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Results: 1-25 | 26-28
Results: 1-25/28
LOCALIZATION OF A FANCONI-ANEMIA GENE TO CHROMOSOME 9P
Authors: SAAR K SCHINDLER D WEGNER RD REIS A WIENKER TF HOEHN H JOENJE H SPERLING K DIGWEED M
Citation: K. Saar et al., LOCALIZATION OF A FANCONI-ANEMIA GENE TO CHROMOSOME 9P, European journal of human genetics, 6(5), 1998, pp. 501-508
THE GENE ENCODING THE ALPHA(1A)-VOLTAGE-DEPENDENT CALCIUM-CHANNEL (CACN1A4) IS NOT A CANDIDATE FOR CAUSING COMMON SUBTYPES OF IDIOPATHIC GENERALIZED EPILEPSY
Authors: SANDER T PETERS C JANZ D BIANCHI A BAUER G WIENKER TF HILDMANN T EPPLEN JT RIESS O
Citation: T. Sander et al., THE GENE ENCODING THE ALPHA(1A)-VOLTAGE-DEPENDENT CALCIUM-CHANNEL (CACN1A4) IS NOT A CANDIDATE FOR CAUSING COMMON SUBTYPES OF IDIOPATHIC GENERALIZED EPILEPSY, Epilepsy research, 29(2), 1998, pp. 115-122
BETA-2 ADRENOCEPTOR GENETIC-VARIATION IS ASSOCIATED WITH GENETIC PREDISPOSITION TO ESSENTIAL-HYPERTENSION - THE BERGEN-BLOOD-PRESSURE-STUDY
Authors: TIMMERMANN B MO R LUFT FC GERDTS E BUSJAHN A OMVIK P LI GH SCHUSTER H WIENKER TF HOEHE MR LUNDJOHANSEN P
Citation: B. Timmermann et al., BETA-2 ADRENOCEPTOR GENETIC-VARIATION IS ASSOCIATED WITH GENETIC PREDISPOSITION TO ESSENTIAL-HYPERTENSION - THE BERGEN-BLOOD-PRESSURE-STUDY, Kidney international, 53(6), 1998, pp. 1455-1460
A CROSS-OVER MEDICATION TRIAL FOR PATIENTS WITH AUTOSOMAL-DOMINANT HYPERTENSION WITH BRACHYDACTYLY
Authors: SCHUSTER H TOKA O TOKA HR BUSJAHN A OZTEKIN O WIENKER TF BILGINTURAN N BAHRING S SKRABAL F HALLER H LUFT FC
Citation: H. Schuster et al., A CROSS-OVER MEDICATION TRIAL FOR PATIENTS WITH AUTOSOMAL-DOMINANT HYPERTENSION WITH BRACHYDACTYLY, Kidney international, 53(1), 1998, pp. 167-172
FAMILIES WITH AUTOSOMAL-DOMINANT BRACHYDACTYLY TYPE-E, SHORT STATURE,AND SEVERE HYPERTENSION
Authors: TOKA HR BAHRING S CHITAYAT D MELBY JC WHITEHEAD R JESCHKE E WIENKER TF TOKA O SCHUSTER H LUFT FC
Citation: Hr. Toka et al., FAMILIES WITH AUTOSOMAL-DOMINANT BRACHYDACTYLY TYPE-E, SHORT STATURE,AND SEVERE HYPERTENSION, Annals of internal medicine, 129(3), 1998, pp. 204-208
CHYMASE GENE LOCUS IS NOT ASSOCIATED WITH MYOCARDIAL-INFARCTION AND IS NOT LINKED TO HEART SIZE OR BLOOD-PRESSURE
Authors: PFEUFER A BUSJAHN A VERGOPOULOS A KNOBLAUCH H URATA H OSTERZIEL KJ MENZ M WIENKER TF FAULHABER HD STEINMETZ A SCHUSTER H DIETZ R LUFT FC
Citation: A. Pfeufer et al., CHYMASE GENE LOCUS IS NOT ASSOCIATED WITH MYOCARDIAL-INFARCTION AND IS NOT LINKED TO HEART SIZE OR BLOOD-PRESSURE, The American journal of cardiology, 82(8), 1998, pp. 979
LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING
Authors: LAASS MW HENNIES HC PREIS S STEVENS HP JUNG M LEIGH IM WIENKER TF REIS A
Citation: Mw. Laass et al., LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING, Human genetics, 101(3), 1997, pp. 376-382
A CROSS-OVER MEDICATION TRIAL OF AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY
Authors: SCHUSTER H TOKA O TOKA HR BUSJAHN A OZTURK O WIENKER TF BILGINTURAN N BAHRING S SKRABAL F HALLER H LUFT FC
Citation: H. Schuster et al., A CROSS-OVER MEDICATION TRIAL OF AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY, Hypertension, 30(3), 1997, pp. 33-33
ALLELIC ASSOCIATION OF JUVENILE ABSENCE EPILEPSY WITH A GLUR5 KAINATERECEPTOR GENE (GRIK1) POLYMORPHISM
Authors: SANDER T HILDMANN T KRETZ R FURST R SAILER U BAUER G SCHMITZ B BECKMANNAGETTA G WIENKER TF JANZ D
