肌萎缩性脊髓侧索硬化症 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "肌萎缩性脊髓侧索硬化症" in Chinese language version.

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alsa.org

Quick Facts About ALS & The ALS Association. The ALS Association. [2022-11-09]. （原始内容存档于2014-08-22）.

architalbiol.org

Silani, Vincenzo; Messina, Stefano; Poletti, Barbara; Morelli, Claudia; Doretti, Alberto; Ticozzi, Nicola; Maderna, Luca. The diagnosis of Amyotrophic Lateral Sclerosis in 2010. Archives Italiennes de Biologie. 2011-03-10, 149 (1) [2022-11-09]. ISSN 0003-9829. doi:10.4449/aib.v149i1.1260. （原始内容存档于2022-11-28）（英语）.
Carlesi, Cecilia; Pasquali, Livia; Piazza, Selina; Gerfo, Annalisa Lo; Ienco, Elena Caldarazzo; Alessi, Rosaria; Fornai, Francesco; Siciliano, Gabriele. Strategies for clinical approach to neurodegeneration in amyotrophic lateral sclerosis. Archives Italiennes de Biologie. 2011-03-10, 149 (1) [2022-11-09]. ISSN 0003-9829. doi:10.4449/aib.v149i1.1267. （原始内容存档于2022-11-04）（英语）.

arvojournals.org

iovs.arvojournals.org

Ahmadi, Mahboobah; Liu, Jing-Xia; Brännström, Thomas; Andersen, Peter M.; Stål, Per; Pedrosa-Domellöf, Fatima. Human Extraocular Muscles in ALS. Investigative Ophthalmology & Visual Science. 2010-07-01, 51 (7) [2022-11-09]. ISSN 1552-5783. doi:10.1167/iovs.09-5030. （原始内容存档于2022-11-09）（英语）.
Liu, Jing-Xia; Brännström, Thomas; Andersen, Peter M.; Pedrosa-Domellöf, Fatima. Different Impact of ALS on Laminin Isoforms in Human Extraocular Muscles versus Limb Muscles. Investigative Ophthalmology & Visual Science. 2011-06-01, 52 (7) [2022-11-09]. ISSN 1552-5783. doi:10.1167/iovs.10-7132. （原始内容存档于2022-11-09）（英语）.

bmj.com

jnnp.bmj.com

Chiò, Adriano; Calvo, Andrea; Moglia, Cristina; Mazzini, Letizia; Mora, Gabriele; Group*, PARALS study. Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study. Journal of Neurology, Neurosurgery & Psychiatry. 2011-07-01, 82 (7) [2022-11-09]. ISSN 0022-3050. PMID 21402743. doi:10.1136/jnnp.2010.235952. （原始内容存档于2022-10-28）（英语）.
Turner, M. R.; Parton, M. J.; Shaw, C. E.; Leigh, P. N.; Al-Chalabi, A. Prolonged survival in motor neuron disease: a descriptive study of the King’s database 1990–2002. Journal of Neurology, Neurosurgery & Psychiatry. 2003-07-01, 74 (7) [2022-11-09]. ISSN 0022-3050. PMC 1738535 . PMID 12810805. doi:10.1136/jnnp.74.7.995. （原始内容存档于2022-11-09）（英语）.
Davenport, R. J.; Swingler, R. J.; Chancellor, A. M.; Warlow, C. P. Avoiding false positive diagnoses of motor neuron disease: lessons from the Scottish Motor Neuron Disease Register.. Journal of Neurology, Neurosurgery & Psychiatry. 1996-02-01, 60 (2) [2022-11-09]. ISSN 0022-3050. PMC 1073793 . PMID 8708642. doi:10.1136/jnnp.60.2.147. （原始内容存档于2022-11-09）（英语）.

bmj.com

McDermott, Christopher J; Shaw, Pamela J. Diagnosis and management of motor neurone disease. BMJ. 2008-03-22, 336 (7645). ISSN 0959-8138. PMC 2270983 . PMID 18356234. doi:10.1136/bmj.39493.511759.BE （英语）.

