Torthaí cuardaigh - Gbadegesin, Rasheed A

Translating genetic findings in hereditary nephrotic syndrome: the missing loops de réir Hall, Gentzon, Gbadegesin, Rasheed A.

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The Genetics of Nephrotic Syndrome de réir Rheault, Michelle N., Gbadegesin, Rasheed A.

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GENETICS OF CHILDHOOD STEROID SENSITIVE NEPHROTIC SYNDROME (SSNS) de réir Karp, Alana M., Gbadegesin, Rasheed A.

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Steroid Regimen for Children with Nephrotic Syndrome Relapse de réir Williams, Anna Elizabeth, Gbadegesin, Rasheed A.

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Aberrant IgM on T cells: biomarker or pathogenic factor in childhood nephrotic syndrome? de réir Chambers, Eileen Tsai, Gbadegesin, Rasheed A.

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Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype de réir Hall, Gentzon, Routh, Jonathan C., Gbadegesin, Rasheed A.

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Genetic Basis of Health Disparity in Childhood Nephrotic Syndrome de réir Varner, Jennifer D., Matory, Ayo, Gbadegesin, Rasheed A.

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Treatment of steroid-resistant nephrotic syndrome in the genomic era de réir Bensimhon, Adam R., Williams, Anna E., Gbadegesin, Rasheed A.

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Case Report: Novel Dietary Supplementation Associated With Kidney Recovery and Reduction in Proteinuria in a Dialysis Dependent Patient Secondary to Steroid Resistant Minimal Chang... de réir Gbadegesin, Rasheed A., Hernandez, Loren P. Herrera, Brophy, Patrick D.

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Vesicoureteral reflux and the extracellular matrix connection de réir Tokhmafshan, Fatima, Brophy, Patrick D., Gbadegesin, Rasheed A., Gupta, Indra R.

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Genetics of Childhood Steroid Sensitive Nephrotic Syndrome: An Update de réir Lane, Brandon M., Cason, Rachel, Esezobor, Christopher Imokhuede, Gbadegesin, Rasheed A.

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Evolutionary genetics and acclimatization in nephrology de réir Adeyemo, Adebowale A., Shriner, Daniel, Bentley, Amy R., Gbadegesin, Rasheed A., Rotimi, Charles N.

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Efficacy of Antibiotic Prophylaxis in Children with Vesicoureteral Reflux: Systematic Review and Meta-Analysis de réir Wang, Hsin-Hsiao S., Gbadegesin, Rasheed A., Foreman, John W., Nagaraj, Shashi K., Wigfall, Delbert R., Wiener, John S., Routh, Jonathan C.

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Case Report: Unusual Aggregation of Different Glomerulopathies in a Family Resolved by Genetic Testing and Reverse Phenotyping de réir Kumar, Reeti, Keskinyan, Vahakn, Stangl, Megan Chryst, Lane, Brandon M., Buckley, Anne F., Barisoni, Laura, Howell, David N., Gbadegesin, Rasheed A.

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Cultivating Research Skills During Clinical Training to Promote Pediatric-Scientist Development de réir Hurst, Jillian H., Barrett, Katherine J., Kelly, Matthew S., Staples, Betty B., McGann, Kathleen A., Cunningham, Coleen K., Reed, Ann M., Gbadegesin, Rasheed A., Permar, Sallie R.

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Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mut... de réir Cason, Rachel K., Williams, Anna, Chryst-Stangl, Megan, Wu, Guanghong, Huggins, Kinsie, Brathwaite, Kaye E., Lane, Brandon M., Greenbaum, Larry A., D’Agati, Vivette D., Gbadegesin, Rasheed A.

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Addressing the physician-scientist pipeline: strategies to integrate research into clinical training programs de réir Permar, Sallie R., Ward, Rebecca A., Barrett, Katherine J., Freel, Stephanie A., Gbadegesin, Rasheed A., Kontos, Christopher D., Hu, Patrick J., Hartmann, Katherine E., Williams, Christopher S., Vyas, Jatin M.

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The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes de réir Hall, Gentzon, Lane, Brandon M., Khan, Kamal, Pediaditakis, Igor, Xiao, Jianqiu, Wu, Guanghong, Wang, Liming, Kovalik, Maria E., Chryst-Stangl, Megan, Davis, Erica E., Spurney, Robert F., Gbadegesin, Rasheed A.

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Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity de réir Hall, Gentzon, Rowell, Janelle, Farinelli, Federica, Gbadegesin, Rasheed A., Lavin, Peter, Wu, Guanghong, Homstad, Alison, Malone, Andrew, Lindsey, Thomas, Jiang, Ruiji, Spurney, Robert, Tomaselli, Gordon F., Kass, David A., Winn, Michelle P.

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Children with vesicoureteric reflux have joint hypermobility and occasional tenascin XB sequence variants de réir Tokhmafshan, Fatima, El Andalousi, Jasmine, Murugapoopathy, Vasikar, Fillion, Marie-Lyne, Campillo, Sarah, Capolicchio, John-Paul, Jednak, Roman, El Sherbiny, Mohamed, Turpin, Sophie, Schalkwijk, Joost, Matsumoto, Ken-Ichi, Brophy, Patrick D., Gbadegesin, Rasheed A., Gupta, Indra R.

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