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Lipid storage disorder
Value of Bronchoalveolar Lavage in Lipidoses with Pulmonary Involvement
Lysosome Lipid Storage Disorder in NCTR-BALB/C Mice
Unraveling the Sterol-Trafficking Defect in Niemann-Pick C Disease
Unraveling the Sterol-Trafficking Defect in Niemann-Pick C Disease
Autophagy, Lipophagy and Lysosomal Lipid Storage Disorders
Regulation of Sphingomyelin Metabolism
New Single Nucleotide Deletion in the SMPD1 Gene Causes Niemann Pick Disease Type a in a Child from Southwest Iran: a Case Report
Gaucher Disease Agents
Gaucher Disease
Neutral Lipid Storage with Acid Lipase Deficiency: a New Variant of Wolman's Disease with Features of the Senior Syndrome
Pluripotent Stem Cells for Disease Modeling and Drug Discovery in Niemann-Pick Type C1
Neuronal Ceroid Lipofuscinosis
Lipid Storage Diseases
Gaucher Disease
Friend Or Foe: Lipid Droplets As Organelles for Protein and Lipid Storage in Cellular Stress Response, Aging and Disease
Results from a 12-Month Open-Label Phase 1/2 Study of Velaglucerase
Lysosomal Storage Diseases: Diagnostic Confirmation and Management of Presymptomatic Individuals Raymond Y
Lipophagy and Lipolysis Status in Lipid Storage and Lipid Metabolism Diseases
Top View
Autophagy in Niemann–Pick C Disease Is Dependent Upon Beclin-1 and Responsive to Lipid Trafficking Defects
Murine Models of Lysosomal Storage Diseases Exhibit Differences in Brain Protein Aggregation and Neuroinflammation
Case Report Renal Failure and Ascites in a Patient with Niemann-Pick Disease: Case Report and Literature Review
Neurometabolic Article: Case Series
[Frontiers in Bioscience 16, 1797-1810, January 1, 2011] 1797
Glycinated Lyso-Glycosphingolipids As New Mass Spectrometry Internal
Niemann-Pick Type C Disease: Molecular Mechanisms of Neurodegeneration and Targets for Therapeutic Intervention
Report of a Rare Lipid Storage and Neurodegenerative Disorder
Niemann-Pick Disease Type A-A Case Report
Autophagy, Lipophagy and Lysosomal Lipid Storage Disorders
Autophagy, Lipophagy and Lysosomal Lipid Storage
Adult Niemann-Pick Disease Type B with Myositis Ossificans: a Case Report
In This Issue Attend
Neurometabolic Disorder with Neuromuscular Manifestation
High Sphingomyelin Levels Induce Lysosomal Damage and Autophagy Dysfunction in Niemann Pick Disease Type A
Metabolomic Studies of Lipid Storage Disorders, with Special Reference to Niemann-Pick Type C Disease: a Critical Review with Future Perspectives
Autophagy and Tau in Niemann-Pick Type C Disease
New Single Nucleotide Deletion in the SMPD1 Gene Causes Niemann Pick Disease Type a in a Child from Southwest Iran: a Case Report
The Hidden Niemann-Pick Type C Patient: Clinical Niches for a Rare Inherited Metabolic
Understanding and Treating Niemann–Pick Type C Disease: Models Matter
The Development of Gene Therapy for Niemann-Pick Type C Disease
Case Report Niemann-Pick Disease: Report of Two Cases and Review of Literature