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Results: 1-8 |
Results: 8
MUTATIONS IN THE FERROCHELATASE GENE OF 4 SPANISH PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA
Authors: GOUYA L SCHNEIDERYIN X RUFENACHT U HERRERO C LECHA M MASCARO JM PUY H DEYBACH JC MINDER EI
Citation: L. Gouya et al., MUTATIONS IN THE FERROCHELATASE GENE OF 4 SPANISH PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA, Journal of investigative dermatology, 111(3), 1998, pp. 406-409
SYSTEMATIC ANALYSIS OF MOLECULAR DEFECTS IN THE FERROCHELATASE GENE FROM PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA
Authors: RUFENACHT UB GOUYA L SCHNEIDERYIN X PUY H SCHAFER BW AQUARON R NORDMANN Y MINDER EI DEYBACH JC
Citation: Ub. Rufenacht et al., SYSTEMATIC ANALYSIS OF MOLECULAR DEFECTS IN THE FERROCHELATASE GENE FROM PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA, American journal of human genetics, 62(6), 1998, pp. 1341-1352
AGE-DEPENDENT REFERENCE VALUES OF URINARY PORPHYRINS IN CHILDREN
Authors: MINDER EI SCHNEIDERYIN X
Citation: Ei. Minder et X. Schneideryin, AGE-DEPENDENT REFERENCE VALUES OF URINARY PORPHYRINS IN CHILDREN, European journal of clinical chemistry and clinical biochemistry, 34(5), 1996, pp. 439-443
HUMAN FERROCHELATASE - A NOVEL MUTATION IN PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA AND AN ISOFORM CAUSED BY ALTERNATIVE SPLICING
Authors: SCHNEIDERYIN X SCHAFER BW TONZ O MINDER EI
Citation: X. Schneideryin et al., HUMAN FERROCHELATASE - A NOVEL MUTATION IN PATIENTS WITH ERYTHROPOIETIC PROTOPORPHYRIA AND AN ISOFORM CAUSED BY ALTERNATIVE SPLICING, Human genetics, 95(4), 1995, pp. 391-396
DEVELOPMENT OF A GAS-CHROMATOGRAPHY - MASS-SPECTROMETRY METHOD FOR DETERMINATION OF KETAMINE IN PLASMA AND ITS APPLICATION TO HUMAN SAMPLES
Authors: FENG N VOLLENWEIDER FX MINDER EI RENTSCH K GRAMPP T VONDERSCHMITT DJ
Citation: N. Feng et al., DEVELOPMENT OF A GAS-CHROMATOGRAPHY - MASS-SPECTROMETRY METHOD FOR DETERMINATION OF KETAMINE IN PLASMA AND ITS APPLICATION TO HUMAN SAMPLES, Therapeutic drug monitoring, 17(1), 1995, pp. 95-100
MOLECULAR DEFECTS IN ERYTHROPOIETIC PROTOPORPHYRIA WITH TERMINAL LIVER-FAILURE
Authors: SCHNEIDERYIN XY SCHAFER BW MOHR P BURG G MINDER EI
Citation: Xy. Schneideryin et al., MOLECULAR DEFECTS IN ERYTHROPOIETIC PROTOPORPHYRIA WITH TERMINAL LIVER-FAILURE, Human genetics, 93(6), 1994, pp. 711-713
RECESSIVE INHERITANCE OF ERYTHROPOIETIC PROTOPORPHYRIA WITH LIVER-FAILURE
Authors: SCHNEIDERYIN X TAKETANI S SCHAFER B MINDER EI
Citation: X. Schneideryin et al., RECESSIVE INHERITANCE OF ERYTHROPOIETIC PROTOPORPHYRIA WITH LIVER-FAILURE, Lancet, 344(8918), 1994, pp. 337-337
LACK OF EFFECT OF ORAL CHARCOAL IN CONGENITAL ERYTHROPOIETIC PORPHYRIA
Authors: MINDER EI SCHNEIDERYIN XY MOLL F
Citation: Ei. Minder et al., LACK OF EFFECT OF ORAL CHARCOAL IN CONGENITAL ERYTHROPOIETIC PORPHYRIA, The New England journal of medicine, 330(15), 1994, pp. 1092-1094
Risultati: 1-8 |