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534 related items for PubMed ID: 15347338

  • 21. Early skin biopsy is helpful for the diagnosis and management of neonatal and infantile erythrodermas.
    Leclerc-Mercier S, Bodemer C, Bourdon-Lanoy E, Larousserie F, Hovnanian A, Brousse N, Fraitag S.
    J Cutan Pathol; 2010 Feb; 37(2):249-55. PubMed ID: 19615015
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  • 22. [Netherton syndrome: a model for studying the regulation of the desquamation process].
    Descargues P, Deraison C, Bonnart C, Hovnanian A.
    Med Sci (Paris); 2005 May; 21(5):457-8. PubMed ID: 15885188
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  • 25. Ichthyosis with confetti: clinics, molecular genetics and management.
    Guerra L, Diociaiuti A, El Hachem M, Castiglia D, Zambruno G.
    Orphanet J Rare Dis; 2015 Sep 17; 10():115. PubMed ID: 26381864
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  • 27. Rapid detection of homozygous mutations in congenital recessive ichthyosis.
    Lugassy J, Hennies HC, Indelman M, Khamaysi Z, Bergman R, Sprecher E.
    Arch Dermatol Res; 2008 Feb 17; 300(2):81-5. PubMed ID: 18034255
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  • 29. Generalized exfoliative erythroderma since birth. Netherton syndrome.
    El Shabrawi-Caelen L, Smolle J, Metze D, Ginter-Hanselmayer G, Raghunath M, Traupe H, Kerl H.
    Arch Dermatol; 2004 Oct 17; 140(10):1275-80. PubMed ID: 15492197
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  • 31. [Netherton syndrome: a type of infantile erythroderma with failure to thrive, immune deficiency, rickets. Report of 3 cases].
    André E, Till M, Descargues P, Cordier MP, Fouilhoux A, Haftek M, Hovnanian A, Lachaux A.
    Arch Pediatr; 2005 Sep 17; 12(9):1364-7. PubMed ID: 15935629
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  • 32. SPINK5 gene mutation and decreased LEKTI activity in three Chinese patients with Netherton's syndrome.
    Zhao Y, Ma ZH, Yang Y, Yang SX, Wu LS, Ding BL, Lin ZM, Wang AP, Bu DF, Tu P.
    Clin Exp Dermatol; 2007 Sep 17; 32(5):564-7. PubMed ID: 17608759
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  • 36. A case of Netherton's syndrome with cerebral infarction.
    Calikoğlu E, Anadolu R, Sanli H, Erdem C.
    Turk J Pediatr; 2001 Sep 17; 43(3):247-9. PubMed ID: 11592518
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  • 37. Ichthyoses: differential diagnosis and molecular genetics.
    Oji V, Traupe H.
    Eur J Dermatol; 2006 Sep 17; 16(4):349-59. PubMed ID: 16935789
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  • 39. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome.
    Chavanas S, Bodemer C, Rochat A, Hamel-Teillac D, Ali M, Irvine AD, Bonafé JL, Wilkinson J, Taïeb A, Barrandon Y, Harper JI, de Prost Y, Hovnanian A.
    Nat Genet; 2000 Jun 17; 25(2):141-2. PubMed ID: 10835624
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