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Genotype-phenotype correlations in SCN8A-related disorders ..:
Schoonjans, An Sofie
;
Johannesen, Katrine M
;
Liu, Yuanyuan
...
boreal:278286. , 2022
Link:
http://hdl.handle.net/2078.1/278286
RT Journal T1
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
UL https://suche.suub.uni-bremen.de/peid=base-ftunistlouisbrus:oai:dial.uclouvain.be:boreal:278286&Exemplar=1&LAN=DE A1 Schoonjans, An Sofie A1 Johannesen, Katrine M A1 Liu, Yuanyuan A1 Koko, Mahmoud A1 Gjerulfsen, Cathrine E A1 Sonnenberg, Lukas A1 Schubert, Julian A1 Fenger, Christina D A1 Eltokhi, Ahmed A1 Rannap, Maert A1 Koch, Nils A A1 Lauxmann, Stephan A1 Krüger, Johanna A1 Kegele, Josua A1 Canafoglia, Laura A1 Franceschetti, Silvana A1 Mayer, Thomas A1 Rebstock, Johannes A1 Zacher, Pia A1 Ruf, Susanne A1 Alber, Michael A1 Sterbova, Katalin A1 Lassuthová, Petra A1 Vlckova, Marketa A1 Lemke, Johannes R A1 Platzer, Konrad A1 Krey, Ilona A1 Heine, Constanze A1 Wieczorek, Dagmar A1 Kroell-Seger, Judith A1 Lund, Caroline A1 Klein, Karl Martin A1 Au, P Y Billie A1 Rho, Jong M A1 Ho, Alice W A1 Masnada, Silvia A1 Veggiotti, Pierangelo A1 Giordano, Lucio A1 Accorsi, Patrizia A1 Hoei-Hansen, Christina E A1 Striano, Pasquale A1 Zara, Federico A1 Verhelst, Helene A1 Verhoeven, Judith S A1 Braakman, Hilde M H A1 van der Zwaag, Bert A1 Harder, Aster V E A1 Brilstra, Eva A1 Pendziwiat, Manuela A1 Lebon, Sebastian A1 Vaccarezza, Maria A1 Le, Ngoc Minh A1 Christensen, Jakob A1 Grønborg, Sabine A1 Scherer, Stephen W A1 Howe, Jennifer A1 Fazeli, Walid A1 Howell, Katherine B A1 Leventer, Richard A1 Stutterd, Chloe A1 Walsh, Sonja A1 Gerard, Marion A1 Gerard, Bénédicte A1 Matricardi, Sara A1 Bonardi, Claudia M A1 Sartori, Stefano A1 Berger, Andrea A1 Hoffman-Zacharska, Dorota A1 Mastrangelo, Massimo A1 Darra, Francesca A1 Vøllo, Arve A1 Motazacker, M Mahdi A1 Lakeman, Phillis A1 Nizon, Mathilde A1 Betzler, Cornelia A1 Altuzarra, Cecilia A1 Caume, Roseline A1 Roubertie, Agathe A1 Gélisse, Philippe A1 Marini, Carla A1 Guerrini, Renzo A1 Bilan, Frederic A1 Tibussek, Daniel A1 Koch-Hogrebe, Margarete A1 Perry, M Scott A1 Ichikawa, Shoji A1 Dadali, Elena A1 Sharkov, Artem A1 Mishina, Irina A1 Abramov, Mikhail A1 Kanivets, Ilya A1 Korostelev, Sergey A1 Kutsev, Sergey A1 Wain, Karen E A1 Eisenhauer, Nancy A1 Wagner, Monisa A1 Savatt, Juliann M A1 Müller-Schlüter, Karen A1 Bassan, Haim A1 Borovikov, Artem A1 Nassogne, Marie-Cécile A1 Destrée, Anne PB Oxford University Press YR 2022 K1 Epilepsy K1 Generalized K1 Epileptic Syndromes K1 Genetic Association Studies K1 Humans K1 Infant K1 Intellectual Disability K1 Mutation K1 NAV1.6 Voltage-Gated Sodium Channel K1 Prognosis K1 Seizures K1 Sodium Channel Blockers K1 SCN8A K1 genetics K1 personalized medicine JF boreal:278286 LK http://hdl.handle.net/2078.1/278286 DO http://hdl.handle.net/2078.1/278286 SF ELIB - SuUB Bremen
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