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Dr Rasheed Adebayo Gbadegesin

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    Collapse Bibliographic 
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Rheault MN, Zhang L, Selewski DT, Kallash M, Tran CL, Seamon M, Katsoufis C, Ashoor I, Hernandez J, Supe-Markovina K, D'Alessandri-Silva C, DeJesus-Gonzalez N, Vasylyeva TL, Formeck C, Woll C, Gbadegesin R, Geier P, Devarajan P, Carpenter SL, Kerlin BA, Smoyer WE. AKI in Children Hospitalized with Nephrotic Syndrome. Clin J Am Soc Nephrol. 2015 Dec 07; 10(12):2110-8. PMID: 26450933.
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    2. Elahi S, Homstad A, Vaidya H, Stout J, Hall G, Wu G, Conlon P, Routh JC, Wiener JS, Ross SS, Nagaraj S, Wigfall D, Foreman J, Adeyemo A, Gupta IR, Brophy PD, Rabinovich CE, Gbadegesin RA. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux. Pediatr Nephrol. 2016 Feb; 31(2):247-53. PMID: 26408188.
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    3. Phelan PJ, Hall G, Wigfall D, Foreman J, Nagaraj S, Malone AF, Winn MP, Howell DN, Gbadegesin R. Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation. Clin Kidney J. 2015 Oct; 8(5):538-42. PMID: 26413278.
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    4. Gbadegesin RA. The author replies. Kidney Int. 2015 Apr; 87(4):859-60. PMID: 25826549.
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    5. Hall G, Gbadegesin RA. Translating genetic findings in hereditary nephrotic syndrome: the missing loops. Am J Physiol Renal Physiol. 2015 Jul 01; 309(1):F24-8. PMID: 25810439.
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    6. 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. The impact of disease duration on quality of life in children with nephrotic syndrome: a Midwest Pediatric Nephrology Consortium study. Pediatr Nephrol. 2015 Sep; 30(9):1467-76. PMID: 25784017.
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    7. 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. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome. J Am Soc Nephrol. 2015 Jul; 26(7):1701-10. PMID: 25349203.
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    8. 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. Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis. Kidney Int. 2014 Dec; 86(6):1253-9. PMID: 25229338.
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    9. Wang HH, Gbadegesin RA, Foreman JW, Nagaraj SK, Wigfall DR, Wiener JS, Routh JC. Efficacy of antibiotic prophylaxis in children with vesicoureteral reflux: systematic review and meta-analysis. J Urol. 2015 Mar; 193(3):963-9. PMID: 25196653.
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    10. 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. A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS. J Am Soc Nephrol. 2015 Apr; 26(4):831-43. PMID: 25145932.
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    11. Selewski DT, Massengill SF, Troost JP, Wickman L, Messer KL, Herreshoff E, Bowers C, Ferris ME, Mahan JD, Greenbaum LA, MacHardy J, Kapur G, Chand DH, Goebel J, Barletta GM, Geary D, Kershaw DB, Pan CG, Gbadegesin R, Hidalgo G, Lane JC, Leiser JD, Song PX, Thissen D, Liu Y, Gross HE, DeWalt DA, Gipson DS. Gaining the Patient Reported Outcomes Measurement Information System (PROMIS) perspective in chronic kidney disease: a Midwest Pediatric Nephrology Consortium study. Pediatr Nephrol. 2014 Dec; 29(12):2347-56. PMID: 24908324.
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    12. 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. Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity. Am J Physiol Renal Physiol. 2014 Jun 15; 306(12):F1442-50. PMID: 24740790.
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    13. 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. Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS. J Am Soc Nephrol. 2014 Sep; 25(9):1991-2002. PMID: 24676636.
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    14. Straatmann C, Ayoob R, Gbadegesin R, Gibson K, Rheault MN, Srivastava T, Tran CL, Gipson DS, Greenbaum LA, Smoyer WE, Vehaskari VM. Treatment outcome of late steroid-resistant nephrotic syndrome: a study by the Midwest Pediatric Nephrology Consortium. Pediatr Nephrol. 2013 Aug; 28(8):1235-41. PMID: 23633037.
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    15. 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. TNXB mutations can cause vesicoureteral reflux. J Am Soc Nephrol. 2013 Jul; 24(8):1313-22. PMID: 23620400.
