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Journal Abstract Search

108 related items for PubMed ID: 9828633

  • 1. [Hereditary benign intraepithelial dyskeratosis].
    Dithmar S, Stulting RD, Grossniklaus HE.
    Ophthalmologe; 1998 Oct; 95(10):684-6. PubMed ID: 9828633
    [Abstract] [Full Text] [Related]

  • 2. Hereditary benign intraepithelial dyskeratosis. A report of two cases from Texas.
    McLean IW, Riddle PJ, Schruggs JH, Jones DB.
    Ophthalmology; 1981 Feb; 88(2):164-8. PubMed ID: 7231902
    [Abstract] [Full Text] [Related]

  • 3. Hereditary benign intraepithelial dyskeratosis: a new case?
    Jham BC, Mesquita RA, Aguiar MC, Carmo MA.
    J Oral Pathol Med; 2007 Jan; 36(1):55-7. PubMed ID: 17181743
    [Abstract] [Full Text] [Related]

  • 4. Hereditary benign intraepithelial dyskeratosis: Report of two cases with prominent oral lesions.
    Haisley-Royster CA, Allingham RR, Klintworth GK, Prose NS.
    J Am Acad Dermatol; 2001 Oct; 45(4):634-6. PubMed ID: 11568764
    [Abstract] [Full Text] [Related]

  • 5. Clinicopathological features of a suspected case of hereditary benign intraepithelial dyskeratosis with bilateral corneas involved: a case report and mini review.
    Cai R, Zhang C, Chen R, Bi Y, Le Q.
    Cornea; 2011 Dec; 30(12):1481-4. PubMed ID: 21993456
    [Abstract] [Full Text] [Related]

  • 6. Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis.
    Soler VJ, Tran-Viet KN, Galiacy SD, Limviphuvadh V, Klemm TP, St Germain E, Fournié PR, Guillaud C, Maurer-Stroh S, Hawthorne F, Suarez C, Kantelip B, Afshari NA, Creveaux I, Luo X, Meng W, Calvas P, Cassagne M, Arné JL, Rozen SG, Malecaze F, Young TL.
    J Med Genet; 2013 Apr; 50(4):246-54. PubMed ID: 23349227
    [Abstract] [Full Text] [Related]

  • 7. Hereditary benign intraepithelial dyskeratosis: an evaluation of diagnostic cytology.
    Cummings TJ, Dodd LG, Eedes CR, Klintworth GK.
    Arch Pathol Lab Med; 2008 Aug; 132(8):1325-8. PubMed ID: 18684035
    [Abstract] [Full Text] [Related]

  • 8. Hereditary Benign Intraepithelial Dyskeratosis: Report of a Case and Re-examination of the Evidence for Locus Heterogeneity.
    Bui T, Young JW, Frausto RF, Markello TC, Glasgow BJ, Aldave AJ.
    Ophthalmic Genet; 2016 Aug; 37(1):76-80. PubMed ID: 24555743
    [Abstract] [Full Text] [Related]

  • 9. A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis.
    Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM.
    Am J Hum Genet; 2001 Feb; 68(2):491-4. PubMed ID: 11170897
    [Abstract] [Full Text] [Related]

  • 10. Chronic keratoconjunctivitis associated with congenital dyskeratosis and erythrokeratodermia variablis. Two rare genodermatoses.
    Merchant A, Zhao TZ, Foster CS.
    Ophthalmology; 1998 Jul; 105(7):1286-91. PubMed ID: 9663235
    [Abstract] [Full Text] [Related]

  • 11. Hereditary benign intraepithelial dyskeratosis: case report.
    Baroni A, Palla M, Aiello FS, Ruocco E, Faccenda F, Vozza A, Satriano RA.
    Int J Dermatol; 2009 Jun; 48(6):627-9. PubMed ID: 19538374
    [No Abstract] [Full Text] [Related]

  • 12. Dyskeratosis congenita with linear areas of severe cutaneous involvement.
    Baselga E, Drolet BA, van Tuinen P, Esterly NB, Happle R.
    Am J Med Genet; 1998 Feb 17; 75(5):492-6. PubMed ID: 9489792
    [Abstract] [Full Text] [Related]

  • 13. Case Series of Patients With Hereditary Benign Intraepithelial Dyskeratosis.
    Seely M, Jackson K, Meeker A, Daluvoy M.
    Cornea; 2022 Nov 01; 41(11):1451-1454. PubMed ID: 36219214
    [Abstract] [Full Text] [Related]

  • 14. Dyskeratosis congenita: oral hyperkeratosis in association with lichenoid reaction.
    Handley TP, Ogden GR.
    J Oral Pathol Med; 2006 Sep 01; 35(8):508-12. PubMed ID: 16918603
    [Abstract] [Full Text] [Related]

  • 15. Dyskeratosis congenita.
    Handley TP, McCaul JA, Ogden GR.
    Oral Oncol; 2006 Apr 01; 42(4):331-6. PubMed ID: 16140563
    [Abstract] [Full Text] [Related]

  • 16. [Dyskeratosis congenita: an update].
    Mialou V, Leblanc T, Peffault de Latour R, Dalle JH, Socié G.
    Arch Pediatr; 2013 Mar 01; 20(3):299-306. PubMed ID: 23352883
    [Abstract] [Full Text] [Related]

  • 17. Retinal vasculopathy in autosomal dominant dyskeratosis congenita due to TINF2 mutation.
    Gleeson M, O'Marcaigh A, Cotter M, Brosnahan D, Vulliamy T, Smith OP.
    Br J Haematol; 2012 Dec 01; 159(5):498. PubMed ID: 23094712
    [No Abstract] [Full Text] [Related]

  • 18. A case of dyskeratosis congenita associated with impaired DNA repair as shown by the comet assay.
    Mazereeuw-Hautier J, Cayrol-Baudouin C, Lachgar S, Pinteaux M, Cambon L, Charveron M, Bonafé J.
    Eur J Dermatol; 1999 Dec 01; 9(7):529-32. PubMed ID: 10523729
    [Abstract] [Full Text] [Related]

  • 19. The presence of Candida albicans in hereditary benign intraepithelial dyskeratosis. An ultrastructural observation.
    Sadeghi EM, Witkop CJ.
    Oral Surg Oral Med Oral Pathol; 1979 Oct 01; 48(4):342-6. PubMed ID: 388275
    [Abstract] [Full Text] [Related]

  • 20. Oral carcinoma in a young man: a case of dyskeratosis congenita.
    Moretti S, Spallanzani A, Chiarugi A, Muscarella G, Battini ML.
    J Eur Acad Dermatol Venereol; 2000 Mar 01; 14(2):123-5. PubMed ID: 10972098
    [Abstract] [Full Text] [Related]

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