セレギリン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "セレギリン" in Japanese language version.

refsWebsite

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38nih.gov

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23doi.org

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5books.google.com

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61^st place

3drugs.com

399^th place

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3worldcat.org

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2fda.gov

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2espacenet.com

800^th place

2,213^th place

1sagepub.com

731^st place

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1inhn.org

low place

1patents.google.com

1,182^nd place

1,387^th place

1thepharmaletter.com

low place

1springer.de

low place

1harvard.edu

18^th place

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1nytimes.com

7^th place

63^rd place

1ecstasy.org

low place

1web.archive.org

1^st place

1lloydinc.com

low place

1veterinarypartner.com

low place

books.google.com

Factor, Steward A.; Weiner, William (2007). Parkinson's Disease: Diagnosis & Clinical Management (2nd ed.). Demos Medical Publishing. pp. 503, 505. ISBN 978-1-934559-87-1
Magyar, Kálmán (2011). “The pharmacology of selegiline”. In Youdim, Moussa. Monoamine Oxidases and Their Inhibitors. International Review of Neurobiology. 100. Academic Press. ISBN 978-0-12-386468-0
Eghianruwa, Kingsley (2014). Essential Drug Data for Rational Therapy in Veterinary Practice. AuthorHouse. pp. 127–128. ISBN 978-1-4918-0010-2
Riviere, Jim E.; Papich, Mark G. (2013). Veterinary Pharmacology and Therapeutics. John Wiley & Sons. pp. 530. ISBN 978-1-118-68590-7
Papich, Mark G. (2015). Saunders Handbook of Veterinary Drugs: Small and Large Animal. Elsevier Health Sciences. p. 722. ISBN 978-0-323-24485-5

