21 results on '"Rouskas, Konstantinos"'
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2. Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
3. Personal Goals, User Engagement, and Meal Adherence within a Personalised AI-Based Mobile Application for Nutrition and Physical Activity.
4. Cerebral Amyloidosis in Individuals with Subjective Cognitive Decline: From Genetic Predisposition to Actual Cerebrospinal Fluid Measurements
5. Periodic veganism in healthy individuals improves blood lipids, reduces low-grade inflammation, but impairs bone health: the FastBio study
6. Identifying novel regulatory effects for clinically relevant genes through the study of the Greek population
7. Weight loss independent association of TCF7 L2 gene polymorphism with fasting blood glucose after Roux-en-Y gastric bypass in type 2 diabetic patients
8. PROTEIN AI Advisor: A Knowledge-Based Recommendation Framework Using Expert-Validated Meals for Healthy Diets
9. Users' Perspective on the AI-Based Smartphone PROTEIN App for Personalized Nutrition and Healthy Living: A Modified Technology Acceptance Model (mTAM) Approach
10. Exploring the impact of the Mediterranean diet on the gut microbiome of individuals with multiple sclerosis
11. Bariatric surgery, lipoprotein metabolism and cardiovascular risk
12. Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome
13. Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human
14. Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome
15. Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer
16. Déterminisme génétique de l’évolution de la glycémie chez les patients obèses et diabétiques après bypass gastrique
17. Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human.
18. Loss‐of‐Function Mutations in MC4R Are Very Rare in the Greek Severely Obese Adult Population
19. Common Variants in FTO, MC4R, TMEM18, PRL, AIF1 , and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population
20. Διερεύνηση της γενετικής προδιάθεσης για παχυσαρκία στον ελληνικό πληθυσμό
21. Genetic Predisposition to Hippocampal Atrophy and Risk of Amnestic Mild Cognitive Impairment and Alzheimer's Dementia.
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