cell.com

Johnson, Janel O.; Mandrioli, Jessica; Benatar, Michael; Abramzon, Yevgeniya; Deerlin, Vivianna M. Van; Trojanowski, John Q.; Gibbs, J. Raphael; Brunetti, Maura; Gronka, Susan; Wuu, Joanne; Ding, Jinhui. Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS. Neuron. 2010-12-09, 68 (5) [2022-11-09]. ISSN 0896-6273. PMC 3032425 . PMID 21145000. doi:10.1016/j.neuron.2010.11.036. （原始内容存档于2013-06-18）（英语）.
DeJesus-Hernandez, Mariely; Mackenzie, Ian R.; Boeve, Bradley F.; Boxer, Adam L.; Baker, Matt; Rutherford, Nicola J.; Nicholson, Alexandra M.; Finch, NiCole A.; Flynn, Heather; Adamson, Jennifer; Kouri, Naomi. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS. Neuron. 2011-10-20, 72 (2) [2022-11-09]. ISSN 0896-6273. PMC 3202986 . PMID 21944778. doi:10.1016/j.neuron.2011.09.011. （原始内容存档于2013-06-16）（英语）.
Buchan, J. Ross; Kolaitis, Regina-Maria; Taylor, J. Paul; Parker, Roy. Eukaryotic Stress Granules Are Cleared by Autophagy and Cdc48/VCP Function. Cell. 2013-06-20, 153 (7). ISSN 0092-8674. PMC 3760148 . PMID 23791177. doi:10.1016/j.cell.2013.05.037 （英语）.
Takahashi, Yuji; Fukuda, Yoko; Yoshimura, Jun; Toyoda, Atsushi; Kurppa, Kari; Moritoyo, Hiroyoko; Belzil, Veronique V.; Dion, Patrick A.; Higasa, Koichiro; Doi, Koichiro; Ishiura, Hiroyuki. ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19. The American Journal of Human Genetics. 2013-11-07, 93 (5). ISSN 0002-9297. PMC 3824132 . PMID 24119685. doi:10.1016/j.ajhg.2013.09.008 （英语）.
Boillée, Séverine; Velde, Christine Vande; Cleveland, Don W. ALS: A Disease of Motor Neurons and Their Nonneuronal Neighbors. Neuron. 2006-10-05, 52 (1) [2022-11-09]. ISSN 0896-6273. PMID 17015226. doi:10.1016/j.neuron.2006.09.018. （原始内容存档于2013-09-30）（英语）.

cnn.com

articles.cnn.com

Stephen Hawking serves as role model for ALS patients. CNN. 2009-04-20 [2015-06-26]. （原始内容存档于2012-09-25）.

corriere.it

Sla, indagini nei club. Pesticidi nel mirino. [2008-10-02]. （原始内容存档于2008年10月3日）.

