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1دورية أكاديمية
المؤلفون: Rui Wu, He Lv, Wei Zhang, Zhaoxia Wang, Yuehuan Zuo, Jing Liu, Yun Yuan
المصدر: BioMed Research International, Vol 2017 (2017)
مصطلحات موضوعية: Medicine
العلاقة: http://dx.doi.org/10.1155/2017/6481367Test; https://doaj.org/toc/2314-6133Test; https://doaj.org/toc/2314-6141Test; https://doaj.org/article/9b0ec8a290254e8480dd7c1b9bb70e5bTest
الإتاحة: https://doi.org/10.1155/2017/6481367Test
https://doaj.org/article/9b0ec8a290254e8480dd7c1b9bb70e5bTest -
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المؤلفون: Yuehuan Zuo, Lingchao Meng, Rui Wu, He Lv, Zhaoxia Wang, Yuanyuan Lu, Yun Yuan, Jing Liu, Wei Zhang
المصدر: Clinical Neuropathology. 37:232-238
مصطلحات موضوعية: Male, 0301 basic medicine, Pathology, medicine.medical_specialty, Biopsy, DNA Mutational Analysis, Mitochondrial trifunctional protein deficiency, Mitochondrial trifunctional protein, medicine.disease_cause, Compound heterozygosity, Pathology and Forensic Medicine, Polyneuropathies, Young Adult, 03 medical and health sciences, Asian People, Sural Nerve, Charcot-Marie-Tooth Disease, Carnitine, medicine, Humans, Amino Acid Sequence, Genetic testing, Mutation, medicine.diagnostic_test, biology, Mitochondrial Trifunctional Protein, business.industry, General Medicine, medicine.disease, Phenotype, Axons, 030104 developmental biology, Neurology, Child, Preschool, Mitochondrial Trifunctional Protein, beta Subunit, biology.protein, Neurology (clinical), business, HADHB
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::019e609ac3460f74fe4ce0fb3e672dd1Test
https://doi.org/10.5414/np301097Test -
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المؤلفون: Wei Zhang, Xiao Liu, Ying Zhu, Yun Yuan, Zhaoxia Wang, Yuehuan Zuo, Jing Liu, Hui-Ting Lin, Jiangxi Xiao
المصدر: Chinese Medical Journal, Vol 131, Iss 12, Pp 1472-1479 (2018)
مصطلحات موضوعية: musculoskeletal diseases, 0301 basic medicine, Pathology, medicine.medical_specialty, lcsh:Medicine, Thigh, Inflammatory myopathy, LMNA, 03 medical and health sciences, 0302 clinical medicine, medicine, Emery-Dreifuss Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Congenital Muscular Dystrophy, Muscle Magnetic Resonance Imaging, Muscular dystrophy, Emery–Dreifuss muscular dystrophy, medicine.diagnostic_test, business.industry, lcsh:R, Magnetic resonance imaging, General Medicine, medicine.disease, 030104 developmental biology, medicine.anatomical_structure, Congenital muscular dystrophy, business, 030217 neurology & neurosurgery, Limb-girdle muscular dystrophy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f22244d32be446309d76b58ffb9e0d84Test
https://doi.org/10.4103/0366-6999.233957Test -
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المؤلفون: Yuanyuan Lu, Suqin Jin, Wei Zhang, Jing Liu, Zhaoxia Wang, Yuehuan Zuo, Yun Yuan, He Lyu
المصدر: Chinese Medical Journal, Vol 130, Iss 9, Pp 1049-1054 (2017)
Chinese Medical Journalمصطلحات موضوعية: Central Nervous System, Male, 0301 basic medicine, Neurology, Gap Junction Beta-1 Protein, DNA Mutational Analysis, lcsh:Medicine, Disease, Gene mutation, Gastroenterology, Connexins, 0302 clinical medicine, Charcot-Marie-Tooth Disease, Genotype, Child, Sanger sequencing, education.field_of_study, General Medicine, Electrophysiology, Phenotype, Child, Preschool, symbols, Connexin 32, Female, Original Article, Adult, X-linked Charcot-Marie-Tooth Type 1, medicine.medical_specialty, Adolescent, Young Adult, 03 medical and health sciences, symbols.namesake, Internal medicine, medicine, Humans, education, Gene, Retrospective Studies, business.industry, lcsh:R, Infant, Retrospective cohort study, Neuropathy, 030104 developmental biology, Mutation, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8aa817f41e29cb2962702f615808b5dTest
http://www.cmj.org/article.asp?issn=0366-6999;year=2017;volume=130;issue=9;spage=1049;epage=1054;aulast=LuTest -
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المؤلفون: Lei Yu, Jing Liu, Yuehuan Zuo, Wei Zhang, Jiangxi Xiao, Qingqing Wang, Zhe Zhang, Meng Yu, Zhaoxia Wang, Yun Yuan
