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Abetalipoproteinemia
Studies on the Absorptive Defect for Triglyceride in Abetalipoproteinemia * P
Bovine Milk Lipoprotein Lipase Transfers Tocopherol to Human Fibroblasts During Triglyceride Hydrolysis in Vitro Maret G
Commonly Used Lipidcentric ICD-10 (ICD-9) Codes
Fat Accumulation in Enterocytes: a Key to the Diagnosis of Abetalipoproteinemia Or Homozygous Hypobetalipoproteinemia
Angioid Streaks Associated with Abetalipoproteinemia
Clinical Reasoning: Complex Ataxia Unpicking the Threads
Pharmacological Targeting of the Atherogenic Dyslipidemia Complex: the Next Frontier in CVD Prevention Beyond Lowering LDL Cholesterol
A Rare Mutation in the APOB Gene Associated with Neurological Manifestations in Familial Hypobetalipoproteinemia
Abetalipoproteinemia
Dyslipidemia Infosheet 6-10-19
Abnormalities of High Density Lipoproteins in Abetalipoproteinemia
Comparison of Three Different Diet-Induced
Studies on the Protein Defect in Tangier Disease
Lipoproteins Alter the Catalytic Behavior of the Platelet-Activating
Low Density Lipoprotein Degradation by Mononuclear Cells from Normal
Abetalipoproteinemia
Mendelian Disorders Among Jews Tables
Severe Hypertriglyceridemia with Pancreatitisthirteen Years
Top View
Current Diagnosis and Management of Abetalipoproteinemia
A Severe Form of Abetalipoproteinemia Caused by New Splicing Mutations
Diagnosis of Inherited Metabolic Disorders Affecting the Nervous System
177 Follow up Case Study for Ninth
Mutations in the Human Lipoprotein Lipase Gene and Their Relationship to Hyperlipidaemia
Rare Dyslipidaemias, from Phenotype to Genotype to Management: a European Atherosclerosis Society Task Force Consensus Statement
1 Non-Alcoholic Steatohepatitis – Diagnostic
Abetalipoproteinemia - a Rare Disease Presenting As Bleeding Disorder
Supplementary Materials Table S1. List of 63 Evaluated Genes Related to Dyslipidemia and Premature Atherosclerosis with Associated Phenotypes
Identification of a Novel MTTP Splice Variant C.394-2A˃C in an Infant with Abetalipoproteinemia
Chylomicron Retention Disease in a Male Infant: a Rare Case from Pakistan
Hypertriglyceridemia and Atherosclerosis Jia Peng, Fei Luo, Guiyun Ruan, Ran Peng and Xiangping Li*
Chylomicron Retention Disease: a Description of a New Mutation in a Very Rare Disease
Abetalipoproteinemia [OMIM#200100]
The Pathology of Tangier Disease a Light and Electron Amicroscopic Study
Prevalence and Incidence of Rare Diseases
Identification of a Variant in APOB Gene As a Major Cause Of
Familial Hypercholesterolemia
Abetalipoproteinemia (Bassen- Kornzweig Disease), 408 Accessory
Normotriglyceridemic Abetalipoproteinemia. Absence of the B- 100 Apolipoprotein
Diagnosis and Clinical Appraisal
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