BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 27862277)

  • 1. Omenn Syndrome Presenting with Striking Erythroderma and Extreme Lymphocytosis in a Newborn.
    Zafar R; Ver Heul A; Beigelman A; Bednarski JJ; Bayliss SJ; Dehner LP; Rosman IS; Coughlin CC
    Pediatr Dermatol; 2017 Jan; 34(1):e37-e39. PubMed ID: 27862277
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Omenn syndrome with mutation in RAG1 gene.
    Jaouad IC; Ouldim K; Ali Ou Alla S; Kriouile Y; Villa A; Sefiani A
    Indian J Pediatr; 2008 Sep; 75(9):944-6. PubMed ID: 19011808
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Clinical phenotype and gene diagnostic analysis of Omenn syndrome].
    Wang YQ; Cui YX; Feng J
    Zhonghua Er Ke Za Zhi; 2013 Jan; 51(1):64-8. PubMed ID: 23527934
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diagnosing Omenn syndrome.
    Cutts L; Bakshi A; Walsh M; Parslew R; Eustace K
    Pediatr Dermatol; 2021 Mar; 38(2):541-543. PubMed ID: 33511666
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exfoliative erythroderma, recurrent infections, generalized lymphadenopathy and hepatosplenomegaly in a newborn: Omenn syndrome.
    Tatli MM; Sarraoglu S; Shermatov K; Gurel MS; Karadag A
    Australas J Dermatol; 2007 May; 48(2):133-4. PubMed ID: 17535207
    [No Abstract]   [Full Text] [Related]  

  • 6. Erythroderma in a newborn infant suggesting Omenn syndrome.
    Ren F; Bai X; Elston DM
    Br J Dermatol; 2020 Sep; 183(3):e63. PubMed ID: 32399979
    [No Abstract]   [Full Text] [Related]  

  • 7. Omenn syndrome: a rare case of neonatal erythroderma.
    Puzenat E; Rohrlich P; Thierry P; Girardin P; Taghian M; Ouachee M; Plouvier E; Fischer A; Humbert P; Aubin F
    Eur J Dermatol; 2007; 17(2):137-9. PubMed ID: 17337397
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Ichtyosiform erythroderma revealing a severe combined immunodeficiency].
    Ghariani Fetoui N; Boussofara L; Hmida D; Mokni S; Mekki N; Ben Mustapha I; Belajouza C; Ghariani N; Picard C; Denguezli M
    Ann Dermatol Venereol; 2020 Feb; 147(2):131-134. PubMed ID: 31973905
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome.
    Chou J; Hanna-Wakim R; Tirosh I; Kane J; Fraulino D; Lee YN; Ghanem S; Mahfouz I; Mégarbané A; Lefranc G; Inati A; Dbaibo G; Giliani S; Notarangelo LD; Geha RS; Massaad MJ
    J Allergy Clin Immunol; 2012 Dec; 130(6):1414-6. PubMed ID: 22841008
    [No Abstract]   [Full Text] [Related]  

  • 10. Cyclosporin treatment improves skin findings in omenn syndrome.
    Caglayan Sozmen S; Isik S; Arikan Ayyildiz Z; Yildiz K; Cakır Y; Ozer E; Asilsoy S; Uzuner N; Karaman O; Anal O
    Pediatr Dermatol; 2015; 32(2):e54-7. PubMed ID: 25727345
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome.
    Dalal I; Tasher D; Somech R; Etzioni A; Garti BZ; Lev D; Cohen S; Somekh E; Leshinsky-Silver E
    Clin Immunol; 2011 Sep; 140(3):284-90. PubMed ID: 21624848
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Omenn syndrome: therapeutic effects of cyclosporin.
    Rego S; Kemp A; Wong M; Knight P
    J Paediatr Child Health; 2006 May; 42(5):319-20. PubMed ID: 16712568
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: a case of Omenn syndrome.
    Cuperus E; Montfrans JMV; Gijn MEV; Bastiaens MT; Willigen MM; Leguit RJ; Brijnzeel-Koomen CA; RusseL IM; Pasmans SG
    Eur J Dermatol; 2017 Jun; 27(3):313-314. PubMed ID: 28414192
    [No Abstract]   [Full Text] [Related]  

  • 14. Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two Siblings.
    Valeri L; Lugli L; Iughetti L; Soresina A; Giliani S; Porta F; Berardi A
    Pediatrics; 2022 Jan; 149(1):. PubMed ID: 34889447
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Omenn Syndrome and DNA recombination defects].
    Yachie A
    Nihon Rinsho Meneki Gakkai Kaishi; 2017; 40(3):179-189. PubMed ID: 28747605
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Omenn syndrome does not live by V(D)J recombination alone.
    Marrella V; Maina V; Villa A
    Curr Opin Allergy Clin Immunol; 2011 Dec; 11(6):525-31. PubMed ID: 22001740
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Atypical Omenn Syndrome Due to RAG2 Gene Mutation, a Case Report.
    Pourvali A; Arshi S; Nabavi M; Bemanian MH; Shokri S; Shahrooei M; Rezaei N; Fallahpour M
    Iran J Immunol; 2019 Dec; 16(4):334-338. PubMed ID: 31885011
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel presentation of Omenn syndrome in association with aniridia.
    Sheehan WJ; Delmonte OM; Miller DT; Roberts AE; Bonilla FA; Morra M; Giliani S; Pai SY; Notarangelo LD; Oettgen HC
    J Allergy Clin Immunol; 2009 Apr; 123(4):966-9. PubMed ID: 19178939
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders.
    Wada T; Takei K; Kudo M; Shimura S; Kasahara Y; Koizumi S; Kawa-Ha K; Ishida Y; Imashuku S; Seki H; Yachie A
    Clin Exp Immunol; 2000 Jan; 119(1):148-55. PubMed ID: 10606976
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.
    Gennery AR; Slatter MA; Rice J; Hoefsloot LH; Barge D; McLean-Tooke A; Montgomery T; Goodship JA; Burt AD; Flood TJ; Abinun M; Cant AJ; Johnson D
    Clin Exp Immunol; 2008 Jul; 153(1):75-80. PubMed ID: 18505430
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.