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Genodermatosis

2008
William L Weston   +2 more
exaly   +2 more sources

Can You Identify the Genodermatosis?

open access: yesActas Dermo-sifiliográficas, 2015
R, Santesteban Muruzábal   +2 more
exaly   +3 more sources

Dupilumab in the treatment of genodermatosis: A systematic review

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2023
SummaryDupilumab interferes with the signaling pathways of IL‐4 and IL‐13 and is effective in treating atopic dermatitis. Specific genodermatoses, including Netherton syndrome, epidermolysis bullosa pruriginosa, and hyper‐IgE syndrome, are Th2 skewed diseases with activation of type 2 inflammation. We performed this systematic review to investigate the
Po-Chien, Wu   +5 more
openaire   +2 more sources

X-linked ichthyosis: An oculocutaneous genodermatosis

Journal of the American Academy of Dermatology, 2010
X-linked ichthyosis (XLI) is an X-linked recessive disorder of cutaneous keratinization with possible extracutaneous manifestations. It was first described as a distinct type of ichthyosis in 1965. XLI is caused by a deficiency in steroid sulfatase activity, which results in abnormal desquamation and a retention hyperkeratosis.
Camila Krysicka Janniger
exaly   +3 more sources

¿Qué genodermatosis es?

open access: yesActas Dermo-sifiliográficas, 2015
R. Santesteban Muruzábal   +2 more
exaly   +2 more sources

Kindler syndrome: a focal adhesion genodermatosis

British Journal of Dermatology, 2009
Kindler syndrome (OMIM 173650) is an autosomal recessive genodermatosis characterized by trauma-induced blistering, poikiloderma, skin atrophy, mucosal inflammation and varying degrees of photosensitivity. Although Kindler syndrome is classified as a subtype of epidermolysis bullosa, it has distinct clinicopathological and molecular abnormalities.
John S McGrath   +2 more
exaly   +4 more sources

Human Leukocyte Antigen in Genodermatosis

International Journal of Dermatology, 1984
ABSTRACT: Tissue typing performed on the lymphocytes of 41 Patients, including: 23 patients with ichthyosis (15 of autosomal dominant and 8 of the x‐linded variety; 8 patients with tuberous sclerosis (epiloia); and 10 patients with acroder‐matitis enteropathica (AEP).
M, Amer, N, Afifi, I, Iskander, N, Diab
openaire   +2 more sources

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