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Journal Abstract Search

241 related items for PubMed ID: 12895008

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
    Düzenli S, Redler S, Müller M, Polat M, Dogruer D, Pasternack SM, Betz RC.
    Clin Exp Dermatol; 2009 Dec; 34(8):e953-6. PubMed ID: 20055871
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  • 4. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B, Hundeiker M.
    Fortschr Med; 1979 Nov 22; 97(44):2018-22. PubMed ID: 511082
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  • 5. 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 22; 64(4):e45-50. PubMed ID: 20659777
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  • 6. Marie Unna hypotrichosis in a Chinese family.
    Wong SN, Giam YC, Lee YS.
    Pediatr Dermatol; 2002 Apr 22; 19(3):250-5. PubMed ID: 12047647
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  • 7. Marie Unna hereditary hypotrichosis.
    Argenziano G, Sammarco E, Rossi A, Delfino M, Calvieri S.
    Eur J Dermatol; 1999 Jun 22; 9(4):278-80. PubMed ID: 10356404
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  • 9. Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity.
    Yan KL, He PP, Yang S, Li M, Yang Q, Ren YQ, Cui Y, Gao M, Xiao FL, Huang W, Zhang XJ.
    Clin Exp Dermatol; 2004 Sep 22; 29(5):460-3. PubMed ID: 15347323
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  • 10. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.
    He PP, Zhang XJ, Yang Q, Li M, Liang YH, Yang S, Yan KL, Cui Y, Shen YY, Wang HY, Sun LD, Du WH, Shen YJ, Xu SJ, Huang W.
    Br J Dermatol; 2004 May 22; 150(5):837-42. PubMed ID: 15149494
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  • 11. Marie Unna congenital hypotrichosis: clinical description, histopathology, scanning electron microscopy of a previously unreported large pedigree.
    Roberts JL, Whiting DA, Henry D, Basler G, Woolf L.
    J Investig Dermatol Symp Proc; 1999 Dec 22; 4(3):261-7. PubMed ID: 10674378
    [Abstract] [Full Text] [Related]

  • 12. [Hypotrichosis congenita hereditaria Maria Unna].
    Wirth G, Bindewald I, Küster W, Goerz G.
    Hautarzt; 1985 Oct 22; 36(10):577-80. PubMed ID: 4066319
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  • 13. Marie-Unna hereditary hypotrichosis: case report and review of the literature.
    Podjasek JO, Hand JL.
    Pediatr Dermatol; 2011 Oct 22; 28(2):202-4. PubMed ID: 21504454
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  • 15. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.
    Lefevre P, Rochat A, Bodemer C, Vabres P, Barrandon Y, de Prost Y, Garner C, Hovnanian A.
    Eur J Hum Genet; 2000 Apr 22; 8(4):273-9. PubMed ID: 10854110
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  • 17. Identification of a novel sporadic U2HR pathogenic variant in a patient with Marie Unna hereditary hypotrichosis.
    Braun T, Wehner M, Teichler A, Betz RC, Hoeger PH.
    Pediatr Dermatol; 2023 Apr 22; 40(3):466-467. PubMed ID: 37012647
    [Abstract] [Full Text] [Related]

  • 18. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
    Cichon S, Kruse R, Hillmer AM, Kukuk G, Anker M, Altland K, Knapp M, Propping P, Nöthen MM.
    Br J Dermatol; 2000 Oct 22; 143(4):811-4. PubMed ID: 11069461
    [Abstract] [Full Text] [Related]

  • 19. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3.
    Yang S, Gao M, Cui Y, Yan KL, Ren YQ, Zhang GL, Wang PG, Xiao FL, Du WH, Liang YH, Sun LD, Xu SJ, Huang W, Zhang XJ.
    J Invest Dermatol; 2005 Oct 22; 125(4):711-4. PubMed ID: 16185270
    [Abstract] [Full Text] [Related]

  • 20. Hereditary hypotrichosis simplex of the scalp.
    Rodríguez Díaz E, Fernández Blasco G, Martín Pascual A, Armijo M.
    Dermatology; 1995 Oct 22; 191(2):139-41. PubMed ID: 8520061
    [Abstract] [Full Text] [Related]

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