Dravet syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Dravet syndrome" in English language version.

refsWebsite

Global rank English rank

32nih.gov

4^th place

21doi.org

2^nd place

8semanticscholar.org

11^th place

8^th place

3dravetfoundation.org

low place

2harvard.edu

18^th place

17^th place

2fda.gov

447^th place

338^th place

2europa.eu

68^th place

117^th place

1books.google.com

3^rd place

1proquest.com

206^th place

124^th place

1dravetfoundation.eu

low place

1archive.today

14^th place

1web.archive.org

1^st place

1nice.org.uk

3,258^th place

2,666^th place

1handle.net

102^nd place

76^th place

1clinicaltrials.gov

5,225^th place

4,062^nd place

1researchgate.net

120^th place

125^th place

1coloradosun.com

low place

7,764^th place

archive.today

"Diagnostic Criteria". Dravet Syndrome Foundation. Archived from the original on 17 March 2015. Retrieved 17 March 2015.

books.google.com

Shorvon SD, Guerrini R, Cook M, eds. (2013). Oxford textbook of epilepsy and epileptic seizures. Oxford: Oxford Univ. Press. p. 13. ISBN 978-0-19-965904-3.

clinicaltrials.gov

"CTG Labs - NCBI". clinicaltrials.gov. Retrieved 2023-10-27.

coloradosun.com

Ingold J (April 8, 2020). "Charlotte Fiji". The Colorado Sun. Retrieved April 13, 2020. 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

