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51. Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study

52. Association of infections and venous thromboembolism in hospitalized children with nephrotic syndrome

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

54. Rationale and design of the Nephrotic Syndrome Study Network (NEPTUNE) Match in glomerular diseases: designing the right trial for the right patient, today

55. A randomized controlled trial of preemptive rituximab to prevent recurrent focal segmental glomerulosclerosis post-kidney transplant (PRI-VENT FSGS): protocol and study design

58. Innovations in MD-only physician-scientist training: experiences from the Burroughs Wellcome Fund physician-scientist institutional award initiative

59. Racial and Ethnic Disparities in Acute Care Utilization Among Patients With Glomerular Disease

60. Age of Onset and Disease Course in Biopsy-Proven Minimal Change Disease: An Analysis From the Cure Glomerulopathy Network

62. Contributors

65. Genetics of childhood steroid-sensitive nephrotic syndrome

68. Cardiovascular Risk Factor Burden and Association With CKD in Ghana and Nigeria

70. Common risk variants in AHI1 are associated with childhood steroid-sensitive nephrotic syndrome

71. Vesicoureteral reflux and the extracellular matrix connection

72. Comparing Kidney Health Outcomes in Children, Adolescents, and Adults With Focal Segmental Glomerulosclerosis

73. Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations

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

75. Cure Glomerulonephropathy Pathology Classification and Core Scoring Criteria, Reproducibility, and Clinicopathologic Correlations

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

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

79. Gaining the Patient Reported Outcomes Measurement Information System (PROMIS) perspective in chronic kidney disease: a midwest pediatric nephrology consortium study

81. Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis

82. Diagnosis, Education, and Care of Patients with APOL1-Associated Nephropathy: A Delphi Consensus and Systematic Review

83. A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

84. Treatment outcome of late steroid-resistant nephrotic syndrome: a study by the Midwest Pediatric Nephrology Consortium

85. Racial-Ethnic Differences in Health-Related Quality of Life among Adults and Children with Glomerular Disease

91. Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomeruosclerosis

92. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

93. Establishing core outcome domains in pediatric kidney disease: report of the Standardized Outcomes in Nephrology—Children and Adolescents (SONG-KIDS) consensus workshops

98. Management of idiopathic childhood nephrotic syndrome in sub-Saharan Africa: Ibadan consensus statement

100. Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome

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