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    16. Gipson DS, Selewski DT, Massengill SF, Wickman L, Messer KL, Herreshoff E, Bowers C, Ferris ME, Mahan JD, Greenbaum LA, MacHardy J, Kapur G, Chand DH, Goebel J, Barletta GM, Geary D, Kershaw DB, Pan CG, Gbadegesin R, Hidalgo G, Lane JC, Leiser JD, Plattner BW, Song PX, Thissen D, Liu Y, Gross HE, DeWalt DA. Gaining the PROMIS perspective from children with nephrotic syndrome: a Midwest pediatric nephrology consortium study. Health Qual Life Outcomes. 2013 Mar 04; 11:30. PMID: 23510630.
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    17. Gbadegesin RA, Winn MP, Smoyer WE. Genetic testing in nephrotic syndrome--challenges and opportunities. Nat Rev Nephrol. 2013 03; 9(3):179-84. PMID: 23321566.
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    18. Akilesh S, Suleiman H, Yu H, Stander MC, Lavin P, Gbadegesin R, Antignac C, Pollak M, Kopp JB, Winn MP, Shaw AS. Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis. J Clin Invest. 2011 Oct; 121(10):4127-37. PMID: 21911940.
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    19. 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. Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis. Kidney Int. 2012 Jan; 81(1):94-9. PMID: 21866090.
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    20. Heeringa SF, Chernin G, Chaki M, Zhou W, Sloan AJ, Ji Z, Xie LX, Salviati L, Hurd TW, Vega-Warner V, Killen PD, Raphael Y, Ashraf S, Ovunc B, Schoeb DS, McLaughlin HM, Airik R, Vlangos CN, Gbadegesin R, Hinkes B, Saisawat P, Trevisson E, Doimo M, Casarin A, Pertegato V, Giorgi G, Prokisch H, Rötig A, Nürnberg G, Becker C, Wang S, Ozaltin F, Topaloglu R, Bakkaloglu A, Bakkaloglu SA, Müller D, Beissert A, Mir S, Berdeli A, Varpizen S, Zenker M, Matejas V, Santos-Ocaña C, Navas P, Kusakabe T, Kispert A, Akman S, Soliman NA, Krick S, Mundel P, Reiser J, Nürnberg P, Clarke CF, Wiggins RC, Faul C, Hildebrandt F. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J Clin Invest. 2011 May; 121(5):2013-24. PMID: 21540551.
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    21. Eckel J, Lavin PJ, Finch EA, Mukerji N, Burch J, Gbadegesin R, Wu G, Bowling B, Byrd A, Hall G, Sparks M, Zhang ZS, Homstad A, Barisoni L, Birbaumer L, Rosenberg P, Winn MP. TRPC6 enhances angiotensin II-induced albuminuria. J Am Soc Nephrol. 2011 Mar; 22(3):526-35. PMID: 21258036.
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    22. Gbadegesin R, Lavin P, Foreman J, Winn M. Pathogenesis and therapy of focal segmental glomerulosclerosis: an update. Pediatr Nephrol. 2011 Jul; 26(7):1001-15. PMID: 21110043.
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    23. Gbadegesin R, Lavin P, Janssens L, Bartkowiak B, Homstad A, Wu G, Bowling B, Eckel J, Potocky C, Abbott D, Conlon P, Scott WK, Howell D, Hauser E, Winn MP. A new locus for familial FSGS on chromosome 2p. J Am Soc Nephrol. 2010 Aug; 21(8):1390-7. PMID: 20616172.
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    24. Gbadegesin R, Zhao S, Charpie J, Brophy PD, Smoyer WE, Lin JJ. Significance of hemolysis on extracorporeal life support after cardiac surgery in children. Pediatr Nephrol. 2009 Mar; 24(3):589-95. PMID: 19002722.
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    25. Gbadegesin R, Bartkowiak B, Lavin PJ, Mukerji N, Wu G, Bowling B, Eckel J, Damodaran T, Winn MP. Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS. Pediatr Nephrol. 2009 Feb; 24(2):281-5. PMID: 18975016.
