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

N J Wilson

Showing results (81-90 of 100) with videos related to

Pageof 10
Sort By:
Internal Medicine Journal|February 12, 2005
Transcatheter closure of a complex postmyocardial infarction ventricular septal defect after surgical patch dehiscenceN J Cutfield, P N Ruygrok, N J Wilson, et al.
The Journal of Pediatrics|November 1, 1992
Autoantibody production after cardiopulmonary bypass with special reference to postpericardiotomy syndromeS A Webber, N J Wilson, M Y Fung, et al.
Circulation|February 7, 2001
Intravenous immunoglobulin in acute rheumatic fever: a randomized controlled trialL M Voss, N J Wilson, J M Neutze, et al.
Molecular Cell Biology Research Communications : MCBRC|November 30, 1999
Expression of a Y559F mutant CSF-1 receptor in M1 myeloid cells: a role for Src kinases in CSF-1 receptor-mediated differentiationD C Marks, X F Csar, N J Wilson, et al.
Journal of the American College of Cardiology|September 19, 1998
Long-term outcome after the mustard repair for simple transposition of the great arteries. 28-year follow-upN J Wilson, P M Clarkson, B G Barratt-Boyes, et al.
The British Journal of Dermatology|December 31, 2013
Heterozygous frameshift mutation in keratin 5 in a family with Galli-Galli diseaseA K Reisenauer, S V Wordingham, J York, et al.
The British Journal of Dermatology|August 8, 2009
Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutationJ K Gass, N J Wilson, F J D Smith, et al.
The British Journal of Dermatology|September 6, 2000
A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe diseaseK Batta, E L Rugg, N J Wilson, et al.
Clinical and Experimental Dermatology|October 28, 2016
Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literatureC Kasparis, D Reid, N J Wilson, et al.
Clinical and Experimental Dermatology|December 18, 2013
A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutationsA Vahlquist, M Virtanen, M Hellström-Pigg, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
Internal Medicine Journal|February 12, 2005
Transcatheter closure of a complex postmyocardial infarction ventricular septal defect after surgical patch dehiscenceN J Cutfield, P N Ruygrok, N J Wilson, et al.
The Journal of Pediatrics|November 1, 1992
Autoantibody production after cardiopulmonary bypass with special reference to postpericardiotomy syndromeS A Webber, N J Wilson, M Y Fung, et al.
Circulation|February 7, 2001
Intravenous immunoglobulin in acute rheumatic fever: a randomized controlled trialL M Voss, N J Wilson, J M Neutze, et al.
Molecular Cell Biology Research Communications : MCBRC|November 30, 1999
Expression of a Y559F mutant CSF-1 receptor in M1 myeloid cells: a role for Src kinases in CSF-1 receptor-mediated differentiationD C Marks, X F Csar, N J Wilson, et al.
Journal of the American College of Cardiology|September 19, 1998
Long-term outcome after the mustard repair for simple transposition of the great arteries. 28-year follow-upN J Wilson, P M Clarkson, B G Barratt-Boyes, et al.
The British Journal of Dermatology|December 31, 2013
Heterozygous frameshift mutation in keratin 5 in a family with Galli-Galli diseaseA K Reisenauer, S V Wordingham, J York, et al.
The British Journal of Dermatology|August 8, 2009
Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutationJ K Gass, N J Wilson, F J D Smith, et al.
The British Journal of Dermatology|September 6, 2000
A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe diseaseK Batta, E L Rugg, N J Wilson, et al.
Clinical and Experimental Dermatology|October 28, 2016
Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literatureC Kasparis, D Reid, N J Wilson, et al.
Clinical and Experimental Dermatology|December 18, 2013
A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutationsA Vahlquist, M Virtanen, M Hellström-Pigg, et al.
Pageof 10