doi.org

dx.doi.org

Kiernan, Matthew C.; Vucic, Steve; Cheah, Benjamin C.; Turner, Martin R.; Eisen, Andrew; Hardiman, Orla; Burrell, James R.; Zoing, Margaret C. Amyotrophic lateral sclerosis. The Lancet. 2011-03-12, 377 (9769) [2022-11-09]. ISSN 0140-6736. PMID 21296405. doi:10.1016/S0140-6736(10)61156-7. （原始内容存档于2014-08-29）（英语）.
Herrando‐Grabulosa, Mireia; Gaja‐Capdevila, Núria; Vela, José M.; Navarro, Xavier. Sigma 1 receptor as a therapeutic target for amyotrophic lateral sclerosis. British Journal of Pharmacology. 2021-03, 178 (6). ISSN 0007-1188. doi:10.1111/bph.15224 （英语）.
Miller, Robert G; Mitchell, J D; Moore, Dan H. Cochrane Neuromuscular Group , 编. Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND). Cochrane Database of Systematic Reviews. 2012-03-14. ISSN 1469-493X. PMC 7055506 . PMID 22419278. doi:10.1002/14651858.CD001447.pub3 （英语）.
McDermott, Christopher J; Shaw, Pamela J. Diagnosis and management of motor neurone disease. BMJ. 2008-03-22, 336 (7645). ISSN 0959-8138. PMC 2270983 . PMID 18356234. doi:10.1136/bmj.39493.511759.BE （英语）.
Rowland, Lewis P. How Amyotrophic Lateral Sclerosis Got Its Name: The Clinical-Pathologic Genius of Jean-Martin Charcot. Archives of Neurology. 2001-03-01, 58 (3). ISSN 0003-9942. doi:10.1001/archneur.58.3.512 （英语）.
Song, Peipei. The Ice Bucket Challenge: The public sector should get ready to promptly promote the sustained development of a system of medical care for and research into rare diseases. Intractable & Rare Diseases Research. 2014, 3 (3) [2022-11-09]. PMC 4214244 . PMID 25364651. doi:10.5582/irdr.2014.01015. （原始内容存档于2022-11-09）.
Phukan, Julie; Pender, Niall P.; Hardiman, Orla. Cognitive impairment in amyotrophic lateral sclerosis. The Lancet Neurology. 2007-11-01, 6 (11) [2022-11-09]. ISSN 1474-4422. PMID 17945153. doi:10.1016/S1474-4422(07)70265-X. （原始内容存档于2011-11-28）（英语）.
Johnson, Janel O.; Mandrioli, Jessica; Benatar, Michael; Abramzon, Yevgeniya; Deerlin, Vivianna M. Van; Trojanowski, John Q.; Gibbs, J. Raphael; Brunetti, Maura; Gronka, Susan; Wuu, Joanne; Ding, Jinhui. Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS. Neuron. 2010-12-09, 68 (5) [2022-11-09]. ISSN 0896-6273. PMC 3032425 . PMID 21145000. doi:10.1016/j.neuron.2010.11.036. （原始内容存档于2013-06-18）（英语）.
Castrillo-Viguera, Carmen; Grasso, Daniela L.; Simpson, Elizabeth; Shefner, Jeremy; Cudkowicz, Merit E. Clinical significance in the change of decline in ALSFRS-R. Amyotrophic Lateral Sclerosis: Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases. 2010, 11 (1-2) [2022-11-09]. ISSN 1471-180X. PMID 19634063. doi:10.3109/17482960903093710. （原始内容存档于2022-11-09）.
Sabatelli, M.; Madia, F.; Conte, A.; Luigetti, M.; Zollino, M.; Mancuso, I.; Monaco, M. Lo; Lippi, G.; Tonali, P. Natural history of young-adult amyotrophic lateral sclerosis. Neurology. 2008-09-16, 71 (12) [2022-11-09]. ISSN 0028-3878. PMID 18596241. doi:10.1212/01.wnl.0000312378.94737.45. （原始内容存档于2022-11-04）（英语）.
Chiò, Adriano; Calvo, Andrea; Moglia, Cristina; Mazzini, Letizia; Mora, Gabriele; Group*, PARALS study. Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study. Journal of Neurology, Neurosurgery & Psychiatry. 2011-07-01, 82 (7) [2022-11-09]. ISSN 0022-3050. PMID 21402743. doi:10.1136/jnnp.2010.235952. （原始内容存档于2022-10-28）（英语）.
Lopez-Lopez, Alan; Gamez, Josep; Syriani, Emilio; Morales, Miguel; Salvado, Maria; Rodríguez, Manuel J.; Mahy, Nicole; Vidal-Taboada, Jose M. CX3CR1 Is a Modifying Gene of Survival and Progression in Amyotrophic Lateral Sclerosis. PLOS ONE. 2014-05-07, 9 (5) [2022-12-09]. ISSN 1932-6203. PMC 4013026 . PMID 24806473. doi:10.1371/journal.pone.0096528. （原始内容存档于2022-11-09）（英语）.
Turner, M. R.; Parton, M. J.; Shaw, C. E.; Leigh, P. N.; Al-Chalabi, A. Prolonged survival in motor neuron disease: a descriptive study of the King’s database 1990–2002. Journal of Neurology, Neurosurgery & Psychiatry. 2003-07-01, 74 (7) [2022-11-09]. ISSN 0022-3050. PMC 1738535 . PMID 12810805. doi:10.1136/jnnp.74.7.995. （原始内容存档于2022-11-09）（英语）.
