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GeNeDis 2020

320,99 €*

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Produktnummer: 16A46404558
Veröffentlichungsdatum: 14.01.2023
EAN: 9783030787899
Sprache: Englisch
Seitenzahl: 452
Produktart: Kartoniert / Broschiert
Herausgeber: Vlamos, Panayiotis
Verlag: Springer Springer International Publishing AG Springer Nature Switzerland
Untertitel: Genetics and Neurodegenerative Diseases
Produktinformationen "GeNeDis 2020"
1-Attitudes and smoking prevalence among undergraduate students in central Greece.- 2-Care of patients with Alzheimer's disease.- 3-Regulation of antioxidant enzymes levels in rat brain.- 4-NIRS-based assessment of cerebral oxygenation during high definition anodal transcranial direct current stimulation in patients with posttraumatic encephalopathy.- 5-Cerebral critical closing pressure at concomitant traumatic brain injury.- 6-The role of inflammatory biomarkers as a diagnostic tool for possible late-life cognitive decline and dementias.- 7-The Development of Antisense RNA Treatments using Engineered Protein Substrates.- 8-Biomarker-driven analysis using high-throughput approaches in neuroinflammation and neurodegenerative diseases.- 9-Sensitive and Stereo specific high-performance liquid chromatographic method for flurbiprofen in human plasma.- 10-Genotypic and Clinical Analysis of a Thalassemia Major Cohort: An Observational Study.- 11-Design and Validation of a New Diagnostic Tool for the Differentiation of Pathological Voices in Parkinsonian Patients.- 12-Effects of an 8-Week Stress Management Program in Women with Breast Cancer: A Randomized Controlled Trial.- 13-The Rosenberg Self-Esteem Scale: Translation and Validation in the Greek Language in Adolescents.- 14-Stress system activation analysis in Greek female adolescents: a bioimpedance study.- 15-Kisspeptin and the genetic obesity interactome.- 16-The importance of diagnostic and prognostic biomarkers identification and classification towards understanding ALS pathogenesis.- 17-Entropy in Cardiac Autonomic Nervous System of Adolescents with General Learning Disabilities or Dyslexia.- 18-Ebola virus disease and current therapeutic strategies; A review.- 19-Hyperbaric Oxygen Therapy effect on "Kinesia Paradoxa" Brain Circuits.- 20-Early and Very Early GRIM19 and MCL1 Expression are Correlated to Late Acquired Prednisolone Effects in a T-Cell Acute Leukemia Cell Line.- 21-Phospholipid Fatty Acid Profile of Spirulina platensis.- 22-Chronic systemic inflammation measured by bioimpedance technology before and after sleeve gastrectomy: a feasibility study.- 23-Synthesis and Biological Evaluation Substituted Thiophene Derivatives.- 24-Force spectroscopy in mechanical protein domains unfolding.- 25-Investigating the genetic component of Parkinson's Disease.- 26-Urticaria from the Neurodermatological Perspective: A Temporal Analysis of Urticaria and Cognition.- 27-Novel Low-Noise CMOS Bioamplifier for the Characterization of Neurodegenerative Diseases.- 28-The Kentucky Inventory of Mindfulness Skills in Greek Undergraduate and Postgraduate Students.- 29-Synthesis, in silico stuiesand biological evaluation of 1, 3 ,4 oxadiazino indole derivatives.- 30-Designing and screening of new schiff bases of indole derivatives for anti-bacterial activity by in-silico methods and docking studies.- 31-Use of vitamin D bolus in fortified juice for improving vitamin D status in children with Cerebral Palsy.-32-Microbes and the games they play.- 33-Impurity Profiling and Identification of 2,6 diisopropylphenol by Raman spectroscopy.- 34-Cultural Accommodation of the Strengthening Families Program for Parents and Young Adolescents 10-14: Greek Phase I & II Study.- 35-The effect of nutrients on Alzheimer's disease biomarkers: A metabolomic approach.- 36-The impact of exercising in the quality of life of people with Aementia-Alzheimer disease.- 37-Advanced Health Technologies and Nanotechnologies in Neurodegenerative Diseases.- 38-Phenotype and genotype study in a case of frontometaphyseal dysplasia 1.- 39-Craniofacial and neurological phenotype in a case of oculodentodigital syndrome.- 40-Clinical and molecular study of common thrombophilia mutation prothrombin G20210A.- 41-Prenatal genetic testing for X-linked hypohidrotic ectodermal dysplasia.- 42-Preimplantation genetic testing for spastic paraplegia type 3.- 43-Synthesis, anti-inflammatory activity and in-silico studies of so
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