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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

130 related items for PubMed ID: 12177510

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. 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
    [Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45. An erythematous rash, diarrhea, failure to thrive, and lymphadenopathy in a 3-month-old girl.
    Sicherer SH, Lederman HM.
    Ann Allergy Asthma Immunol; 1997 Mar; 78(3):253-8. PubMed ID: 9087148
    [No Abstract] [Full Text] [Related]

  • 46. 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]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50. T helper type 2-like cells and therapeutic effects of interferon-gamma in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).
    Schandené L, Ferster A, Mascart-Lemone F, Crusiaux A, Gérard C, Marchant A, Lybin M, Velu T, Sariban E, Goldman M.
    Eur J Immunol; 1993 Jan; 23(1):56-60. PubMed ID: 8419187
    [Abstract] [Full Text] [Related]

  • 51. [On a fatally progressing disease of 3 brothers under the picture of erythrodermia desquamativa Leiner].
    Simon C, Becker V, Wiedemann HR.
    Z Kinderheilkd; 1965 Oct 01; 94(1):12-24. PubMed ID: 4223581
    [No Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 54.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 55. Immune status in two brothers with Omenn's syndrome: no discernible chimerism on FACS analysis using a monoclonal antibody specific for a maternally restricted HLA antigen.
    Tachinami T, Koizumi S, Yachie A, Yamagami M, Yokoi T, Ohno I, Taniguchi N, Takada I, Kawashima A, Okada Y.
    Am J Pediatr Hematol Oncol; 1990 Oct 01; 12(3):343-50. PubMed ID: 2240484
    [Abstract] [Full Text] [Related]

  • 56. 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 01; 27(3):313-314. PubMed ID: 28414192
    [No Abstract] [Full Text] [Related]

  • 57. Newborn screening for severe combined immunodeficiency does not identify bare lymphocyte syndrome.
    Kuo CY, Chase J, Garcia Lloret M, Stiehm ER, Moore T, Aguilera MJ, Lopez Siles J, Church JA.
    J Allergy Clin Immunol; 2013 Jun 01; 131(6):1693-5. PubMed ID: 23453137
    [No Abstract] [Full Text] [Related]

  • 58. Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency.
    Cavazzana-Calvo M, Le Deist F, De Saint Basile G, Papadopoulo D, De Villartay JP, Fischer A.
    J Clin Invest; 1993 Mar 01; 91(3):1214-8. PubMed ID: 8450050
    [Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60. Neonatal and infantile erythroderma: a clinical and follow-up study of 42 cases.
    Al-Dhalimi MA.
    J Dermatol; 2007 May 01; 34(5):302-7. PubMed ID: 17408438
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.