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Current Opinion in Pediatrics|August 9, 2022
Update on glycogen storage disease: primary hepatic involvementTiffany L Freeney Wright, Luis A Umaña, Charina M Ramirez
Journal of Pediatric Gastroenterology and Nutrition|May 3, 2024
Utilization and perspectives of weight loss medications in pediatric metabolic dysfunction-associated steatotic liver diseaseMohit Kehar, Samar H Ibrahim, Charina M Ramirez, et al.
Steroids|September 5, 2020
Delineation of metabolic responses of Npc1-/-nih mice lacking the cholesterol-esterifying enzyme SOAT2 to acute treatment with 2-hydroxypropyl-β-cyclodextrinCharina M Ramirez, Anna M Taylor, Adam M Lopez, et al.
Clinical and Experimental Pharmacology & Physiology|August 14, 2014
Systemic administration of 2-hydroxypropyl-β-cyclodextrin to symptomatic Npc1-deficient mice slows cholesterol sequestration in the major organs and improves liver functionAdam M Lopez, Sandi J Terpack, Kenneth S Posey, et al.
Journal of Lipid Research|December 8, 2009
Cyclodextrin overcomes the transport defect in nearly every organ of NPC1 mice leading to excretion of sequestered cholesterol as bile acidBenny Liu, Charina M Ramirez, Anna M Miller, et al.
Lipids|October 7, 2021
Molecular markers of brain cholesterol homeostasis are unchanged despite a smaller brain mass in a mouse model of cholesteryl ester storage diseaseAmal A Aqul, Charina M Ramirez, Adam M Lopez, et al.
Biochimica Et Biophysica Acta|October 1, 2013
Ontogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann-Pick type C diseaseCharina M Ramirez, Adam M Lopez, Lam Q Le, et al.
Digestive Diseases and Sciences|July 18, 2019
Ontogenesis and Modulation of Intestinal Unesterified Cholesterol Sequestration in a Mouse Model of Niemann-Pick C1 DiseaseAdam M Lopez, Charina M Ramirez, Anna M Taylor, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|January 20, 2021
A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile DuctsKara L Chan, Natasha Varughese, Patricia M Jones, et al.
Journal of Lipid Research|February 4, 2011
Quantitative role of LAL, NPC2, and NPC1 in lysosomal cholesterol processing defined by genetic and pharmacological manipulationsCharina M Ramirez, Benny Liu, Amal Aqul, et al.
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