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Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability.
Epilepsia. 2019 Jan;60(1):155-164. doi: 10.1111/epi.14618. Epub 2018 Dec 7.
Epilepsia. 2019.
PMID: 30525188
Biallelic Variants in the COLGALT1 Gene Causes Severe Congenital Porencephaly: A Case Report.
Teunissen MWA, Kamsteeg EJ, Sallevelt SCEH, Pennings M, Bauer NJC, Vermeulen RJ, Nicolai J.
Teunissen MWA, et al.
Neurol Genet. 2021 Mar 9;7(2):e564. doi: 10.1212/NXG.0000000000000564. eCollection 2021 Apr.
Neurol Genet. 2021.
PMID: 33709034
Free PMC article.
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Autism spectrum disorder and brain volume link through a set of mTOR-related genes.
Arenella M, Mota NR, Teunissen MWA, Brunner HG, Bralten J.
Arenella M, et al. Among authors: teunissen mwa.
J Child Psychol Psychiatry. 2023 Jul;64(7):1007-1014. doi: 10.1111/jcpp.13783. Epub 2023 Mar 15.
J Child Psychol Psychiatry. 2023.
PMID: 36922714
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Effectiveness and tolerability of lacosamide in children with drug resistant epilepsy.
Driessen JT, Wammes-van der Heijden EA, Verschuure P, Fasen KCFM, Teunissen MWA, Majoie HJM.
Driessen JT, et al. Among authors: teunissen mwa.
Epilepsy Behav Rep. 2022 Nov 14;21:100574. doi: 10.1016/j.ebr.2022.100574. eCollection 2023.
Epilepsy Behav Rep. 2022.
PMID: 36545476
Free PMC article.
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ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.
Teunissen MWA, Lewerissa E, van Hugte EJH, Wang S, Ockeloen CW, Koolen DA, Pfundt R, Marcelis CLM, Brilstra E, Howe JL, Scherer SW, Le Guillou X, Bilan F, Primiano M, Roohi J, Piton A, de Saint Martin A, Baer S, Seiffert S, Platzer K, Jamra RA, Syrbe S, Doering JH, Lakhani S, Nangia S, Gilissen C, Vermeulen RJ, Rouhl RPW, Brunner HG, Willemsen MH, Nadif Kasri N.
Teunissen MWA, et al.
Hum Mol Genet. 2023 Jul 4;32(14):2373-2385. doi: 10.1093/hmg/ddad081.
Hum Mol Genet. 2023.
PMID: 37195288
Free PMC article.
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