BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

224 related articles for article (PubMed ID: 21255986)

  • 61. Netherton syndrome showing a large clinical overlap with generalized inflammatory peeling skin syndrome.
    Farooq M; Kurban M; Abbas O; Kibbi AG; Fujimoto A; Fujikawa H; Shimomura Y
    Eur J Dermatol; 2012; 22(3):412-3. PubMed ID: 22562784
    [No Abstract]   [Full Text] [Related]  

  • 62. Successful infliximab treatment in siblings with Netherton syndrome: Unveiling a novel SPINK5 gene variant and literature review.
    Salici NS; Ozcanli A; Rasulova G; Basak AN; Tekgul S; Vural S
    Australas J Dermatol; 2024 May; 65(3):e45-e49. PubMed ID: 38419182
    [TBL] [Abstract][Full Text] [Related]  

  • 63. [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]  

  • 64. A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome.
    Numata S; Teye K; Krol RP; Okamatsu Y; Hashikawa K; Matsuda M; Fortugno P; Di Zenzo G; Castiglia D; Zambruno G; Hamada T; Hashimoto T
    Exp Dermatol; 2016 Jul; 25(7):568-70. PubMed ID: 26997095
    [No Abstract]   [Full Text] [Related]  

  • 65. 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; 32(5):564-7. PubMed ID: 17608759
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C.
    Özyurt K; Atasoy M; Ertaş R; Ulaş Y; Akkuş MR; Kiraz A; Hennies HC
    Turk J Pediatr; 2019; 61(4):604-607. PubMed ID: 31990481
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Netherton syndrome caused by compound heterozygous mutation, c.80A>G mutation in SPINK5 and large-sized genomic deletion mutation, and successful treatment of intravenous immunoglobulin.
    Zhang Z; Pan C; Wei R; Li H; Yang Y; Chen J; Li M; Yao Z
    Mol Genet Genomic Med; 2021 Mar; 9(3):e1600. PubMed ID: 33452875
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Netherton syndrome in one Chinese adult with a novel mutation in the SPINK5 gene and immunohistochemical studies of LEKTI.
    Xi-Bao Z; San-Quan Z; Yu-Qing H; Yu-Wu L; Quan L; Chang-Xing L
    Indian J Dermatol; 2012 Jul; 57(4):265-8. PubMed ID: 22837558
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Ex-vivo gene therapy restores LEKTI activity and corrects the architecture of Netherton syndrome-derived skin grafts.
    Di WL; Larcher F; Semenova E; Talbot GE; Harper JI; Del Rio M; Thrasher AJ; Qasim W
    Mol Ther; 2011 Feb; 19(2):408-16. PubMed ID: 20877344
    [TBL] [Abstract][Full Text] [Related]  

  • 70. 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]  

  • 71. Picture of the month. Comèl-Netherton syndrome without bamboo hair.
    Torchia D; Schachner LA
    Arch Pediatr Adolesc Med; 2011 Aug; 165(8):763. PubMed ID: 21810639
    [No Abstract]   [Full Text] [Related]  

  • 72. A New Splice-site Mutation of
    Erden E; Ceylan AC; Emre S
    Balkan J Med Genet; 2020 Jun; 23(1):91-94. PubMed ID: 32953415
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses.
    Barbieux C; Bonnet des Claustres M; Fahrner M; Petrova E; Tsoi LC; Gouin O; Leturcq F; Nicaise-Roland P; Bole C; Béziat V; Bourrat E; Schilling O; Gudjonsson JE; Hovnanian A
    J Allergy Clin Immunol; 2022 Apr; 149(4):1358-1372. PubMed ID: 34543653
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Par2 inactivation inhibits early production of TSLP, but not cutaneous inflammation, in Netherton syndrome adult mouse model.
    Briot A; Lacroix M; Robin A; Steinhoff M; Deraison C; Hovnanian A
    J Invest Dermatol; 2010 Dec; 130(12):2736-42. PubMed ID: 20703245
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Clinical and genetic characterization of Netherton syndrome due to SPINK5 founder variant in Latvian population.
    Nartisa I; Kirsteina R; Neiburga KD; Zigure S; Ozola L; Grantina I; Micule I; Murmane D; Slisere B; Gailite L; Vilne B; Rots D; Taurina G; Kurjane N
    Pediatr Allergy Immunol; 2023 Apr; 34(4):e13937. PubMed ID: 37102386
    [TBL] [Abstract][Full Text] [Related]  

  • 76. 'Matchstick' eyebrow hairs: a dermoscopic clue to the diagnosis of Netherton syndrome.
    Goujon E; Beer F; Fraitag S; Hovnanian A; Vabres P
    J Eur Acad Dermatol Venereol; 2010 Jun; 24(6):740-1. PubMed ID: 19840201
    [No Abstract]   [Full Text] [Related]  

  • 77. Genetic activation of Nrf2 reduces cutaneous symptoms in a murine model of Netherton syndrome.
    Muzumdar S; Koch M; Hiebert H; Bapst A; Gravina A; Bloch W; Beer HD; Werner S; Schäfer M
    Dis Model Mech; 2020 Jun; 13(5):. PubMed ID: 32457102
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Generation and Clinical Application of Gene-Modified Autologous Epidermal Sheets in Netherton Syndrome: Lessons Learned from a Phase 1 Trial.
    Di WL; Lwin SM; Petrova A; Bernadis C; Syed F; Farzaneh F; Moulding D; Martinez AE; Sebire NJ; Rampling D; Virasami A; Zamiri M; Wang W; Hara H; Kadiyirire T; Abdul-Wahab A; Martinez-Queipo M; Harper JI; McGrath JA; Thrasher AJ; Mellerio JE; Qasim W
    Hum Gene Ther; 2019 Sep; 30(9):1067-1078. PubMed ID: 31288584
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Netherton syndrome--a rare form of inherited ichtyosis].
    Marttila R; Tuomiranta M
    Duodecim; 2012; 128(1):88-93. PubMed ID: 22312831
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Netherton syndrome: a case report and review of the literature.
    Sun JD; Linden KG
    Int J Dermatol; 2006 Jun; 45(6):693-7. PubMed ID: 16796630
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.