Bilaketaren emaitzak - Gbadegesin, Rasheed A

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

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

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

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

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Aberrant IgM on T cells: biomarker or pathogenic factor in childhood nephrotic syndrome? nork 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 nork Hall, Gentzon, Routh, Jonathan C., Gbadegesin, Rasheed A.

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

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Treatment of steroid-resistant nephrotic syndrome in the genomic era nork 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... nork Gbadegesin, Rasheed A., Hernandez, Loren P. Herrera, Brophy, Patrick D.

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

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

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Evolutionary genetics and acclimatization in nephrology nork 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 nork 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 nork 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 nork 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... nork 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 nork 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 nork 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 nork 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 nork 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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