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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 2
1982 3
1983 2
1984 2
1985 2
1986 1
1987 2
1988 2
1989 1
1990 2
1991 6
1992 2
1993 1
1994 1
1995 1
2009 1
2010 1
2011 1
2013 3
2014 1
2015 1
2016 4
2018 1
2019 1
2024 0

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40 results

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Page 1
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.
Stamberger H, Nikanorova M, Willemsen MH, Accorsi P, Angriman M, Baier H, Benkel-Herrenbrueck I, Benoit V, Budetta M, Caliebe A, Cantalupo G, Capovilla G, Casara G, Courage C, Deprez M, Destrée A, Dilena R, Erasmus CE, Fannemel M, Fjær R, Giordano L, Helbig KL, Heyne HO, Klepper J, Kluger GJ, Lederer D, Lodi M, Maier O, Merkenschlager A, Michelberger N, Minetti C, Muhle H, Phalin J, Ramsey K, Romeo A, Schallner J, Schanze I, Shinawi M, Sleegers K, Sterbova K, Syrbe S, Traverso M, Tzschach A, Uldall P, Van Coster R, Verhelst H, Viri M, Winter S, Wolff M, Zenker M, Zoccante L, De Jonghe P, Helbig I, Striano P, Lemke JR, Møller RS, Weckhuysen S. Stamberger H, et al. Among authors: casara g. Neurology. 2016 Mar 8;86(10):954-62. doi: 10.1212/WNL.0000000000002457. Epub 2016 Feb 10. Neurology. 2016. PMID: 26865513 Free article. Review.
99mTc HM-PAO SPECT in pediatric migraine.
Battistella PA, Ruffilli R, Dalla Pozza F, Pitassi I, Casara GL, Boniver C, Suppiej A, Bendagli B, Condini A. Battistella PA, et al. Among authors: casara gl. Headache. 1990 Oct;30(10):646-9. doi: 10.1111/j.1526-4610.1990.hed3010646.x. Headache. 1990. PMID: 2272814
Hypomelanosis of Ito and hemimegalencephaly.
Battistella PA, Peserico A, Bertoli P, Drigo P, Laverda AM, Casara GL. Battistella PA, et al. Among authors: casara gl. Childs Nerv Syst. 1990 Nov;6(7):421-3. doi: 10.1007/BF00302232. Childs Nerv Syst. 1990. PMID: 1669255
Pediatric epilepsy following neonatal seizures symptomatic of stroke.
Suppiej A, Mastrangelo M, Mastella L, Accorsi P, Grazian L, Casara G, Peruzzi C, Carpanelli ML, Janes A, Traverso A, Dalla Bernardina B. Suppiej A, et al. Among authors: casara g. Brain Dev. 2016 Jan;38(1):27-31. doi: 10.1016/j.braindev.2015.05.010. Epub 2015 Jun 6. Brain Dev. 2016. PMID: 26058328
Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly.
Domingues FS, König E, Schwienbacher C, Volpato CB, Picard A, Cantaloni C, Mascalzoni D, Lackner P, Heimbach A, Hoffmann P, Stanzial F, Hicks AA, Parmeggiani L, Benedicenti F, Pellegrin S, Casara G, Pramstaller PP. Domingues FS, et al. Among authors: casara g. Seizure. 2019 Mar;66:81-85. doi: 10.1016/j.seizure.2018.12.021. Epub 2018 Dec 23. Seizure. 2019. PMID: 30818181 Free article.
[Syncope in childhood].
Svaluto Moreolo G, Pellegrino PA, Benetti E, De Martin PG, Milanesi O, Pigato R, Pothen P, Casara G. Svaluto Moreolo G, et al. Among authors: casara g. Pediatr Med Chir. 1984 Sep-Oct;6(5):605-7. Pediatr Med Chir. 1984. PMID: 6535120 Italian.
Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.
Weckhuysen S, Ivanovic V, Hendrickx R, Van Coster R, Hjalgrim H, Møller RS, Grønborg S, Schoonjans AS, Ceulemans B, Heavin SB, Eltze C, Horvath R, Casara G, Pisano T, Giordano L, Rostasy K, Haberlandt E, Albrecht B, Bevot A, Benkel I, Syrbe S, Sheidley B, Guerrini R, Poduri A, Lemke JR, Mandelstam S, Scheffer I, Angriman M, Striano P, Marini C, Suls A, De Jonghe P; KCNQ2 Study Group. Weckhuysen S, et al. Among authors: casara g. Neurology. 2013 Nov 5;81(19):1697-703. doi: 10.1212/01.wnl.0000435296.72400.a1. Epub 2013 Oct 9. Neurology. 2013. PMID: 24107868 Free PMC article.
40 results