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Results: 1-6 |
Results: 6

Authors: STANKOVICS J NAGY A MEHES K MELEGH B
Citation: J. Stankovics et al., UMBILICAL VENOUS CATHETERIZATION AND DEVELOPMENT OF BANTI-SYNDROME - THE POSSIBLE ROLE OF THE FACTOR-V-LEIDEN MUTATION, European journal of pediatrics, 157(8), 1998, pp. 696-696

Authors: MELEGH B STANKOVICS J KIS A NAGY A STORCZ J LOSONCZY H MEHES K
Citation: B. Melegh et al., INCREASED PREVALENCE OF FACTOR-V-LEIDEN MUTATION IN NEONATAL INTRACRANIAL HEMORRHAGE, European journal of pediatrics, 157(3), 1998, pp. 261-261

Authors: STANKOVICS J MOLNAR D BURUS I PINTER Z
Citation: J. Stankovics et al., INFANTILE SIALIC-ACID STORAGE DISEASE DIAGNOSED BY GAS-CHROMATOGRAPHYMASS-SPECTROSCOPY ANALYSES OF URINE SAMPLE, Journal of inherited metabolic disease, 20(5), 1997, pp. 728-729

Authors: STANKOVICS J CRANE AM ANDREWS E WU CH WU GY LEDLEY FD
Citation: J. Stankovics et al., OVEREXPRESSION OF HUMAN METHYLMALONYL COA MUTASE IN MICE AFTER IN-VIVO GENE-TRANSFER WITH ASIALOGLYCOPROTEIN POLYLYSINE DNA COMPLEXES, Human gene therapy, 5(9), 1994, pp. 1095-1104

Authors: YOVANDICH J STANKOVICS J LEDLEY FD
Citation: J. Yovandich et al., LACTOFERRIN-MEDIATED GENE-TRANSFER - USE OF A NONANTIGENIC, DNA-BINDING PROTEIN FOR RECEPTOR TARGETED GENE-THERAPY, Journal of cellular biochemistry, 1994, pp. 231-231

Authors: LEDLEY F STANKOVICS J ANDREWS E WU C WU G
Citation: F. Ledley et al., PRECLINICAL ASSESSMENT OF INVIVO GENE-THERAPY FOR METHYLMALONYL COA MUTASE DEFICIENCY USING ASIALO-GLYCOPROTEIN POLYLYSINE DNA COMPLEXES, Journal of cellular biochemistry, 1993, pp. 238-238
Risultati: 1-6 |