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2020 | 2 |
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Page 1
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood.
Biomedicines. 2020 Oct 28;8(11):456. doi: 10.3390/biomedicines8110456.
Biomedicines. 2020.
PMID: 33126500
Free PMC article.
Clinical spectrum and treatment outcome of 95 children with continuous spikes and waves during sleep (CSWS).
Sonnek B, Döring JH, Mütze U, Schubert-Bast S, Bast T, Balke D, Reuner G, Schuler E, Klabunde-Cherwon A, Hoffmann GF, Kölker S, Syrbe S.
Sonnek B, et al. Among authors: doring jh.
Eur J Paediatr Neurol. 2021 Jan;30:121-127. doi: 10.1016/j.ejpn.2020.10.010. Epub 2020 Oct 24.
Eur J Paediatr Neurol. 2021.
PMID: 33132036
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Deep-Phenotyping the Less Severe Spectrum of PIGT Deficiency and Linking the Gene to Myoclonic Atonic Seizures.
Bayat A, Pendziwiat M, Obersztyn E, Goldenberg P, Zacher P, Döring JH, Syrbe S, Begtrup A, Borovikov A, Sharkov A, Karasińska A, Giżewska M, Mitchell W, Morava E, Møller RS, Rubboli G.
Bayat A, et al. Among authors: doring jh.
Front Genet. 2021 May 11;12:663643. doi: 10.3389/fgene.2021.663643. eCollection 2021.
Front Genet. 2021.
PMID: 34046058
Free PMC article.
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Thirty Years of Orphan Drug Legislation and the Development of Drugs to Treat Rare Seizure Conditions: A Cross Sectional Analysis.
Döring JH, Lampert A, Hoffmann GF, Ries M.
Döring JH, et al.
PLoS One. 2016 Aug 24;11(8):e0161660. doi: 10.1371/journal.pone.0161660. eCollection 2016.
PLoS One. 2016.
PMID: 27557111
Free PMC article.
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