Kallestad, Kristen M.; Hebert, Sadie L.; McDonald, Abby A.; Daniel, Mark L.; Cu, Sharon R.; McLoon, Linda K. Sparing of extraocular muscle in aging and muscular dystrophies: A myogenic precursor cell hypothesis. Experimental Cell Research. 2011-04-01, 317 (6). ISSN 0014-4827. PMC 3072110 . PMID 21277300. doi:10.1016/j.yexcr.2011.01.018 （英语）.
Wingo, Thomas S.; Cutler, David J.; Yarab, Nicole; Kelly, Crystal M.; Glass, Jonathan D. The Heritability of Amyotrophic Lateral Sclerosis in a Clinically Ascertained United States Research Registry. PLOS ONE. 2011-11-22, 6 (11) [2022-12-09]. ISSN 1932-6203. PMC 3222666 . PMID 22132186. doi:10.1371/journal.pone.0027985. （原始内容存档于2022-11-04）（英语）.
Conwit, Robin A. Preventing familial ALS: A clinical trial may be feasible but is an efficacy trial warranted?. Journal of the Neurological Sciences. 2006-12-21, 251 (1). ISSN 0022-510X. PMID 17070848. doi:10.1016/j.jns.2006.07.009 （英语）.
Al-Chalabi, Ammar; Leigh, P. Nigel. Recent advances in amyotrophic lateral sclerosis. Current Opinion in Neurology. 2000-08, 13 (4) [2022-11-09]. ISSN 1350-7540. doi:10.1097/00019052-200008000-00006. （原始内容存档于2022-11-09）（美国英语）.
Battistini, Stefania; Ricci, Claudia; Lotti, Enrico Maria; Benigni, Michele; Gagliardi, Stella; Zucco, Riccardo; Bondavalli, Massimo; Marcello, Norina; Ceroni, Mauro; Cereda, Cristina. Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene. Journal of the Neurological Sciences. 2010-06-15, 293 (1). ISSN 0022-510X. PMID 20385392. doi:10.1016/j.jns.2010.03.009 （英语）.
Andersen, P. M.; Forsgren, L.; Binzer, M.; Nilsson, P.; Ala-Hurula, V.; Keranen, M.- L.; Bergmark, L.; Saarinen, A.; Haltia, T.; Tarvainen, I.; Kinnunen, E. Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation: A clinical and genealogical study of 36 patients. Brain. 1996-08-01, 119 (4) [2022-11-09]. ISSN 0006-8950. doi:10.1093/brain/119.4.1153. （原始内容存档于2022-06-16）（英语）.
DeJesus-Hernandez, Mariely; Mackenzie, Ian R.; Boeve, Bradley F.; Boxer, Adam L.; Baker, Matt; Rutherford, Nicola J.; Nicholson, Alexandra M.; Finch, NiCole A.; Flynn, Heather; Adamson, Jennifer; Kouri, Naomi. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS. Neuron. 2011-10-20, 72 (2) [2022-11-09]. ISSN 0896-6273. PMC 3202986 . PMID 21944778. doi:10.1016/j.neuron.2011.09.011. （原始内容存档于2013-06-16）（英语）.
Majounie, Elisa; Renton, Alan E.; Mok, Kin; Dopper, Elise GP; Waite, Adrian; Rollinson, Sara; Chiò, Adriano; Restagno, Gabriella; Nicolaou, Nayia; Simon-Sanchez, Javier; Swieten, John C. van. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. The Lancet Neurology. 2012-04-01, 11 (4) [2022-11-09]. ISSN 1474-4422. PMC 3322422 . PMID 22406228. doi:10.1016/S1474-4422(12)70043-1. （原始内容存档于2014-02-01）（英语）.
Deng, Han-Xiang; Chen, Wenjie; Hong, Seong-Tshool; Boycott, Kym M.; Gorrie, George H.; Siddique, Nailah; Yang, Yi; Fecto, Faisal; Shi, Yong; Zhai, Hong; Jiang, Hujun. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature. 2011-09, 477 (7363) [2022-11-09]. ISSN 1476-4687. PMC 3169705 . PMID 21857683. doi:10.1038/nature10353. （原始内容存档于2022-11-11）（英语）.
Buchan, J. Ross; Kolaitis, Regina-Maria; Taylor, J. Paul; Parker, Roy. Eukaryotic Stress Granules Are Cleared by Autophagy and Cdc48/VCP Function. Cell. 2013-06-20, 153 (7). ISSN 0092-8674. PMC 3760148 . PMID 23791177. doi:10.1016/j.cell.2013.05.037 （英语）.
Deng, Han-Xiang; Chen, Wenjie; Hong, Seong-Tshool; Boycott, Kym M.; Gorrie, George H.; Siddique, Nailah; Yang, Yi; Fecto, Faisal; Shi, Yong; Zhai, Hong; Jiang, Hujun. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature. 2011-09, 477 (7363) [2022-11-09]. ISSN 1476-4687. PMC 3169705 . PMID 21857683. doi:10.1038/nature10353. （原始内容存档于2022-11-11）（英语）.
Al-Saif, Amr; Al-Mohanna, Futwan; Bohlega, Saeed. A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis. Annals of Neurology. 2011-12, 70 (6) [2022-11-09]. ISSN 1531-8249. PMID 21842496. doi:10.1002/ana.22534. （原始内容存档于2022-11-11）.
