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Charina M. Ramirez

Observed names: Charina M Ramirez, Charina Ramirez
ORCID: 0000-0001-5223-9396
Observed ORCID: 0000-0001-5223-9396
OpenAlex ID: A5022213698
Cyclodextrin overcomes the transport defect in nearly every organ of NPC1 mice leading to excretion of sequestered cholesterol as bile acid
2009 · Benny Liu, Charina M. Ramirez, et al. · Journal of Lipid Research · 172
Weekly Cyclodextrin Administration Normalizes Cholesterol Metabolism in Nearly Every Organ of the Niemann-Pick Type C1 Mouse and Markedly Prolongs Life
2010 · Charina M Ramirez, Benny Liu, et al. · Pediatric Research · 158
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Frequency of the Cholesteryl Ester Storage Disease Common Lipa E8sjm Mutation (C.894G>A) in Various Racial And Ethnic Groups
2013 · Stuart A. Scott, Benny Liu, et al. · Hepatology · 103
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Quantitative role of LAL, NPC2, and NPC1 in lysosomal cholesterol processing defined by genetic and pharmacological manipulations
2011 · Charina M. Ramirez, Benny Liu, et al. · Journal of Lipid Research · 76
The 21st Century Cures Act and Multiuser Electronic Health Record Access: Potential Pitfalls of Information Release
2021 · Simone Arvisais-Anhalt, May Lau, et al. · Journal of Medical Internet Research · 65
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Metabolic dysfunction-associated steatotic liver disease (MASLD) in children with obesity: An Obesity Medicine Association (OMA) and expert joint perspective 2025
2025 · Jennifer Panganiban, Mohit Kehar, et al. · Obesity Pillars · 49
Systemic administration of 2‐hydroxypropyl‐β‐cyclodextrin to symptomatic Npc1‐deficient mice slows cholesterol sequestration in the major organs and improves liver function
2014 · Adam M Lopez, Sandi J Terpack, et al. · Clinical and Experimental Pharmacology and Physiology · 38
Call to action—Pediatric MASLD requires immediate attention to curb health crisis
2025 · Phillipp Hartmann, Marialena Mouzaki, et al. · Hepatology · 17
Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype
2021 · Gregory M. Enns, Zineb Ammous, et al. · Molecular Genetics and Metabolism · 16
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Update on glycogen storage disease: primary hepatic involvement
2022 · Tiffany L. Freeney Wright, Luis A. Umaña, et al. · Current Opinion in Pediatrics · 14
Ontogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann–Pick type C disease
2013 · Charina M. Ramirez, Adam M. Lopez, et al. · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 14
Hepatic Steatosis in the Pediatric Population: An Overview of Pathophysiology, Genetics, and Diagnostic Workup
2021 · Claudia Phen, Charina M. Ramirez · Clinical Liver Disease · 7
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Impact of the loss of caveolin-1 on lung mass and cholesterol metabolism in mice with and without the lysosomal cholesterol transporter, Niemann–Pick type C1
2014 · Dorothy I. Mundy, Adam M. Lopez, et al. · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 6
A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile Ducts
2021 · Kara L Chan, Natasha Varughese, et al. · Pediatric and Developmental Pathology · 5
Delineation of metabolic responses of Npc1 mice lacking the cholesterol-esterifying enzyme SOAT2 to acute treatment with 2-hydroxypropyl-β-cyclodextrin
2020 · Charina M. Ramirez, Anna M. Taylor, et al. · Steroids · 5
Molecular markers of brain cholesterol homeostasis are unchanged despite a smaller brain mass in a mouse model of cholesteryl ester storage disease
2021 · Amal A. Aqul, Charina M. Ramirez, et al. · Lipids · 4
Ontogenesis and Modulation of Intestinal Unesterified Cholesterol Sequestration in a Mouse Model of Niemann–Pick C1 Disease
2019 · Adam M. Lopez, Charina M. Ramirez, et al. · Digestive Diseases and Sciences · 4
Lysosomal Acid Lipase Activity: A Tool for the Detection and Management of Fatty Liver Disease?
2015 · Charina M. Ramirez, Adam M. Lopez, et al. · EBioMedicine · 3
Progression of pulmonary disease and related changes in lung cholesterol metabolism in mice with Niemann–Pick type C1 deficiency
2013 · Charina M. Ramirez, Benny Liu, et al. · Molecular Genetics and Metabolism · 3
Utilization and perspectives of weight loss medications in pediatric metabolic dysfunction‐associated steatotic liver disease
2024 · Mohit Kehar, Samar H. Ibrahim, et al. · Journal of Pediatric Gastroenterology and Nutrition · 2
Vibration‐controlled transient elastography in pediatric metabolic dysfunction‐associated steatotic liver disease: Considerations for risk stratification and clinical use
2026 · Mohit Kehar, Charina Ramirez, et al. · Journal of Pediatric Gastroenterology and Nutrition
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P148: Multimodal characterization of neurological symptoms in Niemann-Pick disease type C
2026 · Raquel van Gool, Merve Koç Yekedüz, et al. · Genetics in Medicine Open
Successful Use of Anifrolumab and Baricitinib Combination Therapy in an Infant with Spondyloenchondrodysplasia with Immune Dysregulation (SPENCD-I)
2025 · Nicole Soucy, Claudia Moreda, et al. · Journal of Human Immunity
Electronic phenotypes to distinguish clinician attention to high body mass index, hypertension, lipid disorders, fatty liver and diabetes in pediatric primary care: Diagnostic accuracy of electronic phenotypes compared to masked comprehensive chart review
2023 · Christy B. Turer, Jenny J. Park, et al. · Pediatric Obesity
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343 Cyclodextrin Overcomes the Sterol Transport Defect in the Liver of the Niemann Pick Type C2 Mouse
2010 · Benny Liu, Charina M. Ramirez, et al. · Gastroenterology
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Works count: 28
Citation count: 760
H-index: 11
I10-index: 11
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