169 results on '"Gabelli, C."'
Search Results
2. The Italian dementia with Lewy bodies study group (DLB-SINdem): toward a standardization of clinical procedures and multicenter cohort studies design
3. The Italian fund for Alzheimer's and other dementias: strategies and objectives to face the dementia challenge
4. The Mutations of Apolipoprotein B Gene Causing Hypobetalipoproteinemia: Molecular and Functional Abnormalities in Apo B-87Padova
5. The association of indwelling urinary catheter with delirium in hospitalized patients and nursing home residents: an explorative analysis from the 'Delirium Day 2015'
6. The Italian dementia with Lewy bodies study group (DLB-SINdem): toward a standardization of clinical procedures and multicenter cohort studies design
7. Apo C-IIPadova: A New Apoprotein Variant in Two Patients with Apo C-II Deficiency Syndrome
8. Apolipoprotein E Modulates the Metabolism of Apolipoprotein B Containing Lipoproteins by Multiple Mechanisms
9. Clinical aspects of lipoprotein disorders
10. Identification of an Italian Kindred with a Variant Apolipoprotein E (E1) Associated with Type III Hyperlipoproteinemia
11. Apolipoprotein C-II Deficiency Syndrome: New Insights into the Molecular Mechanism Leading to the Disease in the Apo C-II Padova Kindred
12. Prevalence and Correlates of Behavioral Disorders in Old Age Subjects with Cognitive Impairment: Results from the ReGAl Project
13. Clinical Features Associated with Delirium Motor Subtypes in Older Inpatients: Results of a Multicenter Study
14. Absolute quantitative evaluation of 123I-FP-CIT: is it possible?
15. Effectiveness of switching to the rivastigmine transdermal patch from oral cholinesterase inhibitors: a naturalistic prospective study in Alzheimer's disease
16. PARAOXONASE 1 GENE POLYMORPHISMS IN ALZHEIMER DISEASE AND VASCULAR DEMENTIA
17. La legionellosi come problema emergente di Sanità Pubblica
18. Hearing loss and cognitive decline in older adults: Questions and answers
19. Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia
20. Ubiqullin 2 mutations in italian patients with amyotrophic lateral sclerosis and frontotemporal dementia
21. Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease
22. Influence of comorbidity and cognitive status on instrumental activities of daily living in amnestic mild cognitive impairment: results from the ReGAl project
23. Le legionellosi come problema emergente di Sanità Pubblica: attività del Gruppo di lavoro della SItI
24. La legionellosi come problema emergente di Sanità Pubblica: attività del Gruppo di lavoro della S.It.I
25. La terapia nella demenza di Alzheimer
26. Plasma protein synthesis in albuminuric patients with and without Type 2 diabetes mellitus
27. Phenotypic expression of heterozygous familial hypobetalipoproteinemia in three kindreds with novel mutations of apolipoprotein B gene
28. LDL-apheresis: Comparison of methods
29. LDL-Aferesi: confronto di metodiche
30. 68 CEREBROTENDINOUS XANTHOMATOSIS IN A COMPOUND HETEROZYGOTE FOR TWO MUTATIONS ON CYP27 GENE: DIAGNOSIS AND TREATMENT
31. NONALCOHOLIC STEATOHEPATITIS IN A FAMILY WITH FAMILIAL HYPOBETALIPOPROTEINEMIA CARRYING A NOVEL SPLICE SITE MUTATION OF APOB GENE
32. POSTPRANDIAL LIPOPROTEIN BEHAVIOR IN MULTIPLE SYMMETRICAL LIPOMATOSIS
33. Rivastigmine: an update on therapeutic efficacy in Alzheimer's disease and other conditions
34. High plasma homocysteine is a risk factor for stroke and congestive heart failure in an elderly italian population
35. Effects of statins on elevated lipoprotein(a) in primary hypercholesterolemia
36. Early onset mental retardation in a subject with cerebrotendinous xanthomatosis
37. Genetic risk factors in coronary heart disease (CHD) and restenosis
38. Changes in HCV Viremia following LDL Apheresis in a HCV Positive Patient with Familial Hypercholesterolemia
39. Lipoprotein(a) and lipoprotein profile in healthy centenarians: a reappraisal of vascular risk factors
40. ApoE4 allele frequency decrease with age and is lowest in centenarians: Results from a study in Northern Italy
41. The frequency of APO(a) atherogenic phenotypes does not decrease in centenarians compared to subjects of different ages
42. Apolipoprotein E genotype and phenotype comparison in a population of dyslipidaemic subjects
43. Metabolic abnormalities and clinical manifestations of familial hypobetalipoproteinemia
44. 2.P.278 Mild hyperhomocysteinemia correlated to folate status in Italian centenarians
45. 4.P.272 Abnormal LDL metabolism in a case of recessive form of familial hypercholesterolemia
46. 4.P.230 Pseudo-hypertriglyceridemia in four kindreds with benign hyperglycerolemia
47. 2.P.133 Lp(a) levels and apo(a) phenotypes in angiographically established coronary heart disease and in controls
48. 1.P.240 Familial hypobetalipoproteinemia caused by a truncated apolipoprotein B (B-33.4) is not protective against carotid artery disease
49. Apolipoprotein E allele polymorphism and ageing: Decreased prevalence of apolipoprotein ε4 allele in old individuals
50. Heterozygous apolipoprotein C-II deficiency: lipoprotein and apoprotein phenotype and Rsal restriction enzyme polymorphism in the Apo C'IIPadova kindred
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