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Items: 1 to 50 of 62

1.

Children with vesico-ureteric reflux have joint hypermobility and occasional TNXB sequence variants.

Tokhmafshan F, El Andalousi J, Murugapoopathy V, Fillion ML, Campillo S, Capolicchio JP, Jednak R, El Sherbiny M, Turpin S, Schalkwijk J, Matsumoto KI, Brophy PD, Gbadegesin RA, Gupta IR.

Can Urol Assoc J. 2019 Nov 5. doi: 10.5489/cuaj.6068. [Epub ahead of print]

PMID:
31702543
2.

Aberrant IgM on T cells: biomarker or pathogenic factor in childhood nephrotic syndrome?

Chambers ET, Gbadegesin RA.

Kidney Int. 2019 Oct;96(4):818-820. doi: 10.1016/j.kint.2019.05.031.

PMID:
31543150
3.

Cultivating Research Skills During Clinical Training to Promote Pediatric-Scientist Development.

Hurst JH, Barrett KJ, Kelly MS, Staples BB, McGann KA, Cunningham CK, Reed AM, Gbadegesin RA, Permar SR.

Pediatrics. 2019 Aug;144(2). pii: e20190745. doi: 10.1542/peds.2019-0745.

PMID:
31363070
4.

Health-related quality of life in glomerular disease.

Canetta PA, Troost JP, Mahoney S, Kogon AJ, Carlozzi N, Bartosh SM, Cai Y, Davis TK, Fernandez H, Fornoni A, Gbadegesin RA, Herreshoff E, Mahan JD, Nachman PH, Selewski DT, Sethna CB, Srivastava T, Tuttle KR, Wang CS, Falk RJ, Gharavi AG, Gillespie BW, Greenbaum LA, Holzman LB, Kretzler M, Robinson BM, Smoyer WE, Guay-Woodford LM, Reeve B, Gipson DS; CureGN Consortium.

Kidney Int. 2019 May;95(5):1209-1224. doi: 10.1016/j.kint.2018.12.018. Epub 2019 Feb 27.

PMID:
30898342
5.

Genetics of Childhood Steroid Sensitive Nephrotic Syndrome: An Update.

Lane BM, Cason R, Esezobor CI, Gbadegesin RA.

Front Pediatr. 2019 Jan 29;7:8. doi: 10.3389/fped.2019.00008. eCollection 2019. Review.

6.

Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study.

Selewski DT, Ambruzs JM, Appel GB, Bomback AS, Matar RB, Cai Y, Cattran DC, Chishti AS, D'Agati VD, D'Alessandri-Silva CJ, Gbadegesin RA, Hogan JJ, Iragorri S, Jennette JC, Julian BA, Khalid M, Lafayette RA, Liapis H, Lugani F, Mansfield SA, Mason S, Nachman PH, Nast CC, Nester CM, Noone DG, Novak J, O'Shaughnessy MM, Reich HN, Rheault MN, Rizk DV, Saha MK, Sanghani NS, Sperati CJ, Sreedharan R, Srivastava T, Swiatecka-Urban A, Twombley K, Vasylyeva TL, Weaver DJ, Yin H, Zee J, Falk RJ, Gharavi AG, Gillespie BW, Gipson DS, Greenbaum LA, Holzman LB, Kretzler M, Robinson BM, Smoyer WE, Flessner M, Guay-Woodford LM, Kiryluk K; CureGN Consortium.

Kidney Int Rep. 2018 Aug 3;3(6):1373-1384. doi: 10.1016/j.ekir.2018.07.021. eCollection 2018 Nov.

7.

Correction to: Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings : A Midwest Pediatric Nephrology Consortium (MWPNC) study.

Pelletier JH, Kumar KR, Engen R, Bensimhon A, Varner JD, Rheault MN, Srivastava T, Straatmann C, Silva C, Davis TK, Wenderfer SE, Gibson K, Selewski D, Barcia J, Weng P, Licht C, Jawa N, Kallash M, Foreman JW, Wigfall DR, Chua AN, Chambers E, Hornik CP, Brewer ED, Nagaraj SK, Greenbaum LA, Gbadegesin RA.

