124 results on '"Charina, M"'
Search Results
2. The 21st Century Cures Act and Multiuser Electronic Health Record Access: Potential Pitfalls of Information Release
3. Ontogenesis and Modulation of Intestinal Unesterified Cholesterol Sequestration in a Mouse Model of Niemann–Pick C1 Disease
4. Adaptive Frame Methods for Magnetohydrodynamic Flows
5. Joint spectral radius and ternary hermite subdivision
6. Multigrid methods: Grid transfer operators and subdivision schemes
7. Regularity of non-stationary subdivision: a matrix approach
8. Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype
9. Molecular markers of brain cholesterol homeostasis are unchanged despite a smaller brain mass in a mouse model of cholesteryl ester storage disease
10. Update on glycogen storage disease: primary hepatic involvement
11. Update on glycogen storage disease: primary hepatic involvement
12. The 21st Century Cures Act and Multiuser Electronic Health Record Access: Potential Pitfalls of Information Release
13. Quantitative role of LAL, NPC2, and NPC1 in lysosomal cholesterol processing defined by genetic and pharmacological manipulations
14. Cyclodextrin overcomes the transport defect in nearly every organ of NPC1 mice leading to excretion of sequestered cholesterol as bile acid
15. The 21st Century Cures Act and Multiuser Electronic Health Record Access: Potential Pitfalls of Information Release (Preprint)
16. Molecular markers of brain cholesterol homeostasis are unchanged despite a smaller brain mass in a mouse model of cholesteryl ester storage disease
17. The 21st Century Cures Act and Multiuser Electronic Health Record Access: Potential Pitfalls of Information Release (Preprint)
18. Ontogenesis and Modulation of Intestinal Unesterified Cholesterol Sequestration in a Mouse Model of Niemann–Pick C1 Disease
19. Hepatic Steatosis in the Pediatric Population: An Overview of Pathophysiology, Genetics, and Diagnostic Workup
20. A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile Ducts
21. Lysosomal Acid Lipase Activity: A Tool for the Detection and Management of Fatty Liver Disease?
22. Systemic administration of 2-hydroxypropyl-β-cyclodextrin to symptomatic Npc1-deficient mice slows cholesterol sequestration in the major organs and improves liver function
23. Hepatic Steatosis in the Pediatric Population: An Overview of Pathophysiology, Genetics, and Diagnostic Workup
24. Delineation of metabolic responses of Npc1(−/−nih) mice lacking the cholesterol-esterifying enzyme SOAT2 to acute treatment with 2-hydroxypropyl-β-cyclodextrin
25. A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile Ducts
26. Delineation of metabolic responses of Npc1 mice lacking the cholesterol-esterifying enzyme SOAT2 to acute treatment with 2-hydroxypropyl-β-cyclodextrin
27. Molecular markers of brain cholesterol homeostasis are unchanged despite a smaller brain mass in a mouse model of cholesteryl ester storage disease.
28. Ontogenesis and Modulation of Intestinal Unesterified Cholesterol Sequestration in a Mouse Model of Niemann–Pick C1 Disease
29. Anisotropic bivariate subdivision with applications to multigrid
30. An algebraic perspective on multivariate tight wavelet frames. II
31. 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
32. Frequency of the cholesteryl ester storage disease commonLIPAE8SJM mutation (c.894G>A) in various racial and ethnic groups
33. Multigrid methods: Grid transfer operators and subdivision schemes
34. Reading Materials Versus Grade Level Is There A Match
35. Unesterified Cholesterol Accumulation in Late Endosomes/Lysosomes Causes Neurodegeneration and Is Prevented by Driving Cholesterol Export from This Compartment
36. Quantitative role of LAL, NPC2, and NPC1 in lysosomal cholesterol processing defined by genetic and pharmacological manipulations
37. Cyclodextrin overcomes the transport defect in nearly every organ of NPC1 mice leading to excretion of sequestered cholesterol as bile acid
38. Persistence of herpes simplex virus DNA in cerebrospinal fluid of neonates with herpes simplex virus encephalitis
39. Systemic administration of 2-hydroxypropyl-β-cyclodextrin to symptomatic Npc1-deficient mice slows cholesterol sequestration in the major organs and improves liver function
40. Regularity of non-stationary subdivision: a matrix approach
41. Ontogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann-Pick type C disease
42. Prolonged Mechanical Ventilation Among Children With Congenital Heart Disease Undergoing Cardiac Surgery In Philippine Heart Center: A Risk Factors Analysis
43. Lysosomal Acid Lipase Activity: A Tool for the Detection and Management of Fatty Liver Disease?
44. Weekly cyclodextrin administration normalizes cholesterol metabolism in nearly every organ of the Niemann-Pick type C1 mouse and markedly prolongs life
45. Inflammatory Myofibroblastic Tumor In The Lung With Feeding Vessel: Mimicking A Congenital Lung Malformation
46. Reproduction of exponential polynomials by multivariate non-stationary subdivision schemes with a general dilation matrix
47. Progression of pulmonary disease and related changes in lung cholesterol metabolism in mice with Niemann–Pick type C1 deficiency
48. 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
49. Ontogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann–Pick type C disease
50. Progression of pulmonary disease and related changes in lung cholesterol metabolism in mice with Niemann–Pick type C1 deficiency
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.