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Results: 1-8 |
Results: 8

Authors: Langhans, B Braunschweiger, I Schweitzer, S Jung, G Inchauspe, G Sauerbruch, T Spengler, U
Citation: B. Langhans et al., Lipidation of T helper sequences from hepatitis C virus core significantlyenhances T-cell activity in vitro, IMMUNOLOGY, 102(4), 2001, pp. 460-465

Authors: Schweitzer, S Schneiders, AM Langhans, B Kraas, W Jung, G Vidalin, O Inchauspe, G Sauerbruch, T Spengler, U
Citation: S. Schweitzer et al., Flow cytometric analysis of peptide binding to major histocampatibility complex class I for hepatitis C virus core T-cell epitopes, CYTOMETRY, 41(4), 2000, pp. 271-278

Authors: Neuberger, JM Schweitzer, S Rolland, MO Burghard, R
Citation: Jm. Neuberger et al., Effect of sodium benzoate in the treatment of atypical nonketotic hyperglycinaemia, J INH MET D, 23(1), 2000, pp. 22-26

Authors: Schweitzer, S Hogge, JP Grimes, M Bear, HD de Paredes, ES
Citation: S. Schweitzer et al., Cowden disease: A cutaneous marker for increased risk of breast cancer, AM J ROENTG, 172(2), 1999, pp. 349-351

Authors: Vaz, FM Scholte, HR Ruiter, J Hussaarts-Odijk, LM Pereira, RR Schweitzer, S de Klerk, JBC Waterham, HR Wanders, RJA
Citation: Fm. Vaz et al., Identification of two novel mutations in OCTN2 of three patients with systemic carnitine deficiency, HUM GENET, 105(1-2), 1999, pp. 157-161

Authors: van der Knaap, MS Jakobs, C Hoffmann, GF Duran, M Muntau, AC Schweitzer, S Kelley, RI Parrot-Roulaud, F Amiel, J De Lonlay, P Rabier, D Eeg-Olofsson, O
Citation: Ms. Van Der Knaap et al., D-2-hydroxyglutaric aciduria: Further clinical delineation, J INH MET D, 22(4), 1999, pp. 404-413

Authors: Renner, C Razeghi, S Uberall, MA Licht, P Wildt, L Dorr, HG Hensen, J Schweitzer, S
Citation: C. Renner et al., Hormone replacement therapy in galactosaemic twins with ovarian failure and severe osteoporosis, J INH MET D, 22(2), 1999, pp. 194-195

Authors: Burwinkel, B Kreuder, J Schweitzer, S Vorgerd, M Gempel, K Gerbitz, KD Kilimann, MW
Citation: B. Burwinkel et al., Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: A novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality, BIOC BIOP R, 261(2), 1999, pp. 484-487
Risultati: 1-8 |