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

Year Number of Results
1993 1
1994 2
1995 1
1996 2
1997 1
2000 1
2001 1
2005 1
2007 5
2008 5
2009 4
2010 4
2011 1
2012 4
2013 10
2014 8
2015 13
2016 11
2017 12
2018 14
2019 8
2020 12
2021 6
2022 7
2023 6
2024 5

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125 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: merkenschlager a. Neurology. 2016 Mar 8;86(10):954-62. doi: 10.1212/WNL.0000000000002457. Epub 2016 Feb 10. Neurology. 2016. PMID: 26865513 Free article. Review.
Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.
Zagaglia S, Selch C, Nisevic JR, Mei D, Michalak Z, Hernandez-Hernandez L, Krithika S, Vezyroglou K, Varadkar SM, Pepler A, Biskup S, Leão M, Gärtner J, Merkenschlager A, Jaksch M, Møller RS, Gardella E, Kristiansen BS, Hansen LK, Vari MS, Helbig KL, Desai S, Smith-Hicks CL, Hino-Fukuyo N, Talvik T, Laugesaar R, Ilves P, Õunap K, Körber I, Hartlieb T, Kudernatsch M, Winkler P, Schimmel M, Hasse A, Knuf M, Heinemeyer J, Makowski C, Ghedia S, Subramanian GM, Striano P, Thomas RH, Micallef C, Thom M, Werring DJ, Kluger GJ, Cross JH, Guerrini R, Balestrini S, Sisodiya SM. Zagaglia S, et al. Among authors: merkenschlager a. Neurology. 2018 Nov 27;91(22):e2078-e2088. doi: 10.1212/WNL.0000000000006567. Epub 2018 Nov 9. Neurology. 2018. PMID: 30413629 Free PMC article.
[Unusual Localisation of a Borrelia Lymphocytoma].
Liebmann N, Sterker I, Sorge I, Opitz S, Merkenschlager A, Gburek-Augustat J. Liebmann N, et al. Among authors: merkenschlager a. Klin Monbl Augenheilkd. 2021 Dec 15. doi: 10.1055/a-1686-9274. Online ahead of print. Klin Monbl Augenheilkd. 2021. PMID: 34911119 German. No abstract available.
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.
Klöckner C, Fernández-Murray JP, Tavasoli M, Sticht H, Stoltenburg-Didinger G, Scholle LM, Bakhtiari S, Kruer MC, Darvish H, Firouzabadi SG, Pagnozzi A, Shukla A, Girisha KM, Narayanan DL, Kaur P, Maroofian R, Zaki MS, Noureldeen MM, Merkenschlager A, Gburek-Augustat J, Cali E, Banu S, Nahar K, Efthymiou S, Houlden H, Jamra RA, Williams J, McMaster CR, Platzer K. Klöckner C, et al. Among authors: merkenschlager a. Brain. 2022 Jun 30;145(6):1916-1923. doi: 10.1093/brain/awac074. Brain. 2022. PMID: 35202461 Free PMC article.
Stress, Stress Reduction and Obesity in Childhood and Adolescence.
Kappes C, Stein R, Körner A, Merkenschlager A, Kiess W. Kappes C, et al. Among authors: merkenschlager a. Horm Res Paediatr. 2023;96(1):88-96. doi: 10.1159/000519284. Epub 2021 Sep 1. Horm Res Paediatr. 2023. PMID: 34469895 Free article. Review.
Late-onset hydrocephalus in a child with Joubert syndrome: a case report.
Fehrenbach MK, Nestler U, Meixensberger J, Bernhard MK, Merkenschlager A, Weise S, Krause M. Fehrenbach MK, et al. Among authors: merkenschlager a. Childs Nerv Syst. 2018 Jul;34(7):1423-1425. doi: 10.1007/s00381-018-3767-0. Epub 2018 Mar 5. Childs Nerv Syst. 2018. PMID: 29508057
125 results