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Results: 1-8 |
Results: 8
SAPOSIN (SAP) A AND SAPOSIN-C ACTIVATE THE DEGRADATION OF GALACTOSYLCERAMIDE IN LIVING CELLS
Authors: HARZER K PATON BC CHRISTOMANOU H CHATELUT M LEVADE T HIRAIWA M OBRIEN JS
Citation: K. Harzer et al., SAPOSIN (SAP) A AND SAPOSIN-C ACTIVATE THE DEGRADATION OF GALACTOSYLCERAMIDE IN LIVING CELLS, FEBS letters, 417(3), 1997, pp. 270-274
MODEL SV40-TRANSFORMED FIBROBLAST LINES FOR METABOLIC STUDIES OF HUMAN PROSAPOSIN AND ACID CERAMIDASE DEFICIENCIES
Authors: CHATELUT M HARZER K CHRISTOMANOU H FEUNTEUN J PIERAGGI MT PATON BC KISHIMOTO Y OBRIEN JS BASILE JP THIERS JC SALVAYRE R LEVADE T
Citation: M. Chatelut et al., MODEL SV40-TRANSFORMED FIBROBLAST LINES FOR METABOLIC STUDIES OF HUMAN PROSAPOSIN AND ACID CERAMIDASE DEFICIENCIES, Clinica chimica acta, 262(1-2), 1997, pp. 61-76
NEUTRAL LIPID STORAGE DISEASE-RESPONSE TO DIETARY INTERVENTION
Authors: KAKOUROU T DROGARI E CHRISTOMANOU H GIANNOULIA A DACOUVOUTETAKIS C
Citation: T. Kakourou et al., NEUTRAL LIPID STORAGE DISEASE-RESPONSE TO DIETARY INTERVENTION, Archives of Disease in Childhood, 77(2), 1997, pp. 184-184
OUCHTERLONY DOUBLE IMMUNODIFFUSION METHOD DEMONSTRATES ABSENCE OF FERRITIN IMMUNOREACTIVITY IN VISCERAL ORGANS FROM 9 PATIENTS WITH NIEMANN-PICK-DISEASE TYPE-C
Authors: CHRISTOMANOU H HARZER K
Citation: H. Christomanou et K. Harzer, OUCHTERLONY DOUBLE IMMUNODIFFUSION METHOD DEMONSTRATES ABSENCE OF FERRITIN IMMUNOREACTIVITY IN VISCERAL ORGANS FROM 9 PATIENTS WITH NIEMANN-PICK-DISEASE TYPE-C, Biochemical and molecular medicine, 58(2), 1996, pp. 176-183
DEFICIENT FERRITIN IMMUNOREACTIVITY IN VISCERAL ORGANS FROM 4 PATIENTS WITH NIEMANN-PICK DISEASE TYPE-C
Authors: CHRISTOMANOU H KELLERMANN J LINK RP HARZER K
Citation: H. Christomanou et al., DEFICIENT FERRITIN IMMUNOREACTIVITY IN VISCERAL ORGANS FROM 4 PATIENTS WITH NIEMANN-PICK DISEASE TYPE-C, Biochemical and molecular medicine, 55(2), 1995, pp. 105-115
DETECTION OF 8 NEW MUTATIONS IN THE ALPHA-GALACTOSIDASE-A GENE IN FABRY-DISEASE
Authors: DAVIES J CHRISTOMANOU H WINCHESTER B MALCOLM S
Citation: J. Davies et al., DETECTION OF 8 NEW MUTATIONS IN THE ALPHA-GALACTOSIDASE-A GENE IN FABRY-DISEASE, Human molecular genetics, 3(4), 1994, pp. 667-669
A FAMILY WITH VISCERAL COURSE OF NIEMANN-PICK DISEASE, MACULAR HALO SYNDROME AND LOW SPHINGOMYELIN DEGRADATION RATE
Authors: SPERL W BART G VANIER MT CHRISTOMANOU H BALDISSERA I STEICHENGERSDORF E PASCHKE E
Citation: W. Sperl et al., A FAMILY WITH VISCERAL COURSE OF NIEMANN-PICK DISEASE, MACULAR HALO SYNDROME AND LOW SPHINGOMYELIN DEGRADATION RATE, Journal of inherited metabolic disease, 17(1), 1994, pp. 93-103
LEPTOMENINGEAL LIPID STORAGE PATTERNS IN FABRY DISEASE
Authors: ELLEDER M CHRISTOMANOU H KUSTERMANNKUHN B HARZER K
Citation: M. Elleder et al., LEPTOMENINGEAL LIPID STORAGE PATTERNS IN FABRY DISEASE, Acta Neuropathologica, 88(6), 1994, pp. 579-582
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