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Results: 1-18 |
Results: 18
ATRIAL DISPERSION OF REFRACTORINESS
Authors: BRACHMANN J KAROLYI L KUBLER W
Citation: J. Brachmann et al., ATRIAL DISPERSION OF REFRACTORINESS, Journal of cardiovascular electrophysiology, 9(8), 1998, pp. 35-39
THE MOLECULAR-GENETIC APPROACH TO BARTTERS-SYNDROME
Authors: KAROLYI L KOCH MC GRZESCHIK KH SEYBERTH HW
Citation: L. Karolyi et al., THE MOLECULAR-GENETIC APPROACH TO BARTTERS-SYNDROME, Journal of molecular medicine, 76(5), 1998, pp. 317-325
DIFFERENTIAL-EFFECTS OF D-SOTALOL ON SUBENDOCARDIAL PURKINJE MYOCYTESISOLATED FROM NORMAL OR 10 TO 14 DAYS POSTINFARCTION CANINE HEARTS - ROLE OF EXTRACELLULAR POTASSIUM CONCENTRATION
Authors: MARSCHANG H SCHOLS W KAROLYI L BEYER T KUBLER W BRACHMANN J
Citation: H. Marschang et al., DIFFERENTIAL-EFFECTS OF D-SOTALOL ON SUBENDOCARDIAL PURKINJE MYOCYTESISOLATED FROM NORMAL OR 10 TO 14 DAYS POSTINFARCTION CANINE HEARTS - ROLE OF EXTRACELLULAR POTASSIUM CONCENTRATION, Journal of cardiovascular pharmacology, 32(2), 1998, pp. 274-283
NOVEL MUTATIONS IN THE THIAZIDE-SENSITIVE NACL COTRANSPORTER GENE IN PATIENTS WITH GITELMAN-SYNDROME WITH PREDOMINANT LOCALIZATION TO THE C-TERMINAL DOMAIN
Authors: LEMMINK HH KNOERS NVAM KAROLYI L VANDIJK H NIAUDET P ANTIGNAC C GUAYWOODFORD LM GOODYER PR CAREL JC HERMES A SEYBERTH HW MONNENS LAH VANDENHEUVEL LPWJ
Citation: Hh. Lemmink et al., NOVEL MUTATIONS IN THE THIAZIDE-SENSITIVE NACL COTRANSPORTER GENE IN PATIENTS WITH GITELMAN-SYNDROME WITH PREDOMINANT LOCALIZATION TO THE C-TERMINAL DOMAIN, Kidney international, 54(3), 1998, pp. 720-730
FETUSES FROM PREECLAMPTIC MOTHERS SHOW REDUCED HEPATIC ERYTHROPOIESIS
Authors: STALLMACH T KAROLYI L LICHTLEN P MAURER M HEBISCH G JOLLER H MARTI HH GASSMANN M
Citation: T. Stallmach et al., FETUSES FROM PREECLAMPTIC MOTHERS SHOW REDUCED HEPATIC ERYTHROPOIESIS, Pediatric research, 43(3), 1998, pp. 349-354
NOVEL MOLECULAR VARIANTS OF THE NA-K-2CL COTRANSPORTER GENE ARE RESPONSIBLE FOR ANTENATAL BARTTER-SYNDROME
Authors: VARGASPOUSSOU R FELDMANN D VOLLMER M KONRAD M KELLY L VANDENHEUVEL LPWJ TEBOURBI L BRANDIS M KAROLYI L HEBERT SC LEMMINK HH DESCHENES G HILDEBRANDT F SEYBERTH HW GUAYWOODFORD LM KNOERS NVAM ANTIGNAC C
Citation: R. Vargaspoussou et al., NOVEL MOLECULAR VARIANTS OF THE NA-K-2CL COTRANSPORTER GENE ARE RESPONSIBLE FOR ANTENATAL BARTTER-SYNDROME, American journal of human genetics, 62(6), 1998, pp. 1332-1340
PRE-NATAL AND POSTNATAL MANAGEMENT OF HYPERPROSTAGLANDIN-E SYNDROME (HPS) FOLLOWING MOLECULAR-GENETIC DIAGNOSIS FROM AMNIOCYTES
Authors: KONRAD M KOCKERLING A LEONHARDT A KAROLYI L SEYBERTH HW
Citation: M. Konrad et al., PRE-NATAL AND POSTNATAL MANAGEMENT OF HYPERPROSTAGLANDIN-E SYNDROME (HPS) FOLLOWING MOLECULAR-GENETIC DIAGNOSIS FROM AMNIOCYTES, Journal of the American Society of Nephrology, 8, 1997, pp. 433-433
NOVEL ROMK (KCNJ1) MUTATIONS IN 2 SPORADIC CASES WITH HYPERPROSTAGLANDIN-E SYNDROME (ANTENATAL BARTTER-SYNDROME)
Authors: KONRAD M HENSEN P KAROLYI L SEYBERTH HW
Citation: M. Konrad et al., NOVEL ROMK (KCNJ1) MUTATIONS IN 2 SPORADIC CASES WITH HYPERPROSTAGLANDIN-E SYNDROME (ANTENATAL BARTTER-SYNDROME), Journal of the American Society of Nephrology, 8, 1997, pp. 1808-1808
A COMMON NKCC2 MUTATION IN COSTA-RICAN BARTTERS-SYNDROME PATIENTS - EVIDENCE FOR A FOUNDER EFFECT
