-
11
المؤلفون: Xue-Li Chang, Jean-Marc Burgunder, Nan-Nan Li, Huihua Li, Eng-King Tan, Rong Peng, Xue-Ye Mao, Jin-Hong Zhang
المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (3)
مصطلحات موضوعية: Adult, Male, China, Adolescent, Genome-wide association study, Single-nucleotide polymorphism, Locus (genetics), Biology, Lower risk, Polymorphism, Single Nucleotide, Cellular and Molecular Neuroscience, Gene Frequency, SNP, Humans, Genetic Predisposition to Disease, Allele, Genetics (clinical), Genetic association, Aged, Genetics, Aged, 80 and over, Parkinson Disease, Middle Aged, LRRK2, Psychiatry and Mental health, Genetic Loci, Case-Control Studies, Female, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4cabfd878480d686ce9c3e900fe100dTest
https://pubmed.ncbi.nlm.nih.gov/21268244Test -
12
المؤلفون: G.-G. Yuan, R. Peng, Jean-Marc Burgunder, Y.-M. Xu, Y.-C. Wang, W.-J. Chen, T. Li, Z.-J. Zhang, Y. Wu, X.-K. An, Y.-R. Gou, J.-H. Zhang
المصدر: European journal of neurology. 15(3)
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, China, Genotype, Population, Glycine, Protein Serine-Threonine Kinases, Arginine, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Gastroenterology, Asian People, Polymorphism (computer science), Risk Factors, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Risk factor, education, Aged, Genetics, Aged, 80 and over, education.field_of_study, Chi-Square Distribution, Polymorphism, Genetic, business.industry, Parkinsonism, Parkinson Disease, Odds ratio, Middle Aged, medicine.disease, LRRK2, Genotype frequency, Neurology, Female, Neurology (clinical), business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4975f753c8b6c3bf2bffa1865817f56Test
https://pubmed.ncbi.nlm.nih.gov/18290841Test -
13
المؤلفون: Benjamin K.C. Ong, Raymond C.S. Seet, Roland Baur, Chew Soh Eng, Shang Huifang, Erle C.H. Lim, Walter Hunziker, Pascal Béguin, Erwin Sigel, Jean-Marc Burgunder
المصدر: Neuromuscular disorders : NMD. 18(8)
مصطلحات موضوعية: musculoskeletal diseases, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, China, DNA, Complementary, Adolescent, Xenopus, Pain, Biology, Compound heterozygosity, medicine.disease_cause, Myotonia, Variable features, Chloride Channels, Internal medicine, medicine, Animals, Humans, Muscle, Skeletal, Exercise, Genetics (clinical), Genetics, Neurologic Examination, CLCN1, Mutation, Myotonia congenita, Electromyography, Reverse Transcriptase Polymerase Chain Reaction, medicine.disease, biology.organism_classification, Electrophysiology, Endocrinology, Neurology, Pediatrics, Perinatology and Child Health, Chloride channel, biology.protein, Oocytes, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0c2fdf4dfca35d7248e8e99f8ec0c33Test
https://pubmed.ncbi.nlm.nih.gov/18579381Test -
14
المؤلفون: Lie Chen, Franziska Joncourt, D. Lang, Sabina Gallati, Jean-Marc Burgunder, X.W. Ran
المصدر: European neurology. 49(4)
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, China, DNA Mutational Analysis, Hypokalemic Periodic Paralysis, Familial periodic paralysis, Bioinformatics, Polymerase Chain Reaction, Genetic determinism, Hypokalemic periodic paralysis, Internal medicine, CACNA1S gene, medicine, Humans, Polymorphism, Single-Stranded Conformational, Polymorphism, Genetic, business.industry, Incidence, Thyrotoxic periodic paralysis, Periodic paralysis, Middle Aged, medicine.disease, Molecular analysis, Endocrinology, Thyrotoxicosis, Neurology, Chromosomes, Human, Pair 1, Mutation, Female, Neurology (clinical), business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91ebc6837362ee450f644b2dde29222cTest
https://pubmed.ncbi.nlm.nih.gov/12736539Test -
15
المؤلفون: Xiaoyan Guo, Yongping Chen, Jean-Marc Burgunder, Wei Song, Xueping Chen, Bei Cao, Rui Huang, JianPeng Li, Bi Zhao, Huifang Shang, Ke Chen
المصدر: Neurobiology of Aging. 34:1709.e7-1709.e8
مصطلحات موضوعية: Adult, Male, China, Aging, EIF4G1 Gene, Population, Vesicular Transport Proteins, Biology, Arginine, Young Adult, VPS35, Humans, VPS35 Gene, Histidine, education, Gene, Aged, Genetics, Vacuolar protein sorting, Aspartic Acid, education.field_of_study, General Neuroscience, Parkinson Disease, Middle Aged, Eukaryotic translation initiation factor 4 gamma, Case-Control Studies, Mutation, Mutation (genetic algorithm), Female, Neurology (clinical), Asparagine, Geriatrics and Gerontology, Eukaryotic Initiation Factor-4G, Developmental Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::236fa32da8eb03d3548d6d3eb9775613Test
https://doi.org/10.1016/j.neurobiolaging.2012.11.003Test