4-Aminopyridine (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "4-Aminopyridine" in English language version.

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  • Albert A, Goldacre R, Phillips J (1948). "455. The strength of heterocyclic bases". Journal of the Chemical Society (Resumed): 2240–2249. doi:10.1039/JR9480002240.
  • Solari A, Uitdehaag B, Giuliani G, Pucci E, Taus C (2002). Solari A (ed.). "Aminopyridines for symptomatic treatment in multiple sclerosis". The Cochrane Database of Systematic Reviews (4): CD001330. doi:10.1002/14651858.CD001330. PMC 7047571. PMID 12804404.
  • Korenke AR, Rivey MP, Allington DR (October 2008). "Sustained-release fampridine for symptomatic treatment of multiple sclerosis". The Annals of Pharmacotherapy. 42 (10): 1458–1465. doi:10.1345/aph.1L028. PMID 18780812. S2CID 207263182.
  • Wu ZZ, Li DP, Chen SR, Pan HL (December 2009). "Aminopyridines potentiate synaptic and neuromuscular transmission by targeting the voltage-activated calcium channel beta subunit". The Journal of Biological Chemistry. 284 (52): 36453–36461. doi:10.1074/jbc.M109.075523. PMC 2794761. PMID 19850918.
  • Yamaguchi S, Rogawski MA (March 1992). "Effects of anticonvulsant drugs on 4-aminopyridine-induced seizures in mice". Epilepsy Research. 11 (1): 9–16. doi:10.1016/0920-1211(92)90016-m. PMID 1563341. S2CID 5772125.
  • Judge SI, Bever CT (July 2006). "Potassium channel blockers in multiple sclerosis: neuronal Kv channels and effects of symptomatic treatment". Pharmacology & Therapeutics. 111 (1): 224–259. doi:10.1016/j.pharmthera.2005.10.006. PMID 16472864.
  • Chang FC, Spriggs DL, Benton BJ, Keller SA, Capacio BR (July 1997). "4-Aminopyridine reverses saxitoxin (STX)- and tetrodotoxin (TTX)-induced cardiorespiratory depression in chronically instrumented guinea pigs". Fundamental and Applied Toxicology. 38 (1): 75–88. doi:10.1006/faat.1997.2328. PMID 9268607. S2CID 17185707.
  • Chen HM, Lin CH, Wang TM (November 1996). "Effects of 4-aminopyridine on saxitoxin intoxication". Toxicology and Applied Pharmacology. 141 (1): 44–48. doi:10.1006/taap.1996.0258. PMID 8917674.
  • Valet M, Quoilin M, Lejeune T, Stoquart G, Van Pesch V, El Sankari S, et al. (November 2019). "Effects of Fampridine in People with Multiple Sclerosis: A Systematic Review and Meta-analysis". CNS Drugs. 33 (11): 1087–1099. doi:10.1007/s40263-019-00671-x. PMID 31612418. S2CID 204543081.
  • Wu ZZ, Li DP, Chen SR, Pan HL (December 2009). "Aminopyridines potentiate synaptic and neuromuscular transmission by targeting the voltage-activated calcium channel beta subunit". The Journal of Biological Chemistry. 284 (52): 36453–36461. doi:10.1074/jbc.M109.075523. PMC 2794761. PMID 19850918.
  • Van Diemen HA, Polman CH, Koetsier JC, Van Loenen AC, Nauta JJ, Bertelsmann FW (June 1993). "4-Aminopyridine in patients with multiple sclerosis: dosage and serum level related to efficacy and safety". Clinical Neuropharmacology. 16 (3): 195–204. doi:10.1097/00002826-199306000-00002. PMID 8504436.
  • Pickett TA, Enns R (March 1996). "Atypical presentation of 4-aminopyridine overdose". Annals of Emergency Medicine. 27 (3): 382–385. doi:10.1016/S0196-0644(96)70277-9. PMID 8599505.
  • Johnson NC, Morgan MW (February 2006). "An unusual case of 4-aminopyridine toxicity". The Journal of Emergency Medicine. 30 (2): 175–177. doi:10.1016/j.jemermed.2005.04.020. PMID 16567254.
  • Gardner TS, Wenis E, Lee J (1954). "The Synthesis of Compounds for the Chemotherapy of Tuberculosis. Iv. The Amide Function". The Journal of Organic Chemistry. 19 (5): 753. doi:10.1021/jo01370a009.

drugs.com

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  • "Fampyra Drug Monograph" (PDF). Health Canada Drug Product Database. Biogen Idec Canada Inc. 26 November 2014. Retrieved 10 October 2017.

hsus.org

medicines.org.uk

medscape.com

nationalmssociety.org

  • "Ampyra". National Multiple Sclerosis Society.

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

dailymed.nlm.nih.gov

njmonline.nl

registrationwala.com

seekingalpha.com

semanticscholar.org

api.semanticscholar.org

  • Korenke AR, Rivey MP, Allington DR (October 2008). "Sustained-release fampridine for symptomatic treatment of multiple sclerosis". The Annals of Pharmacotherapy. 42 (10): 1458–1465. doi:10.1345/aph.1L028. PMID 18780812. S2CID 207263182.
  • Yamaguchi S, Rogawski MA (March 1992). "Effects of anticonvulsant drugs on 4-aminopyridine-induced seizures in mice". Epilepsy Research. 11 (1): 9–16. doi:10.1016/0920-1211(92)90016-m. PMID 1563341. S2CID 5772125.
  • Chang FC, Spriggs DL, Benton BJ, Keller SA, Capacio BR (July 1997). "4-Aminopyridine reverses saxitoxin (STX)- and tetrodotoxin (TTX)-induced cardiorespiratory depression in chronically instrumented guinea pigs". Fundamental and Applied Toxicology. 38 (1): 75–88. doi:10.1006/faat.1997.2328. PMID 9268607. S2CID 17185707.
  • Valet M, Quoilin M, Lejeune T, Stoquart G, Van Pesch V, El Sankari S, et al. (November 2019). "Effects of Fampridine in People with Multiple Sclerosis: A Systematic Review and Meta-analysis". CNS Drugs. 33 (11): 1087–1099. doi:10.1007/s40263-019-00671-x. PMID 31612418. S2CID 204543081.

tga.gov.au

web.archive.org