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Results: 1 to 20 of 127

Similar articles for PubMed (Select 21537821)

1.

Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias.

Suga H, Tsunemi Y, Sugaya M, Shinkuma S, Akiyama M, Shimizu H, Sato S.

Acta Derm Venereol. 2011 Jun;91(4):486-8. doi: 10.2340/00015555-1095. Review. No abstract available.

2.

A large duplication in LIPH underlies autosomal recessive hypotrichosis simplex in four Middle Eastern families.

Nahum S, Pasternack SM, Pforr J, Indelman M, Wollnik B, Bergman R, Nöthen MM, König A, Khamaysi Z, Betz RC, Sprecher E.

Arch Dermatol Res. 2009 Jun;301(5):391-3. doi: 10.1007/s00403-008-0903-9. Epub 2008 Sep 27.

PMID:
18820939
3.

Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).

Naz G, Khan B, Ali G, Azeem Z, Wali A, Ansar M, Ahmad W.

J Dermatol Sci. 2009 Apr;54(1):12-6. doi: 10.1016/j.jdermsci.2008.12.001. Epub 2009 Jan 23.

PMID:
19167195
4.

[Hypotrichosis congenita hereditaria Maria Unna].

Wirth G, Bindewald I, Küster W, Goerz G.

Hautarzt. 1985 Oct;36(10):577-80. German.

PMID:
4066319
5.

Mutations in lipase H gene underlie autosomal recessive hypotrichosis in five Pakistani families.

Kalsoom UE, Habib R, Khan B, Ali G, Ali N, Ansar M, Ahmad W.

Acta Derm Venereol. 2010;90(1):93-4. doi: 10.2340/00015555-0766. No abstract available.

6.

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. doi: 10.1111/j.1365-2230.2011.04014.x. Epub 2011 Mar 21.

PMID:
21426374
7.

Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair.

Horev L, Tosti A, Rosen I, Hershko K, Vincenzi C, Nanova K, Mali A, Potikha T, Zlotogorski A.

J Am Acad Dermatol. 2009 Nov;61(5):813-8. doi: 10.1016/j.jaad.2009.04.020. Epub 2009 Sep 18.

PMID:
19766349
8.

Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.

Tariq M, Ayub M, Jelani M, Basit S, Naz G, Wasif N, Raza SI, Naveed AK, ullah Khan S, Azeem Z, Yasinzai M, Wali A, Ali G, Chishti MS, Ahmad W.

Br J Dermatol. 2009 May;160(5):1006-10. doi: 10.1111/j.1365-2133.2009.09046.x. Epub 2009 Mar 9.

PMID:
19292720
9.

Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis.

Shimomura Y, Sakamoto F, Kariya N, Matsunaga K, Ito M.

J Invest Dermatol. 2006 Jun;126(6):1281-5.

10.

A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis.

Ali G, Chishti MS, Raza SI, John P, Ahmad W.

Hum Genet. 2007 May;121(3-4):319-25. Epub 2007 Feb 27.

PMID:
17333281
11.

Homozygous missense mutation in the LIPH gene causing autosomal recessive hypotrichosis simplex in a Chinese patient.

Liu LH, Wang JW, Chen G, Chang RX, Zhou Y, Tang HY, Zhu J, Wang PG, Yang S, Zhang XJ.

J Dermatol. 2014 Jan;41(1):105-7. doi: 10.1111/1346-8138.12309. Epub 2013 Dec 20. No abstract available.

PMID:
24354445
12.

Hereditary hypotrichosis. A previously undescribed syndrome.

Bentley-Phillips B, Grace HJ.

Br J Dermatol. 1979 Sep;101(3):331-9.

PMID:
508598
13.

Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis.

Shimomura Y, Ito M, Christiano AM.

J Dermatol Sci. 2009 Dec;56(3):205-7. doi: 10.1016/j.jdermsci.2009.08.005. Epub 2009 Nov 4. No abstract available.

14.

Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair.

Pasternack SM, Murugusundram S, Eigelshoven S, Müller M, Kruse R, Lehmann P, Betz RC.

Arch Dermatol Res. 2009 Sep;301(8):621-4. doi: 10.1007/s00403-009-0971-5. Epub 2009 Jun 16.

PMID:
19529952
15.

A missense mutation within the helix initiation motif of the keratin K71 gene underlies autosomal dominant woolly hair/hypotrichosis.

Fujimoto A, Farooq M, Fujikawa H, Inoue A, Ohyama M, Ehama R, Nakanishi J, Hagihara M, Iwabuchi T, Aoki J, Ito M, Shimomura Y.

J Invest Dermatol. 2012 Oct;132(10):2342-9. doi: 10.1038/jid.2012.154. Epub 2012 May 17.

16.

Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance.

Toribio J, Quiñones PA.

Br J Dermatol. 1974 Dec;91(6):687-96. No abstract available.

PMID:
4141628
17.

A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophy.

Indelman M, Bergman R, Lurie R, Richard G, Miller B, Petronius D, Ciubutaro D, Leibu R, Sprecher E.

J Invest Dermatol. 2002 Nov;119(5):1210-3.

18.

The β9 loop domain of PA-PLA1α has a crucial role in autosomal recessive woolly hair/hypotrichosis.

Shinkuma S, Inoue A, Aoki J, Nishie W, Natsuga K, Ujiie H, Nomura T, Abe R, Akiyama M, Shimizu H.

J Invest Dermatol. 2012 Aug;132(8):2093-5. doi: 10.1038/jid.2012.96. Epub 2012 Apr 5. No abstract available.

19.

Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.

Schaffer JV, Bazzi H, Vitebsky A, Witkiewicz A, Kovich OI, Kamino H, Shapiro LS, Amin SP, Orlow SJ, Christiano AM.

J Invest Dermatol. 2006 Jun;126(6):1286-91.

20.

Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis.

Ito T, Shimomura Y, Ogai M, Sakabe J, Tokura Y.

J Dermatol. 2013 Apr;40(4):278-80. doi: 10.1111/1346-8138.12068. Epub 2013 Jan 7. No abstract available.

PMID:
23293922
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