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Items: 49

1.

Distinctive vasculopathy with systemic involvement due to levamisole long-term therapy: a case report.

Aoun B, Alali M, Degheili JA, Sanjad S, Vaquin C, Donadieu J, Ulinski T, Termos S.

J Med Case Rep. 2018 Jul 16;12(1):209. doi: 10.1186/s13256-018-1728-6.

2.

Pamidronate Rescue Therapy for Hypercalcemia in a Child With Williams Syndrome.

Sanjad SA, Aoun B, Yammine H, Bassyouni A, Karam PE.

Front Endocrinol (Lausanne). 2018 May 14;9:240. doi: 10.3389/fendo.2018.00240. eCollection 2018.

3.

Tooth Development Associated with Mutations in Hereditary Vitamin D-Resistant Rickets.

Hanna AE, Sanjad S, Andary R, Nemer G, Ghafari JG.

JDR Clin Trans Res. 2018 Jan;3(1):28-34. doi: 10.1177/2380084417732510. Epub 2017 Sep 20.

PMID:
30938651
4.

Ureteropelvic Junction Obstruction and Parathyroid Adenoma: Coincidence or Link?

Termos S, AlKabbani M, Ulinski T, Sanjad S, Kotobi H, Chalard F, Aoun B.

Case Rep Nephrol. 2017;2017:9852912. doi: 10.1155/2017/9852912. Epub 2017 Oct 17.

5.

Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes.

Andary R, El-Hage-Sleiman AK, Farhat T, Sanjad S, Nemer G.

J Pediatr Endocrinol Metab. 2017 Apr 1;30(4):437-444. doi: 10.1515/jpem-2016-0338.

PMID:
28301319
6.

Chronic peritoneal dialysis in Lebanese children of families with low socioeconomic status.

Aoun B, Ulinski T, Sanjad S, Termos S, Dahrouj M, Fakhoury H, Schmitt CP.

Perit Dial Int. 2015 Jan-Feb;35(1):93-6. doi: 10.3747/pdi.2013.00342. No abstract available.

7.

Severe hypoalphalipoproteinaemia in a child with acute post-streptococcal glomerulonephritis (APSGN).

Alayli MB, Sanjad SA.

BMJ Case Rep. 2013 Nov 5;2013. pii: bcr2013200952. doi: 10.1136/bcr-2013-200952. Review.

8.

Response to steroids in early-onset nephrotic syndrome.

Aoun B, Sanjad S, Schmitt CP, Kalkas G, Fakhoury H, Ulinski T.

Saudi J Kidney Dis Transpl. 2013 May;24(3):590-1. No abstract available.

9.

Congenital nephrotic syndrome and nonsteroidal anti-inflammatory drugs.

Aoun B, Schmitt CP, Ulinski T, Fakhoury H, Kalkas G, Sanjad S.

Indian J Nephrol. 2012 Mar;22(2):152-3. doi: 10.4103/0971-4065.97149. No abstract available.

10.

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.

Boyden LM, Choi M, Choate KA, Nelson-Williams CJ, Farhi A, Toka HR, Tikhonova IR, Bjornson R, Mane SM, Colussi G, Lebel M, Gordon RD, Semmekrot BA, Poujol A, Välimäki MJ, De Ferrari ME, Sanjad SA, Gutkin M, Karet FE, Tucci JR, Stockigt JR, Keppler-Noreuil KM, Porter CC, Anand SK, Whiteford ML, Davis ID, Dewar SB, Bettinelli A, Fadrowski JJ, Belsha CW, Hunley TE, Nelson RD, Trachtman H, Cole TR, Pinsk M, Bockenhauer D, Shenoy M, Vaidyanathan P, Foreman JW, Rasoulpour M, Thameem F, Al-Shahrouri HZ, Radhakrishnan J, Gharavi AG, Goilav B, Lifton RP.

Nature. 2012 Jan 22;482(7383):98-102. doi: 10.1038/nature10814.

11.

Etiology of hypertension in children and adolescents.

Sanjad SA.

J Med Liban. 2010 Jul-Sep;58(3):142-5. Review.

PMID:
21462842
12.

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.

Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, Nayir A, Bakkaloğlu A, Ozen S, Sanjad S, Nelson-Williams C, Farhi A, Mane S, Lifton RP.

