Results 141 to 150 of about 4,844,369 (196)
Magnesium chloride-calcium carbonate treatment in a pregnant patient with severe Darier disease. [PDF]
Yi A, Wang J, Singh D, Konstantinov NK.
europepmc +1 more source
Darier′s disease with perifollicular hypopigmentation
Sornakumar L, Srinivas C
doaj
Persistent Cutaneous Lesions of Darier Disease and Second-Hit Somatic Variants in ATP2A2 Gene.
Atzmony L +9 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
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
B K, Goh, P, Ang, C L, Goh
exaly +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
B K, Goh, P, Ang, C L, Goh
exaly +3 more sources
Darier disease: a case report [PDF]
Darier disease, also known as keratosis follicularis, dyskeratosis follicularis, and benign dyskeratosis, is a rare disorder of keratinisation that primarily affects the skin and, to a lesser extent, the oral mucosa.
Rb Zain
exaly +4 more sources
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
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 ...
Errichetti E., Stinco G.
openaire +1 more source
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 ...
Errichetti E., Stinco G.
openaire +1 more source