doi.org

“Clinical applications of MAO-inhibitors”. Current Medicinal Chemistry 11 (15): 2033–43. (August 2004). doi:10.2174/0929867043364775. PMID 15279566.
“Monoamine oxidase type B inhibitors in early Parkinson's disease: meta-analysis of 17 randomised trials involving 3525 patients”. BMJ 329 (7466): 593. (September 2004). doi:10.1136/bmj.38184.606169.AE. PMC 516655. PMID 15310558.
“Selegiline's neuroprotective capacity revisited”. Journal of Neural Transmission 110 (11): 1273–8. (November 2003). doi:10.1007/s00702-003-0083-x. PMID 14628191.
“Placing transdermal selegiline for major depressive disorder into clinical context: number needed to treat, number needed to harm, and likelihood to be helped or harmed”. Journal of Affective Disorders 151 (2): 409–17. (November 2013). doi:10.1016/j.jad.2013.06.027. PMID 23890583.
Mohammadi MR, Ghanizadeh A, Alaghband-Rad J, Tehranidoost M, Mesgarpour B, Soori H (2004). “Selegiline in comparison with methylphenidate in attention deficit hyperactivity disorder children and adolescents in a double-blind, randomized clinical trial.”. J Child Adolesc Psychopharmacol 14 (3): 418–25. doi:10.1089/cap.2004.14.418. PMID 15650498.
Akhondzadeh S, Tavakolian R, Davari-Ashtiani R, Arabgol F, Amini H (2003). “Selegiline in the treatment of attention deficit hyperactivity disorder in children: a double blind and randomized trial.”. Prog Neuropsychopharmacol Biol Psychiatry 27 (5): 841–5. doi:10.1016/S0278-5846(03)00117-9. PMID 12921918.
Rubinstein S, Malone MA, Roberts W, Logan WJ (2006). “Placebo-controlled study examining effects of selegiline in children with attention-deficit/hyperactivity disorder.”. J Child Adolesc Psychopharmacol 16 (4): 404–15. doi:10.1089/cap.2006.16.404. PMID 16958566.
“Expanding the black box - depression, antidepressants, and the risk of suicide”. The New England Journal of Medicine 356 (23): 2343–6. (June 2007). doi:10.1056/NEJMp078015. PMID 17485726.
“Safety of selegiline (deprenyl) in the treatment of Parkinson's disease”. Drug Safety 19 (1): 11–22. (July 1998). doi:10.2165/00002018-199819010-00002. PMID 9673855.
Csoti, Ilona; Storch, Alexander; Müller, Walter; Jost, Wolfgang H. (December 1, 2012). “Drug interactions with selegiline versus rasagiline”. Basal Ganglia 2 (4, Supplement): S27–S31. doi:10.1016/j.baga.2012.06.003. ISSN 2210-5336.
“Monoamine oxidase inhibitors, opioid analgesics and serotonin toxicity”. British Journal of Anaesthesia 95 (4): 434–41. (October 2005). doi:10.1093/bja/aei210. PMID 16051647.
“Dose linearity study of selegiline pharmacokinetics after oral administration: evidence for strong drug interaction with female sex steroids”. British Journal of Clinical Pharmacology 47 (3): 249–54. (March 1999). doi:10.1046/j.1365-2125.1999.00891.x. PMC 2014223. PMID 10215747.
“Selegiline is a mechanism-based inactivator of CYP2A6 inhibiting nicotine metabolism in humans and mice”. The Journal of Pharmacology and Experimental Therapeutics 324 (3): 992–9. (March 2008). doi:10.1124/jpet.107.133900. PMID 18065502.
“Absorption and presystemic metabolism of selegiline hydrochloride at different regions in the gastrointestinal tract in healthy males”. Pharmaceutical Research 13 (10): 1535–40. (October 1996). doi:10.1023/A:1016035730754. PMID 8899847.
“A new formulation of selegiline: improved bioavailability and selectivity for MAO-B inhibition”. Journal of Neural Transmission 110 (11): 1241–55. (November 2003). doi:10.1007/s00702-003-0036-4. PMID 14628189.
“Selegiline metabolism and cytochrome P450 enzymes: in vitro study in human liver microsomes”. Pharmacology & Toxicology 86 (5): 215–21. (May 2000). doi:10.1034/j.1600-0773.2000.pto860504.x. PMID 10862503.
“Methamphetamine and amphetamine derived from the metabolism of selegiline”. Journal of Forensic Sciences 40 (6): 1100–2. (November 1995). doi:10.1520/JFS13885J. PMID 8522918.
“Contrasting neuroprotective and neurotoxic actions of respective metabolites of anti-Parkinson drugs rasagiline and selegiline”. Neuroscience Letters 355 (3): 169–72. (January 2004). doi:10.1016/j.neulet.2003.10.067. PMID 14732458.
“Are metabolites of l-deprenyl (selegiline) useful or harmful? Indications from preclinical research”. Journal of Neural Transmission. Supplementum 48: 61–73. (January 1, 1996). doi:10.1007/978-3-7091-7494-4_6. ISBN 978-3-211-82891-5. PMID 8988462.
“Clinical pharmacology of rasagiline: a novel, second-generation propargylamine for the treatment of Parkinson disease”. Journal of Clinical Pharmacology 45 (8): 878–94. (August 2005). doi:10.1177/0091270005277935. PMID 16027398.
“2-Methyl-3-butyn-2-ol as an acetylene precursor in the Mannich reaction. A new synthesis of suicide inactivators of monoamine oxidase”. The Journal of Organic Chemistry 42 (15): 2637–7. (July 1977). doi:10.1021/jo00435a026. PMID 874623.
“The potentiation of the anti akinetic effect after L-dopa treatment by an inhibitor of MAO-B, Deprenil”. Journal of Neural Transmission 36 (3–4): 303–26. (1975). doi:10.1007/BF01253131. PMID 1172524.
“Selegiline transdermal system: in the treatment of major depressive disorder”. Drugs 67 (2): 257–65; discussion 266–7. (2007). doi:10.2165/00003495-200767020-00006. PMID 17284087.

drugs.com

“Selegiline”. Drugs.com. February 7, 2016閲覧。
“Selegiline Hydrochloride Monograph for Professionals”. Drugs.com. February 23, 2018閲覧。
“Anipryl Tablets for Animal Use”. Drugs.com. August 31, 2017閲覧。

ecstasy.org

Saunders. “Test results of 30 samples of Ecstasy bought in British clubs between 11/94 and 7/95”. 2020年3月31日閲覧。

espacenet.com

worldwide.espacenet.com

J. Knoll, E. Sanfai, DE 1568277 (1966).
B. Brunova, M. Ferenc, EP 344675 (1989)

fda.gov

accessdata.fda.gov

Selegiline oral label. Updated December 31, 2008
Emsam label Last revised Sept 2014. Index page at FDA

harvard.edu

news.harvard.edu

Cromie (November 7, 2002). “Bodkin is Patching up Depression”. Harvard University Gazette. September 8, 2007閲覧。

inhn.org

Miklya (March 13, 2014). “The History of Selegiline/(-)-Deprenyl the First Selective Inhibitor of B-Type Monoamine Oxidase and The First Synthetic Catecholaminergic Activity Enhancer Substance” (英語). International Network for the History of Neuropsychopharmacology. January 7, 2016閲覧。

lloydinc.com

“Selegiline Treatment of Canine Pituitary-Dependent Hyperadrenocorticism”. Australian Veterinary Journal (2004年). November 29, 2010時点のオリジナルよりアーカイブ。April 8, 2011閲覧。 (PDF)

