Resultats de la cerca - Gbadegesin, Rasheed A

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

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

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

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

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

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

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

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

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

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Evolutionary genetics and acclimatization in nephrology per 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 per 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 per 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 per 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... per 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 per 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 per 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 per 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 per 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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