McIntosh AM, McMahon J, Dibbens LM, Iona X, Mulley JC, Scheffer IE, Berkovic SF (June 2010). "Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study". The Lancet. Neurology. 9 (6): 592–8. doi:10.1016/S1474-4422(10)70107-1. PMID 20447868. S2CID 2676315. ProQuest 314128956.
Couzin-Frankel J (8 April 2015). "Sudden death in epilepsy: Researchers finger possible cause". Science. doi:10.1126/science.aab2456.
Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE (October 2009). "Parental SCN1A mutation mosaicism in familial Dravet syndrome". Clinical Genetics. 76 (4): 398–403. doi:10.1111/j.1399-0004.2009.01208.x. PMID 19673951. S2CID 40396775.
Granata T (April 2011). "Comprehensive care of children with Dravet syndrome". Epilepsia. 52 (Suppl 2): 90–94. doi:10.1111/j.1528-1167.2011.03011.x. PMID 21463289. S2CID 573375.
Lin YJ, Wen CN, Lin YY, Hsieh WC, Chang CC, Chen YH, et al. (January 2020). "Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis". Nature Communications. 11 (1): 315. Bibcode:2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
Ben-Menachem E (July 2011). "Vaccination and the onset of dravet syndrome". Epilepsy Currents. 11 (4): 120–122. doi:10.5698/1535-7511-11.4.120. PMC 3152151. PMID 21852883.
Wallace R (2005). "A plethora of SCN1A mutations: what can they tell us?". Epilepsy Currents. 5 (1): 17–20. doi:10.1111/j.1535-7597.2005.05105.x. PMC 1176321. PMID 16059449.
Sugawara T, Tsurubuchi Y, Agarwala KL, Ito M, Fukuma G, Mazaki-Miyazaki E, et al. (May 2001). "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): 6384–6389. Bibcode:2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.
Steel D, Symonds JD, Zuberi SM, Brunklaus A (November 2017). "Dravet syndrome and its mimics: Beyond SCN1A". Epilepsia. 58 (11): 1807–1816. doi:10.1111/epi.13889. PMID 28880996.
Cardenal-Muñoz E, Auvin S, Villanueva V, Cross JH, Zuberi SM, Lagae L, Aibar JÁ (March 2022). "Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe". Epilepsia Open. 7 (1): 11–26. doi:10.1002/epi4.12569. PMC 8886070. PMID 34882995.
Chiron C, Dulac O (April 2011). "The pharmacologic treatment of Dravet syndrome". Epilepsia. 52 (Suppl 2): 72–75. doi:10.1111/j.1528-1167.2011.03007.x. PMID 21463285. S2CID 39978156.
Brigo F, Igwe SC, Bragazzi NL (September 2022). "Stiripentol add-on therapy for drug-resistant focal epilepsy". The Cochrane Database of Systematic Reviews. 2022 (9): CD009887. doi:10.1002/14651858.CD009887.pub6. PMC 9447417. PMID 36066395.
Devinsky O, Cross JH, Laux L, Marsh E, Miller I, Nabbout R, et al. (May 2017). "Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome". The New England Journal of Medicine. 376 (21): 2011–2020. doi:10.1056/NEJMoa1611618. hdl:20.500.11820/2ed5e0db-7de9-4411-93d7-3a5c388006b9. PMID 28538134. S2CID 86481485.
Hill SF, Meisler MH (2021). "Antisense Oligonucleotide Therapy for Neurodevelopmental Disorders". Developmental Neuroscience. 43 (3–4): 247–252. doi:10.1159/000517686. PMC 8440367. PMID 34412058.
Lersch R, Jannadi R, Grosse L, Wagner M, Schneider MF, von Stülpnagel C, et al. (April 2022). "Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome". The Neuroscientist. 29 (6): 732–750. doi:10.1177/10738584221088244. PMC 10623613. PMID 35414300.
Anwar A, Saleem S, Patel UK, Arumaithurai K, Malik P (June 2019). "Dravet Syndrome: An Overview". Cureus. 11 (6): e5006. doi:10.7759/cureus.5006. PMC 6713249. PMID 31497436.
Berkovic SF (December 2019). "Epileptic encephalopathies of infancy: welcome advances". Lancet. 394 (10216): 2203–2204. doi:10.1016/S0140-6736(19)31239-5. PMID 31862247. S2CID 209394550.
Hurst DL (August 1990). "Epidemiology of severe myoclonic epilepsy of infancy". Epilepsia. 31 (4): 397–400. doi:10.1111/j.1528-1157.1990.tb05494.x. PMID 1695145. S2CID 31868578.
Yakoub M, Dulac O, Jambaqué I, Chiron C, Plouin P (September 1992). "Early diagnosis of severe myoclonic epilepsy in infancy". Brain & Development. 14 (5): 299–303. doi:10.1093/brain/aws151. PMID 1456383.
Aledo-Serrano Á, Mingorance A, Jiménez-Huete A, Toledano R, García-Morales I, Anciones C, Gil-Nagel A (June 2020). "Genetic epilepsies and COVID-19 pandemic: Lessons from the caregiver perspective". Epilepsia. 61 (6): 1312–1314. doi:10.1111/epi.16537. PMC 7276740. PMID 32420620.
Dravet C (April 2011). "The core Dravet syndrome phenotype". Epilepsia. 52 (Suppl 2): 3–9. doi:10.1111/j.1528-1167.2011.02994.x. PMID 21463272. S2CID 41553756.

dravetfoundation.eu

"Síndrome de Dravet: Causas, síntomas y tratamiento". Fundación Síndrome de Dravet (in Spanish). Retrieved 2023-10-27.

dravetfoundation.org

"What is Dravet Syndrome?". Cherry Hill, NJ: Dravet Syndrome Foundation, Inc. 10 January 2022.
"Diagnostic Criteria". Dravet Syndrome Foundation. Archived from the original on 17 March 2015. Retrieved 17 March 2015.
"Dravet Syndrome Foundation: Treatment". Archived from the original on 28 December 2015. Retrieved 1 January 2016.

europa.eu

ema.europa.eu

Fintepla, on ema.europa.eu
Fintepla (fenfluramine). An overview of Fintepla and why it is authorised in the EU, on ema.europa.eu

fda.gov

"Press Announcements - FDA approves first drug comprised of an active ingredient derived from marijuana to treat rare, severe forms of epilepsy". www.fda.gov. Retrieved 27 June 2018.
FDA Approves New Therapy for Dravet Syndrome, on fda.gov

handle.net

hdl.handle.net

Devinsky O, Cross JH, Laux L, Marsh E, Miller I, Nabbout R, et al. (May 2017). "Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome". The New England Journal of Medicine. 376 (21): 2011–2020. doi:10.1056/NEJMoa1611618. hdl:20.500.11820/2ed5e0db-7de9-4411-93d7-3a5c388006b9. PMID 28538134. S2CID 86481485.