Proc Natl Acad Sci U S A. 2009 Nov 10;106(45):19096-101. doi: 10.1073/pnas.0910672106. Epub 2009 Oct 27.

13.

Renal venous thrombosis in a newborn with prothrombotic risk factors.

Muwakkit SA, Saab R, Sanjad SA, Bhar SI, Ishak RS, Samad ZA, Chan AK, Abboud MR.

Blood Coagul Fibrinolysis. 2009 Sep;20(6):458-60. doi: 10.1097/MBC.0b013e32832ca3d8.

PMID:
19542880
14.

Renal tubular acidosis in the arab world.

Sanjad SA.

Saudi J Kidney Dis Transpl. 2003 Jul-Sep;14(3):305-13. No abstract available.

15.
16.

A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype.

Sanjad SA, Hariri A, Habbal ZM, Lifton RP.

Pediatr Nephrol. 2007 Apr;22(4):503-8. Epub 2006 Nov 23.

PMID:
17123117
17.

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.

J Med Genet. 2002 Nov;39(11):796-803.

18.

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.

Transplant Proc. 2001 Aug;33(5):2830-1. No abstract available.

PMID:
11498177
19.

Intensive care and immediate follow-up of children after renal transplantation.

Seikaly MG, Sanjad SA.

Transplant Proc. 2001 Aug;33(5):2821-4. Review. No abstract available.

PMID:
11498173
20.

Improved primary transplant success rates using a triple regimen of cyclosporine microemulsion, mycophenolate mofetil and prednisone.

Khauli RB, Medawar WA, Habbal AA, Birbari AE, Daouk MM, Abdelnoor AM, Uwaydah M, Rahman Bizri A, Sanjad S, Ayvazian PJ, Lovewell T, Stoff JS, Yang Fan P, Bigwood P, Harland R.

Transplant Proc. 2001 Aug;33(5):2776-7. No abstract available.

PMID:
11498156
21.

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.

Hum Genet. 1999 Sep;105(3):240-3.

PMID:
10987651
22.

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.

Nat Genet. 2000 Sep;26(1):71-5.

PMID:
10973252
23.

Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43.

Kelly TE, Blanton S, Saif R, Sanjad SA, Sakati NA.

J Med Genet. 2000 Jan;37(1):63-4. No abstract available.

24.

Bartter syndrome in a neonate: early treatment with indomethacin.

Mourani CC, Sanjad SA, Akatcherian CY.

Pediatr Nephrol. 2000 Feb;14(2):143-5.

PMID:
10684365
25.

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.

Am J Hum Genet. 1999 Dec;65(6):1656-65.

26.

Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.

Al-Jishi E, Meyer BF, Rashed MS, Al-Essa M, Al-Hamed MH, Sakati N, Sanjad S, Ozand PT, Kambouris M.

Clin Genet. 1999 Jun;55(6):444-9.

PMID:
10450861
27.

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.

Science. 1999 Jul 2;285(5424):103-6.

28.

Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinement.

Diaz GA, Gelb BD, Ali F, Sakati N, Sanjad S, Meyer BF, Kambouris M.

Am J Med Genet. 1999 Jul 2;85(1):48-52.

PMID:
10377012
29.

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.

Karet FE, Finberg KE, Nelson RD, Nayir A, Mocan H, Sanjad SA, Rodriguez-Soriano J, Santos F, Cremers CW, Di Pietro A, Hoffbrand BI, Winiarski J, Bakkaloglu A, Ozen S, Dusunsel R, Goodyer P, Hulton SA, Wu DK, Skvorak AB, Morton CC, Cunningham MJ, Jha V, Lifton RP.

Nat Genet. 1999 Jan;21(1):84-90.

PMID:
9916796
30.

Should pediatric kidneys be used in cadaveric kidney transplantation?

Alshaibani K, Raza S, Almeshari K, Alfurayh O, Alahmadi I, Alsabban E, Sanjad S.

Transplant Proc. 1998 Nov;30(7):3123-4. No abstract available.

PMID:
9838380
31.

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.

Transplant Proc. 1998 Nov;30(7):3103-5. No abstract available.

PMID:
9838369
32.

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP.

Nat Genet. 1997 Oct;17(2):171-8.

