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Results: 1-25 | 26-37
Results: 1-25/37
THE REDOX STATUS OF AMINOTHIOLS AS A CLUE TO HOMOCYSTEINE-INDUCED VASCULAR DAMAGE
Authors: KOCH HG GOEBELER M MARQUARDT T ROTH J HARMS E
Citation: Hg. Koch et al., THE REDOX STATUS OF AMINOTHIOLS AS A CLUE TO HOMOCYSTEINE-INDUCED VASCULAR DAMAGE, European journal of pediatrics, 157, 1998, pp. 102-106
VIP SECRETING GANGLIONEUROBLASTOMA CAUSING SECRETORY DIARRHEA IN A CHILD
Authors: ALBERS S KOCH HG SCHELLSCHEIDT J ROTH J RITTER J BRAMSWIG J SCHMID KW SCHAARSCHMIDT K VONLENGERKE HJ WIEG C HARMS E
Citation: S. Albers et al., VIP SECRETING GANGLIONEUROBLASTOMA CAUSING SECRETORY DIARRHEA IN A CHILD, Monatsschrift fur Kinderheilkunde, 146(9), 1998, pp. 838-842
PERSISTENT INFECTION WITH SMALL COLONY VARIANT STRAINS OF STAPHYLOCOCCUS-AUREUS IN PATIENTS WITH CYSTIC-FIBROSIS
Authors: KAHL B HERRMANN M EVERDING AS KOCH HG BECKER K HARMS E PROCTOR RA PETERS G
Citation: B. Kahl et al., PERSISTENT INFECTION WITH SMALL COLONY VARIANT STRAINS OF STAPHYLOCOCCUS-AUREUS IN PATIENTS WITH CYSTIC-FIBROSIS, The Journal of infectious diseases, 177(4), 1998, pp. 1023-1029
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE IB - PHOSPHOMANNOSEISOMERASE DEFICIENCY AND MANNOSE THERAPY
Authors: NIEHUES R HASILIK M ALTON G KORNER C SCHIEBESUKUMAR M KOCH HG ZIMMER KP WU RR HARMS E REITER K VONFIGURA K FREEZE HH HARMS HK MARQUARDT T
Citation: R. Niehues et al., CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE IB - PHOSPHOMANNOSEISOMERASE DEFICIENCY AND MANNOSE THERAPY, The Journal of clinical investigation, 101(7), 1998, pp. 1414-1420
MAPPING OF DROSOPHILA MUTATIONS USING SITE-SPECIFIC MALE RECOMBINATION
Authors: CHEN B CHU T HARMS E GERGEN JP STRICKLAND S
Citation: B. Chen et al., MAPPING OF DROSOPHILA MUTATIONS USING SITE-SPECIFIC MALE RECOMBINATION, Genetics, 149(1), 1998, pp. 157-163
GRAUZONE - A DROSOPHILA GENE ESSENTIAL FOR THE COMPLETION OF FEMALE MEIOSIS AND TRANSLATIONAL REGULATION OF BICOID MESSENGER-RNA
Authors: CHEN B HARMS E GERGEN JP STRICKLAND S
Citation: B. Chen et al., GRAUZONE - A DROSOPHILA GENE ESSENTIAL FOR THE COMPLETION OF FEMALE MEIOSIS AND TRANSLATIONAL REGULATION OF BICOID MESSENGER-RNA, Developmental biology (Print), 198(1), 1998, pp. 97-97
FALSE-POSITIVE GLIADIN AND ENDOMYSIUM ANTIBODIES AND EXOCRINE PANCREATIC INSUFFICIENCY AS PITFALLS IN THE DIFFERENTIAL-DIAGNOSIS OF DUODENAL CROHNS VERSUS CELIAC-DISEASE
Authors: WEBER P ZIMMER KP HUSEMANN S HARMS E
