AAAAAA

   
Results: 1-24 |
Results: 24

Authors: HALANK M WIEMER M TSCHOPE C POLLER W SCHWIMMBECK P HORSTKOTTE D HOFFKEN G
Citation: M. Halank et al., PRECAPILLARY PULMONARY-HYPERTENSION OF UNCERTAIN ETIOLOGY, Deutsche Medizinische Wochenschrift, 123(28-29), 1998, pp. 861-865

Authors: FISHER B DIGNAM J WOLMARK N MAMOUNAS E COSTANTINO J POLLER W FISHER ER WICKERHAM DL DEUTSCH M MARGOLESE R DIMITROV N KAVANAH M
Citation: B. Fisher et al., LUMPECTOMY AND RADIATION-THERAPY FOR THE TREATMENT OF INTRADUCTAL BREAST-CANCER - FINDINGS FROM NATIONAL SURGICAL ADJUVANT BREAST AND BOWELPROJECT B-17, Journal of clinical oncology, 16(2), 1998, pp. 441-452

Authors: GAMBARYAN S WAGNER C SMOLENSKI A WALTER U POLLER W HAASE W KURTZ A LOHMANN SM
Citation: S. Gambaryan et al., ENDOGENOUS OR OVEREXPRESSED CGMP-DEPENDENT PROTEIN-KINASES INHIBIT CAMP-DEPENDENT RENIN RELEASE FROM RAT ISOLATED-PERFUSED KIDNEY, MICRODISSECTED GLOMERULI, AND ISOLATED JUXTAGLOMERULAR CELLS, Proceedings of the National Academy of Sciences of the United Statesof America, 95(15), 1998, pp. 9003-9008

Authors: SCHMITT C OLDENBURG J HAACK A POLLER W BRACKMANN HH SCHWAAB R
Citation: C. Schmitt et al., INVESTIGATION OF FACTOR VIII-ANTIGEN LEVELS OF PATIENTS WITH HEMOPHILIA-A BY A NEW HIGHLY SENSITIVE ENZYME-LINKED-IMMUNOSORBENT-ASSAY (ELISA), Thrombosis and haemostasis, 1997, pp. 120-120

Authors: HAACK A SCHMITT C POLLER W BRACKMANN HH SCHWAAB R
Citation: A. Haack et al., IN-VITRO EXPRESSION STUDIES OF A NEW FUNCTIONALLY ACTIVE B-DOMAIN-TRUNCATED RECOMBINANT FVIII PROTEIN, Thrombosis and haemostasis, 1997, pp. 931-931

Authors: SELTZER SE HOLMAN BL THRALL JH BRAMSON RT POLLER W
Citation: Se. Seltzer et al., ACADEMIC RADIOLOGY IN A NETWORKED ENVIRONMENT, Academic radiology, 3(10), 1996, pp. 865-872

Authors: POLLER W SCHNEIDERRASP S LIEBERT U MERKLEIN F THALHEIMER P HAACK A SCHWAAB R SCHMITT C BRACKMANN HH
Citation: W. Poller et al., STABILIZATION OF TRANSGENE EXPRESSION BY INCORPORATION OF E3 REGION GENES INTO AN ADENOVIRAL FACTOR-IX VECTOR AND BY TRANSIENT ANTI-CD4 TREATMENT OF THE HOST, Gene therapy, 3(6), 1996, pp. 521-530

Authors: GERMING A MACHRAOUI A POLLER W BRAUN BE BARMEYER J
Citation: A. Germing et al., HYPERTRIGLYCERIDEMIA AS A RISK FACTOR FOR CORONARY HEART-DISEASE - ANANGIOGRAPHIC STUDY, Herz, Kreislauf, 28(9), 1996, pp. 282-284

Authors: PAUL M SCHOTT E BOCKER W ORZECHOWSKI HD POLLER W
Citation: M. Paul et al., THE ROLE OF ENDOTHELINS AND THEIR RECEPTORS IN THE CARDIOVASCULAR-SYSTEM, Naunyn-Schmiedeberg's archives of pharmacology, 354(4), 1996, pp. 5-5

Authors: POLLER W BRETZEL RG BOLLEN CC MERKLEIN F FROGUE P HAGER J
Citation: W. Poller et al., ASSOCIATION OF A GLUCAGON RECEPTOR MUTATION IN GERMAN PATIENTS WITH FAMILIAL NIDDM, Diabetes, 45, 1996, pp. 849-849

Authors: HAGER J HANSEN L VAISSE C VIONNET N PHILIPPI A POLLER W VELHO G CARCASSI C CONTU L JULIER C CAMBIEN F PASSA P LATHROP M KINDSVOGEL W DEMENAIS F NISHIMURA E FROGUEL P
Citation: J. Hager et al., A MISSENSE MUTATION IN THE GLUCAGON RECEPTOR GENE IS ASSOCIATED WITH NON-INSULIN-DEPENDENT DIABETES-MELLITUS, Nature genetics, 9(3), 1995, pp. 299-304

