Spastic paraplegia 6 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Spastic paraplegia 6" in English language version.

refsWebsite

Global rank English rank

5nih.gov

4^th place

3doi.org

2^nd place

3worldcat.org

5^th place

2semanticscholar.org

11^th place

8^th place

1rarediseases.org

5,181^st place

3,260^th place

1orpha.net

3,537^th place

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1medscape.com

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636^th place

1hopkinsmedicine.org

5,712^th place

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1ivami.com

low place

1omim.org

4,380^th place

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doi.org

Reed, Johanna A.; Wilkinson, Phillip A.; Patel, Heema; Simpson, Michael A.; Chatonnet, Arnaud; Robay, Dimitri; Patton, Michael A.; Crosby, Andrew H.; Warner, Thomas T. (2005-05-01). "A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia". Neurogenetics. 6 (2): 79–84. doi:10.1007/s10048-004-0209-9. ISSN 1364-6745. PMID 15711826. S2CID 2236413.
Fink, J. K.; Sharp, G. B.; Lange, B. M.; Wu, C. B.; Haley, T.; Otterud, B.; Peacock, M.; Leppert, M. (1995-02-01). "Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family". Neurology. 45 (2): 325–331. doi:10.1212/wnl.45.2.325. ISSN 0028-3878. PMID 7854534. S2CID 33624423.
Rainier, Shirley; Chai, Jing-Hua; Tokarz, Debra; Nicholls, Robert D.; Fink, John K. (2003-10-01). "NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)". American Journal of Human Genetics. 73 (4): 967–971. doi:10.1086/378817. ISSN 0002-9297. PMC 1180617. PMID 14508710.

hopkinsmedicine.org

"Spasticity". www.hopkinsmedicine.org. 2021-08-08. Retrieved 2022-07-01.

ivami.com

"Genetic Testing - familial spastic paraplegia type 6 (Spastic paraplegia type 6 -SPG6-) - Gen NIPA1 . - IVAMI". www.ivami.com. Retrieved 2022-07-01.

medscape.com

emedicine.medscape.com

"Pes Cavus: Practice Essentials, Etiology, Prognosis". 2021-05-07. {{cite journal}}: Cite journal requires |journal= (help)

nih.gov

pubmed.ncbi.nlm.nih.gov

Reed, Johanna A.; Wilkinson, Phillip A.; Patel, Heema; Simpson, Michael A.; Chatonnet, Arnaud; Robay, Dimitri; Patton, Michael A.; Crosby, Andrew H.; Warner, Thomas T. (2005-05-01). "A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia". Neurogenetics. 6 (2): 79–84. doi:10.1007/s10048-004-0209-9. ISSN 1364-6745. PMID 15711826. S2CID 2236413.
Fink, J. K.; Sharp, G. B.; Lange, B. M.; Wu, C. B.; Haley, T.; Otterud, B.; Peacock, M.; Leppert, M. (1995-02-01). "Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family". Neurology. 45 (2): 325–331. doi:10.1212/wnl.45.2.325. ISSN 0028-3878. PMID 7854534. S2CID 33624423.
Rainier, Shirley; Chai, Jing-Hua; Tokarz, Debra; Nicholls, Robert D.; Fink, John K. (2003-10-01). "NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)". American Journal of Human Genetics. 73 (4): 967–971. doi:10.1086/378817. ISSN 0002-9297. PMC 1180617. PMID 14508710.

rarediseases.info.nih.gov

"Spastic paraplegia 6 - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-07-01.

ncbi.nlm.nih.gov

Rainier, Shirley; Chai, Jing-Hua; Tokarz, Debra; Nicholls, Robert D.; Fink, John K. (2003-10-01). "NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)". American Journal of Human Genetics. 73 (4): 967–971. doi:10.1086/378817. ISSN 0002-9297. PMC 1180617. PMID 14508710.

omim.org

"Entry - #600363 - Spastic paraplegia 6, autosomal dominant; SPG6 - OMIM". omim.org. Retrieved 2022-07-01.

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Autosomal dominant spastic paraplegia type 6". www.orpha.net. Retrieved 2022-07-01.{{cite web}}: CS1 maint: numeric names: authors list (link)

rarediseases.org

"Spastic paraplegia 6". 16 June 2022.

semanticscholar.org

api.semanticscholar.org

Reed, Johanna A.; Wilkinson, Phillip A.; Patel, Heema; Simpson, Michael A.; Chatonnet, Arnaud; Robay, Dimitri; Patton, Michael A.; Crosby, Andrew H.; Warner, Thomas T. (2005-05-01). "A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia". Neurogenetics. 6 (2): 79–84. doi:10.1007/s10048-004-0209-9. ISSN 1364-6745. PMID 15711826. S2CID 2236413.
Fink, J. K.; Sharp, G. B.; Lange, B. M.; Wu, C. B.; Haley, T.; Otterud, B.; Peacock, M.; Leppert, M. (1995-02-01). "Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family". Neurology. 45 (2): 325–331. doi:10.1212/wnl.45.2.325. ISSN 0028-3878. PMID 7854534. S2CID 33624423.

worldcat.org

search.worldcat.org

Reed, Johanna A.; Wilkinson, Phillip A.; Patel, Heema; Simpson, Michael A.; Chatonnet, Arnaud; Robay, Dimitri; Patton, Michael A.; Crosby, Andrew H.; Warner, Thomas T. (2005-05-01). "A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia". Neurogenetics. 6 (2): 79–84. doi:10.1007/s10048-004-0209-9. ISSN 1364-6745. PMID 15711826. S2CID 2236413.
Fink, J. K.; Sharp, G. B.; Lange, B. M.; Wu, C. B.; Haley, T.; Otterud, B.; Peacock, M.; Leppert, M. (1995-02-01). "Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family". Neurology. 45 (2): 325–331. doi:10.1212/wnl.45.2.325. ISSN 0028-3878. PMID 7854534. S2CID 33624423.
Rainier, Shirley; Chai, Jing-Hua; Tokarz, Debra; Nicholls, Robert D.; Fink, John K. (2003-10-01). "NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)". American Journal of Human Genetics. 73 (4): 967–971. doi:10.1086/378817. ISSN 0002-9297. PMC 1180617. PMID 14508710.