Results 91 to 100 of about 401 (136)

A two-stage workflow for vitiligo diagnosis: clinical characteristic classification and large language model (LLM)-based report generation. [PDF]

Front Immunol
He K, Xu T, Feng Y, Lu Y, Wang X, Jiang L, Guo S, He Y, Dai W, Zhang W, Zhang J, Lu H, Huang D, Li S.   +13 more
europepmc   +1 more source

A rare presentation of dyschromatosis symmetrica hereditaria in a Canadian context: A case report. [PDF]

SAGE Open Med Case Rep
Czyz S, Jafarian F, Holfeld K.
europepmc   +1 more source

A Case of Dyschromatosis Universalis Hereditaria

The Nishinihon Journal of Dermatology, 1983
TAKEHARA, Naohide, NAKAYAMA, Hidetoshi, MIHARA, Motoyuki, SHIMAO, Shuhei, MATSUMOTO, Isao   +4 more
openaire   +1 more source

Identification of Two Novel Frameshift Mutations of the ADAR1 Gene in Two Chinese Families With Dyschromatosis Symmetrica Hereditaria.

Indian J Dermatol, 2022
Ning X, Xiao S, Zhang Y.
europepmc   +1 more source

A case of dyschromatosis universalis hereditaria.

Skin research, 1984
Shibuya, Kyoko, Kitano, Yukio
openaire   +1 more source

Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations. [PDF]

J Dermatol
Okamura K, Suzuki T.
europepmc   +1 more source

Adermatoglyphia in the Era of Biometrics.

Indian J Dermatol, 2022
De A, Dhar S, Sarda A, Dhar S.
europepmc   +1 more source

Late Onset Amyloid Cutis Dyschromica: An Uncommon Instance. [PDF]

Indian Dermatol Online J
Behera D, Kar HK, Sahu N, Choubey S.
europepmc   +1 more source

Familial Amyloidosis Cutis Dyschromica with GPNMB mutation: A Case Report and Literature Review. [PDF]

Acta Derm Venereol
Untaaveesup S, Borriboon T, Supsrisunjai C.   +2 more
europepmc   +1 more source

A rare case of late-onset amyloidosis cutis dyschromica. [PDF]

JAAD Case Rep
Lau M, Moshiri A, Khalil S, Siegel L.
europepmc   +1 more source