harvard.edu

ui.adsabs.harvard.edu

Lin YJ, Wen CN, Lin YY, Hsieh WC, Chang CC, Chen YH, et al. (January 2020). "Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis". Nature Communications. 11 (1): 315. Bibcode:2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
Sugawara T, Tsurubuchi Y, Agarwala KL, Ito M, Fukuma G, Mazaki-Miyazaki E, et al. (May 2001). "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): 6384–6389. Bibcode:2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.

nice.org.uk

"NICE: Epilepsies: diagnosis and management". The National Institute for Health and Care Excellence (NICE). 11 January 2012. Retrieved 1 January 2016.

nih.gov

pubmed.ncbi.nlm.nih.gov

McIntosh AM, McMahon J, Dibbens LM, Iona X, Mulley JC, Scheffer IE, Berkovic SF (June 2010). "Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study". The Lancet. Neurology. 9 (6): 592–8. doi:10.1016/S1474-4422(10)70107-1. PMID 20447868. S2CID 2676315. ProQuest 314128956.
Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE (October 2009). "Parental SCN1A mutation mosaicism in familial Dravet syndrome". Clinical Genetics. 76 (4): 398–403. doi:10.1111/j.1399-0004.2009.01208.x. PMID 19673951. S2CID 40396775.
Granata T (April 2011). "Comprehensive care of children with Dravet syndrome". Epilepsia. 52 (Suppl 2): 90–94. doi:10.1111/j.1528-1167.2011.03011.x. PMID 21463289. S2CID 573375.
Miller IO, de Menezes MA (April 2019). "SCN1A seizure disorders.". GeneReviews®[Internet]. Seattle: University of Washington. PMID 20301494.
Lin YJ, Wen CN, Lin YY, Hsieh WC, Chang CC, Chen YH, et al. (January 2020). "Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis". Nature Communications. 11 (1): 315. Bibcode:2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
Ben-Menachem E (July 2011). "Vaccination and the onset of dravet syndrome". Epilepsy Currents. 11 (4): 120–122. doi:10.5698/1535-7511-11.4.120. PMC 3152151. PMID 21852883.
Wallace R (2005). "A plethora of SCN1A mutations: what can they tell us?". Epilepsy Currents. 5 (1): 17–20. doi:10.1111/j.1535-7597.2005.05105.x. PMC 1176321. PMID 16059449.
Sugawara T, Tsurubuchi Y, Agarwala KL, Ito M, Fukuma G, Mazaki-Miyazaki E, et al. (May 2001). "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): 6384–6389. Bibcode:2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.
Steel D, Symonds JD, Zuberi SM, Brunklaus A (November 2017). "Dravet syndrome and its mimics: Beyond SCN1A". Epilepsia. 58 (11): 1807–1816. doi:10.1111/epi.13889. PMID 28880996.
Cardenal-Muñoz E, Auvin S, Villanueva V, Cross JH, Zuberi SM, Lagae L, Aibar JÁ (March 2022). "Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe". Epilepsia Open. 7 (1): 11–26. doi:10.1002/epi4.12569. PMC 8886070. PMID 34882995.
Chiron C, Dulac O (April 2011). "The pharmacologic treatment of Dravet syndrome". Epilepsia. 52 (Suppl 2): 72–75. doi:10.1111/j.1528-1167.2011.03007.x. PMID 21463285. S2CID 39978156.
Brigo F, Igwe SC, Bragazzi NL (September 2022). "Stiripentol add-on therapy for drug-resistant focal epilepsy". The Cochrane Database of Systematic Reviews. 2022 (9): CD009887. doi:10.1002/14651858.CD009887.pub6. PMC 9447417. PMID 36066395.
Devinsky O, Cross JH, Laux L, Marsh E, Miller I, Nabbout R, et al. (May 2017). "Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome". The New England Journal of Medicine. 376 (21): 2011–2020. doi:10.1056/NEJMoa1611618. hdl:20.500.11820/2ed5e0db-7de9-4411-93d7-3a5c388006b9. PMID 28538134. S2CID 86481485.
Hill SF, Meisler MH (2021). "Antisense Oligonucleotide Therapy for Neurodevelopmental Disorders". Developmental Neuroscience. 43 (3–4): 247–252. doi:10.1159/000517686. PMC 8440367. PMID 34412058.
Lersch R, Jannadi R, Grosse L, Wagner M, Schneider MF, von Stülpnagel C, et al. (April 2022). "Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome". The Neuroscientist. 29 (6): 732–750. doi:10.1177/10738584221088244. PMC 10623613. PMID 35414300.
Anwar A, Saleem S, Patel UK, Arumaithurai K, Malik P (June 2019). "Dravet Syndrome: An Overview". Cureus. 11 (6): e5006. doi:10.7759/cureus.5006. PMC 6713249. PMID 31497436.
Berkovic SF (December 2019). "Epileptic encephalopathies of infancy: welcome advances". Lancet. 394 (10216): 2203–2204. doi:10.1016/S0140-6736(19)31239-5. PMID 31862247. S2CID 209394550.
Hurst DL (August 1990). "Epidemiology of severe myoclonic epilepsy of infancy". Epilepsia. 31 (4): 397–400. doi:10.1111/j.1528-1157.1990.tb05494.x. PMID 1695145. S2CID 31868578.
Yakoub M, Dulac O, Jambaqué I, Chiron C, Plouin P (September 1992). "Early diagnosis of severe myoclonic epilepsy in infancy". Brain & Development. 14 (5): 299–303. doi:10.1093/brain/aws151. PMID 1456383.
Aledo-Serrano Á, Mingorance A, Jiménez-Huete A, Toledano R, García-Morales I, Anciones C, Gil-Nagel A (June 2020). "Genetic epilepsies and COVID-19 pandemic: Lessons from the caregiver perspective". Epilepsia. 61 (6): 1312–1314. doi:10.1111/epi.16537. PMC 7276740. PMID 32420620.
Dravet C (April 2011). "The core Dravet syndrome phenotype". Epilepsia. 52 (Suppl 2): 3–9. doi:10.1111/j.1528-1167.2011.02994.x. PMID 21463272. S2CID 41553756.

