Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 105

1.

Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.

Dufek S, Cheshire C, Levine AP, Trompeter RS, Issler N, Stubbs M, Mozere M, Gupta S, Klootwijk E, Patel V, Hothi D, Waters A, Webb H, Tullus K, Jenkins L, Godinho L, Levtchenko E, Wetzels J, Knoers N, Teeninga N, Nauta J, Shalaby M, Eldesoky S, Kari JA, Thalgahagoda S, Ranawaka R, Abeyagunawardena A, Adeyemo A, Kristiansen M, Gbadegesin R, Webb NJ, Gale DP, Stanescu HC, Kleta R, Bockenhauer D.

J Am Soc Nephrol. 2019 Jul 1. pii: ASN.2018101054. doi: 10.1681/ASN.2018101054. [Epub ahead of print]

PMID:
31263063
2.

COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.

Kitzler TM, Schneider R, Kohl S, Kolvenbach CM, Connaughton DM, Dai R, Mann N, Nakayama M, Majmundar AJ, Wu CW, Kari JA, El Desoky SM, Senguttuvan P, Bogdanovic R, Stajic N, Valivullah Z, Lek M, Mane S, Lifton RP, Tasic V, Shril S, Hildebrandt F.

Hum Genet. 2019 Jun 22. doi: 10.1007/s00439-019-02042-4. [Epub ahead of print]

PMID:
31230195
3.

Successful Treatment of Recurrent Focal Segmental Glomerulosclerosis After Transplantation in Children: A Single-Center Experience.

Alhasan KA, Alherbish A, Osman A, Kari JA, Almojalli H.

Transplant Proc. 2019 Mar;51(2):517-521. doi: 10.1016/j.transproceed.2019.01.004. Epub 2019 Jan 4.

PMID:
30879580
4.

Preface.

Alhasan KA, Kari JA.

Transplant Proc. 2019 Mar;51(2):487. doi: 10.1016/j.transproceed.2019.01.003. No abstract available.

PMID:
30879573
5.

Short-term outcome associated with disease severity and electrolyte abnormalities among critically ill children with acute kidney injury.

Safder OY, Alhasan KA, Shalaby MA, Khathlan N, Al Rezgan SA, Albanna AS, Kari JA.

BMC Nephrol. 2019 Mar 12;20(1):89. doi: 10.1186/s12882-019-1278-1.

6.

Treatment and long-term outcome in primary distal renal tubular acidosis.

Lopez-Garcia SC, Emma F, Walsh SB, Fila M, Hooman N, Zaniew M, Bertholet-Thomas A, Colussi G, Burgmaier K, Levtchenko E, Sharma J, Singhal J, Soliman NA, Ariceta G, Basu B, Murer L, Tasic V, Tsygin A, Decramer S, Gil-Peña H, Koster-Kamphuis L, La Scola C, Gellermann J, Konrad M, Lilien M, Francisco T, Tramma D, Trnka P, Yüksel S, Caruso MR, Chromek M, Ekinci Z, Gambaro G, Kari JA, König J, Taroni F, Thumfart J, Trepiccione F, Winding L, Wühl E, Ağbaş A, Belkevich A, Vargas-Poussou R, Blanchard A, Conti G, Boyer O, Dursun I, Pınarbaşı AS, Melek E, Miglinas M, Novo R, Mallett A, Milosevic D, Szczepanska M, Wente S, Cheong HI, Sinha R, Gucev Z, Dufek S, Iancu D; European dRTA Consortium , Kleta R, Schaefer F, Bockenhauer D.

Nephrol Dial Transplant. 2019 Jun 1;34(6):981-991. doi: 10.1093/ndt/gfy409.

PMID:
30773598
7.

Genetics of congenital and infantile nephrotic syndrome.

Sharief SN, Hefni NA, Alzahrani WA, Nazer II, Bayazeed MA, Alhasan KA, Safdar OY, El-Desoky SM, Kari JA.

World J Pediatr. 2019 Apr;15(2):198-203. doi: 10.1007/s12519-018-00224-0. Epub 2019 Feb 5.

PMID:
30721404
8.

A case of urinary bladder agenesis and bilateral ectopic ureters: a case report.

Nazer II, Alhashmi G, Sharief SN, Hefni NA, Ibrahim A, El-Desoky SM, Alsayyad AJ, Safdar OY, Kari JA.

BMC Urol. 2018 Sep 26;18(1):83. doi: 10.1186/s12894-018-0396-6.

