations for TMS use in healthy subjects and patient populations, with updates on training, ethical and regulatory issues: Expert GuidelinesSimone Rossi, Andrea Antal, Sven Bestmann, 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.
The New England Journal of Medicine|August 11, 2006
Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibitionRaphaela Goldbach-Mansky, Natalie J Dailey, Scott W Canna, et al.
Pageof 3

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

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
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.
American Journal of Human Genetics|June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutationsJennifer J Johnston, Katie L Lewis, David Ng, et al.
The Journal of Clinical Investigation|August 10, 2023
A phase III randomized crossover trial of plerixafor versus G-CSF for treatment of WHIM syndromeDavid H McDermott, Daniel Velez, Elena Cho, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2016
Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylationChristina Lam, Carlos Ferreira, Donna Krasnewich, et al.
Medrxiv : the Preprint Server for Health Sciences|February 5, 2024
GM1 Gangliosidosis Type II: Results of a 10-Year Prospective StudyPrecilla D'Souza, Cristan Farmer, Jean Johnston, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2024
GM1 gangliosidosis type II: Results of a 10-year prospective studyPrecilla D'Souza, Cristan Farmer, Jean M Johnston, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 27, 2020
Safety and recommendations for TMS use in healthy subjects and patient populations, with updates on training, ethical and regulatory issues: Expert GuidelinesSimone Rossi, Andrea Antal, Sven Bestmann, 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.
The New England Journal of Medicine|August 11, 2006
Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibitionRaphaela Goldbach-Mansky, Natalie J Dailey, Scott W Canna, et al.
Pageof 3