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Journal Abstract Search

161 related items for PubMed ID: 25692760

  • 21. Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients.
    Mazereeuw-Hautier J, Bitoun E, Chevrant-Breton J, Man SY, Bodemer C, Prins C, Antille C, Saurat JH, Atherton D, Harper JI, Kelsell DP, Hovnanian A.
    Br J Dermatol; 2007 May; 156(5):1015-9. PubMed ID: 17381453
    [Abstract] [Full Text] [Related]

  • 22. Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome.
    Yotsumoto S, Hashiguchi T, Chen X, Ohtake N, Tomitaka A, Akamatsu H, Matsunaga K, Shiraishi S, Miura H, Adachi J, Kanzaki T.
    Br J Dermatol; 2003 Apr; 148(4):649-53. PubMed ID: 12752120
    [Abstract] [Full Text] [Related]

  • 23. Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome.
    Griffith AJ, Yang Y, Pryor SP, Park HJ, Jabs EW, Nadol JB, Russell LJ, Wasserman DI, Richard G, Adams JC, Merchant SN.
    Laryngoscope; 2006 Aug; 116(8):1404-8. PubMed ID: 16885744
    [Abstract] [Full Text] [Related]

  • 24. A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome?
    Lazic T, Horii KA, Richard G, Wasserman DI, Antaya RJ.
    Pediatr Dermatol; 2008 Aug; 25(5):535-40. PubMed ID: 18950394
    [Abstract] [Full Text] [Related]

  • 25. Porokeratotic eccrine ostial and dermal duct nevus: a case report and review of the literature.
    Sassmannshausen J, Bogomilsky J, Chaffins M.
    J Am Acad Dermatol; 2000 Aug; 43(2 Pt 2):364-7. PubMed ID: 10901725
    [Abstract] [Full Text] [Related]

  • 26. Porokeratotic eccrine ostial and dermal duct nevus.
    Fernández-Redondo V, Toribio J.
    J Cutan Pathol; 1988 Dec; 15(6):393-5. PubMed ID: 3220997
    [Abstract] [Full Text] [Related]

  • 27. A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation.
    Arndt S, Aschendorff A, Schild C, Beck R, Maier W, Laszig R, Birkenhäger R.
    Otol Neurotol; 2010 Feb; 31(2):210-5. PubMed ID: 20101161
    [Abstract] [Full Text] [Related]

  • 28. Long-standing filiform, blaschkoid papules. Porokeratotic eccrine and ostial dermal duct nevus (PEODDN).
    Koch E, Johnson L, Gehris R.
    JAMA Dermatol; 2013 Jul; 149(7):869-70. PubMed ID: 23752694
    [No Abstract] [Full Text] [Related]

  • 29. A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome.
    Koppelhus U, Tranebjaerg L, Esberg G, Ramsing M, Lodahl M, Rendtorff ND, Olesen HV, Sommerlund M.
    Clin Exp Dermatol; 2011 Mar; 36(2):142-8. PubMed ID: 20846357
    [Abstract] [Full Text] [Related]

  • 30. Mutations of connexin 26 (GJB2) gene in a Chinese keratitis-ichthyosis-deafness syndrome patient with squamous cell carcinoma.
    Liu J, Fang S, Ding Q, Wang Y, Ye T, Zhu H, Zhang X, Li B, Xu Y, Li Z.
    J Dermatol; 2016 Jan; 43(1):104-6. PubMed ID: 26444850
    [No Abstract] [Full Text] [Related]

  • 31. Porokeratotic eccrine ostial and dermal duct nevus - revisited.
    Bhunia D, Ghosh S, Rudra O, Biswas SK.
    Dermatol Online J; 2014 Sep 16; 20(9):. PubMed ID: 25244169
    [Abstract] [Full Text] [Related]

  • 32. Connexin 26 (GJB2) mutations in keratitis-ichthyosis-deafness syndrome presenting with squamous cell carcinoma.
    Sakabe J, Yoshiki R, Sugita K, Haruyama S, Sawada Y, Kabashima R, Bito T, Nakamura M, Tokura Y.
    J Dermatol; 2012 Sep 16; 39(9):814-5. PubMed ID: 22098592
    [No Abstract] [Full Text] [Related]

  • 33. Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness.
    Gerido DA, DeRosa AM, Richard G, White TW.
    Am J Physiol Cell Physiol; 2007 Jul 16; 293(1):C337-45. PubMed ID: 17428836
    [Abstract] [Full Text] [Related]

  • 34. Porokeratotic eccrine and hair follicle nevus: a report of two cases and review of the literature.
    Agulló-Pérez AD, Resano-Abarzuza MÁ, Córdoba-Iturriagagoitia A, Yanguas-Bayona JI.
    An Bras Dermatol; 2017 Jul 16; 92(5 Suppl 1):121-125. PubMed ID: 29267468
    [Abstract] [Full Text] [Related]

  • 35. Ultrapulse carbon dioxide laser treatment of porokeratotic eccrine ostial and dermal duct nevus.
    Jain S, Sardana K, Garg VK.
    Pediatr Dermatol; 2013 Jul 16; 30(2):264-6. PubMed ID: 22339989
    [Abstract] [Full Text] [Related]

  • 36. Porokeratosis palmaris et plantaris disseminata or a disseminated late-onset variant of porokeratotic eccrine ostial and dermal ductal nevus (PEODDN) with follicular involvement.
    Hartman R, Rizzo C, Patel R, Kamino H, Shupack JL.
    Dermatol Online J; 2009 Aug 15; 15(8):8. PubMed ID: 19891916
    [Abstract] [Full Text] [Related]

  • 37. Widespread porokeratotic adnexal ostial nevus: clinical features and proposal of a new name unifying porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus.
    Goddard DS, Rogers M, Frieden IJ, Krol AL, White CR, Jayaraman AG, Robinson-Bostom L, Bruckner AL, Ruben BS.
    J Am Acad Dermatol; 2009 Dec 15; 61(6):1060.e1-14. PubMed ID: 19664847
    [Abstract] [Full Text] [Related]

  • 38. Porokeratotic adnexal ostial nevus: A paradigm of cutaneous mosaicism.
    Kiely L, Ni Mhaolcatha S, Fitzgibbon J, Murphy LA, O'Connor C.
    Clin Case Rep; 2022 Apr 15; 10(4):e05728. PubMed ID: 35432995
    [Abstract] [Full Text] [Related]

  • 39. Trichothiodystrophy-like hair abnormalities in a child with keratitis ichthyosis deafness syndrome.
    De Raeve L, Bonduelle M, Deconinck H, Roseeuw D, Stene JJ.
    Pediatr Dermatol; 2008 Apr 15; 25(4):466-9. PubMed ID: 18789090
    [Abstract] [Full Text] [Related]

  • 40. The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome.
    Mese G, Sellitto C, Li L, Wang HZ, Valiunas V, Richard G, Brink PR, White TW.
    Mol Biol Cell; 2011 Dec 15; 22(24):4776-86. PubMed ID: 22031297
    [Abstract] [Full Text] [Related]

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