ドラベ症候群 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ドラベ症候群" in Japanese language version.

refsWebsite

Global rank Japanese rank

19nih.gov

4^th place

24^th place

14doi.org

2^nd place

6^th place

3dravetfoundation.org

low place

2harvard.edu

18^th place

107^th place

1books.google.com

3^rd place

61^st place

1archive.is

87^th place

39^th place

1web.archive.org

1^st place

1hosp.go.jp

low place

3,375^th place

1nice.org.uk

3,258^th place

1,755^th place

1ice-epilepsy.org

low place

1worldcat.org

5^th place

19^th place

1fda.gov

447^th place

1,043^rd place

1ed.ac.uk

1,871^st place

2,715^th place

1researchgate.net

120^th place

616^th place

1coloradosun.com

low place

archive.is

“Diagnostic Criteria”. Dravet Syndrome Foundation. 17 March 2015時点のオリジナルよりアーカイブ。17 March 2015閲覧。

books.google.com

Oxford textbook of epilepsy and epileptic seizures. Oxford: Oxford Univ. Press. (2013). p. 13. ISBN 978-0-19-965904-3

coloradosun.com

Ingold, John (April 8, 2020). “Charlotte Fiji”. The Colorado Sun. April 13, 2020閲覧。 “"Charlotte Figi, the Colorado Springs girl who, as a gleeful and fragile child, launched a movement that led to sweeping changes in marijuana laws across the globe, has died from complications possibly related to the new coronavirus."”

doi.org

“Parental SCN1A mutation mosaicism in familial Dravet syndrome”. Clinical Genetics 76 (4): 398–403. (October 2009). doi:10.1111/j.1399-0004.2009.01208.x. PMID 19673951.
“Comprehensive care of children with Dravet syndrome”. Epilepsia 52 Suppl 2: 90–4. (April 2011). doi:10.1111/j.1528-1167.2011.03011.x. PMID 21463289.
Couzin-Frankel, Jennifer (8 April 2015). “Sudden death in epilepsy: Researchers finger possible cause”. Science. doi:10.1126/science.aab2456.
“Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis”. Nature Communications 11 (1): 315. (January 2020). Bibcode: 2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
“Vaccination and the onset of dravet syndrome”. Epilepsy Currents 11 (4): 120–2. (July 2011). doi:10.5698/1535-7511-11.4.120. PMC 3152151. PMID 21852883.
“A plethora of SCN1A mutations: what can they tell us?”. Epilepsy Currents 5 (1): 17–20. (2005). doi:10.1111/j.1535-7597.2005.05105.x. PMC 1176321. PMID 16059449.
“A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction”. Proceedings of the National Academy of Sciences of the United States of America 98 (11): 6384–9. (May 2001). Bibcode: 2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.
“The pharmacologic treatment of Dravet syndrome”. Epilepsia 52 Suppl 2: 72–5. (April 2011). doi:10.1111/j.1528-1167.2011.03007.x. PMID 21463285.
Brigo, Francesco; Igwe, Stanley C.; Bragazzi, Nicola Luigi (26 May 2020). “Stiripentol add-on therapy for drug-resistant focal epilepsy”. The Cochrane Database of Systematic Reviews 5: CD009887. doi:10.1002/14651858.CD009887.pub5. ISSN 1469-493X. PMC 7386790. PMID 32468572.
“Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome”. The New England Journal of Medicine 376 (21): 2011–2020. (May 2017). doi:10.1056/NEJMoa1611618. PMID 28538134.
“Epileptic encephalopathies of infancy: welcome advances”. Lancet 394 (10216): 2203–2204. (December 2020). doi:10.1016/S0140-6736(19)31239-5. PMID 31862247.
“Epidemiology of severe myoclonic epilepsy of infancy”. Epilepsia 31 (4): 397–400. (August 1990). doi:10.1111/j.1528-1157.1990.tb05494.x. PMID 1695145.
“Early diagnosis of severe myoclonic epilepsy in infancy”. Brain & Development 14 (5): 299–303. (September 1992). doi:10.1093/brain/aws151. PMID 1456383.
“The core Dravet syndrome phenotype”. Epilepsia 52 Suppl 2: 3–9. (April 2011). doi:10.1111/j.1528-1167.2011.02994.x. PMID 21463272.

dravetfoundation.org

“What is Dravet Syndrome?”. Cherry Hill, NJ: Dravet Syndrome Foundation, Inc.. 2020年12月28日閲覧。
“Diagnostic Criteria”. Dravet Syndrome Foundation. 17 March 2015時点のオリジナルよりアーカイブ。17 March 2015閲覧。
“Dravet Syndrome Foundation: Treatment”. 28 December 2015時点のオリジナルよりアーカイブ。1 January 2016閲覧。

ed.ac.uk

pure.ed.ac.uk

“Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome”. The New England Journal of Medicine 376 (21): 2011–2020. (May 2017). doi:10.1056/NEJMoa1611618. PMID 28538134.

fda.gov

“Press Announcements - FDA approves first drug comprised of an active ingredient derived from marijuana to treat rare, severe forms of epilepsy” (英語). www.fda.gov. 27 June 2018閲覧。

harvard.edu

ui.adsabs.harvard.edu

“Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis”. Nature Communications 11 (1): 315. (January 2020). Bibcode: 2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
“A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction”. Proceedings of the National Academy of Sciences of the United States of America 98 (11): 6384–9. (May 2001). Bibcode: 2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.