9.

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanović R, Stajić N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F.

J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24.

PMID:
30143558
10.

GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome.

Hermle T, Schneider R, Schapiro D, Braun DA, van der Ven AT, Warejko JK, Daga A, Widmeier E, Nakayama M, Jobst-Schwan T, Majmundar AJ, Ashraf S, Rao J, Finn LS, Tasic V, Hernandez JD, Bagga A, Jalalah SM, El Desoky S, Kari JA, Laricchia KM, Lek M, Rehm HL, MacArthur DG, Mane S, Lifton RP, Shril S, Hildebrandt F.

J Am Soc Nephrol. 2018 Aug;29(8):2123-2138. doi: 10.1681/ASN.2017121312. Epub 2018 Jun 29.

PMID:
29959197
11.

Incidence, risk factors, and outcome of neonatal acute kidney injury: a prospective cohort study.

Shalaby MA, Sawan ZA, Nawawi E, Alsaedi S, Al-Wassia H, Kari JA.

Pediatr Nephrol. 2018 Sep;33(9):1617-1624. doi: 10.1007/s00467-018-3966-7. Epub 2018 Jun 5.

PMID:
29869723
12.

Efficiency of Using Pediatrics Emergency Services and Triage Evaluation.

El Desoky S, Mashat S, Bana S, Alama M, Dhabab N, Malibari GM, Halwani M, Albanna AS, Kari JA.

Pediatr Emerg Care. 2018 Jun;34(6):417-421. doi: 10.1097/PEC.0000000000000754.

PMID:
29851918
13.

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.

Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, Hermle T, Warejko JK, Shril S, Airik M, Jobst-Schwan T, Lovric S, Braun DA, Gee HY, Schapiro D, Majmundar AJ, Sadowski CE, Pabst WL, Daga A, van der Ven AT, Schmidt JM, Low BC, Gupta AB, Tripathi BK, Wong J, Campbell K, Metcalfe K, Schanze D, Niihori T, Kaito H, Nozu K, Tsukaguchi H, Tanaka R, Hamahira K, Kobayashi Y, Takizawa T, Funayama R, Nakayama K, Aoki Y, Kumagai N, Iijima K, Fehrenbach H, Kari JA, El Desoky S, Jalalah S, Bogdanovic R, Stajić N, Zappel H, Rakhmetova A, Wassmer SR, Jungraithmayr T, Strehlau J, Kumar AS, Bagga A, Soliman NA, Mane SM, Kaufman L, Lowy DR, Jairajpuri MA, Lifton RP, Pei Y, Zenker M, Kure S, Hildebrandt F.

Nat Commun. 2018 May 17;9(1):1960. doi: 10.1038/s41467-018-04193-w.

14.

Etiology, ethics, and outcomes of chronic kidney disease in neonates.

Kari JA, Sharief SN, El Desoky SM, Alhasan KA, Albanna AS.

Saudi Med J. 2018 Apr;39(4):361-367. doi: 10.15537/smj.2018.4.21712.

15.

Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.

Braun DA, Warejko JK, Ashraf S, Tan W, Daga A, Schneider R, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Nakayama M, Schapiro D, Rao J, Schmidt JM, Hoogstraten CA, Hugo H, Bakkaloglu SA, Kari JA, El Desoky S, Daouk G, Mane S, Lifton RP, Shril S, Hildebrandt F.

Nephrol Dial Transplant. 2019 Mar 1;34(3):485-493. doi: 10.1093/ndt/gfy028.

16.

Urinary neutrophil gelatinase-associated lipocalin (NGAL) and serum cystatin C measurements for early diagnosis of acute kidney injury in children admitted to PICU.

Kari JA, Shalaby MA, Sofyani K, Sanad AS, Ossra AF, Halabi RS, Aljuhani MH, Toffaha WM, Moria FA, Sabry S, Ahmed HA, Alhasan KA, Sharief S, Safdar O.

World J Pediatr. 2018 Apr;14(2):134-142. doi: 10.1007/s12519-017-0110-x. Epub 2018 Feb 20.

PMID:
29464581
17.

HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.

Adeyemo A, Esezobor C, Solarin A, Abeyagunawardena A, Kari JA, El Desoky S, Greenbaum LA, Kamel M, Kallash M, Silva C, Young A, Hunley TE, de Jesus-Gonzalez N, Srivastava T, Gbadegesin R.

