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
Citation: Sa. Sanjad et al., MANAGEMENT OF HYPERLIPIDEMIA IN CHILDREN WITH REFRACTORY NEPHROTIC SYNDROME - THE EFFECT OF STATIN THERAPY, The Journal of pediatrics, 130(3), 1997, pp. 470-474
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
Citation: A. Alabbad et al., CONGENITAL CHLORIDE DIARRHEA - A SINGLE-CENTER EXPERIENCE WITH 10 PATIENTS, Annals of saudi medicine, 15(5), 1995, pp. 466-469
Citation: Sa. Sanjad et al., LIPID-LOWERING AGENTS (LL) DO NOT ALTER THE COURSE OF STEROID-RESISTANT (SR) NEPHROTIC SYNDROME, Pediatric research, 37(4), 1995, pp. 369-369
Authors:
SANJAD SA
KADDOURA RE
NAZER HM
AKHTAR M
SAKATI NA
Citation: Sa. Sanjad et al., FANCONIS-SYNDROME WITH HEPATORENAL GLYCOGENOSIS ASSOCIATED WITH PHOSPHORYLASE-B KINASE-DEFICIENCY, American journal of diseases of children [1960], 147(9), 1993, pp. 957-959