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Your search keyword '"Spina R."' showing total 18 results

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18 results on '"Spina R."'

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1. The surgical treatment of non-metastatic melanoma in a Clinical National Melanoma Registry Study Group (CNMR): a retrospective cohort quality improvement study to reduce the morbidity rates

2. The association between low skeletal muscle mass and delirium: results from the nationwide multi-centre Italian Delirium Day 2017

3. Delirium and Clusters of Older Patients Affected by Multimorbidity in Acute Hospitals

4. Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study

5. Prevalence, associated factors and outcomes of pressure injuries in adult intensive care unit patients: the DecubICUs study

6. Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome

7. rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography

8. MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH 'EXTREME LDL-C PHENOTYPES'

9. Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics

10. Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred

11. Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN)

12. Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study

13. Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia

14. Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population

15. Metabolic disturbances and risk of cancer in the 25 years follow-up of the 'Ventimiglia Heart Study' epidemiological project

16. Novel CREB3L3 Nonsense Mutation in a Family With Dominant Hypertriglyceridemia

17. Prevalence of ANGPTL3 and APOB gene mutations in subjects with combined hypolipidemia

18. Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia

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