34 results on '"Gabelli, C."'
Search Results
2. Clinical aspects of lipoprotein disorders
3. Apolipoprotein C-II Deficiency Syndrome: New Insights into the Molecular Mechanism Leading to the Disease in the Apo C-II Padova Kindred
4. Apo C-IIPadova: A New Apoprotein Variant in Two Patients with Apo C-II Deficiency Syndrome
5. Identification of an Italian Kindred with a Variant Apolipoprotein E (E1) Associated with Type III Hyperlipoproteinemia
6. Apolipoprotein E Modulates the Metabolism of Apolipoprotein B Containing Lipoproteins by Multiple Mechanisms
7. 68 CEREBROTENDINOUS XANTHOMATOSIS IN A COMPOUND HETEROZYGOTE FOR TWO MUTATIONS ON CYP27 GENE: DIAGNOSIS AND TREATMENT
8. NONALCOHOLIC STEATOHEPATITIS IN A FAMILY WITH FAMILIAL HYPOBETALIPOPROTEINEMIA CARRYING A NOVEL SPLICE SITE MUTATION OF APOB GENE
9. Rivastigmine: an update on therapeutic efficacy in Alzheimer's disease and other conditions
10. High plasma homocysteine is a risk factor for stroke and congestive heart failure in an elderly italian population
11. Effects of statins on elevated lipoprotein(a) in primary hypercholesterolemia
12. Early onset mental retardation in a subject with cerebrotendinous xanthomatosis
13. Genetic risk factors in coronary heart disease (CHD) and restenosis
14. Changes in HCV Viremia following LDL Apheresis in a HCV Positive Patient with Familial Hypercholesterolemia
15. Lipoprotein(a) and lipoprotein profile in healthy centenarians: a reappraisal of vascular risk factors
16. ApoE4 allele frequency decrease with age and is lowest in centenarians: Results from a study in Northern Italy
17. The frequency of APO(a) atherogenic phenotypes does not decrease in centenarians compared to subjects of different ages
18. Apolipoprotein E genotype and phenotype comparison in a population of dyslipidaemic subjects
19. Metabolic abnormalities and clinical manifestations of familial hypobetalipoproteinemia
20. 2.P.278 Mild hyperhomocysteinemia correlated to folate status in Italian centenarians
21. 4.P.272 Abnormal LDL metabolism in a case of recessive form of familial hypercholesterolemia
22. 4.P.230 Pseudo-hypertriglyceridemia in four kindreds with benign hyperglycerolemia
23. 2.P.133 Lp(a) levels and apo(a) phenotypes in angiographically established coronary heart disease and in controls
24. 1.P.240 Familial hypobetalipoproteinemia caused by a truncated apolipoprotein B (B-33.4) is not protective against carotid artery disease
25. Apolipoprotein E allele polymorphism and ageing: Decreased prevalence of apolipoprotein ε4 allele in old individuals
26. Heterozygous apolipoprotein C-II deficiency: lipoprotein and apoprotein phenotype and Rsal restriction enzyme polymorphism in the Apo C'IIPadova kindred
27. Efficacy and safety of simvastatin for the treatment of hypercholesterolemia in patients with and without type II diabetes
28. Acute effects of HMG‐CoA reductase inhibitors on biliary lipids in patients with interrupted enterohepatic circulation
29. Apolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patients.
30. Long term-effect of fenofibrate on lipoprotein level and composition in different types of genetic hyperlipidemias
31. A nonsense mutation in the apolipoprotein C-IIPadova gene in a patient with apolipoprotein C-II deficiency.
32. Lipoprotein modifications during dietary treatment in patients with primary type V hyperlipoproteinaemia
33. Abnormal low density lipoprotein metabolism in apolipoprotein E deficiency.
34. Separation of apolipoprotein B species by agarose-acrylamide gel electrophoresis.
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