RachelKateCasonMD

PubMed

• 18 citations
  Genetics of Childhood Steroid Sensitive Nephrotic Syndrome: An Update.
  Brandon M Lane, Rachel Cason, Christopher Imokhuede Esezobor, Rasheed Gbadegesin
  Frontiers in Pediatrics. 2019-01-29
• 7 citations
  Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants inExpand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Ge...
  Rachel K Cason, Anna Williams, Megan Chryst-Stangl, Guanghong Wu, Kinsie Huggins
  Frontiers in Pediatrics. 2022-01-01
• 2 citations
  Atypical recurrent Kawasaki disease with retropharyngeal involvement: A case study and literature review.
  Rachel K Cason, Umakumaran Ponniah, Elizabeth S Makil, Mary C. Niu
  Annals of Pediatric Cardiology. 2020-09-01

Journal Articles

• Monogenic nephrotic syndrome in Nigerian children  
  Esezobor CI, Solarin A, Cason RK, Varner J, Chryst-Ladd M, Lane BM, Ekure E, Gbadegesin RA., Kid Int Rep., 2020
• Genetics of childhood steroid sensitive nephrotic syndrome: an update  
  Lane BM, Cason R, Esezobor CI, Gbadegesin RA, Frontiers in Pediatrics, 1/29/2019

Abstracts/Posters

• Collapsing FSGS in siblings with compound heterozygous variants in NUP93 expand the spectrum of kidney phenotypes associated with nucleoporin gene mutations.
  Cason, RK, Williams AE, Chryst-Stangl M, Wu G, Huggins K, Brathwaite Greenbaum LA, D’Agati VD, Gbadegesin RA., American Society of Nephrology, 11/2021
• A curious case of persistent anemia in a toddler with kidney failure.
  Cason RK, Chua AN, American Dialysis Conference, 3/2021
• Stuck between the stone and a hard place: a unique etiology of acute kidney injury in an infant.
  Smith MD, Cason RK, Wood K, Chua A., Pediatric Hospital Medicine Conference, 7/2019
• Genetic architecture of nephrotic syndrome in African children.
  Cason RK, Varner JD, Chryst-Stangl M, Esezobor C, Solarin A, & Gbadegesin R., Pediatric Academic Societies Meeting, 4/2019
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