124 related articles for article (PubMed ID: 34628647)
1. A homozygous Y131X GPNMB mutation in a Chinese family with amyloidosis cutis dyschromica.
Wang X; Sun J
Int J Dermatol; 2022 Apr; 61(4):e118-e120. PubMed ID: 34628647
[No Abstract] [Full Text] [Related]
2. Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica.
Wang J; Li Y; Xing L; Zhao M; Zhang S; Li Z; Yao Z; Li M
Br J Dermatol; 2019 Dec; 181(6):1327-1329. PubMed ID: 31260093
[No Abstract] [Full Text] [Related]
3. Amyloidosis cutis dyschromica cases caused by GPNMB mutations with different inheritance patterns.
Qin W; Wang H; Zhong W; Bai J; Qiao J; Lin Z
J Dermatol Sci; 2021 Oct; 104(1):48-54. PubMed ID: 34551863
[TBL] [Abstract][Full Text] [Related]
4. Two missense mutations in GPNMB cause autosomal recessive amyloidosis cutis dyschromica in the consanguineous pakistani families.
Rahman OU; Kim J; Mahon C; Jelani M; Kang C
Genes Genomics; 2021 May; 43(5):471-478. PubMed ID: 33687658
[TBL] [Abstract][Full Text] [Related]
5. Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica.
Onoufriadis A; Hsu CK; Eide CR; Nanda A; Orchard GE; Tomita K; Sheriff A; Scott W; Tierney C; Lee JYW; Gomaa NS; Desomchoke R; Lwin SM; Tu WT; Chen LY; Huang HY; Chao SC; Yu-Yun Lee J; Bare Y; Hayday T; Guy AL; Liu L; Lees C; Hirdler T; Lovell P; Xia L; Dayrit JF; Calonje E; Simpson MA; Tolar J; Parsons M; McGrath JA
J Invest Dermatol; 2019 Dec; 139(12):2550-2554.e9. PubMed ID: 31226264
[No Abstract] [Full Text] [Related]
6. [Amyloidosis cutis dyschromica due to homozygous variants of the GPNMB gene in a Chinese pedigree].
Sha Y; Li L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Feb; 38(2):123-126. PubMed ID: 33565062
[TBL] [Abstract][Full Text] [Related]
7. Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.
Yang CF; Lin SP; Chiang CP; Wu YH; H'ng WS; Chang CP; Chen YT; Wu JY
Am J Hum Genet; 2018 Feb; 102(2):219-232. PubMed ID: 29336782
[TBL] [Abstract][Full Text] [Related]
8. Familial amyloidosis cutis dyschromica: a case report.
Dehghani F; Ebrahimzadeh M; Moghimi M; Noorbala MT
Acta Med Iran; 2014; 52(2):163-5. PubMed ID: 24659076
[TBL] [Abstract][Full Text] [Related]
9. Sex differences of Chinese patients with primary localized cutaneous amyloidosis.
Lu P; Wu F; Man M; Rong Z; Zhang Y; Yang B
J Dermatol; 2019 Jul; 46(7):e242-e243. PubMed ID: 30740762
[No Abstract] [Full Text] [Related]
10. Amyloidosis Cutis Dyschromica, a Rare Cause of Hyperpigmentation: A New Case and Literature Review.
Kuseyri O; Haas D; Lang N; Schäkel K; Bettendorf M
Pediatrics; 2017 May; 139(5):. PubMed ID: 28557715
[TBL] [Abstract][Full Text] [Related]
11. [Autosomal-recessive amylosis cutis dyschromica and GPNMB mutations].
Dereure O
Ann Dermatol Venereol; 2018 Oct; 145(10):641-642. PubMed ID: 30098817
[No Abstract] [Full Text] [Related]
12. Case of amyloidosis cutis dyschromica with dermoscopy.
Wang L; Jiang X; Zhang N; Liu L; Zhou H; Liu HJ
J Dermatol; 2019 Feb; 46(2):e77-e79. PubMed ID: 30126033
[No Abstract] [Full Text] [Related]
13. Molecular basis and inheritance patterns of amyloidosis cutis dyschromica.
Chiu FPC; Wessagowit V; Cakmak MF; Doolan BJ; Kootiratrakarn T; Chaowalit P; Bunnag T; Simpson MA; McGrath JA; Onoufriadis A
Clin Exp Dermatol; 2020 Jul; 45(5):650-653. PubMed ID: 32097499
[No Abstract] [Full Text] [Related]
14. Association of amyloidosis cutis dyschromica and familial Mediterranean fever.
Belli AA; Kara A; Dere Y; Yilmaz N
An Bras Dermatol; 2017; 92(5 Suppl 1):21-23. PubMed ID: 29267436
[TBL] [Abstract][Full Text] [Related]
15. Case of amyloidosis cutis dyschromica with palmoplantar keratoderma.
Wang X; Sun J
Australas J Dermatol; 2019 Nov; 60(4):319-320. PubMed ID: 30912135
[No Abstract] [Full Text] [Related]
16. Image Gallery: Cutaneous findings in an adult with X-linked reticulate pigmentary disorder.
Xu Z; Lin Z
Br J Dermatol; 2019 Feb; 180(2):e37. PubMed ID: 30714101
[No Abstract] [Full Text] [Related]
17. Amyloidosis cutis dyschromica treated with acitretin. A case report.
Hennessy K; Kim A; Rodriguez-Waitkus P; Morey G; Seminario-Vidal L
Dermatol Ther; 2020 Nov; 33(6):e13955. PubMed ID: 32621627
[No Abstract] [Full Text] [Related]
18. A Th2 cytokine interleukin-31 signature in a case of sporadic lichen amyloidosis.
Dousset L; Seneschal J; Boniface K; Charreau S; Ezzedine K; Milpied B; Mossalayi MD; McGrath JA; Lecron JC; Taïeb A
Acta Derm Venereol; 2015 Feb; 95(2):223-4. PubMed ID: 24573820
[No Abstract] [Full Text] [Related]
19. Familial primary localized cutaneous amyloidosis results from either dominant or recessive mutations in OSMR.
Wali A; Liu L; Takeichi T; Jelani M; Rahman OU; Heng YK; Thng S; Lee J; Akiyama M; McGrath JA; Betz RC
Acta Derm Venereol; 2015 Nov; 95(8):1005-7. PubMed ID: 25792357
[No Abstract] [Full Text] [Related]
20. Poikiloderma-like primary cutaneous amyloidosis confined to the calves in a Chinese man.
Zeng YP; Jin HZ; Fang K
J Dtsch Dermatol Ges; 2012 Sep; 10(9):663-4. PubMed ID: 22776500
[No Abstract] [Full Text] [Related]
[Next] [New Search]