Citation: P. Weber et al., FALSE-POSITIVE GLIADIN AND ENDOMYSIUM ANTIBODIES AND EXOCRINE PANCREATIC INSUFFICIENCY AS PITFALLS IN THE DIFFERENTIAL-DIAGNOSIS OF DUODENAL CROHNS VERSUS CELIAC-DISEASE, The American journal of gastroenterology, 93(7), 1998, pp. 1177-1179
NEPHROPATHIC CYSTINOSIS (CTNS-LSB) - CONSTRUCTION OF A YAC CONTIG COMPRISING THE REFINED CRITICAL REGION ON CHROMOSOME 17P13
Authors: PETERS U SENGER G RAHLMANN M DUCHESNE I STEC I KOHLER MR WEISSENBACH J LEAL SM KOCH HG DEUFEL T HARMS E
Citation: U. Peters et al., NEPHROPATHIC CYSTINOSIS (CTNS-LSB) - CONSTRUCTION OF A YAC CONTIG COMPRISING THE REFINED CRITICAL REGION ON CHROMOSOME 17P13, European journal of human genetics, 5(1), 1997, pp. 9-14
ULTRASTRUCTURAL-LOCALIZATION OF IGG AND TPO IN AUTOIMMUNE THYROCYTES REFERRING TO THE TRANSCYTOSIS OF IGG AND THE ANTIGEN PRESENTATION OF TPO
Authors: ZIMMER KP SCHEUMANN GFW BRAMSWIG J BOCKER W HARMS E SCHMID KW
Citation: Kp. Zimmer et al., ULTRASTRUCTURAL-LOCALIZATION OF IGG AND TPO IN AUTOIMMUNE THYROCYTES REFERRING TO THE TRANSCYTOSIS OF IGG AND THE ANTIGEN PRESENTATION OF TPO, HISTOCHEM C, 107(2), 1997, pp. 115-120
INTELLECTUAL, NEUROLOGIC, AND NEUROPSYCHOLOGIC OUTCOME IN UNTREATED SUBJECTS WITH NONPHENYLKETONURIA HYPERPHENYLALANINEMIA
Authors: WEGLAGE J ULLRICH K PIETSCH M FUNDERS B GUTTLER F HARMS E
Citation: J. Weglage et al., INTELLECTUAL, NEUROLOGIC, AND NEUROPSYCHOLOGIC OUTCOME IN UNTREATED SUBJECTS WITH NONPHENYLKETONURIA HYPERPHENYLALANINEMIA, Pediatric research, 42(3), 1997, pp. 378-384
TREATMENT OF JUVENILE RHEUMATOID PAUCIART HRITIS WITH SULFASALAZINE
Authors: FROSCH M HERTER B GANSER G ROTH J HARMS E
Citation: M. Frosch et al., TREATMENT OF JUVENILE RHEUMATOID PAUCIART HRITIS WITH SULFASALAZINE, Monatsschrift fur Kinderheilkunde, 145(7), 1997, pp. 724-728
USE OF H-1-NMR SPECTROSCOPY AND COMPUTER-SIMULATIONS TO ANALYZE HISTIDINE PK(A) CHANGES IN A PROTEIN-TYROSINE-PHOSPHATASE - EXPERIMENTAL AND THEORETICAL DETERMINATION OF ELECTROSTATIC PROPERTIES IN A SMALL PROTEIN
Authors: TISHMACK PA BASHFORD D HARMS E VANETTEN RL
Citation: Pa. Tishmack et al., USE OF H-1-NMR SPECTROSCOPY AND COMPUTER-SIMULATIONS TO ANALYZE HISTIDINE PK(A) CHANGES IN A PROTEIN-TYROSINE-PHOSPHATASE - EXPERIMENTAL AND THEORETICAL DETERMINATION OF ELECTROSTATIC PROPERTIES IN A SMALL PROTEIN, Biochemistry, 36(39), 1997, pp. 11984-11994
RHG-CSF RESISTANT NEUTROPENIA IN SLE
Authors: FROSCH M ROTH J HARMS E
Citation: M. Frosch et al., RHG-CSF RESISTANT NEUTROPENIA IN SLE, Annals of the Rheumatic Diseases, 56(6), 1997, pp. 396-396
