Zobrazeno 1 - 10
of 213
pro vyhledávání: '"pruriginosa"'
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 7 (2024)
Externí odkaz:
https://doaj.org/article/8ef8865f1e0c403590775e92c49ca3db
Autor:
Lauren C. LaMonica, MPH, Margaret Lang-Houser, MD, Scott C. Bresler, MD, PhD, Julie E. Mervak, MD
Publikováno v:
JAAD Case Reports, Vol 38, Iss , Pp 82-85 (2023)
Externí odkaz:
https://doaj.org/article/a022f7c2ac19499d9e24a296152c9198
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 11, Pp n/a-n/a (2023)
Abstract Background Variants in COL7A1 cause an extremely rare and clinically heterogeneous syndrome known as dystrophic epidermolysis bullosa pruriginosa (DEB‐Pr). Duplilumab, a fully humanized anti‐IL‐4Ra monoclonal antibody, can inhibit IL
Externí odkaz:
https://doaj.org/article/1e22bebb163144489b2eb986b2825bf4
Publikováno v:
Dermatology Practical & Conceptual, Vol 13, Iss 4 (2023)
Externí odkaz:
https://doaj.org/article/b440ccebec7d4b48bb3516a0c630cb81
Autor:
Maria A. Leonova, Nikolay N. Murashkin
Publikováno v:
Педиатрическая фармакология, Vol 19, Iss 6, Pp 479-483 (2023)
Background. Epidermolisys bullosa pruriginosa is a rare pattern of dystrophic epidermolisys bullosa and characterized by severe itching that accompanies the formation of papules, plaques and nodes primarily on the lower limbs skin and imitating pruri
Externí odkaz:
https://doaj.org/article/aae01313f3b54f528338f868611ecd0e
Autor:
Hong Ha Nguyen, Satoru Shinkuma, Ryota Hayashi, Tatsuya Katsumi, Tomoki Nishiguchi, Ken Natsuga, Yasuyuki Fujita, Riichiro Abe
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 5, Iss 3, Pp 78-87 (2022)
Abstract Objectives Epidermolysis bullosa (EB) is a hereditary disorder characterized by mechanical stress‐induced blistering. The presence of extracutaneous complications such as cardiomyopathy and renal disease observed in severe EB subtypes and
Externí odkaz:
https://doaj.org/article/1851be83fdce4d5282b67b2478ea0cff
Akademický článek
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Publikováno v:
JAAD Case Reports, Vol 16, Iss , Pp 69-71 (2021)
Externí odkaz:
https://doaj.org/article/0e6bdba23d4146fc9fddd2f4083f0cd6
Publikováno v:
Journal of IMAB, Vol 26, Iss 3, Pp 3245-3250 (2020)
Purpose: Epidermolysis bullosa pruriginosa (EBP) is a rare clinical subtype of inherited Epidermolysis bullosa dystrophica (EBD). It is characterized by severe itching and hypertrophic papules affecting the extensor surfaces of the extremities. Mate
Externí odkaz:
https://doaj.org/article/989a1d9d1384446598239c89576b171f
Publikováno v:
JAAD Case Reports, Vol 11, Iss , Pp 112-114 (2021)
Externí odkaz:
https://doaj.org/article/84721fa2c8ea497ca64eac97040d164b