Citation: T. Sander et al., ALLELIC ASSOCIATION OF JUVENILE ABSENCE EPILEPSY WITH A GLUR5 KAINATERECEPTOR GENE (GRIK1) POLYMORPHISM, American journal of medical genetics, 74(4), 1997, pp. 416-421
NEUROVASCULAR COMPRESSION AT THE VENTROLATERAL MEDULLA IN AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY
Authors: NARAGHI R SCHUSTER H TOKA HR BAHRING S TOKA O OZTEKIN O BILGINTURAN N KNOBLAUCH H WIENKER TF BUSJAHN A HALLER H FAHLBUSCH R LUFT FC
Citation: R. Naraghi et al., NEUROVASCULAR COMPRESSION AT THE VENTROLATERAL MEDULLA IN AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY, Stroke, 28(9), 1997, pp. 1749-1754
REFINED MAPPING OF THE EPILEPSY SUSCEPTIBILITY LOCUS EJM1 ON CHROMOSOME-6
Authors: SANDER T BOCKENKAMP B HILDMANN T BLASCZYK R KRETZ R WIENKER TF VOLZ A SCHMITZ B BECKMANNAGETTA G RIESS O EPPLEN JT JANZ D ZIEGLER A
Citation: T. Sander et al., REFINED MAPPING OF THE EPILEPSY SUSCEPTIBILITY LOCUS EJM1 ON CHROMOSOME-6, Neurology, 49(3), 1997, pp. 842-847
LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME (PLS) TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING
Authors: HENNIES HC LAASS MW PREIS S JUNG M STEVENS HP WIENKER TF REIS A
Citation: Hc. Hennies et al., LOCALIZATION OF A GENE FOR PAPILLON-LEFEVRE-SYNDROME (PLS) TO CHROMOSOME 11Q14-Q21 BY HOMOZYGOSITY MAPPING, American journal of human genetics, 61(4), 1997, pp. 64-64
THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21
Authors: SAAR K CHRZANOWSKA KH STUMM M JUNG M NURNBERG G WIENKER TF SEEMANOVA E WEGNER RD REIS A SPERLING K
Citation: K. Saar et al., THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21, American journal of human genetics, 60(3), 1997, pp. 605-610
DELETION AT 12P IN A JAPANESE CHILD WITH BRACHYDACTYLY OVERLAPS THE ASSIGNED LOCUS OF BRACHYDACTYLY WITH HYPERTENSION IN A TURKISH FAMILY
Authors: BAHRING S NAGAI T TOKA HR NITZ I TOKA O AYDIN A MUHL A WIENKER TF SCHUSTER H LUFT FC
Citation: S. Bahring et al., DELETION AT 12P IN A JAPANESE CHILD WITH BRACHYDACTYLY OVERLAPS THE ASSIGNED LOCUS OF BRACHYDACTYLY WITH HYPERTENSION IN A TURKISH FAMILY, American journal of human genetics, 60(3), 1997, pp. 732-735
SEVERE AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY IN A UNIQUE TURKISH KINDRED MAPS TO HUMAN-CHROMOSOME-12
Authors: SCHUSTER H WIENKER TF BAHRING S BILGINTURAN N TOKA HR NEITZEL H JESCHKE E TOKA O GILBERT D LOWE A OTT J HALLER H LUFT FC
Citation: H. Schuster et al., SEVERE AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY IN A UNIQUE TURKISH KINDRED MAPS TO HUMAN-CHROMOSOME-12, Nature genetics, 13(1), 1996, pp. 98-100
CONSTRUCTION OF A PHYSICAL MAP AND ADDITIONAL PHENOTYPING IN AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY, WHICH MAPS TO CHROMOSOME-12
Authors: LUFT FC BAHRING S SCHUSTER H WIENKER TF TOKA H TOKA O NARAGHI R HALLER H
Citation: Fc. Luft et al., CONSTRUCTION OF A PHYSICAL MAP AND ADDITIONAL PHENOTYPING IN AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY, WHICH MAPS TO CHROMOSOME-12, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1515-1515
LINKAGE OF THE GENE FOR THE TRIPLE-A-SYNDROME TO CHROMOSOME 12Q13 NEAR THE TYPE-II KERATIN GENE-CLUSTER
Authors: WEBER A WIENKER TF JUNG M EASTON D DEAN HJ HEINRICHS C REIS A CLARK AJL
Citation: A. Weber et al., LINKAGE OF THE GENE FOR THE TRIPLE-A-SYNDROME TO CHROMOSOME 12Q13 NEAR THE TYPE-II KERATIN GENE-CLUSTER, Human molecular genetics, 5(12), 1996, pp. 2061-2066