INSIGHT INTO THE CATALYTIC MECHANISM OF PTPASES FROM STUDIES OF AN ASP-]GLU MUTANT THAT IS DEFECTIVE IN LEAVING GROUP PROTONATION
Authors: POKALSKY C ZHANG Z HARMS E VANETTEN RL
Citation: C. Pokalsky et al., INSIGHT INTO THE CATALYTIC MECHANISM OF PTPASES FROM STUDIES OF AN ASP-]GLU MUTANT THAT IS DEFECTIVE IN LEAVING GROUP PROTONATION, The FASEB journal, 10(6), 1996, pp. 33-33
EFFECT OF A REDUCED VITAMIN-K SUPPLEMENTATION ON PROTHROMBIN TIME IN PREMATURES AND HIGH-RISK NEONATES
Authors: ROSSI R ALBRECHT O POLLMANN H JORCH G HARMS E
Citation: R. Rossi et al., EFFECT OF A REDUCED VITAMIN-K SUPPLEMENTATION ON PROTHROMBIN TIME IN PREMATURES AND HIGH-RISK NEONATES, Acta paediatrica, 85(6), 1996, pp. 747-749
YEAST ARTIFICIAL CHROMOSOME MAPPING OF THE CYSTINOSIS LOCUS ON CHROMOSOME 17P BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: STEC I PETERS U HARMS E KOEHLER MR SCHMID M DEUFEL T
Citation: I. Stec et al., YEAST ARTIFICIAL CHROMOSOME MAPPING OF THE CYSTINOSIS LOCUS ON CHROMOSOME 17P BY FLUORESCENCE IN-SITU HYBRIDIZATION, Human genetics, 98(3), 1996, pp. 321-322
THE ADDITION OF AMINO-ACIDS AND PHOSPHATE TO HEMODIAFILTRATION SOLUTIONS IN NEWBORNS WITH HYPERAMMONEMIC COMA
Authors: FRUND S KUWERTZBROKING E KOCH HG BULLA M HARMS E
Citation: S. Frund et al., THE ADDITION OF AMINO-ACIDS AND PHOSPHATE TO HEMODIAFILTRATION SOLUTIONS IN NEWBORNS WITH HYPERAMMONEMIC COMA, Clinical nephrology, 46(1), 1996, pp. 64-66
THE SIGNIFICANCE OF THE ALANIN-GLYOXALATE -AMINOTRANSFERASE RESIDUAL ENZYME-ACTIVITY IN TREATMENT OF PRIMARY HYPEROXALURIA - REVIEW OF A FEW CASES
Authors: BULLA M KUWERTZBROKING E FRUND S DURAN M DORLAND L HARMS E
Citation: M. Bulla et al., THE SIGNIFICANCE OF THE ALANIN-GLYOXALATE -AMINOTRANSFERASE RESIDUAL ENZYME-ACTIVITY IN TREATMENT OF PRIMARY HYPEROXALURIA - REVIEW OF A FEW CASES, Nieren- und Hochdruckkrankheiten, 25(12), 1996, pp. 579-588
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I - DETERMINATION OF THE OLIGOSACCHARIDE STRUCTURE OF NEWLY SYNTHESIZED GLYCOPROTEINS BY ANALYSIS OF CALNEXIN BINDING
Authors: MARQUARDT T ULLRICH K NIEHUES R KOCH HG HARMS E
Citation: T. Marquardt et al., CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I - DETERMINATION OF THE OLIGOSACCHARIDE STRUCTURE OF NEWLY SYNTHESIZED GLYCOPROTEINS BY ANALYSIS OF CALNEXIN BINDING, Journal of inherited metabolic disease, 19(2), 1996, pp. 246-250
PRIMARY SCLEROSING CHOLANGITIS AND COLITI S ULCEROSA IN CHILDREN
