Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss von Stover, E H, Borthwick, K J, Bavalia, C, Eady, N, Fritz, D M, Rungroj, N, Giersch, A B S, Morton, C C, Axon, P R, Akil, I, Al-Sabban, E A, Baguley, D M, Bianca, S, Bakkaloglu, A, Bircan, Z, Chauveau, D, Clermont, M-J, Guala, A, Hulton, S A, Kroes, H, Li Volti, G, Mir, S, Mocan, H, Nayir, A, Ozen, S, Rodriguez Soriano, J, Sanjad, S A, Tasic, V, Taylor, C M, Topaloglu, R, Smith, A N, Karet, F E

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Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III von Simon, David B., Bindra, Ranjit S., Mansfield, Traci A., Nelson-Williams, Carol, Mendonca, Erica, Stone, Rosário, Schurman, Scott, Nayir, Ahmet, Alpay, Harika, Bakkaloglu, Aysin, Rodriguez-Soriano, Juan, Morales, Jose M., Sanjad, Sami A., Taylor, C. Mark, Pilz, Daniela, Brem, Andrew, Trachtman, Howard, Griswold, William, Richard, George A., John, Eunice, Lifton, Richard P.

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Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK von SIMON, D. B, KARET, F. E, RODRIGUEZ-SORIANO, J, HAMDAN, J. H, DIPIETRO, A, TRACHTMAN, H, SANJAD, S. A, LIFTON, R. P

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Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness von Karet, Fiona E., Finberg, Karin E., Nelson, Raoul D., Nayir, Ahmet, Mocan, Hilal, Sanjad, Sami A., Rodriguez-Soriano, Juan, Santos, Fernando, Cremers, Cor W.R.J., Pietro, Antonio Di, Hoffbrand, Barry I., Winiarski, Jacek, Bakkaloglu, Aysin, Ozen, Seza, Dusunsel, Ruhan, Goodyer, Paul, Hulton, Sally A., Wu, Doris K., Skvorak, Anne B., Morton, Cynthia C., Cunningham, Michael J., Jha, Vivekanand, Lifton, Richard P.

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Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets von Hanna, A.E., Sanjad, S., Andary, R., Nemer, G., Ghafari, J.G.

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Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing von Smith, Annabel N., Skaug, Jennifer, Choate, Keith A., Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A., Sanjad, Sami A., Al-Sabban, Essam A., Lifton, Richard P., Scherer, Stephen W., Karet, Fiona E.

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Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2 von Simon, D B, Karet, F E, Hamdan, J M, DiPietro, A, Sanjad, S A, Lifton, R P

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Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing ( rdRTA2 ) to 7q33-34 von Karet, Fiona E., Finberg, Karin E., Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A., Sanjad, Sami A., Al-Sabban, Essam A., Medina, Juan F., Lifton, Richard P.

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1201 Whole Exon Deletion in the Claudin 16 Gene, a Novel Mutation in Familial Hypomagnesemia/Hypercalciuria/Nephrocalcinosis (FHHNC) and Sensorineural Deafness (SND) von Sanjad, SA, Lu, Y, Khoury, C, Habbal, Z, Lifton, R

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Management of hyperlipidemia in children with refractory nephrotic syndrome: The effect of statin therapy von Sanjad, Sami A., Al-Abbad, Abbas, Al-Shorafa, Saleh

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Congenital nephrotic syndrome and nonsteroidal anti-inflammatory drugs von Aoun, B, Schmitt, C P, Ulinski, T, Fakhoury, H, Kalkas, G, Sanjad, S

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A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features von Sanjad, S A, Sakati, N A, Abu-Osba, Y K, Kaddoura, R, Milner, R D

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Bartter syndrome in a neonate : early treatment with indomethacin von MOURANI, C. C, SANJAD, S. A, AKATCHERIAN, C. Y

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Intensive care and immediate follow-up of children after renal transplantation von Seikaly, M.G, Sanjad, S.A

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A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity von BURWINKEL, B, SANJAD, S. A, AL-SABBAN, E, AL-ABBAD, A, KILIMANN, M. W

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Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption von SIMON, D. B, YIN LU, MCCREDIE, D, MILFORD, D, SANJAD, S, LIFTON, R. P, CHOATE, K. A, VELAZQUEZ, H, AL-SABBAN, E, PRAGA, M, CASARI, G, BETTINELLI, A, COLUSSI, G, RODRIGUEZ-SORIANO, J

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Renal tubular dysfunction following kidney transplantation: a prospective study in 31 children von Sanjad, S.A, Ibrahim, A, Al Shorafa, S, Al Abbad, A, Khauli, R.B, Shaibani, K.A.P, Al Sabban, E

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Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43 von KELLY, THADDEUS E, BLANTON, SUSAN, SAIF, RAMLA, SANJAD, SAMI A, SAKATI, NADIA A

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Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency von Al-Jishi, E, Meyer, Bf, Rashed, Ms, Al-Essa, M, Al-Hamed, Mh, Sakati, N, Sanjad, S, Ozand, Pt, Kambouris, M

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The kidney transplant program at king faisal specialist hospital and research center: results of the last 10 years von Alshaibani, K, Raza, S, Alfurayh, O, Almeshari, K, Qunibi, W, Alahmadi, I, Alsabban, E, Sanjad, S

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