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Pubmed for Handhelds

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Journal Abstract Search

317 related items for PubMed ID: 511082

  • 21. Monilethrix: three cases.
    Penchaszadeh VB.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):262-4. PubMed ID: 5173278
    [No Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities.
    Farkas K, Nagy N, Kinyó A, Kemény L, Széll M.
    Arch Dermatol Res; 2012 Oct; 304(8):679-81. PubMed ID: 22584530
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  • 25. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
    Wali A, Chishti M, Ayub M, Yasinzai M, Kafaitullah, Ali G, John P, Ahmad W.
    Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
    [Abstract] [Full Text] [Related]

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

  • 27. Hereditary hypotrichosis (Marie Unna type).
    Peachey RD, Wells RS.
    Trans St Johns Hosp Dermatol Soc; 1971 Jul; 57(1):157-66. PubMed ID: 5570254
    [No Abstract] [Full Text] [Related]

  • 28. Marie Unna hypotrichosis in a Chinese family.
    Wong SN, Giam YC, Lee YS.
    Pediatr Dermatol; 2002 Jul; 19(3):250-5. PubMed ID: 12047647
    [Abstract] [Full Text] [Related]

  • 29. Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript.
    Ramot Y, Horev L, Smolovich I, Molho-Pessach V, Zlotogorski A.
    Exp Dermatol; 2010 Aug; 19(8):e320-2. PubMed ID: 20163456
    [Abstract] [Full Text] [Related]

  • 30. 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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  • 33. An unusual defect resembling pili bifurcati.
    Sala F, Crosti C, Bencini PL, Menni S.
    Arch Dermatol; 1985 Jun; 121(6):718. PubMed ID: 4004299
    [No Abstract] [Full Text] [Related]

  • 34. [Erythrodermia ichthyosiformis congenita with hypotrichosis, anhidrosis, deaf-mutism and decreased elimination of various amino acids in the urine].
    Salamon T, Budai V, Lazović O, Macanović K, Volić N.
    Hautarzt; 1974 Sep; 25(9):448-53. PubMed ID: 4617749
    [No Abstract] [Full Text] [Related]

  • 35. 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
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  • 36. Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis.
    Kim JK, Kim E, Baek IC, Kim BK, Cho AR, Kim TY, Song CW, Seong JK, Yoon JB, Stenn KS, Parimoo S, Yoon SK.
    Hum Mol Genet; 2010 Feb 01; 19(3):445-53. PubMed ID: 19897589
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  • 38. Hypotrichosis, hair structure defects, hypercysteine hair and glucosuria: a new genetic syndrome?
    Blume-Peytavi U, Föhles J, Schulz R, Wortmann G, Gollnick H, Orfanos CE.
    Br J Dermatol; 1996 Feb 01; 134(2):319-24. PubMed ID: 8746349
    [Abstract] [Full Text] [Related]

  • 39. Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.
    Whyte MP, Petersen DJ, McAlister WH.
    Am J Med Genet; 1990 Jul 01; 36(3):288-91. PubMed ID: 2363424
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  • 40. An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family.
    Baumer A, Belli S, Trüeb RM, Schinzel A.
    Eur J Hum Genet; 2000 Jun 01; 8(6):443-8. PubMed ID: 10878665
    [Abstract] [Full Text] [Related]

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