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Epileptic phenotypes, electroclinical features and clinical characteristics in 17 children with anti-NMDAR encephalitis.
Eur J Paediatr Neurol. 2017 May;21(3):457-464. doi: 10.1016/j.ejpn.2016.11.016. Epub 2016 Dec 5.
Eur J Paediatr Neurol. 2017.
PMID: 28017557
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: ensslen m.
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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LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs.
Herbst SM, Proepper CR, Geis T, Borggraefe I, Hahn A, Debus O, Haeussler M, von Gersdorff G, Kurlemann G, Ensslen M, Beaud N, Budde J, Gilbert M, Heiming R, Morgner R, Philippi H, Ross S, Strobl-Wildemann G, Muelleder K, Vosschulte P, Morris-Rosendahl DJ, Schuierer G, Hehr U.
Herbst SM, et al. Among authors: ensslen m.
Brain Dev. 2016 Apr;38(4):399-406. doi: 10.1016/j.braindev.2015.10.001. Epub 2015 Oct 19.
Brain Dev. 2016.
PMID: 26494205
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Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation.
Hamilton EM, Polder E, Vanderver A, Naidu S, Schiffmann R, Fisher K, Raguž AB, Blumkin L; H-ABC Research Group; van Berkel CG, Waisfisz Q, Simons C, Taft RJ, Abbink TE, Wolf NI, van der Knaap MS.
Hamilton EM, et al.
Brain. 2014 Jul;137(Pt 7):1921-30. doi: 10.1093/brain/awu110. Epub 2014 Apr 30.
Brain. 2014.
PMID: 24785942
Free PMC article.
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Encephalopathy caused by novel mutations in the CMP-sialic acid transporter, SLC35A1.
Ng BG, Asteggiano CG, Kircher M, Buckingham KJ, Raymond K, Nickerson DA, Shendure J, Bamshad MJ; University of Washington Center for Mendelian Genomics; Ensslen M, Freeze HH.
Ng BG, et al. Among authors: ensslen m.
Am J Med Genet A. 2017 Nov;173(11):2906-2911. doi: 10.1002/ajmg.a.38412. Epub 2017 Aug 29.
Am J Med Genet A. 2017.
PMID: 28856833
Free PMC article.
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[Indications and concept of follow-up care of home-monitoring for premature and risk infants].
Förster KM, Immler S, Ensslen M, Flemmer A, Schulze A, von Poblotzki M, Genzel-Boroviczény O, Heinen F, Hilgendorff A.
Förster KM, et al. Among authors: ensslen m.
Klin Padiatr. 2015 Mar;227(2):72-9. doi: 10.1055/s-0034-1395663. Epub 2015 Mar 9.
Klin Padiatr. 2015.
PMID: 25751680
German.
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Comparison of gene expression profiling between malignant and normal plasma cells with oligonucleotide arrays.
De Vos J, Thykjaer T, Tarte K, Ensslen M, Raynaud P, Requirand G, Pellet F, Pantesco V, Rème T, Jourdan M, Rossi JF, Ørntoft T, Klein B.
De Vos J, et al. Among authors: ensslen m.
Oncogene. 2002 Oct 3;21(44):6848-57. doi: 10.1038/sj.onc.1205868.
Oncogene. 2002.
PMID: 12360412
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Lidamidine inhibits intrinsic contractile patterns of the rat proximal colon.
Decktor DL, Pendleton RG, Ensslen ME, Davis MM.
Decktor DL, et al. Among authors: ensslen me.
Eur J Pharmacol. 1987 Nov 10;143(2):213-9. doi: 10.1016/0014-2999(87)90535-8.
Eur J Pharmacol. 1987.
PMID: 2891549
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