Am J Kidney Dis. 2018 Mar;71(3):399-406. doi: 10.1053/j.ajkd.2017.10.013. Epub 2017 Dec 23.

18.

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.

Warejko JK, Tan W, Daga A, Schapiro D, Lawson JA, Shril S, Lovric S, Ashraf S, Rao J, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Schneider R, Gee HY, Schmidt JM, Vivante A, van der Ven AT, Ityel H, Chen J, Sadowski CE, Kohl S, Pabst WL, Nakayama M, Somers MJG, Rodig NM, Daouk G, Baum M, Stein DR, Ferguson MA, Traum AZ, Soliman NA, Kari JA, El Desoky S, Fathy H, Zenker M, Bakkaloglu SA, Müller D, Noyan A, Ozaltin F, Cadnapaphornchai MA, Hashmi S, Hopcian J, Kopp JB, Benador N, Bockenhauer D, Bogdanovic R, Stajić N, Chernin G, Ettenger R, Fehrenbach H, Kemper M, Munarriz RL, Podracka L, Büscher R, Serdaroglu E, Tasic V, Mane S, Lifton RP, Braun DA, Hildebrandt F.

Clin J Am Soc Nephrol. 2018 Jan 6;13(1):53-62. doi: 10.2215/CJN.04120417. Epub 2017 Nov 10.

19.

Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome.

Rao J, Ashraf S, Tan W, van der Ven AT, Gee HY, Braun DA, Fehér K, George SP, Esmaeilniakooshkghazi A, Choi WI, Jobst-Schwan T, Schneider R, Schmidt JM, Widmeier E, Warejko JK, Hermle T, Schapiro D, Lovric S, Shril S, Daga A, Nayir A, Shenoy M, Tse Y, Bald M, Helmchen U, Mir S, Berdeli A, Kari JA, El Desoky S, Soliman NA, Bagga A, Mane S, Jairajpuri MA, Lifton RP, Khurana S, Martins JC, Hildebrandt F.

J Clin Invest. 2017 Dec 1;127(12):4257-4269. doi: 10.1172/JCI94138. Epub 2017 Oct 23.

20.

Outcome of pediatric acute kidney injury: a multicenter prospective cohort study.

Kari JA, Alhasan KA, Shalaby MA, Khathlan N, Safdar OY, Al Rezgan SA, El Desoky S, Albanna AS.

Pediatr Nephrol. 2018 Feb;33(2):335-340. doi: 10.1007/s00467-017-3786-1. Epub 2017 Sep 15.

PMID:
28917005
21.

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.

Daga A, Majmundar AJ, Braun DA, Gee HY, Lawson JA, Shril S, Jobst-Schwan T, Vivante A, Schapiro D, Tan W, Warejko JK, Widmeier E, Nelson CP, Fathy HM, Gucev Z, Soliman NA, Hashmi S, Halbritter J, Halty M, Kari JA, El-Desoky S, Ferguson MA, Somers MJG, Traum AZ, Stein DR, Daouk GH, Rodig NM, Katz A, Hanna C, Schwaderer AL, Sayer JA, Wassner AJ, Mane S, Lifton RP, Milosevic D, Tasic V, Baum MA, Hildebrandt F.

Kidney Int. 2018 Jan;93(1):204-213. doi: 10.1016/j.kint.2017.06.025. Epub 2017 Oct 12.

22.

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.

Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F.

Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14.

23.

Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia.

Lipska-Ziętkiewicz BS, Gellermann J, Boyer O, Gribouval O, Ziętkiewicz S, Kari JA, Shalaby MA, Ozaltin F, Dusek J, Melk A, Bayazit AK, Massella L, Hyla-Klekot L, Habbig S, Godron A, Szczepańska M, Bieniaś B, Drożdż D, Odeh R, Jarmużek W, Zachwieja K, Trautmann A, Antignac C, Schaefer F; PodoNet Consortium.

PLoS One. 2017 Aug 10;12(8):e0180926. doi: 10.1371/journal.pone.0180926. eCollection 2017.

24.

Impact of acute kidney injury on long-term mortality and progression to chronic kidney disease among critically ill children.

Al-Otaibi NG, Zeinelabdin M, Shalaby MA, Khathlan N, Mashat GD, Zahrani AA, NoorSaeed SM, Shalabi NM, Alhasan KA, Sharief SN, Albanna AS, Kari JA.

Saudi Med J. 2017 Feb;38(2):138-142. doi: 10.15537/smj.2017.2. 16012.

25.

Facial swelling in a child on chronic hemodialysis: Answers.