Authors: KURTZ CL KAROLYI L SEYBERTH HW KOCH MC VARGAS R FELDMANN D VOLLMER M KNOERS NVAM MADRIGAL G GUAYWOODFORD LM
Citation: Cl. Kurtz et al., A COMMON NKCC2 MUTATION IN COSTA-RICAN BARTTERS-SYNDROME PATIENTS - EVIDENCE FOR A FOUNDER EFFECT, Journal of the American Society of Nephrology, 8(11), 1997, pp. 1706-1711
MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997)
Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPWJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997), Human molecular genetics, 6(4), 1997, pp. 650-650
MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY
Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 6(1), 1997, pp. 17-26
MUTATIONS IN THE ROMK GENE IN ANTENATAL BARTTER-SYNDROME ARE ASSOCIATED WITH IMPAIRED K+ CHANNEL FUNCTION
Authors: DERST C KONRAD M KOCKERLING A KAROLYI L DESCHENES G DAUT J KARSCHIN A SEYBERTH HW
Citation: C. Derst et al., MUTATIONS IN THE ROMK GENE IN ANTENATAL BARTTER-SYNDROME ARE ASSOCIATED WITH IMPAIRED K+ CHANNEL FUNCTION, Biochemical and biophysical research communications, 230(3), 1997, pp. 641-645
PHENOTYPIC VARIABILITY AND GENETIC-HETEROGENEITY IN BARTTER-SYNDROME
Authors: VARGAS R ANTIGNAC C JEAN G FORESTIER L NIAUDET P FELDMANN D DESCHENES G KAROLYI L SEYBERTH HW MADRIGAL G HILDEBRANDT F KNOERS NVAM GUAYWOODFORD LM HEBERT SC
Citation: R. Vargas et al., PHENOTYPIC VARIABILITY AND GENETIC-HETEROGENEITY IN BARTTER-SYNDROME, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1881-1881
GITELMANS-SYNDROME IS GENETICALLY DISTINCT FROM OTHER FORMS OF BARTTERS-SYNDROME
Authors: KAROLYI L ZIEGLER A POLLAK M FISCHBACH M GRZESCHIK KH KOCH MC SEYBERTH HW
Citation: L. Karolyi et al., GITELMANS-SYNDROME IS GENETICALLY DISTINCT FROM OTHER FORMS OF BARTTERS-SYNDROME, Pediatric nephrology, 10(5), 1996, pp. 551-554
THE IMPLANTABLE CARDIOVERTER DEFIBRILLATO R (ICD) - DEVELOPMENT TO PRESENT AND PERSPECTIVES FOR THE FUTURE/
Authors: BRACHMANN J HILBEL T SCHOLS W BEYER T SCHWEIZER M STERNS L KAROLYI L MELICHERCIK J FREIGANG KD KUBLER W
Citation: J. Brachmann et al., THE IMPLANTABLE CARDIOVERTER DEFIBRILLATO R (ICD) - DEVELOPMENT TO PRESENT AND PERSPECTIVES FOR THE FUTURE/, Herz, 19(5), 1994, pp. 246-250
THE IMPLANTABLE CARDIOVERTER DEFIBRILLATO R (ICD) - DEVELOPMENT TO PRESENT AND PERSPECTIVES FOR THE FUTURE/
Authors: BRACHMANN J HILBEL T SCHOLS W BEYER T SCHWEIZER M STERNS L KAROLYI L MELICHERCIK J FREIGANG KD KUBLER W
Citation: J. Brachmann et al., THE IMPLANTABLE CARDIOVERTER DEFIBRILLATO R (ICD) - DEVELOPMENT TO PRESENT AND PERSPECTIVES FOR THE FUTURE/, Herz, 19(5), 1994, pp. 246-250
AUGMENTATION OF FETAL GRANULOPOIESIS WITH CHORIOAMNIONITIS DURING THE2ND TRIMESTER OF GESTATION
Authors: STALLMACH T KAROLYI L
Citation: T. Stallmach et L. Karolyi, AUGMENTATION OF FETAL GRANULOPOIESIS WITH CHORIOAMNIONITIS DURING THE2ND TRIMESTER OF GESTATION, Human pathology, 25(3), 1994, pp. 244-247
REGULARITY OF SPONTANEOUSLY OCCURRING VENTRICULAR TACHYCARDIAS AND ITS INFLUENCE ON STABILITY-CRITERIA FOR DETECTION
Authors: BRACHMANN J STERNS LD HILBEL T BEYER T SCHOELS W RUFRICHTER J KAROLYI L MERKELY B
Citation: J. Brachmann et al., REGULARITY OF SPONTANEOUSLY OCCURRING VENTRICULAR TACHYCARDIAS AND ITS INFLUENCE ON STABILITY-CRITERIA FOR DETECTION, Circulation, 88(4), 1993, pp. 353-353
Risultati: 1-18 |