Results 91 to 100 of about 1,447 (168)

Pioneers in Dermatology and Venereology: An interview with Professor Dan Lipsker

Journal of the European Academy of Dermatology and Venereology, Volume 39, Issue 11, Page 1878-1880, November 2025.
Dan Lipsker
wiley   +1 more source

Topographical variations in the skin barrier and their role in disease pathogenesis

Journal of the European Academy of Dermatology and Venereology, Volume 39, Issue 7, Page 1228-1238, July 2025.
Unlike the gut, the skin appears uniform at first glance. However, histological and molecular biological research has revealed significant regional variations in the composition and function of its main barrier elements. In this review, we describe the topographical differences of four barrier elements in healthy skin: microbiome, chemical, physical ...
Z. Dajnoki, A. Kapitány, K. Eyerich, S. Eyerich, D. Törőcsik, A. Szegedi   +5 more
wiley   +1 more source

An Uncommon Presentation of Darier-White Disease with Hystrix-like Palmoplantar Keratoderma [PDF]

, 2021
Darier-White disease is a relatively common autosomal dominant genodermatosis caused by mutation in the ATP2A2 gene. It is characterized by multiple warty papules coalescing into plaques in the seborrheic areas and by specific histological skin changes ...
Ellenbogen, Eran, Gat, Andrea, Goldberg, Ilan, Jammal, Anwar, Martinez, Helena, Pessach, Yakov, Sprecher, Eli   +6 more
core   +1 more source

A Rare Clinical Presentation of Darier’s Disease

Case Reports in Dermatological Medicine, 2013
Darier’s disease, also known as keratosis follicularis or dyskeratosis follicularis, is a rare disorder of keratinization. It is an autosomal dominant genodermatosis with high penetrance and variable expressivity.
Mybera Ferizi, Antigona Begolli-Gerqari, Bostjan Luzar, Fisnik Kurshumliu, Mergita Ferizi   +4 more
doaj   +1 more source

Debilitating Darier\u27s disease [PDF]

, 2007
Darier\u27s disease is an inherited dermatitis that is due to a mutation in the ATP2A2 gene. This mutation causes disrupted signaling within cells and leads to a skin condition that is resistant to many dermatologic treatments.
David W. Brodell, Lawrence E. Frisch, Robert Brodell   +2 more
core   +1 more source

Spinal anesthesia in a patient with Darier’s disease: A case report

, 2023
Ibrahim Boğa, Truong Van Can
openalex   +2 more sources

Kaposi's varicelliform eruption in a patient with darier's disease: A rare case report

Clinical Dermatology Review
Darier's disease is a rare autosomal dominant disorder, characterized clinically by the appearance of multiple, pruritic, discrete, and scaly papules affecting seborrheic areas coupled with palmar pits, nail changes, and mucosal involvement ...
Trishala Shirahatti, H Bangaru
doaj   +1 more source

Novel and recurrent ATP2A2 mutations in Japanese patients with Darier’s disease [PDF]

, 2016
2016-11Darier’s disease (DD, keratosis follicularis: OMIM#124200) is an autosomal dominant skin disorder characterized by multiple dark brown keratotic plaques and warty papules covered by thick crusts. Most cases of DD are caused by mutations in ATP2A2,
67690, 67691, 67692, 67693, 67694, 67695, 67696, 67697, 67698, 67699, 67700, 67701, 67702, 67703, Akiyama, Masashi, Fujio, Yumi, Hino, Haruko, Kagami, Shinji, Konohana, Izumi, Miura, Shunsuke, Mukai, Hideki, Nakamura, Yuki, Noda, Kana, Okuno, Yusuke, Otani, Ayako, Sugiura, Kazumitsu, Takama, Hiromichi, Takeichi, Takuya   +27 more
core  

Solitary Mastocytoma in Pediatrics. Case Report and Literature Review

Revista Finlay, 2020
The mastocytoma is a genodermatosis of unknown etiology, so it is included in the group of rare or uncommon diseases; it usually appears in childhood or at birth.
Juan Carlos Yanes Macías, Mery Rosa Betancourt Trujillo, Lino Arístides Sánchez Galván   +2 more
doaj   +2 more sources

Darier’s Disease Misdiagnosed as Severe Seborrheic Dermatitis [PDF]

, 2011
Jessica L. Schwartz, Tony S. Clinton
openalex   +1 more source