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John B Mee

Showing results (11-20 of 14) with videos related to

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The British Journal of Dermatology|April 2, 2024
Combined rituximab and belimumab to treat recalcitrant epidermolysis bullosa aquisita associated with systemic lupus erythematosusThomas J Tull, Emma C Benton, Kristina Semkova, et al.
The American Journal of Pathology|September 19, 2009
Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activationJoey E Lai-Cheong, Maddy Parsons, Akio Tanaka, et al.
Frontiers in Immunology|December 29, 2025
Clinical correlation of anti-desmoglein antibody dynamics in pemphigus treated with rituximabVishvan Naidu, Harshita A Jain, Ali Yalcinkaya, et al.
The Journal of Investigative Dermatology|February 19, 2010
A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplexRichard W Groves, Lu Liu, Patricia J Dopping-Hepenstal, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
The British Journal of Dermatology|April 2, 2024
Combined rituximab and belimumab to treat recalcitrant epidermolysis bullosa aquisita associated with systemic lupus erythematosusThomas J Tull, Emma C Benton, Kristina Semkova, et al.
The American Journal of Pathology|September 19, 2009
Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activationJoey E Lai-Cheong, Maddy Parsons, Akio Tanaka, et al.
Frontiers in Immunology|December 29, 2025
Clinical correlation of anti-desmoglein antibody dynamics in pemphigus treated with rituximabVishvan Naidu, Harshita A Jain, Ali Yalcinkaya, et al.
The Journal of Investigative Dermatology|February 19, 2010
A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplexRichard W Groves, Lu Liu, Patricia J Dopping-Hepenstal, et al.
Pageof 2