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1دورية أكاديمية
المؤلفون: Quang Tuan Rémy Nguyen, Juan Dario Ortigoza Escobar, Jean-Marc Burgunder, Caterina Mariotti, Carsten Saft, Lena Elisabeth Hjermind, Katia Youssov, G. Bernhard Landwehrmeyer, Anne-Catherine Bachoud-Lévi
المصدر: Frontiers in Neurology, Vol 13 (2022)
مصطلحات موضوعية: Huntington's disease, chorea, phenocopy, diagnosis, differential diagnosis, guidelines, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2022.891800/fullTest; https://doaj.org/toc/1664-2295Test
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2دورية أكاديمية
المؤلفون: Quang Tuan Rémy Nguyen, Juan Dario Ortigoza Escobar, Jean-Marc Burgunder, Caterina Mariotti, Carsten Saft, Lena Elisabeth Hjermind, Katia Youssov, G. Bernhard Landwehrmeyer, Anne-Catherine Bachoud-Lévi
المصدر: Frontiers in Neurology, Vol 13 (2022)
مصطلحات موضوعية: Huntington's disease, chorea, phenocopy, diagnosis, differential diagnosis, guidelines, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fneur.2022.817753/fullTest; https://doaj.org/toc/1664-2295Test
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المؤلفون: Quang Tuan Rémy Nguyen, Juan Dario Ortigoza Escobar, Jean-Marc Burgunder, Caterina Mariotti, Carsten Saft, Lena Elisabeth Hjermind, Katia Youssov, G. Bernhard Landwehrmeyer, Anne-Catherine Bachoud-Lévi
مصطلحات موضوعية: Neurology and Neuromuscular Diseases, Neurogenetics, Huntington's disease, chorea, phenocopy, diagnosis, differential diagnosis, guidelines, daily clinical practice
الإتاحة: https://doi.org/10.3389/fneur.2022.817753.s001Test
https://figshare.com/articles/dataset/Table_1_Combining_Literature_Review_With_a_Ground_Truth_Approach_for_Diagnosing_Huntington_s_Disease_Phenocopy_DOCX/19151516Test -
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المؤلفون: Fengyin Liang, Shichang Li, Jean-Marc Burgunder, Guangqing Xu, Qinmei Wang, Yixuan Zeng, Xi-Lin Lu, Wenyuan Guo, Zhong Pei, Jie-Bin Zhou, Ji-Yan Pang, Yi Huang, Simei Long, Luyang Feng
المصدر: Drug Design, Development and Therapy
مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Huntingtin, Mutant, Pharmaceutical Science, Protein aggregation, Neuroprotection, molecular target, Small Molecule Libraries, xyloketal derivatives, 03 medical and health sciences, Protein Aggregates, Huntington's disease, mutant Huntingtin, Drug Discovery, mental disorders, medicine, Huntingtin Protein, Animals, protein misfolding, Caenorhabditis elegans, Pyrans, Original Research, Pharmacology, Genetics, Drug Design, Development and Therapy, biology, Chorea, biology.organism_classification, medicine.disease, Cell biology, nervous system diseases, Molecular Docking Simulation, Disease Models, Animal, 030104 developmental biology, Huntington Disease, Neuroprotective Agents, medicine.symptom, Huntington’s disease
وصف الملف: text/html
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc8fcea67e2258c9d419944fe7fc01e0Test
https://pubmed.ncbi.nlm.nih.gov/27110099Test -
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المؤلفون: Jean-Marc Burgunder
المصدر: Therapeutic Advances in Neurological Disorders, Vol 6 (2013)
مصطلحات موضوعية: Pharmacology, medicine.medical_specialty, business.industry, Reviews, Chorea, Disease, medicine.disease, lcsh:RC346-429, Task (project management), Neurology, Huntington's disease, Medicine, Neurology (clinical), medicine.symptom, business, Psychiatry, lcsh:Neurology. Diseases of the nervous system
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06cae59c3730e5edef31ec7e2af1725fTest
https://doaj.org/article/6ec96d981dcf49e7bff7984060af877bTest -
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المؤلفون: Yongping Chen, R. Huang, X. P. Chen, K. Chen, J. Yang, Jean-Marc Burgunder, B. Zhao, Wei Song, Huifang Shang, Z.-Z. Zheng
المصدر: European journal of neurology. 21(1)
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, China, Adolescent, Aura, DNA Mutational Analysis, Nerve Tissue Proteins, medicine.disease_cause, Gastroenterology, Exon, Young Adult, Chorea, Internal medicine, medicine, Humans, In patient, Insertion, Age of Onset, Child, Gene, Genetics, Mutation, business.industry, Membrane Proteins, Paroxysmal dyskinesia, musculoskeletal system, Dystonia, Neurology, cardiovascular system, Female, Neurology (clinical), business, PRRT2
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c13f88ff53a02f70117dcfeae1035222Test
https://pubmed.ncbi.nlm.nih.gov/23496026Test