ROLE OF T-CELL RECEPTOR DELTA-GENE IN SUSCEPTIBILITY TO CELIAC-DISEASE (VOL 74, PG 93, 1996)
Authors: ROSCHMANN E WIENKER TF VOLK BA
Citation: E. Roschmann et al., ROLE OF T-CELL RECEPTOR DELTA-GENE IN SUSCEPTIBILITY TO CELIAC-DISEASE (VOL 74, PG 93, 1996), Journal of molecular medicine, 74(5), 1996, pp. 279-279
ROLE OF T-CELL RECEPTOR DELTA-GENE IN SUSCEPTIBILITY TO CELIAC-DISEASE
Authors: ROSCHMANN E WIENKER TF VOLK BA
Citation: E. Roschmann et al., ROLE OF T-CELL RECEPTOR DELTA-GENE IN SUSCEPTIBILITY TO CELIAC-DISEASE, Journal of molecular medicine, 74(2), 1996, pp. 93-98
EXCLUSION OF LINKAGE BETWEEN IDIOPATHIC GENERALIZED EPILEPSIES AND THE GABA(A) RECEPTOR ALPHA-1 AND GAMMA-2 SUBUNIT GENE-CLUSTER ON CHROMOSOME-5
Authors: SANDER T HILDMANN T JANZ D WIENKER TF BIANCHI A BAUER G SAILER U SCARAMELLI A NEITZEL H SCHMITZ B BAILEY MES BECKMANNAGETTA G JOHNSON KJ DARLISON MG
Citation: T. Sander et al., EXCLUSION OF LINKAGE BETWEEN IDIOPATHIC GENERALIZED EPILEPSIES AND THE GABA(A) RECEPTOR ALPHA-1 AND GAMMA-2 SUBUNIT GENE-CLUSTER ON CHROMOSOME-5, Epilepsy research, 23(3), 1996, pp. 235-244
AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY IN A TURKISH KINDRED RESEMBLES ESSENTIAL-HYPERTENSION
Authors: SCHUSTER H WIENKER TF TOKA HR BAHRING S JESCHKE E TOKA O BUSJAHN A HEMPEL A TAHLHAMMER C OELKERS W KUNZE J BILGINTURAN N HALLER H LUFT FC
Citation: H. Schuster et al., AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY IN A TURKISH KINDRED RESEMBLES ESSENTIAL-HYPERTENSION, Hypertension, 28(6), 1996, pp. 1085-1092
COMMON SUBTYPES OF IDIOPATHIC GENERALIZED EPILEPSIES - LACK OF LINKAGE TO D20S19 CLOSE TO CANDIDATE LOCI (EBN1, EEGV1) ON CHROMOSOME-20
Authors: SANDER T HILDMANN T WIENKER TF RAMEL C BECKMANNAGETTA G BIANCHI A SAILER U BEREK K BAUER G NEITZEL H SCHMITZ B DURNER M JOHNSON KJ JANZ D
Citation: T. Sander et al., COMMON SUBTYPES OF IDIOPATHIC GENERALIZED EPILEPSIES - LACK OF LINKAGE TO D20S19 CLOSE TO CANDIDATE LOCI (EBN1, EEGV1) ON CHROMOSOME-20, American journal of medical genetics, 67(1), 1996, pp. 31-39
THE PHENOTYPIC SPECTRUM RELATED TO THE HUMAN EPILEPSY SUSCEPTIBILITY GENE EJM1
Authors: SANDER T HILDMANN T JANZ D WIENKER TF NEITZEL H BIANCHI A BAUER G SAILER U BEREK K SCHMITZ B BECKMANNAGETTA G
Citation: T. Sander et al., THE PHENOTYPIC SPECTRUM RELATED TO THE HUMAN EPILEPSY SUSCEPTIBILITY GENE EJM1, Annals of neurology, 38(2), 1995, pp. 210-217
REFINEMENT OF MAP POSITION OF THE HUMAN GLUR6 KAINATE RECEPTOR GENE (GRIK2) AND LACK OF ASSOCIATION AND LINKAGE WITH IDIOPATHIC GENERALIZEDEPILEPSIES
Authors: SANDER T JANZ D RAMEL C ROSS CA PASCHEN W HILDMANN T WIENKER TF BIANCHI A BAUER G SAILER U BEREK K NEITZEL H VOLZ A ZIEGLER A SCHMITZ B BECKMANNAGETTA G
Citation: T. Sander et al., REFINEMENT OF MAP POSITION OF THE HUMAN GLUR6 KAINATE RECEPTOR GENE (GRIK2) AND LACK OF ASSOCIATION AND LINKAGE WITH IDIOPATHIC GENERALIZEDEPILEPSIES, Neurology, 45(9), 1995, pp. 1713-1720
AN ANGIOTENSIN-CONVERTING ENZYME GENE VARIANT IS ASSOCIATED WITH ACUTE MYOCARDIAL-INFARCTION IN WOMEN BUT NOT IN MEN
Authors: SCHUSTER H WIENKER TF STREMMLER U NOLL B STEINMETZ A LUFT FC
Citation: H. Schuster et al., AN ANGIOTENSIN-CONVERTING ENZYME GENE VARIANT IS ASSOCIATED WITH ACUTE MYOCARDIAL-INFARCTION IN WOMEN BUT NOT IN MEN, The American journal of cardiology, 76(8), 1995, pp. 601
Risultati: 1-25 | 26-28