Results 91 to 100 of about 2,444 (225)

Darier disease: Current insights and challenges in pathogenesis and management

open access: yesJournal of the European Academy of Dermatology and Venereology, Volume 39, Issue 5, Page 942-951, May 2025.
Darier disease (DD) is characterized by the following: Disrupted Ca2+ gradients, impaired desmosomes, impaired keratinocyte differentiation, type 17 inflammation, DC and LC ↓, Th17 cells ↑. DD treatment: First line: keratinocyte focused and/or anti‐inflammatory. Second line: experimental approaches like specific targeting of the inflammatory infiltrate.
Monika Ettinger   +8 more
wiley   +1 more source

Comparative oncology: The paradigmatic example of canine and human mast cell neoplasms [PDF]

open access: yes, 2019
In humans, advanced mast cell (MC) neoplasms are rare malignancies with a poor prognosis. Only a few preclinical models are available, and current treatment options are limited. In dogs, MC neoplasms are the most frequent malignant skin tumours.
Arock M.   +13 more
core   +1 more source

A Rare Clinical Presentation of Darier’s Disease

open access: yesCase 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   +4 more
doaj   +1 more source

VEGF-induced intracellular Ca2+ oscillations are down-regulated and do not stimulate angiogenesis in breast cancer-derived endothelial colony forming cells. [PDF]

open access: yes, 2017
Endothelial colony forming cells (ECFCs) represent a population of truly endothelial precursors that promote the angiogenic switch in solid tumors, such as breast cancer (BC).
Biggiogera Marco   +13 more
core   +1 more source

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

open access: yesClinical 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

Calcium signaling in epithelium : Special focus on Hailey-Hailey and Darier diseases, neurofibromatosis 1 and transitional cell carcinoma [PDF]

open access: yes, 2008
This study utilized normal and defective epithelial cell cultures and epidermal skin samples to examine intra- and intercellular calcium signaling. The main interests of this thesis were Hailey-Hailey disease (HHD), Darier disease (DD), neurofibromatosis
Leinonen, Pekka
core  

Erythroderma: analysis of 247 cases [PDF]

open access: yes, 1995
The profile of 247 patients with erythroderma during a 23 year period from January, 1962 through March, 1985, with a follow-up period ranging from 1 to 26 years were analysed.
Aoki, Valéria   +5 more
core   +4 more sources

Mixed Variant of Acrokeratosis verruciformis of Hopf: A rare entity [PDF]

open access: yes, 2021
Acrokeratosis verruciformis of Hopf (AKV) is a rare autosomal dominant genodermatosis of unknown etiology. Here we present a case of a 20-year-female with multiple skin-colored flat papules over the dorsum of hands and feet interspersed with multiple ...
Abhay Vilas Deshmukh   +3 more
core   +1 more source

A dermatoglyphic investigation of selected skin disorders [PDF]

open access: yes, 1994
This investigation involved the study of qualitative and quantitative digital and palmar traits in patients with various selected skin disorders and normal control subjects.
Blackwell, David
core  

Solitary Mastocytoma in Pediatrics. Case Report and Literature Review

open access: yesRevista 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   +2 more
doaj   +2 more sources

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