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dyschromatosis symmetrica hereditaria相关文献:
Dyschromatosis symmetrica hereditaria and reticulate acropigmentation of Kitamura: An update.
Kono M, Akiyama M.
J Dermatol Sci. 2019 Feb;93(2):75-81. doi: 10.1016/j.jdermsci.2019.01.004. Epub 2019 Jan 15.
PMID:30692041
Dyschromatosis symmetrica hereditaria.
Hayashi M, Suzuki T.
J Dermatol. 2013 May;40(5):336-43. doi: 10.1111/j.1346-8138.2012.01661.x. Epub 2012 Sep 14.
PMID:22974014
Dyschromatosis universalis hereditaria.
Murthy AB, Palaniappan V, Karthikeyan K, Anbarasan V.
Int J Dermatol. 2023 Oct;62(10):1218-1227. doi: 10.1111/ijd.16817. Epub 2023 Aug 27.
PMID:37634201
Dyschromatosis symmetrica hereditaria: A clue to early diagnosis of Aicardi-Goutieres syndrome.
Ahmed F, Do N, Vanderver AL, Treat JR.
Pediatr Dermatol. 2024 Jan-Feb;41(1):156-157. doi: 10.1111/pde.15437. Epub 2023 Sep 28.
PMID:37770123
A Novel Mutation of the ADAR1 Gene in a Chinese Family with Dyschromatosis Symmetrica Hereditaria and Literature Review.
Ge H, Zhang N, Chen X, Wang M, Ye T.
Clin Cosmet Investig Dermatol. 2024 Nov 30;17:2687-2700. doi: 10.2147/CCID.S475880. eCollection 2024.
PMID:39633902
A Case Report of Dyschromatosis Symmetrica Hereditaria with Glucose-6-Phosphate Dehydrogenase Deficiency.
Wang P, Tang C, Zhao Y, Wang P.
Clin Cosmet Investig Dermatol. 2023 Apr 19;16:1047-1050. doi: 10.2147/CCID.S407052. eCollection 2023.
PMID:37155515
Investigation of the pathogenesis of ADAR1 gene in dyschromatosis symmetrica hereditaria.
Zhang J, Jiang C, Wang Z, Fang B, He J, Li M.
Exp Dermatol. 2024 Feb;33(2):e15031. doi: 10.1111/exd.15031.
PMID:38375898
Dyschromatosis.
Urabe K, Hori Y.
Semin Cutan Med Surg. 1997 Mar;16(1):81-5. doi: 10.1016/s1085-5629(97)80039-9.
PMID:9125769
Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases.
Oyama M, Shimizu H, Ohata Y, Tajima S, Nishikawa T.
Br J Dermatol. 1999 Mar;140(3):491-6. doi: 10.1046/j.1365-2133.1999.02716.x.
PMID:10233273
Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China.
He PP, He CD, Cui Y, Yang S, Xu HH, Li M, Yuan WT, Gao M, Liang YH, Li CR, Xu SJ, Chen JJ, Chen HD, Huang W, Zhang XJ.
Br J Dermatol. 2004 Apr;150(4):633-9. doi: 10.1111/j.0007-0963.2004.05861.x.
PMID:15099357
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