hosp.go.jp

shizuokamind.hosp.go.jp

“2. てんかん症候群”. てんかん情報センター (国立病院機構静岡てんかん・神経医療センター) 2022年1月5日閲覧。

ice-epilepsy.org

“SCN1A Patients Advised to Avoid Sodium Channel Blockers”. Calgary, Canada: Intractable Childhood Epilepsy Alliance. 1 January 2016閲覧。

nice.org.uk

“NICE: Epilepsies: diagnosis and management”. The National Institute for Health and Care Excellence (NICE). 1 January 2016閲覧。

nih.gov

pubmed.ncbi.nlm.nih.gov

“Parental SCN1A mutation mosaicism in familial Dravet syndrome”. Clinical Genetics 76 (4): 398–403. (October 2009). doi:10.1111/j.1399-0004.2009.01208.x. PMID 19673951.
“Comprehensive care of children with Dravet syndrome”. Epilepsia 52 Suppl 2: 90–4. (April 2011). doi:10.1111/j.1528-1167.2011.03011.x. PMID 21463289.
“Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis”. Nature Communications 11 (1): 315. (January 2020). Bibcode: 2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
“Vaccination and the onset of dravet syndrome”. Epilepsy Currents 11 (4): 120–2. (July 2011). doi:10.5698/1535-7511-11.4.120. PMC 3152151. PMID 21852883.
“A plethora of SCN1A mutations: what can they tell us?”. Epilepsy Currents 5 (1): 17–20. (2005). doi:10.1111/j.1535-7597.2005.05105.x. PMC 1176321. PMID 16059449.
“A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction”. Proceedings of the National Academy of Sciences of the United States of America 98 (11): 6384–9. (May 2001). Bibcode: 2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.
“The pharmacologic treatment of Dravet syndrome”. Epilepsia 52 Suppl 2: 72–5. (April 2011). doi:10.1111/j.1528-1167.2011.03007.x. PMID 21463285.
Brigo, Francesco; Igwe, Stanley C.; Bragazzi, Nicola Luigi (26 May 2020). “Stiripentol add-on therapy for drug-resistant focal epilepsy”. The Cochrane Database of Systematic Reviews 5: CD009887. doi:10.1002/14651858.CD009887.pub5. ISSN 1469-493X. PMC 7386790. PMID 32468572.
“Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome”. The New England Journal of Medicine 376 (21): 2011–2020. (May 2017). doi:10.1056/NEJMoa1611618. PMID 28538134.
“Epileptic encephalopathies of infancy: welcome advances”. Lancet 394 (10216): 2203–2204. (December 2020). doi:10.1016/S0140-6736(19)31239-5. PMID 31862247.
“Epidemiology of severe myoclonic epilepsy of infancy”. Epilepsia 31 (4): 397–400. (August 1990). doi:10.1111/j.1528-1157.1990.tb05494.x. PMID 1695145.
“Early diagnosis of severe myoclonic epilepsy in infancy”. Brain & Development 14 (5): 299–303. (September 1992). doi:10.1093/brain/aws151. PMID 1456383.
“The core Dravet syndrome phenotype”. Epilepsia 52 Suppl 2: 3–9. (April 2011). doi:10.1111/j.1528-1167.2011.02994.x. PMID 21463272.

ncbi.nlm.nih.gov

“SCN1A seizure disorders.”. GeneReviews®[Internet]. Seattle: University of Washington. (April 2019)
“Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis”. Nature Communications 11 (1): 315. (January 2020). Bibcode: 2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
“Vaccination and the onset of dravet syndrome”. Epilepsy Currents 11 (4): 120–2. (July 2011). doi:10.5698/1535-7511-11.4.120. PMC 3152151. PMID 21852883.
“A plethora of SCN1A mutations: what can they tell us?”. Epilepsy Currents 5 (1): 17–20. (2005). doi:10.1111/j.1535-7597.2005.05105.x. PMC 1176321. PMID 16059449.
“A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction”. Proceedings of the National Academy of Sciences of the United States of America 98 (11): 6384–9. (May 2001). Bibcode: 2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.
Brigo, Francesco; Igwe, Stanley C.; Bragazzi, Nicola Luigi (26 May 2020). “Stiripentol add-on therapy for drug-resistant focal epilepsy”. The Cochrane Database of Systematic Reviews 5: CD009887. doi:10.1002/14651858.CD009887.pub5. ISSN 1469-493X. PMC 7386790. PMID 32468572.

researchgate.net

“Bernardo Dalla Bernardina | University of Verona (UNIVR)” (英語). ResearchGate. researchgate. 2020年12月28日閲覧。

web.archive.org

“Dravet Syndrome Foundation: Treatment”. 28 December 2015時点のオリジナルよりアーカイブ。1 January 2016閲覧。

worldcat.org

search.worldcat.org

Brigo, Francesco; Igwe, Stanley C.; Bragazzi, Nicola Luigi (26 May 2020). “Stiripentol add-on therapy for drug-resistant focal epilepsy”. The Cochrane Database of Systematic Reviews 5: CD009887. doi:10.1002/14651858.CD009887.pub5. ISSN 1469-493X. PMC 7386790. PMID 32468572.