ncbi.nlm.nih.gov

Miller IO, de Menezes MA (April 2019). "SCN1A seizure disorders.". GeneReviews®[Internet]. Seattle: University of Washington. PMID 20301494.
Lin YJ, Wen CN, Lin YY, Hsieh WC, Chang CC, Chen YH, et al. (January 2020). "Oil-in-water emulsion adjuvants for pediatric influenza vaccines: a systematic review and meta-analysis". Nature Communications. 11 (1): 315. Bibcode:2020NatCo..11..315L. doi:10.1038/s41467-019-14230-x. PMC 6965081. PMID 31949137.
Ben-Menachem E (July 2011). "Vaccination and the onset of dravet syndrome". Epilepsy Currents. 11 (4): 120–122. doi:10.5698/1535-7511-11.4.120. PMC 3152151. PMID 21852883.
Wallace R (2005). "A plethora of SCN1A mutations: what can they tell us?". Epilepsy Currents. 5 (1): 17–20. doi:10.1111/j.1535-7597.2005.05105.x. PMC 1176321. PMID 16059449.
Sugawara T, Tsurubuchi Y, Agarwala KL, Ito M, Fukuma G, Mazaki-Miyazaki E, et al. (May 2001). "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): 6384–6389. Bibcode:2001PNAS...98.6384S. doi:10.1073/pnas.111065098. PMC 33477. PMID 11371648.
Cardenal-Muñoz E, Auvin S, Villanueva V, Cross JH, Zuberi SM, Lagae L, Aibar JÁ (March 2022). "Guidance on Dravet syndrome from infant to adult care: Road map for treatment planning in Europe". Epilepsia Open. 7 (1): 11–26. doi:10.1002/epi4.12569. PMC 8886070. PMID 34882995.
Brigo F, Igwe SC, Bragazzi NL (September 2022). "Stiripentol add-on therapy for drug-resistant focal epilepsy". The Cochrane Database of Systematic Reviews. 2022 (9): CD009887. doi:10.1002/14651858.CD009887.pub6. PMC 9447417. PMID 36066395.
Hill SF, Meisler MH (2021). "Antisense Oligonucleotide Therapy for Neurodevelopmental Disorders". Developmental Neuroscience. 43 (3–4): 247–252. doi:10.1159/000517686. PMC 8440367. PMID 34412058.
Lersch R, Jannadi R, Grosse L, Wagner M, Schneider MF, von Stülpnagel C, et al. (April 2022). "Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome". The Neuroscientist. 29 (6): 732–750. doi:10.1177/10738584221088244. PMC 10623613. PMID 35414300.
Anwar A, Saleem S, Patel UK, Arumaithurai K, Malik P (June 2019). "Dravet Syndrome: An Overview". Cureus. 11 (6): e5006. doi:10.7759/cureus.5006. PMC 6713249. PMID 31497436.
Aledo-Serrano Á, Mingorance A, Jiménez-Huete A, Toledano R, García-Morales I, Anciones C, Gil-Nagel A (June 2020). "Genetic epilepsies and COVID-19 pandemic: Lessons from the caregiver perspective". Epilepsia. 61 (6): 1312–1314. doi:10.1111/epi.16537. PMC 7276740. PMID 32420620.

