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Journal Abstract Search

258 related items for PubMed ID: 23974601

  • 1. Vohwinkel syndrome with mental retardation.
    Mercy P, Singh A, Ghorpade AK, Das MN, Upadhyay A, Keswani N.
    Indian J Dermatol Venereol Leprol; 2013; 79(5):725. PubMed ID: 23974601
    [No Abstract] [Full Text] [Related]

  • 2. A new variant of Vohwinkel syndrome: a case report.
    Seirafi H, Khezri S, Morowati S, Kamyabhesari K, Mirzaeipour M, Khezri F.
    Dermatol Online J; 2011 Mar 15; 17(3):3. PubMed ID: 21426869
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  • 3. Vohwinkel syndrome, ichthyosiform variant--by Camisa--case report.
    Corte LD, Silva MV, Oliveira CF, Vetoratto G, Steglich RB, Borges J.
    An Bras Dermatol; 2013 Mar 15; 88(6 Suppl 1):206-8. PubMed ID: 24346921
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  • 5. Vohwinkel syndrome: ichthyosiform variant in a family.
    Reinehr CPH, Peruzzo J, Cestari T.
    An Bras Dermatol; 2018 Mar 15; 93(5):723-725. PubMed ID: 30156625
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  • 6. D66H mutation in GJB2 gene in a Chinese family with classical Vohwinkel syndrome.
    Qiu Y, Wang Z, Chen N, Song Y, Wang Z, Zhang L.
    Indian J Dermatol Venereol Leprol; 2012 Mar 15; 78(5):640-2. PubMed ID: 22960825
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  • 10. Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia.
    Wei S, Zhou Y, Zhang TD, Huang ZM, Zhang XB, Zhu HL, Liang BH, Lin L, Deng L.
    Clin Exp Dermatol; 2011 Jun 15; 36(4):399-405. PubMed ID: 21198793
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  • 11. [Vohwinkel syndrome. Hearing loss and keratoderma on the hands and feet].
    Dippold S, Butsch F, Schopf R, Keilmann A.
    HNO; 2013 Jul 15; 61(7):617-9. PubMed ID: 23247752
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  • 12. Low-dose isotretinoin prevents digital amputation in loricrin keratoderma (Vohwinkel syndrome with ichthyosis).
    Nico MMS, Fernandes JD.
    J Dtsch Dermatol Ges; 2017 Jun 15; 15(6):665-667. PubMed ID: 28591443
    [No Abstract] [Full Text] [Related]

  • 13. Suppressing AP1 factor signaling in the suprabasal epidermis produces a keratoderma phenotype.
    Rorke EA, Adhikary G, Young CA, Roop DR, Eckert RL.
    J Invest Dermatol; 2015 Jan 15; 135(1):170-180. PubMed ID: 25050598
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  • 15. Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?
    Steijlen PM, Neumann HA, der Kinderen DJ, Smeets DF, van der Kerkhof PC, Happle R.
    J Am Acad Dermatol; 1994 May 15; 30(5 Pt 2):893-8. PubMed ID: 8169270
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  • 16. Unique autosomal recessive variant of palmoplantar keratoderma associated with hearing loss not caused by known mutations.
    Hegazi MA, Manou S, Sakr H, Camp GV.
    An Bras Dermatol; 2017 May 15; 92(5 Suppl 1):154-158. PubMed ID: 29267478
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  • 17. An apparently new mental retardation syndrome in three elderly sisters.
    Viljoen DL, Kallis J, Voges S, Marais AS, van Vuuren I.
    Clin Genet; 1991 Jul 15; 40(1):6-11. PubMed ID: 1884519
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  • 19. A family of Bart-Pumphrey syndrome.
    Gönül M, Gül Ü, Hizli P, Hizli Ö.
    Indian J Dermatol Venereol Leprol; 2012 Jul 15; 78(2):178-81. PubMed ID: 22421650
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  • 20. Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
    Paes-Alves AF, Azevêdo ES, Sousa MG, Almeida-Melo N, Oliveira-Filho OJ.
    Am J Med Genet; 1991 Nov 01; 41(2):141-52. PubMed ID: 1785624
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