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31
المؤلفون: Christian Wider, Jean-Marc Burgunder, Jean-Marc Good
المصدر: Forum Médical Suisse ‒ Swiss Medical Forum. 15
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::21d65cab494697617cd20d550db4193bTest
https://doi.org/10.4414/fms.2015.02458Test -
32
المصدر: Parkinsonism & Related Disorders. 46:e33
مصطلحات موضوعية: Gerontology, Neurology, Huntington's disease, business.industry, Cross-sectional study, Medicine, Neurology (clinical), Geriatrics and Gerontology, business, China, medicine.disease
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e5bc5c81b56e8edda02a58518a9f18d3Test
https://doi.org/10.1016/j.parkreldis.2017.11.107Test -
33
المؤلفون: X.-H. Hu, Y.-W. Zhang, D.-F. Fang, Huifang Shang, Jean-Marc Burgunder, X. P. Chen, S.-S. Zhang
المصدر: European Journal of Neurology. 17:846-851
مصطلحات موضوعية: Dystonia, medicine.medical_specialty, business.industry, Focal dystonia, medicine.disease, Hospital Anxiety and Depression Scale, Neurology, Internal medicine, medicine, Physical therapy, Anxiety, Neurology (clinical), Cervical dystonia, Family history, Age of onset, medicine.symptom, business, Depression (differential diagnoses)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::216f76dcd5489b967c6086f16fead54aTest
https://doi.org/10.1111/j.1468-1331.2009.02944.xTest -
34
المؤلفون: Wei Song, Yongping Chen, Rui Huang, Bei Cao, Jean-Marc Burgunder, Huifang Shang, Ke Chen, Bi Zhao, Jing Yang
المصدر: Parkinsonism & Related Disorders. 19:1043-1045
مصطلحات موضوعية: Adult, Male, China, medicine.medical_specialty, Blepharospasm, Polymorphism, Single Nucleotide, Gastroenterology, Young Adult, Methionine, Polymorphism (computer science), Internal medicine, Genotype, medicine, Humans, SNP, Cervical dystonia, Genetic Association Studies, Torticollis, Genetic association, Dystonia, Genetics, business.industry, Brain-Derived Neurotrophic Factor, Valine, Middle Aged, medicine.disease, Minor allele frequency, Neurology, Female, Neurology (clinical), Geriatrics and Gerontology, medicine.symptom, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a28b1d59197fca70bb86b85bb04e20eTest
https://doi.org/10.1016/j.parkreldis.2013.06.004Test -
35
المؤلفون: Jin-Hong Zhang, Xingkai An, Wenjun Chen, Yingru Gou, Yan Wu, Jean-Marc Burgunder, Yanming Xu, Guanggu Yuan, Yingcheng Wang, Rong Peng, Xue-Ye Mao, Zijuan Zhang
المصدر: Movement Disorders. 24:1902-1905
مصطلحات موضوعية: medicine.medical_specialty, education.field_of_study, Pathology, Parkinson's disease, business.industry, Population, Late onset, Odds ratio, medicine.disease, Gastroenterology, LRRK2, Central nervous system disease, Neurology, Internal medicine, Cohort, Medicine, Neurology (clinical), Risk factor, business, education
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::777ee45cb14245bc8d90b0ba2b8fcabfTest
https://doi.org/10.1002/mds.22371Test -
36
المؤلفون: Huifang Shang, Zu-Ming Luo, Shu-Hui Wu, Shu-Shan Zhang, Yuan Yang, Qin Chen, Xueping Chen, Yang-Wei Zhang, Jean-Marc Burgunder
المصدر: Movement Disorders. 23:1472-1475
مصطلحات موضوعية: Male, Myoclonus, China, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, RNA Stability, Nonsense mutation, Gene mutation, Biology, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Frameshift mutation, Exon, SGCE, Sarcoglycans, medicine, Humans, RNA, Messenger, Child, Frameshift Mutation, Dystonia, Genetics, Exons, medicine.disease, Introns, Stop codon, Pedigree, Mutagenesis, Insertional, Phenotype, Neurology, Codon, Nonsense, Dystonic Disorders, Mutation (genetic algorithm), Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f29b383d1b454920c3367ff1697e3eTest
https://doi.org/10.1002/mds.22008Test -
37
المؤلفون: Lie Chen, Jean-Marc Burgunder
المصدر: Cell Biology International. 29:506-513
مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Utrophin, Sarcoplasm, Cell Culture Techniques, Fluorescent Antibody Technique, Dystrophin, Dystrophin-associated protein complex, Dystroglycan, medicine, Humans, Protein Isoforms, Dystroglycans, Muscle, Skeletal, Sarcolemma, biology, Skeletal muscle, Cell Differentiation, Cell Biology, General Medicine, musculoskeletal system, Clone Cells, medicine.anatomical_structure, Biochemistry, biology.protein, Pikachurin, Laminin
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5115e085c6a4c0d704f143e45f9e9837Test
https://doi.org/10.1016/j.cellbi.2005.01.009Test -
38
المصدر: Experimental Neurology. 193:234-237
مصطلحات موضوعية: Rats, Sprague-Dawley, Lesion, Parkinsonian Disorders, Developmental Neuroscience, Dopamine, Basal ganglia, medicine, Animals, skin and connective tissue diseases, biology, Motor Cortex, Rats, Subthalamic nucleus, Parvalbumins, medicine.anatomical_structure, Gene Expression Regulation, nervous system, Neurology, biology.protein, GABAergic, Female, sense organs, Primary motor cortex, medicine.symptom, Neuroscience, Parvalbumin, medicine.drug, Motor cortex
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30ae995ea176ca8003cfb7243c9c5a30Test
https://doi.org/10.1016/j.expneurol.2004.12.007Test -
39
المؤلفون: Huifang Shang, D. Lang, Jean-Marc Burgunder, A. Kaelin-Lang, N. Clerc
المصدر: European Journal of Neurology. 12:131-138
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Pathology, Disease, Polymerase Chain Reaction, Torsion dystonia, Exon, SGCE, Sarcoglycans, Internal medicine, otorhinolaryngologic diseases, medicine, Humans, Age of Onset, Family history, GTP Cyclohydrolase, Polymorphism, Single-Stranded Conformational, Dystonia, Polymorphism, Genetic, Genetic heterogeneity, business.industry, medicine.disease, nervous system diseases, Neurology, Dystonic Disorders, Mutation, Female, Neurology (clinical), Age of onset, business, Molecular Chaperones
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6f50cc9fb3b5283bceda48d9c588551Test
https://doi.org/10.1111/j.1468-1331.2004.00974.xTest -
40
المؤلفون: Jean-Marc Burgunder, M. Weber, Th Lauterburg, Irene Tobler
المصدر: Neuroscience Letters. 358:17-20
مصطلحات موضوعية: medicine.medical_specialty, Substantia nigra, Dynorphin, Motor Activity, Biology, Rats, Sprague-Dawley, Dopamine receptor D1, Dopamine, Dopamine receptor D2, Internal medicine, medicine, Animals, Neurotransmitter Agents, Tyrosine hydroxylase, General Neuroscience, Dopaminergic, Brain, Circadian Rhythm, Rats, Receptors, Neurotransmitter, Ventral tegmental area, Endocrinology, medicine.anatomical_structure, Gene Expression Regulation, Neuroscience, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10fdecc9b1ec678973c8488de23457cdTest
https://doi.org/10.1016/j.neulet.2003.12.053Test