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portada Genedis 2020: Genetics and Neurodegenerative Diseases
Type
Physical Book
Illustrated by
Publisher
Language
English
Pages
435
Format
Paperback
Dimensions
25.4 x 17.8 x 2.3 cm
Weight
0.78 kg.
ISBN13
9783030787899

Genedis 2020: Genetics and Neurodegenerative Diseases

Panayiotis Vlamos (Illustrated by) · Springer · Paperback

Genedis 2020: Genetics and Neurodegenerative Diseases - Vlamos, Panayiotis

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£ 338.38

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Synopsis "Genedis 2020: Genetics and Neurodegenerative Diseases"

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 G2

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