Authors: POLLER W WILLNOW TE HILPERT J HERZ J
Citation: W. Poller et al., DIFFERENTIAL RECOGNITION OF ALPHA(1)-ANTITRYPSIN-ELASTASE AND ALPHA(1)-ANTICHYMOTRYPSIN-CATHEPSIN-G COMPLEXES BY THE LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN, The Journal of biological chemistry, 270(6), 1995, pp. 2841-2845

Authors: KALININ VN SCHMIDT W POLLER W OLEK K
Citation: Vn. Kalinin et al., A POINT MUTATION IN THE ND1 MITOCHONDRIAL GENE IDENTIFIED IN A TYPE-II DIABETIC PATIENT, Genetika, 31(8), 1995, pp. 1180-1182

Authors: HAGER J VAISSE C VIONNET N PHILIPPI A POLLER W CAMBIEN F PASSA P JULIER C VELHO G KINDSVOGEL W DEMENAIS F FROGUEL P
Citation: J. Hager et al., A MISSENSE MUTATION IN THE GLUCAGON RECEPTOR GENE IS LINKED TO FAMILIAL NIDDM, Diabetologia, 37, 1994, pp. 10000016-10000016

Authors: HAGER J BLANCHE H SUN F VAXILLAIRE NVM POLLER W COHEN D CZERNICHOW P VELHO G ROBERT JJ COHEN N FROGUEL P
Citation: J. Hager et al., 6 MUTATIONS IN THE GLUCOKINASE GENE IDENTIFIED IN MODY BY USING A NONRADIOACTIVE SENSITIVE SCREENING TECHNIQUE, Diabetes, 43(5), 1994, pp. 730-733

Authors: HAGER J VAISSE C VIONNET N POLLER W KINDSVOGEL W FROGUEL P
Citation: J. Hager et al., MUTATION SCANNING OF THE GLUCAGON RECEPTOR IN NIDDM PATIENTS, Diabetes, 43, 1994, pp. 10000004-10000004

Authors: FABER JP POLLER W WEIDINGER S KIRCHGESSER M SCHWAAB R BIDLINGMAIER F OLEK K
Citation: Jp. Faber et al., IDENTIFICATION AND DNA-SEQUENCE ANALYSIS OF 15 NEW ALPHA(1)-ANTITRYPSIN VARIANTS, INCLUDING 2 PI-ASTERISK-Q0 ALLELES AND ONE DEFICIENT PI-ASTERISK-M ALLELE, American journal of human genetics, 55(6), 1994, pp. 1113-1121

Authors: POLLER W FABER JP WEIDINGER S TIEF K SCHOLZ S FISCHER M OLEK K KIRCHGESSER M HEIDTMANN HH
Citation: W. Poller et al., A LEUCINE-TO-PROLINE SUBSTITUTION CAUSES A DEFECTIVE ALPHA(1)-ANTICHYMOTRYPSIN ALLELE ASSOCIATED WITH FAMILIAL OBSTRUCTIVE LUNG-DISEASE, Genomics, 17(3), 1993, pp. 740-743

Authors: POLLER W SCHATZ H
Citation: W. Poller et H. Schatz, MOLECULAR-GENETIC ANALYSIS OF NIDDM - STATUS AND PROSPECTS, Experimental and clinical endocrinology, 101(2), 1993, pp. 58-68

Authors: FABER JP POLLER W OLEK K BAUMANN U CARLSON J LINDMARK B ERIKSSON S
Citation: Jp. Faber et al., THE MOLECULAR-BASIS OF ALPHA(1)-ANTICHYMOTRYPSIN DEFICIENCY IN A HETEROZYGOTE WITH LIVER AND LUNG-DISEASE, Journal of hepatology, 18(3), 1993, pp. 313-321

Authors: FISHER B COSTANTINO J REDMOND C FISHER E MARGOLESE R DIMITROV N WOLMARK N WICKERHAM DL DEUTSCH M ORE L MAMOUNAS E POLLER W KAVANAH M
Citation: B. Fisher et al., LUMPECTOMY COMPARED WITH LUMPECTOMY AND RADIATION-THERAPY FOR THE TREATMENT OF INTRADUCTAL BREAST-CANCER, The New England journal of medicine, 328(22), 1993, pp. 1581-1586

Authors: HAGER J FROQUEL P VELHO G OLEK K POLLER W
Citation: J. Hager et al., GENE SCANNING OF GLUCOKINASE IN GERMAN EARLY AND LATE AGE-OF-ONSET NIDDM FAMILIES, Diabetologia, 36, 1993, pp. 10000084-10000084

Authors: POLLER W FABER JP WEIDINGER S TIEF K SCHOLZ S OLEK K HEIDTMANN HH
Citation: W. Poller et al., MOLECULAR-BASIS OF A DEFECTIVE ALPHA-1-ANTICHYMOTRYPSIN PHENOTYPE (BOCHUM-I) ASSOCIATED WITH FAMILIAL CHRONIC OBSTRUCTIVE LUNG-DISEASE, The American review of respiratory disease, 147(4), 1993, pp. 677-677

Authors: VOSS B POLLER W WIETHEGE T BOHM S BRAUN DE BAUR X
Citation: B. Voss et al., ELEVATED LAMINI P1 CONCENTRATIONS IN SERA OF PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY-DISEASE, The American review of respiratory disease, 147(4), 1993, pp. 869-869
Risultati: 1-24 |