Results 21 to 30 of about 4,844,369 (196)
Combination of Naltrexone and Isotretinoin for the Treatment of Darier Disease. [PDF]
Darier disease (DD) is an autosomal-dominant genodermatosis in which mutations in the ATP2A2 gene result in impaired intercellular adhesion and epidermal blistering.
Costa T +3 more
europepmc +2 more sources
Increased activation of ErbB and NF-κB signalling pathways in Darier disease affected skin. [PDF]
Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 3, Page 506-509, March 2026.
Ernst N, Ludwig RJ, Vorobyev A.
europepmc +2 more sources
Exacerbation of Darier disease with lithium therapy [PDF]
Darier disease is an autosomal dominant blistering disorder linked to mutation of the endoplasmic reticulum calcium pump, SERCA2, which compromises keratinocyte adhesion and differentiation.
Simpson, Cory L, Tamazian, Shant
core +1 more source
Darier disease and Hailey-Hailey disease are severe, monogenetic dermatological disorders with mutations affecting all cells, making them liable to exhibit extra-dermal symptoms.
Philip Curman +5 more
doaj +1 more source
Vertebral sarcoidosis with associated Darier-Roussy disease manifesting as acute back pain
Introduction: Sarcoidosis is a systemic granulomatous disease of unknown etiology, with a heterogenous clinical manifestation, progression, and prognosis.
Mohamad Syafeeq Faeez Md Noh +5 more
doaj +1 more source
Unilateral and pruritic papules: segmental Darier-White disease [PDF]
Darier-White disease is an uncommon disorder, which presents in a localized pattern in about 10% of patients, usually without nail, mucosa, or acral involvement.
Puente, Nieves +3 more
core +3 more sources
ATP2A2 SINE Insertion in an Irish Terrier with Darier Disease and Associated Infundibular Cyst Formation. [PDF]
A 4-month-old female Irish Terrier presented with a well demarcated ulcerative and crusting lesion in the right ear canal. Histological analysis revealed epidermal hyperplasia with severe acantholysis affecting all suprabasal layers of the epidermis ...
Monika Linek +19 more
core +2 more sources
Type 1 Segmental Darier Disease: Case Report and Discussion of the Treatment Options
Darier disease is a rare type of autosomal dominant genodermatosis, and it is caused by a mutation in the gene coding for the endoplasmic reticulum membrane calcium pump Ca2+-ATPase type 2, leading to compromised intercellular adhesion.
Sahar Hasan Alsharif +2 more
doaj +1 more source
Carbon dioxide laser treatment for Darier disease [PDF]
Hasina Maredia, MD +3 more
doaj +2 more sources
Heterozygous ATP2A2 missense variant identified in a Shih Tzu with Darier disease. [PDF]
Darier disease is caused by heterozygous loss of function variants in the ATP2A2 gene encoding the endoplasmic/sarcoplasmic reticulum Ca2+ pump ATP2A2.
Rich, Naomi +11 more
core +2 more sources

