Search Results - Lerche, Holger

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  1. 1
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    Long-term clinical course and treatment outcomes of individuals with Nodding Syndrome by Kegele, Josua (Author) , Wagner, Thomas (Author) , Kowenski, Teresa (Author) , Wiesmayr, Matthias (Author) , Gatterer, Christian (Author) , Alber, Michael (Author) , Matuja, Wiliam (Author) , Schmutzhard, Erich (Author) , Lerche, Holger (Author) , Winkler, Andrea S. (Author) ,


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  2. 2
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    Direct fluorescent labeling of NF186 and NaV1.6 in living primary neurons using bioorthogonal click chemistry: tools and resources by Stajković, Nevena (Author) , Liu, Yuanyuan (Author) , Arsić, Aleksandra (Author) , Meng, Ning (Author) , Lyu, Hang (Author) , Zhang, Nan (Author) , Grimm, Dirk (Author) , Lerche, Holger (Author) , Nikić-Spiegel, Ivana (Author) ,


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  3. 3
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    Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy by Park, Joohyun (Author) , Tucci, Arianna (Author) , Cipriani, Valentina (Author) , Demidov, German (Author) , Rocca, Clarissa (Author) , Senderek, Jan (Author) , Butryn, Michaela (Author) , Velic, Ana (Author) , Lam, Tanya (Author) , Galanaki, Evangelia (Author) , Cali, Elisa (Author) , Vestito, Letizia (Author) , Maroofian, Reza (Author) , Deininger, Natalie (Author) , Rautenberg, Maren (Author) , Admard, Jakob (Author) , Hahn, Gesa-Astrid (Author) , Bartels, Claudius (Author) , Os, Nienke J. H. van (Author) , Horvath, Rita (Author) , Chinnery, Patrick F. (Author) , Tiet, May Yung (Author) , Hewamadduma, Channa (Author) , Hadjivassiliou, Marios (Author) , Tofaris, George K. (Author) , Wood, Nicholas (Author) , Hayer, Stefanie Nicole (Author) , Bender, Friedemann (Author) , Menden, Benita (Author) , Cordts, Isabell (Author) , Klein, Katrin (Author) , Nguyen, Huu Phuc (Author) , Krauss, Joachim K. (Author) , Blahak, Christian (Author) , Strom, Tim M. (Author) , Sturm, Marc (Author) , Warrenburg, Bart Petrus Christoffel van de (Author) , Lerche, Holger (Author) , Maček, Boris (Author) , Synofzik, Matthis (Author) , Ossowski, Stephan (Author) , Timmann-Braun, Dagmar (Author) , Wolf, Marc (Author) , Smedley, Damian (Author) , Rieß, Olaf (Author) , Schöls, Ludger (Author) , Houlden, Henry (Author) , Haack, Tobias (Author) , Hengel, Holger (Author) ,


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    Predicting functional effects of missense variants in voltage-gated sodium and calcium channels by Heyne, Henrike (Author) , Baez-Nieto, David (Author) , Iqbal, Sumaiya (Author) , Palmer, Duncan S. (Author) , Brunklaus, Andreas (Author) , May, Patrick (Author) , Johannesen, Katrine M. (Author) , Lauxmann, Stephan (Author) , Lemke, Johannes R. (Author) , Møller, Rikke S. (Author) , Pérez-Palma, Eduardo (Author) , Scholl, Ute I. (Author) , Syrbe, Steffen (Author) , Lerche, Holger (Author) , Lal, Dennis (Author) , Campbell, Arthur J. (Author) , Wang, Hao-Ran (Author) , Pan, Jen (Author) , Daly, Mark J. (Author) ,


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    Novel KCNQ3 muation in a large family with benign familial neonatal epilepsy: a rare cause of neonatal seizures by Maljevic, Snezana (Author) , Vejzovic, Sabina (Author) , Bernhard, Matthias K. (Author) , Bertsche, Astrid (Author) , Weise, Sebastian (Author) , Döcker, Miriam (Author) , Lerche, Holger (Author) , Lemke, Johannes R. (Author) , Merkenschlager, Andreas (Author) , Syrbe, Steffen (Author) ,


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