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Results: 1-20 |
Results: 20
LOW-NOISE OPERATION OF INTEGRATED YBA2CU3O7 MAGNETOMETERS IN STATIC MAGNETIC-FIELDS
Authors: KREY S DAVID B ECKART R DOSSEL O
Citation: S. Krey et al., LOW-NOISE OPERATION OF INTEGRATED YBA2CU3O7 MAGNETOMETERS IN STATIC MAGNETIC-FIELDS, Applied physics letters, 72(24), 1998, pp. 3205-3207
INTEGRATED YBA2CU3O7 MAGNETOMETERS FOR BIOMAGNETIC APPLICATIONS
Authors: KREY S SUBKE KO REIMER D SCHILLING M SCHARNWEBER R DAVID B
Citation: S. Krey et al., INTEGRATED YBA2CU3O7 MAGNETOMETERS FOR BIOMAGNETIC APPLICATIONS, Applied superconductivity, 5(7-12), 1997, pp. 213-219
DEFECTIVE DIMERIZATION OF VON-WILLEBRAND-FACTOR - A NEW CLASS OF MUTATIONS IN VWD TYPE-2 AND TYPE-3
Authors: SCHNEPPENHEIM R BRASSARD J BUDDE U KREY S SCHWAAB R OLDENBURG J
Citation: R. Schneppenheim et al., DEFECTIVE DIMERIZATION OF VON-WILLEBRAND-FACTOR - A NEW CLASS OF MUTATIONS IN VWD TYPE-2 AND TYPE-3, Thrombosis and haemostasis, 1997, pp. 1585-1585
DELTA-C IN EXON-18 OF THE VON-WILLEBRAND-FACTOR GENE IS THE MOST COMMON MUTATION IN PATIENTS WITH SEVERE VON-WILLEBRAND-DISEASE TYPE-3 IN POLAND
Authors: GAZDA H BUDDE U KREY S ROKICKAMILEWSKA R SCHNEPPENHEIM R
Citation: H. Gazda et al., DELTA-C IN EXON-18 OF THE VON-WILLEBRAND-FACTOR GENE IS THE MOST COMMON MUTATION IN PATIENTS WITH SEVERE VON-WILLEBRAND-DISEASE TYPE-3 IN POLAND, Blood, 90(10), 1997, pp. 3132-3132
HIGH-T-C SQUID MAGNETOMETERS FOR BIOMAGNETIC MEASUREMENTS
Authors: DAVID B GRUNDLER D KREY S DOORMANN V ECKART R KRUMME JP RABE G DOESSEL O
Citation: B. David et al., HIGH-T-C SQUID MAGNETOMETERS FOR BIOMAGNETIC MEASUREMENTS, Superconductor science and technology, 9(4A), 1996, pp. 96-99
RESULTS OF A SCREENING FOR VON-WILLEBRAND DISEASE TYPE 2N PATIENTS WITH SUSPECTED HEMOPHILIA-A OR VAN WILLEBRAND DISEASE TYPE-1
Authors: SCHNEPPENHEIM R BUDDE U KREY S DREWKE E BERGMANN F LECHLER E OLDENBURG J SCHWAAB R
Citation: R. Schneppenheim et al., RESULTS OF A SCREENING FOR VON-WILLEBRAND DISEASE TYPE 2N PATIENTS WITH SUSPECTED HEMOPHILIA-A OR VAN WILLEBRAND DISEASE TYPE-1, Thrombosis and haemostasis, 76(4), 1996, pp. 598-602
PREVALENCE OF FACTOR-V LEIDEN IN CHILDREN WITH THROMBOEMBOLISM
Authors: ASCHKA I AUMANN V BERGMANN F BUDDE U EBERL W ECKHOFDONOVAN S KREY S NOWAKGOTTL U SCHOBESS R SUTOR AH WENDISCH J SCHNEPPENHEIM R
Citation: I. Aschka et al., PREVALENCE OF FACTOR-V LEIDEN IN CHILDREN WITH THROMBOEMBOLISM, European journal of pediatrics, 155(12), 1996, pp. 1009-1014
