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 *

57 related articles for article (PubMed ID: 8712290)

  • 1. Significance of interdigitating reticulum cells in Omenn's syndrome.
    Bahadoran P; Rieux-Laucat F; Canioni D; Le Deist F; Fischer A; Brousse N
    Am J Surg Pathol; 1996 Aug; 20(8):1032. PubMed ID: 8712290
    [No Abstract]   [Full Text] [Related]  

  • 2. Omenn's reticulosis associated with the nephrotic syndrome.
    Rybojad M; Cambiaghi S; Moraillon I; Vignon-Pennmen MD; Morel P; Baudoin V; Loirat C
    Br J Dermatol; 1996 Jul; 135(1):124-7. PubMed ID: 8776375
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome.
    Rieux-Laucat F; Bahadoran P; Brousse N; Selz F; Fischer A; Le Deist F; De Villartay JP
    J Clin Invest; 1998 Jul; 102(2):312-21. PubMed ID: 9664072
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [So-called Omenn syndrome. A contribution to pathogenesis and histomorphology].
    Heymer B; Friedrich W; Vossbeck S; Negri G; Müller-Hermelink HK
    Pathologe; 1993 Dec; 14(6):334-40. PubMed ID: 8121886
    [No Abstract]   [Full Text] [Related]  

  • 5. Successful unrelated umbilical cord blood transplantation in a child with Omenn's syndrome.
    Benito A; Diaz MA; Alonso F; Fontán G; Madero L
    Pediatr Hematol Oncol; 1999; 16(4):361-6. PubMed ID: 10407874
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fatal cytomegalovirus myocarditis in an infant with Omenn's syndrome.
    Chan Tack TA; Sandy S; Chan-Tack KM
    Pediatr Infect Dis J; 2006 Aug; 25(8):759-60. PubMed ID: 16874187
    [No Abstract]   [Full Text] [Related]  

  • 7. Treatment with cyclosporin A in a patient with Omenn's syndrome.
    Meyer-Bahlburg A; Haas JP; Haase R; Eschrich U; Wawer A; Frank L; Marsch WCh; Burdach S; Horneff G
    Arch Dis Child; 2002 Sep; 87(3):231-3. PubMed ID: 12193438
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Neonatal erythrodermia - early manifestation of Omenn's syndrome].
    Wozniakowska-Gesicka T; Wisniewska-Ligier M; Borowska-Rybus B
    Med Wieku Rozwoj; 2002; 6(1):23-9. PubMed ID: 12177510
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The lymph node pathology of Omenn's syndrome.
    Martin JV; Willoughby PB; Giusti V; Price G; Cerezo L
    Am J Surg Pathol; 1995 Sep; 19(9):1082-7. PubMed ID: 7661282
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Omenn's syndrome--pathologic arguments in favor of a graft versus host pathogenesis: a report of nine cases.
    Jouan H; Le Deist F; Nezelof C
    Hum Pathol; 1987 Nov; 18(11):1101-8. PubMed ID: 3679186
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rituximab for the treatment of post-bone marrow transplantation refractory hemolytic anemia in a child with Omenn's syndrome.
    Silvana B; Antonella LM; Basilia P; Trombetta D; Saija A; Salpietro C
    Pediatr Transplant; 2007 Aug; 11(5):552-6. PubMed ID: 17631027
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Omenn's Syndrome: A rare primary immunodeficiency disorder.
    Elnour IB; Ahmed S; Halim K; Nirmala V
    Sultan Qaboos Univ Med J; 2007 Aug; 7(2):133-8. PubMed ID: 21748095
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Omenn's syndrome: lessons from a red baby.
    Katugampola RP; Morgan G; Khetan R; Williams N; Blackford S
    Clin Exp Dermatol; 2008 Jul; 33(4):425-8. PubMed ID: 18498405
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An unusual case of severe combined immunodeficiency with hypereosinophilia.
    Dams ET; Mascart-Lemone F; Schandené L; van der Meer JW
    J Intern Med; 1997 Sep; 242(3):267-9. PubMed ID: 9350173
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel RAG1 mutation in a case of severe combined immunodeficiency.
    Zhang J; Quintal L; Atkinson A; Williams B; Grunebaum E; Roifman CM
    Pediatrics; 2005 Sep; 116(3):e445-9. PubMed ID: 16061569
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome.
    Tabori U; Mark Z; Amariglio N; Etzioni A; Golan H; Biloray B; Toren A; Rechavi G; Dalal I
    Clin Genet; 2004 Apr; 65(4):322-6. PubMed ID: 15025726
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Omenn's syndrome.
    Nazzari G; Drago F; Crovato F
    Int J Dermatol; 1997 Feb; 36(2):141-4. PubMed ID: 9109017
    [No Abstract]   [Full Text] [Related]  

  • 18. Omenn's syndrome and related combined immunodeficiency syndromes: diagnostic considerations in infants with persistent erythroderma and failure to thrive.
    Pupo RA; Tyring SK; Raimer SS; Wirt DP; Brooks EG; Goldblum RM
    J Am Acad Dermatol; 1991 Aug; 25(2 Pt 2):442-6. PubMed ID: 1832695
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fatal late-onset EBV-associated post transplant lymphoproliferative disease after umbilical cord blood transplantation due to persistent mixed chimerism and severe delay in T-cell recovery in a patient with Omenn's syndrome.
    Meyer-Bahlburg A; Winkler J; Meerbach A; Holzhausen HJ; Wawer A; Diwan O; Wutzler P; Horneff G; Burdach S
    Bone Marrow Transplant; 2004 Aug; 34(3):283-4. PubMed ID: 15195075
    [No Abstract]   [Full Text] [Related]  

  • 20. Severe combined immunodeficiency syndrome associated with colonic stenosis.
    López-Herrera G; Garibay-Escobar A; Alvarez-Zavala BJ; Esparza-García A; Galindo-Rujana ME; Flores-Romo L; Estrada-García I; Hernández-Pando R; Estrada-Parra S; Santos-Argumedo L
    Arch Med Res; 2004; 35(4):348-58. PubMed ID: 15325511
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.