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    26. Lavin PJ, Gbadegesin R, Damodaran TV, Winn MP. Therapeutic targets in focal and segmental glomerulosclerosis. Curr Opin Nephrol Hypertens. 2008 Jul; 17(4):386-92. PMID: 18660675.
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    27. Chernin G, Heeringa SF, Gbadegesin R, Liu J, Hinkes BG, Vlangos CN, Vega-Warner V, Hildebrandt F. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome. Pediatr Nephrol. 2008 Sep; 23(9):1455-60. PMID: 18543005.
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    28. Heeringa SF, Vlangos CN, Chernin G, Hinkes B, Gbadegesin R, Liu J, Hoskins BE, Ozaltin F, Hildebrandt F. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome. Nephrol Dial Transplant. 2008 Nov; 23(11):3527-33. PMID: 18503012.
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    29. Amodu OK, Oyedeji SI, Ntoumi F, Orimadegun AE, Gbadegesin RA, Olumese PE, Omotade OO. Complexity of the msp2 locus and the severity of childhood malaria, in south-western Nigeria. Ann Trop Med Parasitol. 2008 Mar; 102(2):95-102. PMID: 18318931.
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    30. Hinkes B, Vlangos C, Heeringa S, Mucha B, Gbadegesin R, Liu J, Hasselbacher K, Ozaltin F, Hildebrandt F. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome. J Am Soc Nephrol. 2008 Feb; 19(2):365-71. PMID: 18216321.
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    31. Gbadegesin R, Kudelka T, Gadegbeku CA, Brophy P, Smoyer WE, Lin JJ. Arterial compliance in adolescents and young adults receiving chronic hemodialysis. Ren Fail. 2008; 30(6):591-6. PMID: 18661408.
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    32. Gbadegesin R, Hinkes BG, Hoskins BE, Vlangos CN, Heeringa SF, Liu J, Loirat C, Ozaltin F, Hashmi S, Ulmer F, Cleper R, Ettenger R, Antignac C, Wiggins RC, Zenker M, Hildebrandt F. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS). Nephrol Dial Transplant. 2008 Apr; 23(4):1291-7. PMID: 18065803.
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    33. Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K, Hangan D, Ozaltin F, Zenker M, Hildebrandt F. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2). Pediatrics. 2007 Apr; 119(4):e907-19. PMID: 17371932.
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    34. Gbadegesin R, Hinkes B, Vlangos C, Mucha B, Liu J, Hopcian J, Hildebrandt F. Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome. Pediatr Nephrol. 2007 Apr; 22(4):509-13. PMID: 17216259.
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    35. Hinkes B, Wiggins RC, Gbadegesin R, Vlangos CN, Seelow D, Nürnberg G, Garg P, Verma R, Chaib H, Hoskins BE, Ashraf S, Becker C, Hennies HC, Goyal M, Wharram BL, Schachter AD, Mudumana S, Drummond I, Kerjaschki D, Waldherr R, Dietrich A, Ozaltin F, Bakkaloglu A, Cleper R, Basel-Vanagaite L, Pohl M, Griebel M, Tsygin AN, Soylu A, Müller D, Sorli CS, Bunney TD, Katan M, Liu J, Attanasio M, O'toole JF, Hasselbacher K, Mucha B, Otto EA, Airik R, Kispert A, Kelley GG, Smrcka AV, Gudermann T, Holzman LB, Nürnberg P, Hildebrandt F. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nat Genet. 2006 Dec; 38(12):1397-405. PMID: 17086182.
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    36. Gbadegesin RA, Cotton SA, Watson CJ, Brenchley PE, Webb NJ. Association between ICAM-1 Gly-Arg polymorphism and renal parenchymal scarring following childhood urinary tract infection. Int J Immunogenet. 2006 Feb; 33(1):49-53. PMID: 16426244.
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    37. Amodu OK, Olumese PE, Gbadegesin RA, Ayoola OO, Adeyemo AA. The influence of individual preventive measures on the clinical severity of malaria among Nigerian children. Acta Trop. 2006 Mar; 97(3):370-2. PMID: 16438924.
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    38. Asinobi AO, Gbadegesin RA, Ogunkunle OO. Increased steroid responsiveness of young children with nephrotic syndrome in Nigeria. Ann Trop Paediatr. 2005 Sep; 25(3):199-203. PMID: 16156985.
