These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 8170853)

  • 1. 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]  

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

  • 3. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Netherton syndrome associated with idiopathic congenital hemihypertrophy.
    Yerebakan O; Uğuz A; Keser I; Lüleci G; Ciftçioğlu MA; Başaran E; Alpsoy E
    Pediatr Dermatol; 2002; 19(4):345-8. PubMed ID: 12220283
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Congenital reticular ichthyosiform erythroderma.
    Dvorakova V; Watson RM; Terron-Kwiatkowski A; Andrew N; Irvine AD
    Clin Exp Dermatol; 2016 Jul; 41(5):576-7. PubMed ID: 26801004
    [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. Clinico-immunological heterogeneity in Comèl-Netherton syndrome.
    Van Gysel D; Koning H; Baert MR; Savelkoul HF; Neijens HJ; Oranje AP
    Dermatology; 2001; 202(2):99-107. PubMed ID: 11306829
    [TBL] [Abstract][Full Text] [Related]  

  • 17. LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome.
    Ong C; O'Toole EA; Ghali L; Malone M; Smith VV; Callard R; Harper JI
    Br J Dermatol; 2004 Dec; 151(6):1253-7. PubMed ID: 15606522
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 140(10):1275-80. PubMed ID: 15492197
    [No Abstract]   [Full Text] [Related]  

  • 19. Netherton syndrome: report of identical twins presenting with severe atopic dermatitis.
    Kilic G; Guler N; Ones U; Tamay Z; Guzel P
    Eur J Pediatr; 2006 Sep; 165(9):594-7. PubMed ID: 16670861
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosis.
    Sprecher E; Chavanas S; DiGiovanna JJ; Amin S; Nielsen K; Prendiville JS; Silverman R; Esterly NB; Spraker MK; Guelig E; de Luna ML; Williams ML; Buehler B; Siegfried EC; Van Maldergem L; Pfendner E; Bale SJ; Uitto J; Hovnanian A; Richard G
    J Invest Dermatol; 2001 Aug; 117(2):179-87. PubMed ID: 11511292
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.