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Results:
1-14
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Results: 14
Authors:
SIMON DB
LIFTON RP
Citation: Db. Simon et Rp. Lifton, ION TRANSPORTER MUTATIONS IN GITELMANS AND BARTTERS SYNDROMES, Current opinion in nephrology and hypertension, 7(1), 1998, pp. 43-47
Authors:
SIMON DB
LIFTON RP
Citation: Db. Simon et Rp. Lifton, MUTATIONS IN NA(K)CL TRANSPORTERS IN GITELMANS AND BARTTERS-SYNDROMES, Current opinion in cell biology, 10(4), 1998, pp. 450-454
Authors:
SIMON DB
BINDRA RS
MANSFIELD TA
NELSONWILLIAMS C
MENDONCA E
STONE R
SCHURMAN S
NAYIR A
ALPAY H
BAKKALOGLU A
RODRIGUEZSORIANO J
MORALES JM
SANJAD SA
TAYLOR CM
PILZ D
BREM A
TRACHTMAN H
GRISWOLD W
RICHARD GA
JOHN E
LIFTON RP
Citation: Db. Simon et al., MUTATIONS IN THE CHLORIDE CHANNEL GENE, CLCNKB, CAUSE BARTTERS-SYNDROME TYPE-III, Nature genetics, 17(2), 1997, pp. 171-178
Authors:
MANSFIELD TA
SIMON DB
FARFEL Z
BIA M
TUCCI JR
LEBEL M
GUTKIN M
VIALETTES B
CHRISTOFILIS MA
KAUPPINENMAKELIN R
MAYAN H
RISCH N
LIFTON RP
Citation: Ta. Mansfield et al., MULTILOCUS LINKAGE OF FAMILIAL HYPERKALEMIA AND HYPERTENSION, PSEUDOHYPOALDOSTERONISM TYPE-II, TO CHROMOSOMES 1Q31-42 AND 17P11-Q21, Nature genetics, 16(2), 1997, pp. 202-205
Authors:
MANSFIELD TA
SIMON DB
FARFEL Z
BIA M
TUCCI JR
LEBEL M
GUTKIN M
VIALETTES B
CHRISTOFILIS MA
KAUPPIUNENMAKELIN R
MAYAN H
RISCH N
LIFTON RP
Citation: Ta. Mansfield et al., LINKAGE OF FAMILIAL HYPERKALEMIA AND HYPERTENSION, PSEUDOHYPOALDOSTERONISM TYPE-II, TO 1Q31-42 AND 17P11-Q21, Hypertension, 30(3), 1997, pp. 38-38
Authors:
SIMON DB
KARET FE
RODRIGUEZSORIANO J
HAMDAN JH
DIPIETRO A
TRACHTMAN H
SANJAD SA
LIFTON RP
Citation: Db. Simon et al., GENETIC-HETEROGENEITY OF BARTTERS-SYNDROME REVEALED BY MUTATIONS IN THE K+ CHANNEL, ROMK, Nature genetics, 14(2), 1996, pp. 152-156
Authors:
SIMON DB
KARET FE
HAMDAN JM
DIPIETRO A
SANJAD SA
LIFTON RP
Citation: Db. Simon et al., BARTTERS-SYNDROME, HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA, IS CAUSED BY MUTATIONS IN THE NA-K-2CL COTRANSPORTER NKCC2, Nature genetics, 13(2), 1996, pp. 183-188
Authors:
SIMON DB
NELSONWILLIAMS C
BIA MJ
ELLISON D
KARET FE
MOLINA AM
VAARA I
IWATA F
CUSHNER HM
KOOLEN M
GAINZA FJ
GITELMAN HJ
LIFTON RP
Citation: Db. Simon et al., GITELMANS VARIANT OF BARTTERS-SYNDROME, INHERITED HYPOKALEMIC ALKALOSIS, IS CAUSED BY MUTATIONS IN THE THIAZIDE-SENSITIVE NA-CL COTRANSPORTER, Nature genetics, 12(1), 1996, pp. 24-30
Authors:
SIMON DB
FARHI A
MAHNESMITH R
LIFTON RP
Citation: Db. Simon et al., INHERITED SUSCEPTIBILITY TO HIV NEPHROPATHY IN AFRICAN-AMERICANS, Journal of the American Society of Nephrology, 7(9), 1996, pp. 486-486
Authors:
SIMON DB
KARET FE
RUDIN A
TRACHTMAN H
FISCHBACH M
CALO L
HULTON S
SECHI G
UNWIN R
LIFTON RP
Citation: Db. Simon et al., THE MOLECULAR-BASIS OF INHERITED HYPOKALEMIC ALKALOSIS - BARTTERS ANDGITELMANS SYNDROMES, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1871-1871
Authors:
SIMON DB
FARHI A
MAHNENSMITH R
LIFTON RP
Citation: Db. Simon et al., GENETIC CONTRIBUTION TO THE RISK OF END-STAGE RENAL-DISEASE IN AFRICAN-AMERICANS, Journal of the American Society of Nephrology, 7(9), 1996, pp. 3090-3090
Authors:
SIMON DB
LIFTON RP
Citation: Db. Simon et Rp. Lifton, THE MOLECULAR-BASIS OF INHERITED HYPOKALEMIC ALKALOSIS - BARTTERS ANDGITELMANS SYNDROMES, American journal of physiology. Renal, fluid and electrolyte physiology, 40(5), 1996, pp. 961-966
Authors:
SIMON DB
KARET FE
HAMDAN JM
DIPIETRO A
LIFTON RP
Citation: Db. Simon et al., BARTTERS-SYNDROME IS CAUSED BY MUTATIONS IN THE NA-K-2CL COTRANSPORTER, Hypertension, 28(3), 1996, pp. 30-30
Authors:
SIMON DB
FARFEL Z
ELLISON D
BIA M
TUCCI J
LIFTON RP
Citation: Db. Simon et al., EXAMINATION OF THE THIAZIDE-SENSITIVE NA-CL COTRANSPORTER AS A CANDIDATE GENE IN GORDONS SYNDROME, Journal of the American Society of Nephrology, 6(3), 1995, pp. 632-632
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