BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 1534889)

  • 1. What syndrome is this? Netherton syndrome.
    Krafchik BR
    Pediatr Dermatol; 1992 Jun; 9(2):157-60. PubMed ID: 1534889
    [No Abstract]   [Full Text] [Related]  

  • 2. Congenital erythroderma.
    Claus S; Terliesner N; Simon JC; Treudler R
    J Dtsch Dermatol Ges; 2016 Apr; 14(4):435-7. PubMed ID: 26972371
    [No Abstract]   [Full Text] [Related]  

  • 3. Netherton syndrome revisited.
    Seraly MP; Sheehan M; Collins M; Mostow E
    Pediatr Dermatol; 1994 Mar; 11(1):61-4. PubMed ID: 8170853
    [No Abstract]   [Full Text] [Related]  

  • 4. Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndrome.
    Sprecher E; Tesfaye-Kedjela A; Ratajczak P; Bergman R; Richard G
    Clin Exp Dermatol; 2004 Sep; 29(5):513-7. PubMed ID: 15347338
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome.
    Hausser I; Anton-Lamprecht I
    Pediatr Dermatol; 1996; 13(3):183-99. PubMed ID: 8806118
    [TBL] [Abstract][Full Text] [Related]  

  • 6. NETHERTON'S DISEASE; TRICHORRHEXIS INVAGINATA (BAMBOO HAIR), CONGENITAL ICHTHYOSIFORM ERYTHRODERMA AND THE ATOPIC DIATHESIS. A HISTOPATHOLOGIC STUDY.
    WILKINSON RD; CURTIS GH; HAWK WA
    Arch Dermatol; 1964 Jan; 89():46-54. PubMed ID: 14070837
    [No Abstract]   [Full Text] [Related]  

  • 7. [Congenital exfoliative erythroderma].
    Mégarbané H; Tomb R; Klein-Tomb L; Mégarbané A
    Ann Dermatol Venereol; 2004 Feb; 131(2):211-2. PubMed ID: 15026755
    [No Abstract]   [Full Text] [Related]  

  • 8. Guess what! Comèl-Netherton syndrome.
    Wilke S; Hoffmann R; Happle R; Freyschmidt-Paul P
    Eur J Dermatol; 2001; 11(4):381-2. PubMed ID: 11458927
    [No Abstract]   [Full Text] [Related]  

  • 9. Comèl-Netherton syndrome.
    Okkerse A; Oranje AP; de Laat PC
    Br J Dermatol; 1994 Nov; 131(5):725-6. PubMed ID: 7999614
    [No Abstract]   [Full Text] [Related]  

  • 10. Netherton syndrome presenting as congenital psoriasis.
    Shwayder T; Banerjee S
    Pediatr Dermatol; 1997; 14(6):473-6. PubMed ID: 9436849
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ichthyosiform erythroderma and ichthyosis vulgaris. Occurrence in a Negro family.
    FLIEGELMAN MT
    Arch Dermatol; 1962 Aug; 86():222-5. PubMed ID: 13893598
    [No Abstract]   [Full Text] [Related]  

  • 12. UNILATERAL ICHTHYOSIFORM ERYTHRODERMA.
    ROSSMAN RE; SHAPIRO EM; FREEMAN RG
    Arch Dermatol; 1963 Nov; 88():567-71. PubMed ID: 14060072
    [No Abstract]   [Full Text] [Related]  

  • 13. [Hereditary ichthyosis].
    Piérard GE; Hermanns-Lê T; Deleixhe-Mauhin F; Piérard-Franchimont C
    Rev Med Liege; 1994 Sep; 49(9):503-8. PubMed ID: 7939021
    [No Abstract]   [Full Text] [Related]  

  • 14. An unusual dermatitis with annular lesions.
    Cernik C; Trevino J; Janik M
    Pediatr Dermatol; 2008; 25(2):253-4. PubMed ID: 18429793
    [No Abstract]   [Full Text] [Related]  

  • 15. A case of a Japanese neonate with congenital ichthyosiform erythroderma diagnosed as Netherton syndrome.
    Mizuno Y; Suga Y; Haruna K; Muramatsu S; Hasegawa T; Kohroh K; Shimizu T; Komatsu N; Ogawa H; Ikeda S
    Clin Exp Dermatol; 2006 Sep; 31(5):677-80. PubMed ID: 16901309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Abnormal hair growth in a child with atopy.
    Piliang MP; Guenthner S; Treadwell PA
    Arch Dermatol; 2001 Nov; 137(11):1521-6. PubMed ID: 11708964
    [No Abstract]   [Full Text] [Related]  

  • 17. [CONGENITAL ICHTHYOSIFORM ERYTHRODERMA].
    BOLGERT M; DUPERRAT B; TINTHOIN JF
    Bull Soc Fr Dermatol Syphiligr; 1965; 72():125-6. PubMed ID: 14335363
    [No Abstract]   [Full Text] [Related]  

  • 18. Severe hypernatremic dehydration in an infant with Netherton syndrome.
    Stoll C; Alembik Y; Tchomakov D; Messer J; Heid E; Boehm N; Calvas P; Hovnanian A
    Genet Couns; 2001; 12(3):237-43. PubMed ID: 11693786
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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; 12(9):1364-7. PubMed ID: 15935629
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comel-Netherton syndrome: evolution of manifestation in a 20-year follow-up and phenotypic overlap with peeling skin syndrome type B.
    Schneider I; Sebök B; Kosztolányi G; Szekeres G
    Acta Derm Venereol; 2000 May; 80(3):209-10. PubMed ID: 10954215
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.