Al-Sabban E - Search Results

1

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.

Simon DB, Lu Y, Choate KA, Velazquez H, Al-Sabban E, Praga M, Casari G, Bettinelli A, Colussi G, Rodriguez-Soriano J, McCredie D, Milford D, Sanjad S, Lifton RP. Simon DB, et al. Science. 1999 Jul 2;285(5424):103-6. doi: 10.1126/science.285.5424.103. Science. 1999. PMID: 10390358

2

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.

Smith AN, Skaug J, Choate KA, Nayir A, Bakkaloglu A, Ozen S, Hulton SA, Sanjad SA, Al-Sabban EA, Lifton RP, Scherer SW, Karet FE. Smith AN, et al. Nat Genet. 2000 Sep;26(1):71-5. doi: 10.1038/79208. Nat Genet. 2000. PMID: 10973252

3

Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.

Karet FE, Finberg KE, Nayir A, Bakkaloglu A, Ozen S, Hulton SA, Sanjad SA, Al-Sabban EA, Medina JF, Lifton RP. Karet FE, et al. Am J Hum Genet. 1999 Dec;65(6):1656-65. doi: 10.1086/302679. Am J Hum Genet. 1999. PMID: 10577919 Free PMC article.

4

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.

Stover EH, Borthwick KJ, Bavalia C, Eady N, Fritz DM, Rungroj N, Giersch AB, Morton CC, Axon PR, Akil I, Al-Sabban EA, Baguley DM, Bianca S, Bakkaloglu A, Bircan Z, Chauveau D, Clermont MJ, Guala A, Hulton SA, Kroes H, Li Volti G, Mir S, Mocan H, Nayir A, Ozen S, Rodriguez Soriano J, Sanjad SA, Tasic V, Taylor CM, Topaloglu R, Smith AN, Karet FE. Stover EH, et al. Among authors: al sabban ea. J Med Genet. 2002 Nov;39(11):796-803. doi: 10.1136/jmg.39.11.796. J Med Genet. 2002. PMID: 12414817 Free PMC article.

5

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity.

Burwinkel B, Sanjad SA, Al-Sabban E, Al-Abbad A, Kilimann MW. Burwinkel B, et al. Hum Genet. 1999 Sep;105(3):240-3. doi: 10.1007/s004390051095. Hum Genet. 1999. PMID: 10987651

6

Renal tubular dysfunction following kidney transplantation: a prospective study in 31 children.

Sanjad SA, Ibrahim A, Al Shorafa S, Al Abbad A, Khauli RB, Shaibani KA, Al Sabban E. Sanjad SA, et al. Transplant Proc. 2001 Aug;33(5):2830-1. doi: 10.1016/s0041-1345(01)02208-4. Transplant Proc. 2001. PMID: 11498177 Clinical Trial. No abstract available.

7

Primary hyperoxaluria type 1: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children.

Sanjad SA, Al-Abbad A, Al-Sabban E. Sanjad SA, et al. Among authors: al sabban e. Ann Saudi Med. 1999 Jan-Feb;19(1):4-7. doi: 10.5144/0256-4947.1999.4. Ann Saudi Med. 1999. PMID: 17337975 Free article.

8

Congenital chloride diarrhea: A single center experience with ten patients.

Al-Abbad A, Nazer H, Sanjad SA, Al-Sabban E. Al-Abbad A, et al. Ann Saudi Med. 1995 Sep;15(5):466-9. doi: 10.5144/0256-4947.1995.466. Ann Saudi Med. 1995. PMID: 17590642 Free article.

9

Should pediatric kidneys be used in cadaveric kidney transplantation?

Alshaibani K, Raza S, Almeshari K, Alfurayh O, Alahmadi I, Alsabban E, Sanjad S. Alshaibani K, et al. Transplant Proc. 1998 Nov;30(7):3123-4. doi: 10.1016/s0041-1345(98)00962-2. Transplant Proc. 1998. PMID: 9838380 No abstract available.

10

The kidney transplant program at King Faisal Specialist Hospital and Research Center: results of the last 10 years.

Alshaibani K, Raza S, Alfurayh O, Almeshari K, Qunibi W, Alahmadi I, Alsabban E, Sanjad S. Alshaibani K, et al. Transplant Proc. 1998 Nov;30(7):3103-5. doi: 10.1016/s0041-1345(98)00950-6. Transplant Proc. 1998. PMID: 9838369 No abstract available.

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