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    39. Amodu OK, Adeyemo AA, Ayoola OO, Gbadegesin RA, Orimadegun AE, Akinsola AK, Olumese PE, Omotade OO. Genetic diversity of the msp-1 locus and symptomatic malaria in south-west Nigeria. Acta Trop. 2005 Sep; 95(3):226-32. PMID: 16023985.
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    40. Amodu OK, Gbadegesin RA, Ralph SA, Adeyemo AA, Brenchley PE, Ayoola OO, Orimadegun AE, Akinsola AK, Olumese PE, Omotade OO. 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? Acta Trop. 2005 Sep; 95(3):248-55. PMID: 16002039.
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    41. Asinobi AO, Gbadegesin RA, Shittu OB. A review of cases of posterior urethral valves seen at the University College Hospital, Ibadan (Nigeria). Pediatr Med Chir. 2004 Nov-Dec; 26(6):430-3. PMID: 16363768.
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    42. Olumese PE, Amodu OK, Björkman A, Adeyemo AA, Gbadegesin RA, Walker O. Chloroquine resistance of Plasmodium falciparum is associated with severity of disease in Nigerian children. Trans R Soc Trop Med Hyg. 2002 Jul-Aug; 96(4):418-20. PMID: 12497979.
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    43. Gbadegesin RA, Watson CJ, Cotton SA, Brenchley PE, Webb NJ. A PCR-RFLP typing method for adhesion molecule gene polymorphisms and allele frequencies in a normal UK population. Eur J Immunogenet. 2002 Apr; 29(2):109-11. PMID: 11918635.
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    44. Gbadegesin RA, Cotton SA, Coupes BM, Awan A, Brenchley PE, Webb NJ. Plasma and urinary soluble adhesion molecule expression is increased during first documented acute pyelonephritis. Arch Dis Child. 2002 Mar; 86(3):218-21. PMID: 11861252.
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    45. Cotton SA, Gbadegesin RA, Williams S, Brenchley PE, Webb NJ. Role of TGF-beta1 in renal parenchymal scarring following childhood urinary tract infection. Kidney Int. 2002 Jan; 61(1):61-7. PMID: 11786085.
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    46. Omokhodion SI, Ladipo JK, Odebode TO, Ajao OG, Famewo CE, Lagundoye SB, Sanusi A, Gbadegesin RA. The Ibadan conjoined twins: a report of omphalopagus twins and a review of cases reported in Nigeria over 60 years. Ann Trop Paediatr. 2001 Sep; 21(3):263-70. PMID: 11579866.
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    47. Olumese PE, Gbadegesin RA, Adeyemo AA, Brown B, Walker A. Neurological features of cerebral malaria in Nigerian children. Ann Trop Paediatr. 1999 Dec; 19(4):321-5. PMID: 10716024.
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    48. Olumese PE, Björkman A, Gbadegesin RA, Adeyemo AA, Walker O. Comparative efficacy of intramuscular artemether and intravenous quinine in Nigerian children with cerebral malaria. Acta Trop. 1999 Oct 15; 73(3):231-6. PMID: 10546840.
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    49. Asinobi AO, Gbadegesin RA, Adeyemo AA, Akang EE, Arowolo FA, Abiola OA, Osinusi K. The predominance of membranoproliferative glomerulonephritis in childhood nephrotic syndrome in Ibadan, Nigeria. West Afr J Med. 1999 Jul-Sep; 18(3):203-6. PMID: 10593158.
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    50. Adeyemo AA, Sodeinde O, Gbadegesin RA, Ademowo OG. Breastfeeding and bloody diarrhoea in young children. J Trop Pediatr. 1998 02; 44(1):52-3. PMID: 9538609.
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    51. Amodu OK, Adeyemo AA, Olumese PE, Gbadegesin RA. Intraleucocytic malaria pigment and clinical severity of malaria in children. Trans R Soc Trop Med Hyg. 1998 Jan-Feb; 92(1):54-6. PMID: 9692152.
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    52. Sodeinde O, Gbadegesin RA, Ademowo OG, Adeyemo AA. Lack of association between falciparum malaria parasitemia and acute diarrhea in Nigerian children. Am J Trop Med Hyg. 1997 Dec; 57(6):702-5. PMID: 9430531.