nih.gov

pubmed.ncbi.nlm.nih.gov

“Clinical applications of MAO-inhibitors”. Current Medicinal Chemistry 11 (15): 2033–43. (August 2004). doi:10.2174/0929867043364775. PMID 15279566.
“Monoamine oxidase type B inhibitors in early Parkinson's disease: meta-analysis of 17 randomised trials involving 3525 patients”. BMJ 329 (7466): 593. (September 2004). doi:10.1136/bmj.38184.606169.AE. PMC 516655. PMID 15310558.
“Selegiline's neuroprotective capacity revisited”. Journal of Neural Transmission 110 (11): 1273–8. (November 2003). doi:10.1007/s00702-003-0083-x. PMID 14628191.
“Placing transdermal selegiline for major depressive disorder into clinical context: number needed to treat, number needed to harm, and likelihood to be helped or harmed”. Journal of Affective Disorders 151 (2): 409–17. (November 2013). doi:10.1016/j.jad.2013.06.027. PMID 23890583.
Mohammadi MR, Ghanizadeh A, Alaghband-Rad J, Tehranidoost M, Mesgarpour B, Soori H (2004). “Selegiline in comparison with methylphenidate in attention deficit hyperactivity disorder children and adolescents in a double-blind, randomized clinical trial.”. J Child Adolesc Psychopharmacol 14 (3): 418–25. doi:10.1089/cap.2004.14.418. PMID 15650498.
Akhondzadeh S, Tavakolian R, Davari-Ashtiani R, Arabgol F, Amini H (2003). “Selegiline in the treatment of attention deficit hyperactivity disorder in children: a double blind and randomized trial.”. Prog Neuropsychopharmacol Biol Psychiatry 27 (5): 841–5. doi:10.1016/S0278-5846(03)00117-9. PMID 12921918.
Rubinstein S, Malone MA, Roberts W, Logan WJ (2006). “Placebo-controlled study examining effects of selegiline in children with attention-deficit/hyperactivity disorder.”. J Child Adolesc Psychopharmacol 16 (4): 404–15. doi:10.1089/cap.2006.16.404. PMID 16958566.
“Deprenyl (selegiline), a selective MAO-B inhibitor with active metabolites; effects on locomotor activity, dopaminergic neurotransmission and firing rate of nigral dopamine neurons”. The Journal of Pharmacology and Experimental Therapeutics 259 (2): 841–7. (November 1991). PMID 1658311.
“Expanding the black box - depression, antidepressants, and the risk of suicide”. The New England Journal of Medicine 356 (23): 2343–6. (June 2007). doi:10.1056/NEJMp078015. PMID 17485726.
“Safety of selegiline (deprenyl) in the treatment of Parkinson's disease”. Drug Safety 19 (1): 11–22. (July 1998). doi:10.2165/00002018-199819010-00002. PMID 9673855.
“Monoamine oxidase inhibitors, opioid analgesics and serotonin toxicity”. British Journal of Anaesthesia 95 (4): 434–41. (October 2005). doi:10.1093/bja/aei210. PMID 16051647.
“Dose linearity study of selegiline pharmacokinetics after oral administration: evidence for strong drug interaction with female sex steroids”. British Journal of Clinical Pharmacology 47 (3): 249–54. (March 1999). doi:10.1046/j.1365-2125.1999.00891.x. PMC 2014223. PMID 10215747.
“The selegiline transdermal system (emsam): a therapeutic option for the treatment of major depressive disorder”. P & T 33 (4): 212–46. (April 2008). PMC 2730099. PMID 19750165.
“Selegiline is a mechanism-based inactivator of CYP2A6 inhibiting nicotine metabolism in humans and mice”. The Journal of Pharmacology and Experimental Therapeutics 324 (3): 992–9. (March 2008). doi:10.1124/jpet.107.133900. PMID 18065502.
“Absorption and presystemic metabolism of selegiline hydrochloride at different regions in the gastrointestinal tract in healthy males”. Pharmaceutical Research 13 (10): 1535–40. (October 1996). doi:10.1023/A:1016035730754. PMID 8899847.
“A new formulation of selegiline: improved bioavailability and selectivity for MAO-B inhibition”. Journal of Neural Transmission 110 (11): 1241–55. (November 2003). doi:10.1007/s00702-003-0036-4. PMID 14628189.
“Selegiline metabolism and cytochrome P450 enzymes: in vitro study in human liver microsomes”. Pharmacology & Toxicology 86 (5): 215–21. (May 2000). doi:10.1034/j.1600-0773.2000.pto860504.x. PMID 10862503.
“Methamphetamine and amphetamine derived from the metabolism of selegiline”. Journal of Forensic Sciences 40 (6): 1100–2. (November 1995). doi:10.1520/JFS13885J. PMID 8522918.
“Contrasting neuroprotective and neurotoxic actions of respective metabolites of anti-Parkinson drugs rasagiline and selegiline”. Neuroscience Letters 355 (3): 169–72. (January 2004). doi:10.1016/j.neulet.2003.10.067. PMID 14732458.
“Are metabolites of l-deprenyl (selegiline) useful or harmful? Indications from preclinical research”. Journal of Neural Transmission. Supplementum 48: 61–73. (January 1, 1996). doi:10.1007/978-3-7091-7494-4_6. ISBN 978-3-211-82891-5. PMID 8988462.
“Clinical pharmacology of rasagiline: a novel, second-generation propargylamine for the treatment of Parkinson disease”. Journal of Clinical Pharmacology 45 (8): 878–94. (August 2005). doi:10.1177/0091270005277935. PMID 16027398.
“2-Methyl-3-butyn-2-ol as an acetylene precursor in the Mannich reaction. A new synthesis of suicide inactivators of monoamine oxidase”. The Journal of Organic Chemistry 42 (15): 2637–7. (July 1977). doi:10.1021/jo00435a026. PMID 874623.
“Phenylisopropylmethylpropinylamine (E-250), a new spectrum psychic energizer”. Archives Internationales de Pharmacodynamie et de Therapie 155 (1): 154–64. (May 1965). PMID 4378644.
“Comparative pharmacological analysis of the optical isomers of phenyl-isopropyl-methyl-propinylamine (E-250)”. Acta Physiologica Academiae Scientiarum Hungaricae 32 (4): 377–87. (1967). PMID 5595908.
“The potentiation of the anti akinetic effect after L-dopa treatment by an inhibitor of MAO-B, Deprenil”. Journal of Neural Transmission 36 (3–4): 303–26. (1975). doi:10.1007/BF01253131. PMID 1172524.
“Selegiline transdermal system: in the treatment of major depressive disorder”. Drugs 67 (2): 257–65; discussion 266–7. (2007). doi:10.2165/00003495-200767020-00006. PMID 17284087.
“Emsam: the first year”. Psychiatry 4 (6): 19–21. (June 2007). PMC 2921248. PMID 20711332.

