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djmonstermos Gallagher [3 articles]

Recent papers posted to djmonstermos library by the author Gallagher. You can also see everyones Gallagher.
  • Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
    Nature genetics, Vol. 13, No. 2. (June 1996), pp. 214-218.
    by SW Eber, JM Gonzalez, ML Lux, AL Scarpa, WT Tse, M Dornwell, J Herbers, W Kugler, R Ozcan, A Pekrun, PG Gallagher, W Schröter, BG Forget, SE Lux
    posted to anemia by djmonstermo on 2008-07-11 04:12:21 as **
  • Slow subcutaneous human intravenous immunoglobulin in the treatment of antibody immunodeficiency: use of an old method with a new product.
    The Journal of allergy and clinical immunology, Vol. 101, No. 6 Pt 1. (June 1998), pp. 848-849.
    by ER Stiehm, AM Casillas, JZ Finkelstein, KT Gallagher, PM Groncy, RH Kobayashi, JM Oleske, RL Roberts, ET Sandberg, ME Wakim
    posted to immunodeficiency by djmonstermo on 2008-07-04 04:44:52 as **
  • Randomized clinical trial of intramuscular vs oral methylprednisolone in the treatment of asthma exacerbations following discharge from an emergency department.
    Chest, Vol. 126, No. 2. (August 2004), pp. 362-368.
    by M Lahn, P Bijur, EJ Gallagher
    posted to asthma by djmonstermo on 2008-07-04 03:19:54 as **
    • Bemerkung: Sie können diese Seite wie folgt zitieren: http://www.citeulike.org/user/djmonstermo/author/Gallagher

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