Sawan ZA, El-Desoky SM, Shalaby MA, Bockenhauer D, Kari JA.

Pediatr Nephrol. 2017 Aug;32(8):1351-1353. doi: 10.1007/s00467-016-3525-z. Epub 2016 Nov 17. No abstract available.

PMID:
27858195
26.

Facial swelling in a child on chronic hemodialysis: Questions.

Sawan ZA, El-Desoky SM, Shalaby MA, Bockenhauer D, Kari JA.

Pediatr Nephrol. 2017 Aug;32(8):1349-1350. doi: 10.1007/s00467-016-3523-1. Epub 2016 Nov 17. No abstract available.

PMID:
27858194
27.

Prevalence of hypertension, obesity, hematuria and proteinuria amongst healthy adolescents living in Western Saudi Arabia.

Hothan KA, Alasmari BA, Alkhelaiwi OK, Althagafi KM, Alkhaldi AA, Alfityani AK, Aladawi MM, Sharief SN, El Desoky S, Kari JA.

Saudi Med J. 2016 Oct;37(10):1120-6. doi: 10.15537/smj.2016.10.14784.

28.

Serum cystatin is a useful marker for the diagnosis of acute kidney injury in critically ill children: prospective cohort study.

Safdar OY, Shalaby M, Khathlan N, Elattal B, Bin Joubah M, Bukahri E, Saber M, Alahadal A, Aljariry H, Gasim S, Hadadi A, Alqahtani A, Awleyakhan R, Kari JA.

BMC Nephrol. 2016 Sep 13;17(1):130. doi: 10.1186/s12882-016-0346-z.

29.

Efficiency of Using Pediatrics Emergency Services and Triage Evaluation.

El Desoky S, Mashat S, Bana S, Alama M, Dhabab N, Malibari GM, Halwani M, Albanna AS, Kari JA.

Pediatr Emerg Care. 2016 Jun 2. [Epub ahead of print]

PMID:
27261954
30.

Prevalence of Hyperparathyroidism, Mineral and Bone Disorders in Children with Advanced Chronic Kidney Disease.

El Desoky S, Farag YM, Safdar E, Shalaby MA, Singh AK, Kari JA.

Indian J Pediatr. 2016 May;83(5):420-5. doi: 10.1007/s12098-015-1986-x. Epub 2016 Jan 30.

PMID:
26830276
31.

Erratum to: Steroid-resistant nephrotic syndrome in a child with dysmorphic features: Answers.

Safdar OY, El-Desoky SM, Bockenhauer D, Sebire N, Kari JA.

Pediatr Nephrol. 2016 Jul;31(7):1199. No abstract available.

PMID:
26820663
32.

Can pre-implantation biopsies predict renal allograft function in pediatric renal transplant recipients?

Kari JA, Ma AL, Dufek S, Mohamed I, Mamode N, Sebire NJ, Marks SD.

Saudi Med J. 2015 Nov;36(11):1299-304. doi: 10.15537/smj.2015.11.12976.

33.

Paradoxical increase in blood pressure following bilateral native nephrectomy.

Ajlan BA, Safdar OY, Shalabi M, Kari JA.

Clin Case Rep. 2015 Jul;3(7):553-7. doi: 10.1002/ccr3.296. Epub 2015 May 18.

34.

Potentially lethal ACE-inhibitor-induced angioedema in a child.

Bukhari E, Safdar OY, Shalaby M, AlSharif SM, Alsufiany K, Kari JA.

Clin Case Rep. 2015 Jun;3(6):427-30. doi: 10.1002/ccr3.265. Epub 2015 Apr 9.

35.

Urinary tract infection in children younger than 5 years. Etiology and associated urological anomalies.

Garout WA, Kurdi HS, Shilli AH, Kari JA.

Saudi Med J. 2015 Apr;36(4):497-501. doi: 10.15537/smj.2015.4.10770.

36.

Predictors of renal replacement therapy and mortality in children with chronic kidney disease.

Kari JA, El Desoky SM, Farag YM, Singh AK.

Saudi Med J. 2015 Jan;36(1):32-9. doi: 10.15537/smj.2015.1.9774.

37.

Angioplasty for renovascular hypertension in 78 children.

Kari JA, Roebuck DJ, McLaren CA, Davis M, Dillon MJ, Hamilton G, Shroff R, Marks SD, Tullus K.

Arch Dis Child. 2015 May;100(5):474-8. doi: 10.1136/archdischild-2013-305886. Epub 2014 Dec 19.