proquest.com

search.proquest.com

McIntosh AM, McMahon J, Dibbens LM, Iona X, Mulley JC, Scheffer IE, Berkovic SF (June 2010). "Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study". The Lancet. Neurology. 9 (6): 592–8. doi:10.1016/S1474-4422(10)70107-1. PMID 20447868. S2CID 2676315. ProQuest 314128956.

researchgate.net

"Bernardo Dalla Bernardina | University of Verona (UNIVR)". ResearchGate.

semanticscholar.org

api.semanticscholar.org

McIntosh AM, McMahon J, Dibbens LM, Iona X, Mulley JC, Scheffer IE, Berkovic SF (June 2010). "Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study". The Lancet. Neurology. 9 (6): 592–8. doi:10.1016/S1474-4422(10)70107-1. PMID 20447868. S2CID 2676315. ProQuest 314128956.
Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE (October 2009). "Parental SCN1A mutation mosaicism in familial Dravet syndrome". Clinical Genetics. 76 (4): 398–403. doi:10.1111/j.1399-0004.2009.01208.x. PMID 19673951. S2CID 40396775.
Granata T (April 2011). "Comprehensive care of children with Dravet syndrome". Epilepsia. 52 (Suppl 2): 90–94. doi:10.1111/j.1528-1167.2011.03011.x. PMID 21463289. S2CID 573375.
Chiron C, Dulac O (April 2011). "The pharmacologic treatment of Dravet syndrome". Epilepsia. 52 (Suppl 2): 72–75. doi:10.1111/j.1528-1167.2011.03007.x. PMID 21463285. S2CID 39978156.
Devinsky O, Cross JH, Laux L, Marsh E, Miller I, Nabbout R, et al. (May 2017). "Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome". The New England Journal of Medicine. 376 (21): 2011–2020. doi:10.1056/NEJMoa1611618. hdl:20.500.11820/2ed5e0db-7de9-4411-93d7-3a5c388006b9. PMID 28538134. S2CID 86481485.
Berkovic SF (December 2019). "Epileptic encephalopathies of infancy: welcome advances". Lancet. 394 (10216): 2203–2204. doi:10.1016/S0140-6736(19)31239-5. PMID 31862247. S2CID 209394550.
Hurst DL (August 1990). "Epidemiology of severe myoclonic epilepsy of infancy". Epilepsia. 31 (4): 397–400. doi:10.1111/j.1528-1157.1990.tb05494.x. PMID 1695145. S2CID 31868578.
Dravet C (April 2011). "The core Dravet syndrome phenotype". Epilepsia. 52 (Suppl 2): 3–9. doi:10.1111/j.1528-1167.2011.02994.x. PMID 21463272. S2CID 41553756.

web.archive.org

"Dravet Syndrome Foundation: Treatment". Archived from the original on 28 December 2015. Retrieved 1 January 2016.