Results 121 to 130 of about 957 (153)
Association of oligophrenia and dyskeratoses: a clinical investigation and an enquiry into its implications [PDF]
, 1954 Ewing, J.A.
core
Some of the next articles are maybe not open access.
Related searches:
Related searches:
The Journal of Dermatology, 2016
AbstractDarier disease (DD) is a type of inherited keratinizing disorder that exhibits autosomal dominant inheritance. DD is caused by the mutations of ATP2A2, which encodes an endoplasmic reticulum calcium pump, sarco/endoplasmic reticulum ATPase type 2 (SERCA2).
Atsushi, Takagi +2 more
openaire +2 more sources
AbstractDarier disease (DD) is a type of inherited keratinizing disorder that exhibits autosomal dominant inheritance. DD is caused by the mutations of ATP2A2, which encodes an endoplasmic reticulum calcium pump, sarco/endoplasmic reticulum ATPase type 2 (SERCA2).
Atsushi, Takagi +2 more
openaire +2 more sources
Darier's (Darier–White) disease/keratosis follicularis
International Journal of Dermatology, 2004Darier’s (Darier–White) disease/keratosis follicularis was initially reported in the year 1889 by Darier and White independently. Darier’s disease has since (for over a century) fascinated research workers. 1–12 Almost all cases of the disease are attributed to mutations in the sarcoplasmic endoreticulum Ca 2+ -ATPase isoform-2 (SERCA-2).
Virendra N, Sehgal, Govind, Srivastava
openaire +2 more sources
Archives of Dermatology, 1964
Four cases of Darier's disease (keratosis follicularis) with unusual acral hemorrhagic lesions are presented and discussed. It is suggested that the lesions represent hemorrhage into lacunae secondary to trauma.
W N, JONES, T E, NIX, W H, CLARK
openaire +2 more sources
Four cases of Darier's disease (keratosis follicularis) with unusual acral hemorrhagic lesions are presented and discussed. It is suggested that the lesions represent hemorrhage into lacunae secondary to trauma.
W N, JONES, T E, NIX, W H, CLARK
openaire +2 more sources
British Journal of Dermatology, 1995
Darier's disease is an inherited disorder with well-recognized patterns of presentation. Lesions commonly affect the trunk and flexures. The diagnosis is based on the typical clinical appearance and histology showing acantholytic dyskeratosis. We report two unusual cases with prominent nodular, comedonal lesions on the face and scalp.
E K, Derrick, C R, Darley, S, Burge
openaire +2 more sources
Darier's disease is an inherited disorder with well-recognized patterns of presentation. Lesions commonly affect the trunk and flexures. The diagnosis is based on the typical clinical appearance and histology showing acantholytic dyskeratosis. We report two unusual cases with prominent nodular, comedonal lesions on the face and scalp.
E K, Derrick, C R, Darley, S, Burge
openaire +2 more sources
International Journal of Dermatology, 2000
A 48‐year‐old Caucasian man recounted the onset of keratotic papules on the trunk at the age of 8 years, with subsequent spread to the forearms, scalp, and forehead. His most severe disease was present on the legs. He complained of pain, itching, and noted exacerbations in the summer and with sweating.
R, Katta, J, Reed, J E, Wolf
openaire +2 more sources
A 48‐year‐old Caucasian man recounted the onset of keratotic papules on the trunk at the age of 8 years, with subsequent spread to the forearms, scalp, and forehead. His most severe disease was present on the legs. He complained of pain, itching, and noted exacerbations in the summer and with sweating.
R, Katta, J, Reed, J E, Wolf
openaire +2 more sources
2015
Darier’s disease (DD) is an autosomal dominant disease induced by haplo-insufficiency with variable expressivity but with complete penetrance in adults. Considerable variation in severity and in clinical manifestation was found between families. Lesions are hyperkeratotic, greasy papules, which are skin colored, yellow, or brown, that may coalesce into
Federico Bardazzi +2 more
openaire +1 more source
Darier’s disease (DD) is an autosomal dominant disease induced by haplo-insufficiency with variable expressivity but with complete penetrance in adults. Considerable variation in severity and in clinical manifestation was found between families. Lesions are hyperkeratotic, greasy papules, which are skin colored, yellow, or brown, that may coalesce into
Federico Bardazzi +2 more
openaire +1 more source
2018
Darier’s disease is an uncommon, autosomal-dominant inherited disorder. It is characterized by greasy, hyperkeratotic, skin-colored, or yellowish-brown papules that show a characteristic dermatoscopic pattern which consists of a central yellowish-brownish area of different morphologies (“star-like,” branched, polygonal, or roundish-oval), generally ...
Enzo Errichetti, Giuseppe Stinco
openaire +3 more sources
Darier’s disease is an uncommon, autosomal-dominant inherited disorder. It is characterized by greasy, hyperkeratotic, skin-colored, or yellowish-brown papules that show a characteristic dermatoscopic pattern which consists of a central yellowish-brownish area of different morphologies (“star-like,” branched, polygonal, or roundish-oval), generally ...
Enzo Errichetti, Giuseppe Stinco
openaire +3 more sources