المصدر: Chinese Medical Journal, Vol 129, Iss 12, Pp 1419-1424 (2016)
Chinese Medical Journalمصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Adolescent, Genotype, Heart block, lcsh:Medicine, Kearns-Sayre Syndrome, Brain Magnetic Resonance Imaging, Heart Conduction Block, 030204 cardiovascular system & hematology, DNA, Mitochondrial, Kearns–Sayre syndrome, White matter, 03 medical and health sciences, 0302 clinical medicine, medicine, Humans, Child, Muscle biopsy, medicine.diagnostic_test, Bundle branch block, business.industry, lcsh:R, Brain, Magnetic resonance imaging, General Medicine, medicine.disease, Magnetic Resonance Imaging, Heart Block, medicine.anatomical_structure, Child, Preschool, Original Article, Female, Electrical conduction system of the heart, Age of onset, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dd09c47c242fed4d9fc080179981f2aTest
https://doi.org/10.4103/0366-6999.183417Test -
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المؤلفون: Jing Liu, He Lv, Wei Zhang, Lu Wang, Zhaoxia Wang, Yuehuan Zuo, Yun Yuan
المصدر: Journal of the Neurological Sciences. 358:153-157
مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Adolescent, Genotype, Neural Conduction, MFN2, Sural nerve, Gene mutation, Nerve conduction velocity, GTP Phosphohydrolases, Cohort Studies, Mitochondrial Proteins, Young Adult, Myelin, Sural Nerve, Charcot-Marie-Tooth Disease, medicine, Humans, Axon, Child, Pathological, business.industry, Anatomy, Middle Aged, Median nerve, Median Nerve, Phenotype, medicine.anatomical_structure, Neurology, Child, Preschool, Mutation, Female, Neurology (clinical), business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2acb07a57dec501aa774953bb11626dfTest
https://doi.org/10.1016/j.jns.2015.08.1528Test -
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المؤلفون: Yuehuan Zuo, Xiao Liu, Yining Huang, Wei Sun, Zhaoxia Wang, Jiangxi Xiao, He Lv, Yun Yuan, Wei Zhang
المصدر: Journal of the Neurological Sciences. 354:63-69
مصطلحات موضوعية: Adult, Male, Mutation, Missense, CADASIL, Disease, Gene mutation, Leukoencephalopathy, Young Adult, Exon, Asian People, medicine, Humans, Missense mutation, Genetic Testing, Receptor, Notch3, Pathological, Aged, Genetics, Receptors, Notch, business.industry, Middle Aged, medicine.disease, Neurology, Mutation (genetic algorithm), Female, Neurology (clinical), business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc01ff04cc540f8daf007e58343d7900Test
https://doi.org/10.1016/j.jns.2015.04.047Test -
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المؤلفون: Yun Yuan, Zhaoxia Wang, Rui Wu, He Lv, Wei Zhang, Yuehuan Zuo, Jing Liu
المصدر: BioMed Research International, Vol 2017 (2017)
BioMed Research Internationalمصطلحات موضوعية: Adult, Male, 0301 basic medicine, China, Pathology, medicine.medical_specialty, Adolescent, Article Subject, lcsh:Medicine, Sural nerve, Nerve fiber, Biology, General Biochemistry, Genetics and Molecular Biology, Cohort Studies, Young Adult, 03 medical and health sciences, Myelin, 0302 clinical medicine, Asian People, Charcot-Marie-Tooth Disease, Peripheral myelin protein 22, medicine, Humans, Child, Pathological, Onion bulb formation, General Immunology and Microbiology, lcsh:R, Infant, General Medicine, Middle Aged, medicine.disease, 030104 developmental biology, medicine.anatomical_structure, nervous system, Child, Preschool, Female, Age of onset, Polyneuropathy, 030217 neurology & neurosurgery, Research Article
وصف الملف: text/xhtml
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b94fa30af51cfcaf575508367f289cdTest
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المؤلفون: Wei, Zhang, Mande, Kang, Yawen, Zhao, Fan, Li, Junlong, Shu, Yuehuan, Zuo, Jing, Liu, Yining, Huang, Yun, Yuan
المصدر: Zhonghua yi xue za zhi. 95(23)
مصطلحات موضوعية: Male, Sex Characteristics, Heart Diseases, Incidence, Stroke, Asian People, alpha-Galactosidase, Hypertension, Mutation, Fabry Disease, Humans, Neuralgia, Female, Kidney Diseases
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::13c6625975d102abbe2a6c423b584efdTest
https://pubmed.ncbi.nlm.nih.gov/26712400Test