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    53. Adeyemo AA, Gbadegesin RA, Omotade OO. Major congenital malformations among neonatal referrals to a Nigerian university hospital. East Afr Med J. 1997 Nov; 74(11):699-701. PMID: 9557439.
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    54. Amodu OK, Adeyemo AA, Olumese PE, Ketiku O, Gbadegesin RA. Intraleucocyte malaria pigment in asymptomatic and uncomplicated malaria. East Afr Med J. 1997 Nov; 74(11):714-6. PMID: 9557443.
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    55. Sodeinde O, Adeyemo AA, Gbadegesin RA, Ademowo OG. Persistent diarrhoea in Nigerian children aged less than five years: a hospital-based study. J Diarrhoeal Dis Res. 1997 Sep; 15(3):155-60. PMID: 9473879.
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    56. Adeyemo AA, Sodeinde O, Gbadegesin RA, Ademowo OG. Breastfeeding and bloody diarrhoea in young children in Ibadan, Nigeria. J Trop Pediatr. 1997 08; 43(4):235-6. PMID: 9283128.
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    57. Gbadegesin RA, Adeyemo AA, Asinobi AO. Deaths in childhood nephrotic syndrome in Ibadan, Nigeria. J Trop Pediatr. 1997 Aug; 43(4):248-9. PMID: 9283132.
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    58. Nafiu OO, Olumese PE, Gbadegesin RA, Osinusi K. Intraosseous infusion in an emergency situation: a case report. Ann Trop Paediatr. 1997 Jun; 17(2):175-7. PMID: 9230983.
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    59. Olumese PE, Adeyemo AA, Ademowo OG, Gbadegesin RA, Sodeinde O, Walker O. The clinical manifestations of cerebral malaria among Nigerian children with the sickle cell trait. Ann Trop Paediatr. 1997 Jun; 17(2):141-5. PMID: 9230977.
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    60. Gbadegesin RA, Adeyemo AA, Asinobi AO, Osinusi K. Inaccuracy of the Schwartz formula in estimating glomerular filtration rate in Nigerian children. Ann Trop Paediatr. 1997 Jun; 17(2):179-85. PMID: 9230984.
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    61. Olumese PE, Adeyemo AA, Gbadegesin RA, Walker O. Retinal haemorrhage in cerebral malaria. East Afr Med J. 1997 May; 74(5):285-7. PMID: 9337004.
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    62. Gbadegesin RA, Sodeinde O, Adeyemo AA, Ademowo OG. Body temperature is a poor predictor of malaria parasitaemia in children with acute diarrhoea. Ann Trop Paediatr. 1997 Mar; 17(1):89-94. PMID: 9176584.
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    63. Sodeinde O, Adeyemo AA, Gbadegesin RA, Olaleye BO, Ajayi-Obe KE, Ademowo OG. Interaction between acute diarrhoea and falciparum malaria in Nigerian children. J Diarrhoeal Dis Res. 1996 Dec; 14(4):269-73. PMID: 9203790.
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    64. Olumese PE, Sodeinde O, Gbadegesin RA, Nafiu O, Oguche S, Walker O. Respiratory distress adversely affects the outcome of childhood cerebral malaria. Trans R Soc Trop Med Hyg. 1995 Nov-Dec; 89(6):634. PMID: 8594678.
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    65. Gbadegesin RA, Asinobi AO, Osinusi K, Adeyemo AA. Is the height/plasma creatinine formula of Schwartz useful as a screening test in detecting Nigeria children with low GFR? West Afr J Med. 1995 Oct-Dec; 14(4):242-5. PMID: 8634231.
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    66. Akindele JA, Gbadegesin RA. Outbreak of neonatal Klebsiella septicaemia at the University College Hospital, Ibadan, Nigeria. Appraisal of predisposing factors and preventive measures. Trop Geogr Med. 1994; 46(3):151-3. PMID: 7941004.
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    67. Adeyemo AA, Gbadegesin RA, Onyemenem TN, Ekweozor CC. Urinary tract pathogens and antimicrobial sensitivity patterns in children in Ibadan, Nigeria. Ann Trop Paediatr. 1994; 14(4):271-4. PMID: 7880087.
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