Søgeresultater - Gbadegesin, Rasheed A

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

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

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

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

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

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

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

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

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

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Evolutionary genetics and acclimatization in nephrology af 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 af 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 af 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 af 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... af 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 af 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 af 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 af 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 af 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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