Authors: WEBER P ZIMMER KP HARMS E
Citation: P. Weber et al., PRIMARY SCLEROSING CHOLANGITIS AND COLITI S ULCEROSA IN CHILDREN, Monatsschrift fur Kinderheilkunde, 144(4), 1996, pp. 370-373
THE EFFECT OF THE ACTIVE-SITE HISTIDINE MUTATIONS ON THE CATALYTIC ACTIVITY OF HUMAN HEART LACTATE-DEHYDROGENASE
Authors: BURGNER JW WILSBACHER L BARNARD J HARMS E
Citation: Jw. Burgner et al., THE EFFECT OF THE ACTIVE-SITE HISTIDINE MUTATIONS ON THE CATALYTIC ACTIVITY OF HUMAN HEART LACTATE-DEHYDROGENASE, The FASEB journal, 9(6), 1995, pp. 1264-1264
IMMUNOGENICITY AND SAFETY OF A MONOVALENT, MULTICOMPONENT ACELLULAR PERTUSSIS-VACCINE IN 15-MONTH 6-YEAR-OLD GERMAN CHILDREN
Authors: STEHR K HEININGER U UHLENBUSCH R ANGERSBACH P HACKELL J ECKHARDT T BAHRINIPOUR M FALKENBERG N HARMS E HOPFNER J KALUZA D LUBBEN U LUDWIG M MICHAELIS E RUGGEBERG F SCHOTOLA H STEINBERG H VEHSE H WOLSCHNER H
Citation: K. Stehr et al., IMMUNOGENICITY AND SAFETY OF A MONOVALENT, MULTICOMPONENT ACELLULAR PERTUSSIS-VACCINE IN 15-MONTH 6-YEAR-OLD GERMAN CHILDREN, European journal of pediatrics, 154(3), 1995, pp. 209-214
ULTRASTRUCTURAL, IMMUNOCYTOCHEMICAL AND STEREOLOGICAL INVESTIGATION OF HEPATOCYTES IN A PATIENT WITH THE MUTATION OF THE ORNITHINE TRANSCARBAMYLASE GENE
Authors: ZIMMER KP MATSUDA I MATSUURA T MORI M COLOMBO JP FAHIMI HD KOCH HG ULLRICH K HARMS E
Citation: Kp. Zimmer et al., ULTRASTRUCTURAL, IMMUNOCYTOCHEMICAL AND STEREOLOGICAL INVESTIGATION OF HEPATOCYTES IN A PATIENT WITH THE MUTATION OF THE ORNITHINE TRANSCARBAMYLASE GENE, European journal of cell biology, 67(1), 1995, pp. 73-83
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME (CDGS) - GLYCOSYLATION, FOLDING AND INTRACELLULAR-TRANSPORT OF NEWLY SYNTHESIZED GLYCOPROTEINS
Authors: MARQUARDT T ULLRICH K ZIMMER P HASILIK A DEUFEL T HARMS E
Citation: T. Marquardt et al., CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME (CDGS) - GLYCOSYLATION, FOLDING AND INTRACELLULAR-TRANSPORT OF NEWLY SYNTHESIZED GLYCOPROTEINS, European journal of cell biology, 66(3), 1995, pp. 268-273
A NOVEL POINT MUTATION AT CODON-269 OF THE ORNITHINE TRANSCARBAMYLASE(OTC) GENE CAUSING NEONATAL ONSET OF OTC DEFICIENCY
Authors: ZIMMER KP MATSUURA T COLOMBO JP KOCH HG ULLRICH K DEUFEL T HARMS E MATSUDA I
Citation: Kp. Zimmer et al., A NOVEL POINT MUTATION AT CODON-269 OF THE ORNITHINE TRANSCARBAMYLASE(OTC) GENE CAUSING NEONATAL ONSET OF OTC DEFICIENCY, Journal of inherited metabolic disease, 18(3), 1995, pp. 356-357
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