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Journal Abstract Search

175 related items for PubMed ID: 10971339

  • 1. Congenital hypotrichosis due to short anagen.
    Barraud-Klenovsek MM, Trüeb RM.
    Br J Dermatol; 2000 Sep; 143(3):612-7. PubMed ID: 10971339
    [Abstract] [Full Text] [Related]

  • 2. Hereditary hypotrichosis of the scalp.
    Hess RO, Uno H.
    Am J Med Genet; 1991 May 01; 39(2):125-9. PubMed ID: 2063912
    [Abstract] [Full Text] [Related]

  • 3. 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 01; 4(3):261-7. PubMed ID: 10674378
    [Abstract] [Full Text] [Related]

  • 4. Hereditary hypotrichosis simplex of the scalp.
    Rodríguez Díaz E, Fernández Blasco G, Martín Pascual A, Armijo M.
    Dermatology; 1995 Dec 01; 191(2):139-41. PubMed ID: 8520061
    [Abstract] [Full Text] [Related]

  • 5. Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance.
    Toribio J, Quiñones PA.
    Br J Dermatol; 1974 Dec 01; 91(6):687-96. PubMed ID: 4141628
    [No Abstract] [Full Text] [Related]

  • 6. Congenital hypotrichosis and milia: report of a large family suggesting X-linked dominant inheritance.
    Rapelanoro R, Taïeb A, Lacombe D.
    Am J Med Genet; 1994 Oct 01; 52(4):487-90. PubMed ID: 7747764
    [Abstract] [Full Text] [Related]

  • 7. Marie Unna hereditary hypotrichosis.
    Argenziano G, Sammarco E, Rossi A, Delfino M, Calvieri S.
    Eur J Dermatol; 1999 Jun 01; 9(4):278-80. PubMed ID: 10356404
    [Abstract] [Full Text] [Related]

  • 8. A sporadic case of congenital hypotrichosis simplex of the scalp: difficulties in diagnosis and classification.
    Cambiaghi S, Barbareschi M.
    Pediatr Dermatol; 1999 Jun 01; 16(4):301-4. PubMed ID: 10469417
    [Abstract] [Full Text] [Related]

  • 9. Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
    Ibsen HH, Clemmensen OJ, Brandrup F.
    Acta Derm Venereol; 1991 Jun 01; 71(4):349-51. PubMed ID: 1681656
    [Abstract] [Full Text] [Related]

  • 10. Autosomal recessive hypotrichosis with loose anagen hairs associated with TKFC mutations.
    Onoufriadis A, Cabezas A, Ng JCF, Canales J, Costas MJ, Ribeiro JM, Rodrigues JR, McAleer MA, Castelo-Soccio L, Simpson MA, Fraternali F, Irvine AD, Cameselle JC, McGrath JA.
    Br J Dermatol; 2021 May 01; 184(5):935-943. PubMed ID: 32790068
    [Abstract] [Full Text] [Related]

  • 11. Hereditary hypotrichosis simplex: report of a family.
    Al Aboud K, Al Hawsawi K, Al Aboud D, Al Githami A.
    Clin Exp Dermatol; 2002 Nov 01; 27(8):654-6. PubMed ID: 12472539
    [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 01; 16(1):11-5. PubMed ID: 7648037
    [Abstract] [Full Text] [Related]

  • 13. Loose anagen hair syndrome: an underdiagnosed condition in males.
    Pham CM, Krejci-Manwaring J.
    Pediatr Dermatol; 2010 Mar 01; 27(4):408-9. PubMed ID: 20653870
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Autosomal dominant ectodermal dysplasia.
    Jorgenson RJ, Dowben JS, Dowben SL.
    J Craniofac Genet Dev Biol; 1987 Jun 01; 7(4):403-12. PubMed ID: 3429615
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 132(10):2342-2349. PubMed ID: 22592156
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 152A(10):2628-33. PubMed ID: 20814945
    [Abstract] [Full Text] [Related]

  • 18. [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
    [Abstract] [Full Text] [Related]

  • 19. [Hereditary congenital hypotrichosis, Marie Unna type].
    Chlebarov S.
    Z Hautkr; 1985 Apr 01; 60(7):583-96. PubMed ID: 4002769
    [Abstract] [Full Text] [Related]

  • 20. Hereditary hypotrichosis. A previously undescribed syndrome.
    Bentley-Phillips B, Grace HJ.
    Br J Dermatol; 1979 Sep 01; 101(3):331-9. PubMed ID: 508598
    [Abstract] [Full Text] [Related]

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