脊髓性肌萎缩伴进行性肌阵挛性癫痫 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "脊髓性肌萎缩伴进行性肌阵挛性癫痫" in Chinese language version.

refsWebsite

Global rank Chinese rank

7nih.gov

4^th place

5^th place

5doi.org

2^nd place

23^rd place

2web.archive.org

1^st place

2worldcat.org

5^th place

12^th place

1archive.org

6^th place

4^th place

archive.org (Global: 6^th place; Chinese: 4^th place)

Jankovic, J.; Rivera, V. M. Hereditary myoclonus and progressive distal muscular atrophy. Annals of Neurology. 1979, 6 (3): 227–231. PMID 534421. doi:10.1002/ana.410060309.

doi.org (Global: 2^nd place; Chinese: 23^rd place)

Haliloglu, G.; Chattopadhyay, A.; Skorodis, L.; Manzur, A.; Mercuri, E.; Talim, B.; Akçören, Z.; Renda, Y.; Muntoni, F.; Topaloğlu, H. Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy: Report of New Cases and Review of the Literature. Neuropediatrics. 2002, 33 (6): 314–319. PMID 12571787. doi:10.1055/s-2002-37087.
Zhou, J.; Tawk, M.; Tiziano, F. D.; Veillet, J.; Bayes, M.; Nolent, F.; Garcia, V.; Servidei, S.; Bertini, E.; Castro-Giner, F.; Renda, Y.; Carpentier, S. P.; Andrieu-Abadie, N.; Gut, I.; Levade, T.; Topaloglu, H.; Melki, J. Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy is Caused by Mutations in ASAH1. The American Journal of Human Genetics. 2012, 91 (1): 5–14. PMC 3397266 . PMID 22703880. doi:10.1016/j.ajhg.2012.05.001.
Gan, Joanna J.; Garcia, Virginie; Tian, Jane; Tagliati, Michele; Parisi, Joseph E.; Chung, Jeffrey M.; Lewis, Richard; Baloh, Robert; Levade, Thierry; Pierson, Tyler Mark. Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsy. Neuromuscular Disorders. 2015-12-01, 25 (12): 959–963. ISSN 0960-8966. PMID 26526000. doi:10.1016/j.nmd.2015.09.007 （英语）.
Jankovic, J.; Rivera, V. M. Hereditary myoclonus and progressive distal muscular atrophy. Annals of Neurology. 1979, 6 (3): 227–231. PMID 534421. doi:10.1002/ana.410060309.
Park, Jae-Ho; Schuchman, Edward H. Acid ceramidase and human disease. Biochimica et Biophysica Acta. December 2006, 1758 (12): 2133–2138. ISSN 0006-3002. PMID 17064658. doi:10.1016/j.bbamem.2006.08.019.

nih.gov (Global: 4^th place; Chinese: 5^th place)

ncbi.nlm.nih.gov

Haliloglu, G.; Chattopadhyay, A.; Skorodis, L.; Manzur, A.; Mercuri, E.; Talim, B.; Akçören, Z.; Renda, Y.; Muntoni, F.; Topaloğlu, H. Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy: Report of New Cases and Review of the Literature. Neuropediatrics. 2002, 33 (6): 314–319. PMID 12571787. doi:10.1055/s-2002-37087.
Zhou, J.; Tawk, M.; Tiziano, F. D.; Veillet, J.; Bayes, M.; Nolent, F.; Garcia, V.; Servidei, S.; Bertini, E.; Castro-Giner, F.; Renda, Y.; Carpentier, S. P.; Andrieu-Abadie, N.; Gut, I.; Levade, T.; Topaloglu, H.; Melki, J. Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy is Caused by Mutations in ASAH1. The American Journal of Human Genetics. 2012, 91 (1): 5–14. PMC 3397266 . PMID 22703880. doi:10.1016/j.ajhg.2012.05.001.
Gan, Joanna J.; Garcia, Virginie; Tian, Jane; Tagliati, Michele; Parisi, Joseph E.; Chung, Jeffrey M.; Lewis, Richard; Baloh, Robert; Levade, Thierry; Pierson, Tyler Mark. Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsy. Neuromuscular Disorders. 2015-12-01, 25 (12): 959–963. ISSN 0960-8966. PMID 26526000. doi:10.1016/j.nmd.2015.09.007 （英语）.
Jankovic, J.; Rivera, V. M. Hereditary myoclonus and progressive distal muscular atrophy. Annals of Neurology. 1979, 6 (3): 227–231. PMID 534421. doi:10.1002/ana.410060309.
Park, Jae-Ho; Schuchman, Edward H. Acid ceramidase and human disease. Biochimica et Biophysica Acta. December 2006, 1758 (12): 2133–2138. ISSN 0006-3002. PMID 17064658. doi:10.1016/j.bbamem.2006.08.019.
Morell, Pierre; Quarles, Richard H. The Myelin Sheath. Basic Neurochemistry: Molecular, Cellular and Medical Aspects. 6th Edition. 1999 [2019-09-21]. （原始内容存档于2020-11-11）（英语）.

ghr.nlm.nih.gov

Reference, Genetics Home. Spinal muscular atrophy with progressive myoclonic epilepsy. Genetics Home Reference. [2018-09-24]. （原始内容存档于2020-10-01）（英语）.

web.archive.org (Global: 1^st place; Chinese: 1^st place)

Reference, Genetics Home. Spinal muscular atrophy with progressive myoclonic epilepsy. Genetics Home Reference. [2018-09-24]. （原始内容存档于2020-10-01）（英语）.
Morell, Pierre; Quarles, Richard H. The Myelin Sheath. Basic Neurochemistry: Molecular, Cellular and Medical Aspects. 6th Edition. 1999 [2019-09-21]. （原始内容存档于2020-11-11）（英语）.

worldcat.org (Global: 5^th place; Chinese: 12^th place)

Gan, Joanna J.; Garcia, Virginie; Tian, Jane; Tagliati, Michele; Parisi, Joseph E.; Chung, Jeffrey M.; Lewis, Richard; Baloh, Robert; Levade, Thierry; Pierson, Tyler Mark. Acid ceramidase deficiency associated with spinal muscular atrophy with progressive myoclonic epilepsy. Neuromuscular Disorders. 2015-12-01, 25 (12): 959–963. ISSN 0960-8966. PMID 26526000. doi:10.1016/j.nmd.2015.09.007 （英语）.
Park, Jae-Ho; Schuchman, Edward H. Acid ceramidase and human disease. Biochimica et Biophysica Acta. December 2006, 1758 (12): 2133–2138. ISSN 0006-3002. PMID 17064658. doi:10.1016/j.bbamem.2006.08.019.

脊髓性肌萎缩伴进行性肌阵挛性癫痫 (Chinese Wikipedia)

archive.org (Global: 6th place; Chinese: 4th place)

doi.org (Global: 2nd place; Chinese: 23rd place)

nih.gov (Global: 4th place; Chinese: 5th place)