Pediatr Nephrol. 2019 Mar;34(3):539. doi: 10.1007/s00467-018-4103-3.

PMID:
30443740
8.

Genetic Basis of Health Disparity in Childhood Nephrotic Syndrome.

Varner JD, Matory A, Gbadegesin RA.

Am J Kidney Dis. 2018 Nov;72(5 Suppl 1):S22-S25. doi: 10.1053/j.ajkd.2018.06.022. Review.

PMID:
30343718
9.

Treatment of steroid-resistant nephrotic syndrome in the genomic era.

Bensimhon AR, Williams AE, Gbadegesin RA.

Pediatr Nephrol. 2019 Nov;34(11):2279-2293. doi: 10.1007/s00467-018-4093-1. Epub 2018 Oct 2. Review.

PMID:
30280213
10.

The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes.

Hall G, Lane BM, Khan K, Pediaditakis I, Xiao J, Wu G, Wang L, Kovalik ME, Chryst-Stangl M, Davis EE, Spurney RF, Gbadegesin RA.

J Am Soc Nephrol. 2018 Aug;29(8):2110-2122. doi: 10.1681/ASN.2017121338. Epub 2018 Jul 12.

11.

Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings.

Pelletier JH, Kumar KR, Engen R, Bensimhon A, Varner JD, Rheault MN, Srivastava T, Straatmann C, Silva C, Davis TK, Wenderfer SE, Gibson K, Selewski D, Barcia J, Weng P, Licht C, Jawa N, Kallash M, Foreman JW, Wigfall DR, Chua AN, Chambers E, Hornik CP, Brewer ED, Nagaraj SK, Greenbaum LA, Gbadegesin RA.

Pediatr Nephrol. 2018 Oct;33(10):1773-1780. doi: 10.1007/s00467-018-3994-3. Epub 2018 Jul 7. Erratum in: Pediatr Nephrol. 2019 Mar;34(3):539.

12.

Responsiveness of the PROMIS® measures to changes in disease status among pediatric nephrotic syndrome patients: a Midwest pediatric nephrology consortium study.

Selewski DT, Troost JP, Cummings D, Massengill SF, Gbadegesin RA, Greenbaum LA, Shatat IF, Cai Y, Kapur G, Hebert D, Somers MJ, Trachtman H, Pais P, Seifert ME, Goebel J, Sethna CB, Mahan JD, Gross HE, Herreshoff E, Liu Y, Carlozzi NE, Reeve BB, DeWalt DA, Gipson DS.

Health Qual Life Outcomes. 2017 Aug 23;15(1):166. doi: 10.1186/s12955-017-0737-2.

13.

Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.

Hall G, Routh JC, Gbadegesin RA.

Am J Kidney Dis. 2017 Jul;70(1):8-10. doi: 10.1053/j.ajkd.2017.03.017. Epub 2017 Apr 26. No abstract available.

14.

The Genetics of Nephrotic Syndrome.

Rheault MN, Gbadegesin RA.

J Pediatr Genet. 2016 Mar;5(1):15-24. doi: 10.1055/s-0035-1557109. Epub 2015 Aug 13. Review.

15.

Genetics of childhood steroid-sensitive nephrotic syndrome.

Karp AM, Gbadegesin RA.

Pediatr Nephrol. 2017 Sep;32(9):1481-1488. doi: 10.1007/s00467-016-3456-8. Epub 2016 Jul 29. Review.

16.

Vesicoureteral reflux and the extracellular matrix connection.

Tokhmafshan F, Brophy PD, Gbadegesin RA, Gupta IR.

Pediatr Nephrol. 2017 Apr;32(4):565-576. doi: 10.1007/s00467-016-3386-5. Epub 2016 May 2. Review.

17.

Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux.

Elahi S, Homstad A, Vaidya H, Stout J, Hall G, Wu G, Conlon P Jr, Routh JC, Wiener JS, Ross SS, Nagaraj S, Wigfall D, Foreman J, Adeyemo A, Gupta IR, Brophy PD, Rabinovich CE, Gbadegesin RA.