PMID:
25527520
38.

Rituximab for troublesome cases of childhood nephrotic syndrome.

Safdar OY, Aboualhameael A, Kari JA.

World J Clin Pediatr. 2014 Nov 8;3(4):69-75. doi: 10.5409/wjcp.v3.i4.69. eCollection 2014 Nov 8. Review.

39.

Outcome of acute kidney injury in pediatric patients admitted to the intensive care unit.

Shalaby M, Khathlan N, Safder O, Fadel F, Farag YM, Singh AK, Kari JA.

Clin Nephrol. 2014 Dec;82(6):379-86.

PMID:
25412199
40.

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.

Sadowski CE, Lovric S, Ashraf S, Pabst WL, Gee HY, Kohl S, Engelmann S, Vega-Warner V, Fang H, Halbritter J, Somers MJ, Tan W, Shril S, Fessi I, Lifton RP, Bockenhauer D, El-Desoky S, Kari JA, Zenker M, Kemper MJ, Mueller D, Fathy HM, Soliman NA; SRNS Study Group, Hildebrandt F.

J Am Soc Nephrol. 2015 Jun;26(6):1279-89. doi: 10.1681/ASN.2014050489. Epub 2014 Oct 27.

41.
42.

Reply to RE: Steroid-resistant nephrotic syndrome: impact of genetic testing.

Kari JA.

Ann Saudi Med. 2014 May-Jun;34(3):270. doi: 10.5144/0256.4947.2014.270. No abstract available.

43.

The case | Renal tubular acidosis and eye findings.

Kari JA, El Desoky SM, Singh AK, Gari MA, Kleta R, Bockenhauer D.

Kidney Int. 2014 Jul;86(1):217-8. doi: 10.1038/ki.2013.320. No abstract available.

44.

Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years.

Kari JA, Montini G, Bockenhauer D, Brennan E, Rees L, Trompeter RS, Tullus K, Van't Hoff W, Waters A, Ashton E, Lench N, Sebire NJ, Marks SD.

Pediatr Nephrol. 2014 Nov;29(11):2173-80. doi: 10.1007/s00467-014-2856-x. Epub 2014 Jun 6.

45.

Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.

Lovric S, Fang H, Vega-Warner V, Sadowski CE, Gee HY, Halbritter J, Ashraf S, Saisawat P, Soliman NA, Kari JA, Otto EA, Hildebrandt F; Nephrotic Syndrome Study Group.

Clin J Am Soc Nephrol. 2014 Jun 6;9(6):1109-16. doi: 10.2215/CJN.09010813. Epub 2014 Apr 17.

46.

Pediatric CKD and cardiovascular disease.

Safder O, Al sharif S, Kari JA.

Cardiovasc Hematol Disord Drug Targets. 2014;14(3):177-84. Review.

PMID:
24720458
47.

Steroid-resistant nephrotic syndrome in a child with dysmorphic features: answers.

Safdar O, El-Desoky SM, Bockenhauer D, Sebire N, Sabire N, Kari JA.

Pediatr Nephrol. 2014 May;29(5):839-40; quiz 837-8. doi: 10.1007/s00467-014-2754-2. Epub 2014 Jan 29. No abstract available. Erratum in: Pediatr Nephrol. 2014 May;29(5):945. Sabire, Neil [corrected to Sebire, Neil]. Pediatr Nephrol. 2016 Jul;31(7):1199. Safder, Osama Y [corrected to Safdar, Osama Y].

PMID:
24474578
48.

Steroid-resistant nephrotic syndrome: impact of genetic testing.

Kari JA, El-Desoky SM, Gari M, Malik K, Vega-Warner V, Lovric S, Bockenhauer D.

Ann Saudi Med. 2013 Nov-Dec;33(6):533-8. doi: 10.5144/0256-4947.2013.533.

49.

Quality of life among children with beta-thalassemia major treated in Western Saudi Arabia.

Ayoub MD, Radi SA, Azab AM, Abulaban AA, Balkhoyor AH, Bedair SW, Aljaouni SK, Kari JA.

Saudi Med J. 2013 Dec;34(12):1281-6.

PMID:
24343469
50.

Vesicoureteric reflux in children.

Kari JA, El-Desoky SM, Basnawi F, Bahrawi O.

Urol Ann. 2013 Oct;5(4):232-6. doi: 10.4103/0974-7796.120292.

Supplemental Content

Support Center