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Monogenic variants in dystonia: an exome-wide sequencing study.
Lancet Neurol. 2020 Nov;19(11):908-918. doi: 10.1016/S1474-4422(20)30312-4.
Lancet Neurol. 2020.
PMID: 33098801
Free PMC article.
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.
von Stülpnagel C, Ensslen M, Møller RS, Pal DK, Masnada S, Veggiotti P, Piazza E, Dreesmann M, Hartlieb T, Herberhold T, Hughes E, Koch M, Kutzer C, Hoertnagel K, Nitanda J, Pohl M, Rostásy K, Haack TB, Stöhr K, Kluger G, Borggraefe I.
von Stülpnagel C, et al. Among authors: herberhold t.
Eur J Paediatr Neurol. 2017 May;21(3):530-541. doi: 10.1016/j.ejpn.2017.01.001. Epub 2017 Jan 14.
Eur J Paediatr Neurol. 2017.
PMID: 28109652
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Stability of 0.5% Glucose-Containing Balanced Electrolyte Solutions for Patients on Ketogenic Diets: A Laboratory Study.
Heiderich S, Dennhardt N, Hartmann H, Kluger GJ, Sümpelmann R, Herberhold T.
Heiderich S, et al. Among authors: herberhold t.
Neuropediatrics. 2020 Dec;51(6):397-400. doi: 10.1055/s-0040-1715634. Epub 2020 Aug 25.
Neuropediatrics. 2020.
PMID: 32842160
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Ectopic craniopharyngioma.
Kordes U, Flitsch J, Hagel C, Goebell E, Schwarz R, Herberhold T, von Bueren AO, Rutkowski S, Müller HL.
Kordes U, et al. Among authors: herberhold t.
Klin Padiatr. 2011 May;223(3):176-7. doi: 10.1055/s-0031-1273743. Epub 2011 Apr 1.
Klin Padiatr. 2011.
PMID: 21462099
No abstract available.
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