Pediatr Nephrol. 2016 Feb;31(2):247-53. doi: 10.1007/s00467-015-3203-6. Epub 2015 Sep 25.

18.

The author replies.

Gbadegesin RA.

Kidney Int. 2015 Apr;87(4):859-60. doi: 10.1038/ki.2015.39. No abstract available.

19.

Translating genetic findings in hereditary nephrotic syndrome: the missing loops.

Hall G, Gbadegesin RA.

Am J Physiol Renal Physiol. 2015 Jul 1;309(1):F24-8. doi: 10.1152/ajprenal.00683.2014. Epub 2015 Mar 25. Review.

20.

The impact of disease duration on quality of life in children with nephrotic syndrome: a Midwest Pediatric Nephrology Consortium study.

Selewski DT, Troost JP, Massengill SF, Gbadegesin RA, Greenbaum LA, Shatat IF, Cai Y, Kapur G, Hebert D, Somers MJ, Trachtman H, Pais P, Seifert ME, Goebel J, Sethna CB, Mahan JD, Gross HE, Herreshoff E, Liu Y, Song PX, Reeve BB, DeWalt DA, Gipson DS.

Pediatr Nephrol. 2015 Sep;30(9):1467-76. doi: 10.1007/s00467-015-3074-x. Epub 2015 Mar 18.

21.

HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.

Gbadegesin RA, Adeyemo A, Webb NJ, Greenbaum LA, Abeyagunawardena A, Thalgahagoda S, Kale A, Gipson D, Srivastava T, Lin JJ, Chand D, Hunley TE, Brophy PD, Bagga A, Sinha A, Rheault MN, Ghali J, Nicholls K, Abraham E, Janjua HS, Omoloja A, Barletta GM, Cai Y, Milford DD, O'Brien C, Awan A, Belostotsky V, Smoyer WE, Homstad A, Hall G, Wu G, Nagaraj S, Wigfall D, Foreman J, Winn MP; Mid-West Pediatric Nephrology Consortium.

J Am Soc Nephrol. 2015 Jul;26(7):1701-10. doi: 10.1681/ASN.2014030247. Epub 2014 Oct 27.

22.

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.

Malone AF, Phelan PJ, Hall G, Cetincelik U, Homstad A, Alonso AS, Jiang R, Lindsey TB, Wu G, Sparks MA, Smith SR, Webb NJ, Kalra PA, Adeyemo AA, Shaw AS, Conlon PJ, Jennette JC, Howell DN, Winn MP, Gbadegesin RA.

Kidney Int. 2014 Dec;86(6):1253-9. doi: 10.1038/ki.2014.305. Epub 2014 Sep 17.

23.

Efficacy of antibiotic prophylaxis in children with vesicoureteral reflux: systematic review and meta-analysis.

Wang HH, Gbadegesin RA, Foreman JW, Nagaraj SK, Wigfall DR, Wiener JS, Routh JC.

J Urol. 2015 Mar;193(3):963-9. doi: 10.1016/j.juro.2014.08.112. Epub 2014 Sep 6. Review.

24.

A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.

Hall G, Gbadegesin RA, Lavin P, Wu G, Liu Y, Oh EC, Wang L, Spurney RF, Eckel J, Lindsey T, Homstad A, Malone AF, Phelan PJ, Shaw A, Howell DN, Conlon PJ, Katsanis N, Winn MP.

J Am Soc Nephrol. 2015 Apr;26(4):831-43. doi: 10.1681/ASN.2013101053. Epub 2014 Aug 21.

25.

Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity.

Hall G, Rowell J, Farinelli F, Gbadegesin RA, Lavin P, Wu G, Homstad A, Malone A, Lindsey T, Jiang R, Spurney R, Tomaselli GF, Kass DA, Winn MP.

Am J Physiol Renal Physiol. 2014 Jun 15;306(12):F1442-50. doi: 10.1152/ajprenal.00212.2013. Epub 2014 Apr 16.

26.

Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.

