Literature DB >> 2802660

Universal inherited melanodyschromatosis: a case of melanosis universalis hereditaria?

A Rebora, A Parodi.   

Abstract

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Year:  1989        PMID： 2802660

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN： 0003-987X


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  5 in total

1.  Universal acquired melanosis in siblings.

Authors:  Snehansu Chakraborti; Tarak Nath Ghosh; Shankha Subhra Nag; Arvind Kumar Singh; Piyali Mitra
Journal:  Indian J Pediatr       Date:  2012-08       Impact factor: 1.967

2.  Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity.

Authors:  Fang Xiao-Kai; He Yue-Xi; Li Yan-Jia; Chen Li-Rong; Wang He-Peng; Sun Qing
Journal:  An Bras Dermatol       Date:  2017 May-Jun       Impact factor: 1.896

3.  Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Authors:  Zhi-Qiang Wang; Lizhen Si; Quan Tang; Debao Lin; Zhangjie Fu; Jing Zhang; Bin Cui; Yufei Zhu; Xianghua Kong; Min Deng; Yu Xia; Heng Xu; Weidong Le; Landian Hu; Xiangyin Kong
Journal:  Am J Hum Genet       Date:  2009-04-16       Impact factor: 11.025

4.  Familial progressive hyperpigmentation: a case report.

Authors:  Monica Yadav; Sugandha Ghonasgi; Rohit Shah; S M Meghana
Journal:  Case Rep Dent       Date:  2012-04-18

5.  Adrenal function and MC1R gene analysis in a prepubertal girl with generalized hyperpigmentation: case report.

Authors:  Aleksandra Rojek; Marek Niedziela
Journal:  Arch Med Sci       Date:  2013-02-28       Impact factor: 3.318
  5 in total

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