172 related articles for article (PubMed ID: 9114612)
21. Ultrastructural findings in progressive macular hypomelanosis indicate decreased melanin production.
Relyveld GN; Dingemans KP; Menke HE; Bos JD; Westerhof W
J Eur Acad Dermatol Venereol; 2008 May; 22(5):568-74. PubMed ID: 18266692
[TBL] [Abstract][Full Text] [Related]
22. Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria.
Cui YX; Xia XY; Zhou Y; Gao L; Shang XJ; Ni T; Wang WP; Fan XB; Yin HL; Jiang SJ; Yao B; Hu YA; Wang G; Li XJ
PLoS One; 2013; 8(11):e79808. PubMed ID: 24224009
[TBL] [Abstract][Full Text] [Related]
23. Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria.
Binitha MP; Thomas D; Asha LK
Indian J Dermatol Venereol Leprol; 2006; 72(4):300-2. PubMed ID: 16880579
[TBL] [Abstract][Full Text] [Related]
24. The PER3
Chen H; Yang P; Yang D; Wang D; Lu M; Li Y; Zhong Z; Zhang J; Zeng Z; Liu Z; Zeng X; Jia X; Xing Q; Zhou D
J Mol Med (Berl); 2023 Mar; 101(3):279-294. PubMed ID: 36790533
[TBL] [Abstract][Full Text] [Related]
25. Dyschromatosis universalis hereditaria: a case report.
Udayashankar C; Nath AK
Dermatol Online J; 2011 Feb; 17(2):2. PubMed ID: 21382285
[TBL] [Abstract][Full Text] [Related]
26. Hypomelanosis of Ito: electron microscopical observations on two new cases.
Cavallari V; Ussia AF; Siragusa M; Schepis C
J Dermatol Sci; 1996 Oct; 13(1):87-92. PubMed ID: 8902659
[TBL] [Abstract][Full Text] [Related]
27. Differences in the melanosome distribution within the epidermal melanin units and its association with the impairing background of leukoderma in vitiligo and halo nevi: a retrospective study.
Xiong XX; Ding GZ; Zhao WE; Li X; Ling YT; Sun L; Gong QL; Lu Y
Arch Dermatol Res; 2017 Jul; 309(5):323-333. PubMed ID: 28314912
[TBL] [Abstract][Full Text] [Related]
28. Treatment of reticulate acropigmentation of Kitamura with azelaic acid. An immunohistochemical and electron microscopic study.
Kameyama K; Morita M; Sugaya K; Nishiyama S; Hearing VJ
J Am Acad Dermatol; 1992 May; 26(5 Pt 2):817-20. PubMed ID: 1613143
[TBL] [Abstract][Full Text] [Related]
29. Retyping and molecular pathology diagnosis of dyschromatosis universalis hereditaria.
Zhou D; Yang P; Chen H
Exp Dermatol; 2023 Sep; 32(9):1334-1343. PubMed ID: 37353900
[TBL] [Abstract][Full Text] [Related]
30. The effect of the NMDA receptor-dependent signaling pathway on cell morphology and melanosome transfer in melanocytes.
Ni J; Wang N; Gao L; Li L; Zheng S; Liu Y; Ozukum M; Nikiforova A; Zhao G; Song Z
J Dermatol Sci; 2016 Dec; 84(3):296-304. PubMed ID: 27596138
[TBL] [Abstract][Full Text] [Related]
31. Inhibition of melanosome transfer from melanocytes to keratinocytes by lectins and neoglycoproteins in an in vitro model system.
Minwalla L; Zhao Y; Cornelius J; Babcock GF; Wickett RR; Le Poole IC; Boissy RE
Pigment Cell Res; 2001 Jun; 14(3):185-94. PubMed ID: 11434566
[TBL] [Abstract][Full Text] [Related]
32. The distribution of melanocytes and the degradation of melanosomes in fetal hair follicles.
Xiao L; Zhang RZ; Zhu WY
Micron; 2019 Apr; 119():109-116. PubMed ID: 30711746
[TBL] [Abstract][Full Text] [Related]
33. Dyschromatosis universalis hereditaria: two cases in a Chinese family.
Wang G; Li CY; Gao TW; Liu YF
Clin Exp Dermatol; 2005 Sep; 30(5):494-6. PubMed ID: 16045675
[TBL] [Abstract][Full Text] [Related]
34. Dyschromatosis universalis hereditaria.
Murthy AB; Palaniappan V; Karthikeyan K; Anbarasan V
Int J Dermatol; 2023 Oct; 62(10):1218-1227. PubMed ID: 37634201
[TBL] [Abstract][Full Text] [Related]
35. A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association.
Kumar S; Bhoyar P; Mahajan BB
Indian Dermatol Online J; 2015; 6(2):105-9. PubMed ID: 25821732
[TBL] [Abstract][Full Text] [Related]
36. Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria.
Cao L; Zhang R; Yong L; Chen S; Zhang H; Chen W; Xu Q; Ge H; Mao Y; Zhen Q; Yu Y; Hu X; Sun L
BMC Med Genomics; 2021 Jun; 14(1):168. PubMed ID: 34174894
[TBL] [Abstract][Full Text] [Related]
37. Acquired pigmented macules in human piebald lesions. Ultrastructure of melanocytes in hypomelanotic skin.
Fukai K; Hamada T; Ishii M; Kitajima J; Terao Y
Acta Derm Venereol; 1989; 69(6):524-7. PubMed ID: 2575329
[TBL] [Abstract][Full Text] [Related]
38. Ultrastructure of early pigmentary changes in Dowling-Degos' disease.
Grosshans E; Geiger JM; Hanau D; Jelen G; Heid E
J Cutan Pathol; 1980 Apr; 7(2):77-87. PubMed ID: 7372882
[TBL] [Abstract][Full Text] [Related]
39. Density of dopa-positive melanocytes in dyschromatosis symmetrica hereditaria.
Hata S; Yokomi I
Dermatologica; 1985; 171(1):27-9. PubMed ID: 2411610
[TBL] [Abstract][Full Text] [Related]
40. Dyschromatosis Universalis Hereditaria with Oral Leukokeratosis--A Case of Mistaken Identity and Review of the Literature.
Sorensen RH; Werner KA; Kobayashi TT
Pediatr Dermatol; 2015; 32(6):e283-7. PubMed ID: 26269252
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
