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Sauerbruch, T
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Authors:
Schweitzer, S
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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
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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:
Vaz, FM
Scholte, HR
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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
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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