116 related articles for article (PubMed ID: 22082473)
1. Marie-Unna hereditary hypotrichosis or autosomal recessive hereditary hypotrichosis with woolly hair: the diagnostic dilemma of labeling cases with hypotrichosis.
Aboud KA; Aboud DA
Pediatr Dermatol; 2011; 28(6):750-751. PubMed ID: 22082473
[No Abstract] [Full Text] [Related]
2. Marie-Unna hereditary hypotrichosis: case report and review of the literature.
Podjasek JO; Hand JL
Pediatr Dermatol; 2011; 28(2):202-4. PubMed ID: 21504454
[TBL] [Abstract][Full Text] [Related]
3. Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
Green J; Fitzpatrick E; de Berker D; Forrest SM; Sinclair RD
J Investig Dermatol Symp Proc; 2003 Jun; 8(1):121-5. PubMed ID: 12895008
[TBL] [Abstract][Full Text] [Related]
4. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
Spiegl B; Hundeiker M
Fortschr Med; 1979 Nov; 97(44):2018-22. PubMed ID: 511082
[TBL] [Abstract][Full Text] [Related]
5. Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutation.
Mansur AT; Elcioglu NH; Redler S; Serdar ZA; Cetinel S; Betz RC; Akarsu NA
Am J Med Genet A; 2010 Oct; 152A(10):2628-33. PubMed ID: 20814945
[TBL] [Abstract][Full Text] [Related]
6. Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan.
Takeichi T; Tanahashi K; Taki T; Kono M; Sugiura K; Akiyama M
Br J Dermatol; 2017 Jul; 177(1):290-292. PubMed ID: 27641630
[No Abstract] [Full Text] [Related]
7. Marie-unna hereditary hypotrichosis.
Srinivas SM; Hiremagalore R
Int J Trichology; 2014 Oct; 6(4):182-4. PubMed ID: 25368478
[TBL] [Abstract][Full Text] [Related]
8. Marie Unna hereditary hypotrichosis.
Argenziano G; Sammarco E; Rossi A; Delfino M; Calvieri S
Eur J Dermatol; 1999 Jun; 9(4):278-80. PubMed ID: 10356404
[TBL] [Abstract][Full Text] [Related]
9. [Hereditary congenital hypotrichosis, Marie Unna type].
Chlebarov S
Z Hautkr; 1985 Apr; 60(7):583-96. PubMed ID: 4002769
[TBL] [Abstract][Full Text] [Related]
10. Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review.
Mizukami Y; Hayashi R; Tsuruta D; Shimomura Y; Sugawara K
J Dermatol; 2018 May; 45(5):613-617. PubMed ID: 29464811
[TBL] [Abstract][Full Text] [Related]
11. Hereditary hypotrichosis (Marie-Unna type) (two cases).
Hutchinson PE; Wells RS
Proc R Soc Med; 1975 Aug; 68(8):534-5. PubMed ID: 1202498
[No Abstract] [Full Text] [Related]
12. Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance.
Souied E; Amalric P; Chauvet ML; Chevallier C; Le Hoang P; Munnich A; Kaplan J
Ophthalmic Genet; 1995 Mar; 16(1):11-5. PubMed ID: 7648037
[TBL] [Abstract][Full Text] [Related]
13. Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report.
Redler S; Kruse R; Eigelshoven S; Hanneken S; Refke M; Wen Y; Zhang X; Cichon S; Betz RC; Nöthen MM
J Am Acad Dermatol; 2011 Apr; 64(4):e45-50. PubMed ID: 20659777
[TBL] [Abstract][Full Text] [Related]
14. Marie Unna hypotrichosis in a Chinese family.
Wong SN; Giam YC; Lee YS
Pediatr Dermatol; 2002; 19(3):250-5. PubMed ID: 12047647
[TBL] [Abstract][Full Text] [Related]
15. Light and scanning electron microscopic examination of late changes in hair with hereditary trichodysplasia (Marie Unna hypotrichosis).
Celik HH; Surucu SH; Aldur MM; Ozdemir BM; Karaduman AA; Cumhur MM
Saudi Med J; 2004 Nov; 25(11):1648-51. PubMed ID: 15573195
[TBL] [Abstract][Full Text] [Related]
16. Novel mutation in LIPH in a Lebanese patient with autosomal recessive woolly hair/hypotrichosis.
Sleiman MB; Sleiman MB; Abbas O; Btadini W; Najjar T; Tofaili M; Chedraoui A; Khalil S; Kibbi AG; Kurban M
J Dermatol; 2015 Aug; 42(8):822-4. PubMed ID: 26046953
[No Abstract] [Full Text] [Related]
17. Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.
Khan S; Habib R; Mir H; Umm-e-Kalsoom ; Naz G; Ayub M; Shafique S; Yamin T; Ali N; Basit S; Wasif N; Kamran-Ul-Hassan Naqvi S; Ali G; Wali A; Ansar M; Ahmad W
Clin Exp Dermatol; 2011 Aug; 36(6):652-4. PubMed ID: 21426374
[TBL] [Abstract][Full Text] [Related]
18. Hereditary hypotrichosis (Marie-Unna type) and juvenile macular degeneration (Stargardt's maculopathy).
Marren P; Wilson C; Dawber RP; Walshe MM
Clin Exp Dermatol; 1992 May; 17(3):189-91. PubMed ID: 1451298
[TBL] [Abstract][Full Text] [Related]
19. Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families.
Ahmad F; Sharif S; Furqan Ubaid M; Shah K; Khan MN; Umair M; Azeem Z; Ahmad W
Congenit Anom (Kyoto); 2018 Jan; 58(1):24-28. PubMed ID: 28425126
[TBL] [Abstract][Full Text] [Related]
20. A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosis.
Liu LH; Chen G; Wang JW; Liu SX; Wang JB; Zhou FS; Zhu J; Sun LD; Gao M; Wang PG; Yang S; Zhang XJ
Clin Exp Dermatol; 2013 Oct; 38(7):796-8. PubMed ID: 23773027
[No Abstract] [Full Text] [Related]
[Next] [New Search]
