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المؤلفون: Jean-Marc Burgunder, Mario Wiesendanger, Deborah J. Serrien
المصدر: Serrien, Deborah J.; Burgunder, Jean-Marc; Wiesendanger, Mario (2002). Control of manipulative forces during unimanual and bimanual tasks in patients with Huntington’s disease. Experimental brain research, 143(3), pp. 328-334. Springer 10.1007/s00221-001-0992-6 <http://dx.doi.org/10.1007/s00221-001-0992-6Test>
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, 610 Medicine & health, medicine.disease_cause, Functional Laterality, Weight-bearing, Weight-Bearing, Physical medicine and rehabilitation, Huntington's disease, Hand strength, medicine, Humans, In patient, Muscle, Skeletal, Hand Strength, General Neuroscience, Motor control, Brain, Body movement, Middle Aged, medicine.disease, Control subjects, Hand, Sagittal plane, Motor Skills Disorders, medicine.anatomical_structure, Huntington Disease, Female, Psychology, Neuroscience, Muscle Contraction
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2762cb16107196a4fca0bdf495451136Test
http://doc.rero.ch/record/315362/files/221_2001_Article_992.pdfTest -
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المؤلفون: Simeon Schaub, Iris-Katharina Penner, Bettina Fischer-Barnicol, Jean-Marie Annoni, Özgür Yaldizli, Bettina Frey, Jana Pöttgen, Sara Bagutti, Dominik Zwahlen, Mireille Neuhaus, Marie‐ Dominique Martory, Jean-Marc Burgunder
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Multiple Sclerosis, Anxiety, Neuropsychological Tests, 050105 experimental psychology, 03 medical and health sciences, 0302 clinical medicine, Cognition, Social cognition, Theory of mind, Medicine, Raw score, Humans, 0501 psychology and cognitive sciences, Effects of sleep deprivation on cognitive performance, Psychiatry, Social Behavior, 610 Medicine & health, Depression (differential diagnoses), Facial affect, business.industry, Depression, Multiple sclerosis, 05 social sciences, Middle Aged, medicine.disease, Neurology, Social Perception, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Clinical psychology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f51514869fd2dba4bdd97ab979c21dc7Test
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المؤلفون: Stefan Mühlebach, Jean-Marc Nuoffer, Jean-Marc Burgunder, Lorenz Risch, Lia Bally, Zeno Stanga, Carla Aeberhard, E Aubry
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Mitochondrial Diseases, Endocrinology, Diabetes and Metabolism, Rest, Population, Nutritional Status, Disease, Clinical nutrition, Diet Surveys, Risk Assessment, 03 medical and health sciences, 0302 clinical medicine, Quality of life, Risk Factors, Internal medicine, 540 Chemistry, medicine, Humans, Mass Screening, Resting energy expenditure, 030212 general & internal medicine, Prospective Studies, Prospective cohort study, education, 610 Medicine & health, Aged, education.field_of_study, Nutrition and Dietetics, business.industry, Malnutrition, Middle Aged, medicine.disease, Parenteral nutrition, Nutrition Assessment, Case-Control Studies, Physical therapy, Quality of Life, 570 Life sciences, biology, Female, business, Energy Metabolism, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a067fa1adc33724279c88e4b774f142Test
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المؤلفون: Jean-Marc Burgunder, S. Vez, Jean-Marie Annoni, David A. Magezi, B. Frey, J. Kohli
المصدر: Neuropsychologia. 119
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, genetic structures, Cognitive Neuroscience, media_common.quotation_subject, Experimental and Cognitive Psychology, Disease, Striatum, Audiology, Neuropsychological Tests, behavioral disciplines and activities, 050105 experimental psychology, Cohort Studies, 03 medical and health sciences, Behavioral Neuroscience, 0302 clinical medicine, Huntington's disease, Perception, Basal ganglia, medicine, Humans, 0501 psychology and cognitive sciences, 610 Medicine & health, media_common, 05 social sciences, Cognition, Time perception, Middle Aged, medicine.disease, Huntington Disease, Time Perception, Auditory Perception, Disease Progression, Female, Psychology, 030217 neurology & neurosurgery, psychological phenomena and processes, Stroop effect
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::833de38c5e83ffcb7703d1a76602a4c1Test
https://pubmed.ncbi.nlm.nih.gov/30142378Test -
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المؤلفون: Michel Fardeau, Shari Fallet, Silvia Torelli, Norma B. Romero, C Pollitt, Gillian Storey, Caroline Sewry, Paola Prandini, Rumaisa Bashir, Thomas Voit, Derek J. Blake, Louise V.B. Anderson, Kate Bushby, Susan C. Brown, Volker Straub, Y Yuva, Isabelle Richard, Francesco Muntoni, Ralf Herrmann, Matthew A. Benson, Jean-Marc Burgunder, Martin Brockington
المصدر: Brockington, Martin; Yuva, Yeliz; Prandini, Paola; Brown, Susan C.; Torelli, Silvia; Benson, Matthew A.; Herrmann, Ralf; Anderson, Louise V.B.; Bashir, Rumaisa; Burgunder, Jean-Marc; Fallet, Shari; Romero, Norma; Fardeau, Michel; Straub, Volker; Storey, Gillian; Pollitt, Christine; Richard, Isabelle; Sewry, Caroline A.; Bushby, Kate; Voit, Thomas; ... (2001). Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Human molecular genetics, 10(25), pp. 2851-2859. Oxford University Press 10.1093/hmg/10.25.2851 <http://dx.doi.org/10.1093/hmg/10.25.2851Test>
مصطلحات موضوعية: Adult, Male, Adolescent, Genotype, Genetic Linkage, Blotting, Western, 610 Medicine & health, Polymerase Chain Reaction, Muscular Dystrophies, Muscle hypertrophy, Immunoenzyme Techniques, Fukuyama congenital muscular dystrophy, Genetics, medicine, Humans, Pentosyltransferases, Age of Onset, Muscular dystrophy, Child, Dystroglycans, Walker–Warburg syndrome, Molecular Biology, Genetics (clinical), DNA Primers, Membrane Glycoproteins, Fukutin-related protein, biology, Calpain, Infant, Proteins, General Medicine, Middle Aged, medicine.disease, Fukutin, Pedigree, Cytoskeletal Proteins, Phenotype, Haplotypes, Child, Preschool, Mutation, biology.protein, Congenital muscular dystrophy, Female, Laminin, Chromosomes, Human, Pair 19, Microsatellite Repeats, Limb-girdle muscular dystrophy
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8637abdd8a7da6e9a9ecb905ca82f74cTest
http://doc.rero.ch/record/297949/files/dde309.pdfTest