DEFECTIVE DIMERIZATION OF VON-WILLEBRAND-FACTOR SUBUNITS DUE TO A CYS-]ARG MUTATION IN TYPE-IID VON-WILLEBRAND DISEASE
Authors: SCHNEPPENHEIM R BRASSARD J KREY S BUDDE U KUNICKI TJ HOLMBERG L WARE J RUGGERI ZM
Citation: R. Schneppenheim et al., DEFECTIVE DIMERIZATION OF VON-WILLEBRAND-FACTOR SUBUNITS DUE TO A CYS-]ARG MUTATION IN TYPE-IID VON-WILLEBRAND DISEASE, Proceedings of the National Academy of Sciences of the United Statesof America, 93(8), 1996, pp. 3581-3586
IDENTIFICATION OF A SINGLE-BASE DELETION (DELTA-C08565 8566) IN A PATIENT WITH VON-WILLEBRAND DISEASE TYPE 2A (SUBTYPE IIE)/
Authors: SCHNEPPENHEIM R BUDDE U KREY S DREWKE E
Citation: R. Schneppenheim et al., IDENTIFICATION OF A SINGLE-BASE DELETION (DELTA-C08565 8566) IN A PATIENT WITH VON-WILLEBRAND DISEASE TYPE 2A (SUBTYPE IIE)/, Blood, 88(10), 1996, pp. 1294-1294
BIOMAGNETIC MEASUREMENTS WITH AN INTEGRATED YBA2CU3O7 MAGNETOMETER INA HAND-HELD CRYOSTAT
Authors: SCHILLING M KREY S SCHARNWEBER R
Citation: M. Schilling et al., BIOMAGNETIC MEASUREMENTS WITH AN INTEGRATED YBA2CU3O7 MAGNETOMETER INA HAND-HELD CRYOSTAT, Applied physics letters, 69(18), 1996, pp. 2749-2751
LOW-NOISE YBA2CU3O7-X SQUID MAGNETOMETERS OPERATED WITH ADDITIONAL POSITIVE FEEDBACK
Authors: DRUNG D DANTSKER E LUDWIG F KOCH H KLEINER R CLARKE J KREY S REIMER D DAVID B DOESSEL O
Citation: D. Drung et al., LOW-NOISE YBA2CU3O7-X SQUID MAGNETOMETERS OPERATED WITH ADDITIONAL POSITIVE FEEDBACK, Applied physics letters, 68(13), 1996, pp. 1856-1858
A VARIANT OF VON-WILLEBRAND-DISEASE (TYPE 2N) RESEMBLING PHENOTYPICALLY MILD OR MODERATELY SEVERE HEMOPHILIA
Authors: DREWKE E KREY S SCHNEPPENHEIM R BUNDE U
Citation: E. Drewke et al., A VARIANT OF VON-WILLEBRAND-DISEASE (TYPE 2N) RESEMBLING PHENOTYPICALLY MILD OR MODERATELY SEVERE HEMOPHILIA, Infusionstherapie und Transfusionsmedizin, 22, 1995, pp. 48-50
IDENTIFICATION OF A CANDIDATE MISSENSE MUTATION IN A FAMILY WITH VON-WILLEBRAND-DISEASE TYPE-IIC
Authors: SCHNEPPENHEIM R THOMAS KB KREY S BUDDE U JESSAT U SUTOR AH ZIEGER B
Citation: R. Schneppenheim et al., IDENTIFICATION OF A CANDIDATE MISSENSE MUTATION IN A FAMILY WITH VON-WILLEBRAND-DISEASE TYPE-IIC, Human genetics, 95(6), 1995, pp. 681-686
PREVALENCE OF APC-RESISTANCE IN CHILDREN
Authors: ASCHKA I KREY S BERGMANN F BUDDE U EBERL W ECKHOFDONOVAN S KREUZ W NOWAKGOTTL U PLENDL H SCHOBESS R SCHNEPPENHEIM R