Gbadegesin RA, Hall G, Adeyemo A, Hanke N, Tossidou I, Burchette J, Wu G, Homstad A, Sparks MA, Gomez J, Jiang R, Alonso A, Lavin P, Conlon P, Korstanje R, Stander MC, Shamsan G, Barua M, Spurney R, Singhal PC, Kopp JB, Haller H, Howell D, Pollak MR, Shaw AS, Schiffer M, Winn MP.

J Am Soc Nephrol. 2014 Sep;25(9):1991-2002. doi: 10.1681/ASN.2013090976. Epub 2014 Mar 27.

27.

TNXB mutations can cause vesicoureteral reflux.

Gbadegesin RA, Brophy PD, Adeyemo A, Hall G, Gupta IR, Hains D, Bartkowiak B, Rabinovich CE, Chandrasekharappa S, Homstad A, Westreich K, Wu G, Liu Y, Holanda D, Clarke J, Lavin P, Selim A, Miller S, Wiener JS, Ross SS, Foreman J, Rotimi C, Winn MP.

J Am Soc Nephrol. 2013 Jul;24(8):1313-22. doi: 10.1681/ASN.2012121148. Epub 2013 Apr 25.

28.

Genetic testing in nephrotic syndrome--challenges and opportunities.

Gbadegesin RA, Winn MP, Smoyer WE.

Nat Rev Nephrol. 2013 Mar;9(3):179-84. doi: 10.1038/nrneph.2012.286. Epub 2013 Jan 15. Review.

29.

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.

Gbadegesin RA, Lavin PJ, Hall G, Bartkowiak B, Homstad A, Jiang R, Wu G, Byrd A, Lynn K, Wolfish N, Ottati C, Stevens P, Howell D, Conlon P, Winn MP.

Kidney Int. 2012 Jan;81(1):94-9. doi: 10.1038/ki.2011.297. Epub 2011 Aug 24.

30.

Complexity of the msp2 locus and the severity of childhood malaria, in south-western Nigeria.

Amodu OK, Oyedeji SI, Ntoumi F, Orimadegun AE, Gbadegesin RA, Olumese PE, Omotade OO.

Ann Trop Med Parasitol. 2008 Mar;102(2):95-102. doi: 10.1179/136485908X252340.

PMID:
18318931
31.

The influence of individual preventive measures on the clinical severity of malaria among Nigerian children.

Amodu OK, Olumese PE, Gbadegesin RA, Ayoola OO, Adeyemo AA.

Acta Trop. 2006 Mar;97(3):370-2. Epub 2006 Jan 24. No abstract available.

PMID:
16438924
32.

Association between ICAM-1 Gly-Arg polymorphism and renal parenchymal scarring following childhood urinary tract infection.

Gbadegesin RA, Cotton SA, Watson CJ, Brenchley PE, Webb NJ.

Int J Immunogenet. 2006 Feb;33(1):49-53.

PMID:
16426244
33.

A review of cases of posterior urethral valves seen at the University College Hospital, Ibadan (Nigeria).

Asinobi AO, Gbadegesin RA, Shittu OB.

Pediatr Med Chir. 2004 Nov-Dec;26(6):430-3.

PMID:
16363768
34.

Increased steroid responsiveness of young children with nephrotic syndrome in Nigeria.

Asinobi AO, Gbadegesin RA, Ogunkunle OO.

Ann Trop Paediatr. 2005 Sep;25(3):199-203.

PMID:
16156985
35.

Genetic diversity of the msp-1 locus and symptomatic malaria in south-west Nigeria.

Amodu OK, Adeyemo AA, Ayoola OO, Gbadegesin RA, Orimadegun AE, Akinsola AK, Olumese PE, Omotade OO.

Acta Trop. 2005 Sep;95(3):226-32.

PMID:
16023985
36.

Plasmodium falciparum malaria in south-west Nigerian children: is the polymorphism of ICAM-1 and E-selectin genes contributing to the clinical severity of malaria?

Amodu OK, Gbadegesin RA, Ralph SA, Adeyemo AA, Brenchley PE, Ayoola OO, Orimadegun AE, Akinsola AK, Olumese PE, Omotade OO.

Acta Trop. 2005 Sep;95(3):248-55.

PMID:
16002039
37.

