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PUBMED FOR HANDHELDS

Journal Abstract Search


109 related items for PubMed ID: 4223581

  • 41. Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin.
    Israeli S, Zamir H, Sarig O, Bergman R, Sprecher E.
    J Invest Dermatol; 2011 Mar; 131(3):779-81. PubMed ID: 21191406
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  • 47. [Staphylococcal and toxic "burned skin" syndromes].
    Lelis II.
    Vestn Dermatol Venerol; 1984 Oct; (10):47-9. PubMed ID: 6240172
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  • 48. A case report of severe dermatitis, allergies, and metabolic wasting (SAM syndrome).
    Rodríguez Tejero A, Tercedor Sánchez J, Montero Vilchez T, López Delgado D, Arias Santiago S, Molina Leyva A.
    Pediatr Dermatol; 2020 May; 37(3):576-578. PubMed ID: 32126589
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  • 49. Diagnostic next generation sequencing in neonatal erythroderma.
    Cuperus E, Sigurdsson V, van den Akker PC, Bolling MC, van Gijn ME, Pasmans SGMA.
    J Dtsch Dermatol Ges; 2021 Apr; 19(4):612-614. PubMed ID: 33103336
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  • 50. [On the clinical picture of mast-cell erythroderma].
    Haensch R, Ippen H.
    Hautarzt; 1968 Sep; 19(9):403-7. PubMed ID: 4234541
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  • 51. Erythema toxicum neonatorum.
    Schwartz RA, Janniger CK.
    Cutis; 1996 Aug; 58(2):153-5. PubMed ID: 8864602
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  • 52. [Congenital erythrodermal states in childhood].
    Levi L, Caputo R.
    G Ital Dermatol Minerva Dermatol; 1968 Aug; 109(4):229-44. PubMed ID: 4240024
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  • 57. [What is your diagnosis? Sézary cells].
    Viollier AF, Viollier EH.
    Schweiz Rundsch Med Prax; 1984 Oct 09; 73(41):1227-8. PubMed ID: 6238395
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  • 60. Neglecting dermatitis neglecta.
    Burgdorf WH, Duncan WC.
    Arch Dermatol; 2010 Apr 09; 146(4):452-3. PubMed ID: 20404246
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