PMID:
9326936
33.

Hereditary and acquired renal tubular disorders: the saudi experience.

Sanjad SA.

Saudi J Kidney Dis Transpl. 1997 Jul-Sep;8(3):247-59. No abstract available.

34.

Management of hyperlipidemia in children with refractory nephrotic syndrome: the effect of statin therapy.

Sanjad SA, al-Abbad A, al-Shorafa S.

J Pediatr. 1997 Mar;130(3):470-4.

PMID:
9063427
35.

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad SA, Lifton RP.

Nat Genet. 1996 Oct;14(2):152-6.

PMID:
8841184
36.

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.

Simon DB, Karet FE, Hamdan JM, DiPietro A, Sanjad SA, Lifton RP.

Nat Genet. 1996 Jun;13(2):183-8.

PMID:
8640224
37.

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

Al-Abbad A, Nazer H, Sanjad SA, Al-Sabban E.

Ann Saudi Med. 1995 Sep;15(5):466-9.

38.

Kidney transplantations at King Faisal Specialist Hospital and Research Centre.

Lundgren G, Al-Furayh O, Akhtar M, Barri Y, Collste H, Al-Meshari K, Qunibi W, Al-Sabban E, Sanjad S, Al-Shaibani K, Sheth K, Taher S.

Ann Saudi Med. 1994 Jan;14(1):5-11.

39.

Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency.

Sanjad SA, Kaddoura RE, Nazer HM, Akhtar M, Sakati NA.

Am J Dis Child. 1993 Sep;147(9):957-9.

PMID:
8362811
40.

Five-years' experience with cadaveric kidney transplantation at King Faisal Specialist Hospital and Research Center, Riyadh.

Lundgren G, Alfurayh O, Duffy BB, Nicholls P, Qunibi W, al-Sabban E, Sanjad S, Taher S.

Transplant Proc. 1992 Oct;24(5):1840. No abstract available.

PMID:
1412873
41.

The kidney transplantation program at King Faisal Specialist Hospital and Research Centre, Riyadh.

Lundgren G, Alfurayh O, Collste C, Duffy BB, Nicholls P, al-Sabban E, Sanjad S, Taher S, Qunibi W.

Transplant Proc. 1992 Feb;24(1):336-8. No abstract available.

PMID:
1539302
42.

A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

Sanjad SA, Sakati NA, Abu-Osba YK, Kaddoura R, Milner RD.

Arch Dis Child. 1991 Feb;66(2):193-6.

43.

Renal hypoprostaglandism, hypertension, and type IV renal tubular acidosis reversed by furosemide.

Sanjad SA, Keenan BS, Hill LL.

Ann Intern Med. 1983 Nov;99(5):624-7.

PMID:
6579876
44.

Severe hypertension, hyperkalemia, and renal tubular acidosis responding to dietary sodium restriction.

Sanjad SA, Mansour FM, Hernandez RH, Hill LL.

Pediatrics. 1982 Mar;69(3):317-24.

PMID:
7063287
45.

Childhood acute leukemia: a search for occult extramedullary disease prior to discontinuation of chemotherapy.

Mahoney DH Jr, Gonzales ET, Ferry GD, Sanjad SA, von Noorden GK, Fernbach DJ.

Cancer. 1981 Nov 1;48(9):1964-6.

PMID:
6945902
46.

Acute glomerulonephritis in children: a review of 153 cases.

Sanjad S, Tolaymat A, Whitworth J, Levin S.

South Med J. 1977 Oct;70(10):1202-6.

PMID:
333598
47.

Oral treatment of acrodermatitis enteropathica with zinc sulfate.

Der Kaloustian VM, Musallam SS, Sanjad SA, Murib A, Hammad WD, Idriss ZH.

Am J Dis Child. 1976 Apr;130(4):421-3.

PMID:
946739
48.

Nephropathy, an underestimated complication of methicillin therapy.

Sanjad SA, Haddad GG, Nassar VH.

J Pediatr. 1974 Jun;84(6):873-7. No abstract available.

PMID:
4826627
49.

Urinary tract lithiasis in children.

Sanjad S, Alterbarmakian V.

J Med Liban. 1973;26(1):31-9. No abstract available.

PMID:
4718006

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