Results 171 to 180 of about 9,158,896 (219)
DARIER'S DISEASE OF THE LARYNX [PDF]
Archives of Otolaryngology - Head and Neck Surgery, 1955 DARIER'S disease is a rare but wellrecognized dermatologic disorder of unknown etiology characterized by papular, vesicular, and occasionally ulcerating lesions of the skin, particularly of the face, extremities, and inguinal region. Although it most frequently occurs in childhood, examples in infancy 1 as well as adulthood 2 have been recorded.
Edwin R. Fisher, Stephen L. Kyler
openaire +2 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Journal of the European Academy of Dermatology and Venereology, 2020
Darier disease is an autosomal dominant skin disease characterized by keratotic greasy papules and plaques, primarily in seborrheic and intertriginous areas. Darier disease is caused by mutations in ATP2A2 that encodes a sarco/endoplasmic reticulum Ca2+ -
A. Agematsu +11 more
semanticscholar +1 more source
Darier disease is an autosomal dominant skin disease characterized by keratotic greasy papules and plaques, primarily in seborrheic and intertriginous areas. Darier disease is caused by mutations in ATP2A2 that encodes a sarco/endoplasmic reticulum Ca2+ -
A. Agematsu +11 more
semanticscholar +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
Dermatoglyphics in Darier's disease
British Journal of Dermatology, 1997Palmar and fingerprints were taken from 70 patients with Darier's disease and 409 normal controls. The dermatoglyphic characteristics of each group were determined and comparisons were made between them. Dermatoglyphic abnormalities were found; some confirmed previous findings and some were novel, but they are too small in degree and frequency to be of
Sam Shuster, D Blackwell
openaire +3 more sources
Variable response to low‐dose naltrexone in patients with Darier disease: a case series
Journal of the European Academy of Dermatology and Venereology, 2019Darier disease is a rare autosomal‐dominant genodermatosis with a loss of function of a Ca2+‐ATPase pump (SERCA2‐pump). Clinically, the disease is characterized by red–brown keratotic papules mainly in seborrhoeic areas and has only limited and ...
D. Boehmer +4 more
semanticscholar +1 more source
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).
Govind Srivastava, Virendra N. Sehgal
openaire +3 more sources
Darier's disease and psychosis
Psychiatry Research, 1996There are some reports in the literature about the comorbidity of Darier's Disease (keratosis follicularis) and psychiatric illness (e.g. mental retardation or affective disorders). Here we present evidence that schizophreniform psychosis may also be associated with Darier's Disease.
Hellwig, Bernhard +2 more
openaire +3 more sources
Archives of Dermatology, 1993
To the Editor.— While examining 34 individuals with Darier's disease from three large pedigrees in the southern tier of New York State, we found five individuals, all from one pedigree (DD-He) who had hemorrhagic bullae and red and black macules with jagged borders on the hands and feet (Figs 1 and 2).
Lowell A. Goldsmith +3 more
openaire +3 more sources
To the Editor.— While examining 34 individuals with Darier's disease from three large pedigrees in the southern tier of New York State, we found five individuals, all from one pedigree (DD-He) who had hemorrhagic bullae and red and black macules with jagged borders on the hands and feet (Figs 1 and 2).
Lowell A. Goldsmith +3 more
openaire +3 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.
Thomas E. Nix +2 more
openaire +3 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.
Thomas E. Nix +2 more
openaire +3 more sources
British Journal of Dermatology, 2005
Darier's disease is a rare, dominantly inherited genodermatosis. Although it has been well studied in caucasians, very little is known about the clinical spectrum of this disorder among Asians.To determine the demographic and clinical profile of Asian patients with Darier's disease.This is a retrospective study of all new cases of Darier's disease seen
Boon Kee Goh, Por Ang, Chee-Leok Goh
openaire +3 more sources
Darier's disease is a rare, dominantly inherited genodermatosis. Although it has been well studied in caucasians, very little is known about the clinical spectrum of this disorder among Asians.To determine the demographic and clinical profile of Asian patients with Darier's disease.This is a retrospective study of all new cases of Darier's disease seen
Boon Kee Goh, Por Ang, Chee-Leok Goh
openaire +3 more sources