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Results:
1-12
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Results: 12
Authors:
SCHUMANN K
LEBEAU A
GRESSER U
GUNTHER T
VORMANN J
Citation: K. Schumann et al., ON THE ORIGIN OF THE INCREASED TISSUE IRON CONTENT IN GRADED MAGNESIUM-DEFICIENCY STATES IN THE RAT, British Journal of Nutrition, 77(3), 1997, pp. 475-490
Authors:
GATHOF BS
GEISSLER J
WINGEN AM
GRESSER U
Citation: Bs. Gathof et al., NOVEL INITIATION CODON MUTATION MET1THR IDENTIFIED IN A PATIENT WITH PARTIAL HYPOXANTHINE-GUANINE PHOSPHORIBOSYL-TRANSFERASE (HPRT) DEFICIENCY - HPRT HEIDELBERG, Human mutation, 7(2), 1996, pp. 184-184
Authors:
GATHOF BS
SOMMER M
PODSKARBI T
REICHARDT J
BRAUN A
GRESSER U
SHIN YS
Citation: Bs. Gathof et al., CHARACTERIZATION OF 2 STOP CODON MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 MALE GALACTOSEMIC PATIENTS WITH SEVERE CLINICAL MANIFESTATION (VOL 96, PG 721, 1995), Human genetics, 97(5), 1996, pp. 699-699
Authors:
SHIN YS
GATHOF BS
PODSKARBI T
SOMMER M
GIUGLIANI R
GRESSER U
Citation: Ys. Shin et al., 3 MISSENSE MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 FAMILIES WITH MILD GALACTOSEMIA, European journal of pediatrics, 155(5), 1996, pp. 393-397
Authors:
PODSKARBI T
KOHLMETZ T
GATHOF BS
KLEINLEIN B
BIEGER WP
GRESSER U
SHIN YS
Citation: T. Podskarbi et al., MOLECULAR CHARACTERIZATION OF DUARTE-1 AND DUARTE-2 VARIANTS OF GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE, Journal of inherited metabolic disease, 19(5), 1996, pp. 638-644
Authors:
GATHOF BS
SOMMER M
PODSKARBI T
REICHARDT J
BRAUN A
GRESSER U
SHIN YS
Citation: Bs. Gathof et al., CHARACTERIZATION OF 2 STOP CODON MUTATIONS IN THE GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE GENE OF 3 MALE GALACTOSEMIC PATIENTS WITH SEVERE CLINICAL MANIFESTATION, Human genetics, 96(6), 1995, pp. 721-725
Authors:
GROSS M
GATHOF BS
KOLLE P
GRESSER U
Citation: M. Gross et al., CAPILLARY ELECTROPHORESIS FOR SCREENING OF ADENYLOSUCCINATE LYASE DEFICIENCY, Electrophoresis, 16(10), 1995, pp. 1927-1929
Authors:
SHIN YS
GRESSER U
Citation: Ys. Shin et U. Gresser, FIRST ASIAN-EUROPEAN WORKSHOP ON INBORN-ERRORS OF METABOLISM - FOREWORD, Journal of inherited metabolic disease, 17(1), 1994, pp. 122-122
Authors:
WAGNER DR
ECKERT F
GRESSER U
LANDTHALER M
MIDDEKE M
ZOLLNER N
Citation: Dr. Wagner et al., DEPOSITS OF PARAPROTEIN IN SMALL VESSELS AS A CAUSE OF SKIN ULCERS INWALDENSTROMS MACROGLOBULINEMIA, The Clinical investigator, 72(1), 1993, pp. 46-49
Authors:
GROSS M
GRESSER U
Citation: M. Gross et U. Gresser, ERGOMETER EXERCISE IN MYOADENYLATE DEAMINASE DEFICIENT PATIENTS, The Clinical investigator, 71(6), 1993, pp. 461-465
Authors:
DEVRIES JX
WALTERSACK I
ITTENSOHN A
WEBER E
EMPL H
GRESSER U
ZOLLNER N
Citation: Jx. Devries et al., BENZBROMARONE HYDROXYLATION IN MAN - DEFECTIVE FORMATION OF THE 6-HYDROXYBENZBROMARONE METABOLITE, The Clinical investigator, 71(11), 1993, pp. 947-952
Authors:
KAMILLI I
GRESSER U
GATHOF BS
GROBNER W
Citation: I. Kamilli et al., PARTIAL HGPRT-DEFICIENCY, PHEOCHROMOCYTOMA AND ERYTHROCYTOSIS, Journal of inherited metabolic disease, 16(2), 1993, pp. 484-485
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