Citation: I. Aschka et al., PREVALENCE OF APC-RESISTANCE IN CHILDREN, Thrombosis and haemostasis, 73(6), 1995, pp. 1121-1121
COMPOUND HETEROZYGOSITY FOR DELTA-C AND MUTATIONS IN THE FACTOR-VIII BINDING DOMAIN OF VON-WILLEBRAND-FACTOR, AND THE DESCRIPTION OF A NOVEL MUTATION (E24K), CORRELATED WITH A MORE SEVERE FORM OF VON-WILLEBRANDS DISEASE TYPE NORMANDY
Authors: SCHNEPPENHEIM R BUDDE U KREY S DREWKE E BERGMANN F LECHLER E OLDENBURG J SCHWAAB R
Citation: R. Schneppenheim et al., COMPOUND HETEROZYGOSITY FOR DELTA-C AND MUTATIONS IN THE FACTOR-VIII BINDING DOMAIN OF VON-WILLEBRAND-FACTOR, AND THE DESCRIPTION OF A NOVEL MUTATION (E24K), CORRELATED WITH A MORE SEVERE FORM OF VON-WILLEBRANDS DISEASE TYPE NORMANDY, Thrombosis and haemostasis, 73(6), 1995, pp. 1169-1169
GENETIC-HETEROGENEITY OF SEVERE VON-WILLEBRAND DISEASE TYPE-III IN THE GERMAN POPULATION
Authors: SCHNEPPENHEIM R KREY S BERGMANN F BOCK D BUDDE U LANGE M LINDE R MITTLER U MEILI E MERTES G OLEK K PLENDL H SIMEONI E
Citation: R. Schneppenheim et al., GENETIC-HETEROGENEITY OF SEVERE VON-WILLEBRAND DISEASE TYPE-III IN THE GERMAN POPULATION, Human genetics, 94(6), 1994, pp. 640-652
MAPPING OF THE LOCUS FOR TRANSFERRIN RECEPTOR BY LINKAGE ANALYSIS
Authors: KREY S COX S BRYANT S GAL A
Citation: S. Krey et al., MAPPING OF THE LOCUS FOR TRANSFERRIN RECEPTOR BY LINKAGE ANALYSIS, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 38-38
THE LOCUS FOR CELLULAR RETINOL-BINDING PROTEIN I MAPS BETWEEN D3S14 AND D3S47 ON 3Q A 3RD ALLELE OF THE TAQI RFLP
Authors: KREY S GAL A
Citation: S. Krey et A. Gal, THE LOCUS FOR CELLULAR RETINOL-BINDING PROTEIN I MAPS BETWEEN D3S14 AND D3S47 ON 3Q A 3RD ALLELE OF THE TAQI RFLP, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 38-39
AUTOSOMAL-DOMINANT SECTOR RETINITIS-PIGMENTOSA DUE TO A POINT MUTATION PREDICTING AN ASN-15-SER SUBSTITUTION OF RHODOPSIN
Authors: KRANICH H BARTKOWSKI S DENTON MJ KREY S DICKINSON P DUVIGNEAU C GAL A
Citation: H. Kranich et al., AUTOSOMAL-DOMINANT SECTOR RETINITIS-PIGMENTOSA DUE TO A POINT MUTATION PREDICTING AN ASN-15-SER SUBSTITUTION OF RHODOPSIN, Human molecular genetics, 2(6), 1993, pp. 813-814
HOMOZYGOUS AND HETEROZYGOUS DELETIONS OF THE VON-WILLEBRAND-FACTOR GENE IN GERMANY
Authors: SCHNEPPENHEIM R KREY S LANGE M BUDDE U PLENDL H BOCK D
Citation: R. Schneppenheim et al., HOMOZYGOUS AND HETEROZYGOUS DELETIONS OF THE VON-WILLEBRAND-FACTOR GENE IN GERMANY, Thrombosis and haemostasis, 69(6), 1993, pp. 1179-1179
Risultati: 1-20 |