Canlyniadau Chwilio - Gbadegesin, Rasheed A

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

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

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

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

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

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

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

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

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

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Evolutionary genetics and acclimatization in nephrology gan 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 gan 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 gan 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 gan 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... gan 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 gan 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 gan 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 gan 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 gan 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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