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

nytimes.com

Duffy, Mary (3 December 2002). “Patch Raises New Hope For Beating Depression”. The New York Times. ISSN 0362-4331

patents.google.com

J. Hermann Nee Voeroes, Z. Ecsery, G. Sabo, L. Arvai, L. Nagi, O. Orban, E. Sanfai, アメリカ合衆国特許第 4,564,706号 (1986)

sagepub.com

jcp.sagepub.com

“Clinical pharmacology of rasagiline: a novel, second-generation propargylamine for the treatment of Parkinson disease”. Journal of Clinical Pharmacology 45 (8): 878–94. (August 2005). doi:10.1177/0091270005277935. PMID 16027398.

springer.de

link.springer.de

“The potentiation of the anti akinetic effect after L-dopa treatment by an inhibitor of MAO-B, Deprenil”. Journal of Neural Transmission 36 (3–4): 303–26. (1975). doi:10.1007/BF01253131. PMID 1172524.

thepharmaletter.com

“Sanofi Extends Holding in Chinoin”. The Pharma Letter (September 19, 1993). 2020年3月31日閲覧。

veterinarypartner.com

Lundgren. “Canine Cognitive Dysfunction”. Veterinary Partner. April 8, 2011閲覧。

web.archive.org

“Selegiline Treatment of Canine Pituitary-Dependent Hyperadrenocorticism”. Australian Veterinary Journal (2004年). November 29, 2010時点のオリジナルよりアーカイブ。April 8, 2011閲覧。 (PDF)

worldcat.org

search.worldcat.org

Csoti, Ilona; Storch, Alexander; Müller, Walter; Jost, Wolfgang H. (December 1, 2012). “Drug interactions with selegiline versus rasagiline”. Basal Ganglia 2 (4, Supplement): S27–S31. doi:10.1016/j.baga.2012.06.003. ISSN 2210-5336.
Duffy, Mary (3 December 2002). “Patch Raises New Hope For Beating Depression”. The New York Times. ISSN 0362-4331

worldcat.org

Saunders, Nicholas; Heron, Liz (1993). E for Ecstasy. London: N. Saunders. ISBN 978-0-9501628-8-1. OCLC 29388575 ^{[要ページ番号]}