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Journal Abstract Search

430 related items for PubMed ID: 16403385

  • 21.
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  • 23. Lamellar ichthyosis with a novel homozygous C-terminal mutation in the transglutaminase-1 gene.
    Rodríguez-Pazos L, Ginarte M, Vega-Gliemmo A, Toribio J.
    Int J Dermatol; 2009 Nov; 48(11):1195-7. PubMed ID: 20064174
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  • 24. Stratum corneum hydration and flexibility are useful parameters to indicate clinical severity of congenital ichthyosis.
    Tomita Y, Akiyama M, Shimizu H.
    Exp Dermatol; 2005 Aug; 14(8):619-24. PubMed ID: 16026584
    [Abstract] [Full Text] [Related]

  • 25. Self-healing collodion membrane and mild nonbullous congenital ichthyosiform erythroderma due to 2 novel mutations in the ALOX12B gene.
    Harting M, Brunetti-Pierri N, Chan CS, Kirby J, Dishop MK, Richard G, Scaglia F, Yan AC, Levy ML.
    Arch Dermatol; 2008 Mar; 144(3):351-6. PubMed ID: 18347291
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  • 26. A mother and two children with nonbullous congenital ichthyosiform erythroderma.
    Rossmann-Ringdahl I, Anton-Lamprecht I, Swanbeck G.
    Arch Dermatol; 1986 May; 122(5):559-64. PubMed ID: 3707173
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  • 27. Genotype of autosomal recessive congenital ichthyosis from a tertiary care center in India.
    Chiramel MJ, Mathew L, Athirayath R, Chapla A, Sathishkumar D, Mani T, Danda S, George R.
    Pediatr Dermatol; 2022 May; 39(3):420-424. PubMed ID: 35412663
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  • 29. New mutations in the transglutaminase 1 gene in three families with lamellar ichthyosis.
    Cao X, Lin Z, Yang H, Bu D, Tu P, Chen L, Wu H, Yang Y.
    Clin Exp Dermatol; 2009 Dec; 34(8):904-9. PubMed ID: 19486042
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  • 30. Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis.
    Fachal L, Rodríguez-Pazos L, Ginarte M, Beiras A, Suárez-Peñaranda JM, Toribio J, Carracedo Á, Vega A.
    Int J Dermatol; 2012 Apr; 51(4):427-30. PubMed ID: 22435431
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  • 31. Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child.
    Benmously-Mlika R, Zaouak A, Mrad R, Laaroussi N, Abdelhak S, Hovnanian A, Mokhtar I.
    Int J Dermatol; 2014 Dec; 53(12):1478-80. PubMed ID: 25209454
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  • 32. Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients.
    Pigg MH, Bygum A, Gånemo A, Virtanen M, Brandrup F, Zimmer AD, Hotz A, Vahlquist A, Fischer J.
    Acta Derm Venereol; 2016 Nov 02; 96(7):932-937. PubMed ID: 27025581
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  • 33. Fibroblast apoptosis in a patient affected by lamellar ichthyosis.
    Tavian D, Colombo R, Misiti F, Ena P, Ena L, Sampaolese B, Giardina B, Clementi ME.
    J Cutan Pathol; 2009 Apr 02; 36(4):417-24. PubMed ID: 19278426
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  • 35. Congenital ichthyosiform erythroderma: particulate staining pattern of TGK.
    Hashimoto K, Tanaka K, Misra I, Shwayder T, Moiin A.
    J Dermatol; 1999 Dec 02; 26(12):791-6. PubMed ID: 10659499
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  • 36.
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  • 37. Specific TGM1 mutation profiles in bathing suit and self-improving collodion ichthyoses: phenotypic and genotypic data from 9 patients with dynamic phenotypes of autosomal recessive congenital ichthyosis.
    Bourrat E, Blanchet-Bardon C, Derbois C, Cure S, Fischer J.
    Arch Dermatol; 2012 Oct 02; 148(10):1191-5. PubMed ID: 22801880
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  • 38. Structural changes in epidermal scale and appendages as indicators of defective TGM1 activity.
    Rice RH, Crumrine D, Uchida Y, Gruber R, Elias PM.
    Arch Dermatol Res; 2005 Sep 02; 297(3):127-33. PubMed ID: 16133457
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  • 39. Novel ABCA-12 mutations leading to recessive congenital ichthyosis.
    Peterson H, Lofgren S, Bremmer S, Krol A.
    Pediatr Dermatol; 2013 Sep 02; 30(6):e236-7. PubMed ID: 22299640
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  • 40. Plasminogen activator inhibitor-2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross-linking into the cornified cell envelope by transglutaminase-1.
    Oji V, Oji ME, Adamini N, Walker T, Aufenvenne K, Raghunath M, Traupe H.
    Br J Dermatol; 2006 May 02; 154(5):860-7. PubMed ID: 16634887
    [Abstract] [Full Text] [Related]

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