Chloroquine resistance of Plasmodium falciparum is associated with severity of disease in Nigerian children.

Olumese PE, Amodu OK, Björkman A, Adeyemo AA, Gbadegesin RA, Walker O.

Trans R Soc Trop Med Hyg. 2002 Jul-Aug;96(4):418-20.

PMID:
12497979
38.

A PCR-RFLP typing method for adhesion molecule gene polymorphisms and allele frequencies in a normal UK population.

Gbadegesin RA, Watson CJ, Cotton SA, Brenchley PE, Webb NJ.

Eur J Immunogenet. 2002 Apr;29(2):109-11.

PMID:
11918635
39.

Plasma and urinary soluble adhesion molecule expression is increased during first documented acute pyelonephritis.

Gbadegesin RA, Cotton SA, Coupes BM, Awan A, Brenchley PE, Webb NJ.

Arch Dis Child. 2002 Mar;86(3):218-21.

40.

Role of TGF-beta1 in renal parenchymal scarring following childhood urinary tract infection.

Cotton SA, Gbadegesin RA, Williams S, Brenchley PE, Webb NJ.

Kidney Int. 2002 Jan;61(1):61-7.

41.

The Ibadan conjoined twins: a report of omphalopagus twins and a review of cases reported in Nigeria over 60 years.

Omokhodion SI, Ladipo JK, Odebode TO, Ajao OG, Famewo CE, Lagundoye SB, Sanusi A, Gbadegesin RA.

Ann Trop Paediatr. 2001 Sep;21(3):263-70. Review.

PMID:
11579866
42.

Neurological features of cerebral malaria in Nigerian children.

Olumese PE, Gbadegesin RA, Adeyemo AA, Brown B, Walker A.

Ann Trop Paediatr. 1999 Dec;19(4):321-5.

PMID:
10716024
43.

The predominance of membranoproliferative glomerulonephritis in childhood nephrotic syndrome in Ibadan, Nigeria.

Asinobi AO, Gbadegesin RA, Adeyemo AA, Akang EE, Arowolo FA, Abiola OA, Osinusi K.

West Afr J Med. 1999 Jul-Sep;18(3):203-6.

PMID:
10593158
44.

Comparative efficacy of intramuscular artemether and intravenous quinine in Nigerian children with cerebral malaria.

Olumese PE, Björkman A, Gbadegesin RA, Adeyemo AA, Walker O.

Acta Trop. 1999 Oct 15;73(3):231-6.

PMID:
10546840
45.

Intraleucocytic malaria pigment and clinical severity of malaria in children.

Amodu OK, Adeyemo AA, Olumese PE, Gbadegesin RA.

Trans R Soc Trop Med Hyg. 1998 Jan-Feb;92(1):54-6.

PMID:
9692152
46.

Intraleucocyte malaria pigment in asymptomatic and uncomplicated malaria.

Amodu OK, Adeyemo AA, Olumese PE, Ketiku O, Gbadegesin RA.

East Afr Med J. 1997 Nov;74(11):714-6.

PMID:
9557443
47.

Major congenital malformations among neonatal referrals to a Nigerian university hospital.

Adeyemo AA, Gbadegesin RA, Omotade OO.

East Afr Med J. 1997 Nov;74(11):699-701.

PMID:
9557439
48.

Breastfeeding and bloody diarrhoea in young children.

Adeyemo AA, Sodeinde O, Gbadegesin RA, Ademowo OG.

J Trop Pediatr. 1998 Feb;44(1):52-3. doi: 10.1093/tropej/44.1.52. No abstract available.

PMID:
9538609
49.

Persistent diarrhoea in Nigerian children aged less than five years: a hospital-based study.

Sodeinde O, Adeyemo AA, Gbadegesin RA, Ademowo OG.

J Diarrhoeal Dis Res. 1997 Sep;15(3):155-60.

PMID:
9473879
50.

Lack of association between falciparum malaria parasitemia and acute diarrhea in Nigerian children.

Sodeinde O, Gbadegesin RA, Ademowo OG, Adeyemo AA.

Am J Trop Med Hyg. 1997 Dec;57(6):702-5.

PMID:
9430531

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