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

R Ratnavel

Showing results (11-20 of 19) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 19 results.
Clinical and Experimental Dermatology|July 26, 2002
Case 3: Multiple familial pilomatrixomaS A Grabczynska, P Budny, E Calonje, et al.
British Journal of Rheumatology|July 1, 1993
Rheumatoid arthritis in a patient with primary hypogammaglobulinaemiaR Hermaszewski, R Ratnavel, A D Webster, et al.
Clinical and Experimental Dermatology|March 12, 2011
Current application of National Institute for Health and Clinical Excellence (NICE) guidance in the management of patients with severe psoriasis: a clinical audit against NICE guidance in seven National Health Service specialist dermatology units in EnglandA Bewley, R Cerio, M Clement, et al.
The British Journal of Dermatology|December 12, 2001
Vancomycin-induced linear IgA disease with autoantibodies to BP180 and LAD285R A Palmer, G Ogg, J Allen, et al.
Bone Marrow Transplantation|May 25, 1999
Extracorporeal photopheresis (ECP) in the treatment of chronic graft-versus-host disease (GVHD)F J Child, R Ratnavel, P Watkins, et al.
Human Molecular Genetics|June 1, 1995
Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneityD P Kelsell, H P Stevens, R Ratnavel, et al.
Cancer Genetics and Cytogenetics|November 19, 2003
Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instabilityN A Alam, P Gorman, E E M Jaeger, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Clinical and Experimental Dermatology|July 26, 2002
Case 3: Multiple familial pilomatrixomaS A Grabczynska, P Budny, E Calonje, et al.
British Journal of Rheumatology|July 1, 1993
Rheumatoid arthritis in a patient with primary hypogammaglobulinaemiaR Hermaszewski, R Ratnavel, A D Webster, et al.
Clinical and Experimental Dermatology|March 12, 2011
Current application of National Institute for Health and Clinical Excellence (NICE) guidance in the management of patients with severe psoriasis: a clinical audit against NICE guidance in seven National Health Service specialist dermatology units in EnglandA Bewley, R Cerio, M Clement, et al.
The British Journal of Dermatology|December 12, 2001
Vancomycin-induced linear IgA disease with autoantibodies to BP180 and LAD285R A Palmer, G Ogg, J Allen, et al.
Bone Marrow Transplantation|May 25, 1999
Extracorporeal photopheresis (ECP) in the treatment of chronic graft-versus-host disease (GVHD)F J Child, R Ratnavel, P Watkins, et al.
Human Molecular Genetics|June 1, 1995
Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneityD P Kelsell, H P Stevens, R Ratnavel, et al.
Cancer Genetics and Cytogenetics|November 19, 2003
Germline deletions of EXO1 do not cause colorectal tumors and lesions which are null for EXO1 do not have microsatellite instabilityN A Alam, P Gorman, E E M Jaeger, et al.
The Journal of Investigative Dermatology|February 1, 1997
Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplexF J Smith, L D Corden, E L Rugg, et al.
Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.
Pageof 2