Wu, Chi-Hong; Fallini, Claudia; Ticozzi, Nicola; Keagle, Pamela J.; Sapp, Peter C.; Piotrowska, Katarzyna; Lowe, Patrick; Koppers, Max; McKenna-Yasek, Diane; Baron, Desiree M.; Kost, Jason E. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis. Nature. 2012-08, 488 (7412) [2022-11-09]. ISSN 1476-4687. PMC 3575525 . PMID 22801503. doi:10.1038/nature11280. （原始内容存档于2022-11-09）（英语）.
Takahashi, Yuji; Fukuda, Yoko; Yoshimura, Jun; Toyoda, Atsushi; Kurppa, Kari; Moritoyo, Hiroyoko; Belzil, Veronique V.; Dion, Patrick A.; Higasa, Koichiro; Doi, Koichiro; Ishiura, Hiroyuki. ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19. The American Journal of Human Genetics. 2013-11-07, 93 (5). ISSN 0002-9297. PMC 3824132 . PMID 24119685. doi:10.1016/j.ajhg.2013.09.008 （英语）.
Kim, Hong Joo; Kim, Nam Chul; Wang, Yong-Dong; Scarborough, Emily A.; Moore, Jennifer; Diaz, Zamia; MacLea, Kyle S.; Freibaum, Brian; Li, Songqing; Molliex, Amandine; Kanagaraj, Anderson P. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. Nature. 2013-03, 495 (7442) [2022-11-09]. ISSN 1476-4687. PMC 3756911 . PMID 23455423. doi:10.1038/nature11922. （原始内容存档于2022-11-11）（英语）.
Bruijn, Lucie I.; Houseweart, Megan K.; Kato, Shinsuke; Anderson, Karen L.; Anderson, Scott D.; Ohama, Eisaku; Reaume, Andrew G.; Scott, Rick W.; Cleveland, Don W. Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1. Science. 1998-09-18, 281 (5384) [2022-11-09]. ISSN 0036-8075. doi:10.1126/science.281.5384.1851. （原始内容存档于2022-11-09）（英语）.
Reaume, Andrew G.; Elliott, Jeffrey L.; Hoffman, Eric K.; Kowall, Neil W.; Ferrante, Robert J.; Siwek, Donald R.; Wilcox, Heide M.; Flood, Dorothy G.; Beal, M. Flint; Brown, Robert H.; Scott, Richard W. Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury. Nature Genetics. 1996-05, 13 (1) [2022-11-09]. ISSN 1546-1718. doi:10.1038/ng0596-43. （原始内容存档于2022-11-09）（英语）.
Furukawa, Yoshiaki; Fu, Ronggen; Deng, Han-Xiang; Siddique, Teepu; O'Halloran, Thomas V. Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice. Proceedings of the National Academy of Sciences. 2006-05-02, 103 (18) [2022-11-09]. ISSN 0027-8424. PMC 1447524 . PMID 16636274. doi:10.1073/pnas.0602048103. （原始内容存档于2022-11-09）（英语）.
Boillée, Séverine; Velde, Christine Vande; Cleveland, Don W. ALS: A Disease of Motor Neurons and Their Nonneuronal Neighbors. Neuron. 2006-10-05, 52 (1) [2022-11-09]. ISSN 0896-6273. PMID 17015226. doi:10.1016/j.neuron.2006.09.018. （原始内容存档于2013-09-30）（英语）.
Manuel, Marin; Heckman, C. J. Stronger is not always better: Could a bodybuilding dietary supplement lead to ALS?. Experimental Neurology. 2011-03-01, 228 (1) [2022-11-09]. ISSN 0014-4886. PMC 3049458 . PMID 21167830. doi:10.1016/j.expneurol.2010.12.007. （原始内容存档于2015-09-24）（英语）.
Carunchio, Irene; Curcio, Livia; Pieri, Massimo; Pica, Francesca; Caioli, Silvia; Viscomi, Maria Teresa; Molinari, Marco; Canu, Nadia; Bernardi, Giorgio; Zona, Cristina. Increased levels of p70S6 phosphorylation in the G93A mouse model of Amyotrophic Lateral Sclerosis and in valine-exposed cortical neurons in culture. Experimental Neurology. 2010-11-01, 226 (1). ISSN 0014-4886. doi:10.1016/j.expneurol.2010.08.033 （英语）.
Fernández-Borges, Natalia; Eraña, Hasier; Elezgarai, Saioa R.; Harrathi, Chafik; Gayosso, Mayela; Castilla, Joaquín. Infectivity versus Seeding in Neurodegenerative Diseases Sharing a Prion-Like Mechanism. International Journal of Cell Biology. 2013-09-25, 2013 [2022-11-09]. ISSN 1687-8876. PMC 3800648 . PMID 24187553. doi:10.1155/2013/583498. （原始内容存档于2022-11-09）（英语）.
Holtcamp, Wendee. The Emerging Science of BMAA: Do Cyanobacteria Contribute to Neurodegenerative Disease?. Environmental Health Perspectives. 2012-03-01, 120 (3) [2022-11-09]. PMC 3295368 . PMID 22382274. doi:10.1289/ehp.120-a110. （原始内容存档于2022-11-09）.
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