P 145 Deficient body structural description in apraxia von Dafsari, H. Salimi, Dovern, A., Fink, G.R., Weiss, P.H.

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Genotype-phenotype correlation in seven motor neuron disease families with novel ALS2 mutations von Sprute, R, Jergas, H, Ölmez, A, Alawbathani, S, Karasoy, H, Salimi Dafsari, H, Becker, K, Daimagüeler, H-S, Nürnberg, P, Muntoni, F, Topaloglu, H, Uyanik, G, Cirak, S

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The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification von Becker Lena-Luise, Salimi, Dafsari Hormos, Schallner Jens, Abdin Dalia, Seifert, Michael, Petit, Florence, Smol, Thomas, Bok Levinus, Rodan Lance, Krapels Ingrid, Spranger, Stephanie, Weschke Bernhard, Johnson, Katherine, Straub Volker, Kaindl, Angela M, Di Donato Nataliya, von der Hagen Maja, Cirak Sebahattin

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Clinical features and genotype–phenotype correlations in epilepsy patients with de novo DYNC1H1 variants von Cuccurullo, Claudia, Cerulli Irelli, Emanuele, Ugga, Lorenzo, Riva, Antonella, D'Amico, Alessandra, Cabet, Sara, Lesca, Gaetan, Bilo, Leonilda, Zara, Federico, Iliescu, Catrinel, Barca, Diana, Fung, France, Helbig, Katherine, Ortiz‐Gonzalez, Xilma, Schelhaas, Helenius J., Willemsen, Marjolein H., Linden, Inge, Canafoglia, Laura, Courage, Carolina, Gommaraschi, Samuele, Gonzalez‐Alegre, Pedro, Bardakjian, Tanya, Syrbe, Steffen, Schuler, Elisabeth, Lemke, Johannes R., Vari, Stella, Roende, Gitte, Bak, Mads, Huq, Mahbulul, Powis, Zoe, Johannesen, Katrine M., Hammer, Trine Bjørg, Møller, Rikke S., Rabin, Rachel, Pappas, John, Zupanc, Mary L., Zadeh, Neda, Cohen, Julie, Naidu, Sakkubai, Krey, Ilona, Saneto, Russell, Thies, Jenny, Licchetta, Laura, Tinuper, Paolo, Bisulli, Francesca, Minardi, Raffaella, Bayat, Allan, Villeneuve, Nathalie, Molinari, Florence, Salimi Dafsari, Hormos, Moller, Birk, Le Roux, Marie, Houdayer, Clara, Vecchi, Marilena, Mammi, Isabella, Fiorini, Elena, Proietti, Jacopo, Ferri, Sofia, Cantalupo, Gaetano, Battaglia, Domenica Immacolata, Gambardella, Maria Luigia, Contaldo, Ilaria, Brogna, Claudia, Trivisano, Marina, De Dominicis, Angela, Bova, Stefania Maria, Gardella, Elena, Striano, Pasquale, Coppola, Antonietta

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Deficient body structural description contributes to apraxic end-position errors in imitation von Dafsari, Hormos Salimi, Dovern, Anna, Fink, Gereon R., Weiss, Peter H.

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Risk of meningomyelocele mediated by the common 22q11.2 deletion von Vong, Keng Ioi, Lee, Sangmoon, Au, Kit Sing, Crowley, T Blaine, Capra, Valeria, Martino, Jeremiah, Haller, Meade, Araújo, Camila, Machado, Hélio R, George, Renee, Gerding, Bryn, James, Kiely N, Stanley, Valentina, Jiang, Nan, Alu, Kameron, Meave, Naomi, Nidhiry, Anna S, Jiwani, Fiza, Tang, Isaac, Nisal, Ashna, Jhamb, Ishani, Patel, Arzoo, Patel, Aakash, McEvoy-Venneri, Jennifer, Barrows, Chelsea, Shen, Celina, Ha, Yoo-Jin, Howarth, Robyn, Strain, Madison, Ashley-Koch, Allison Elizabeth, Azam, Matloob, Mumtaz, Sara, Bot, Gyang Markus, Finnell, Richard H, Kibar, Zoha, Marwan, Ahmed I, Melikishvili, Gia, Meltzer, Hal S, Mutchinick, Osvaldo M, Stevenson, David A, Mroczkowski, Henry J, Ostrander, Betsy, Schindewolf, Erica, Moldenhauer, Julie, Zackai, Elaine H, Emanuel, Beverly S, Garcia-Minaur, Sixto, Nowakowska, Beata A, Stevenson, Roger E, Zaki, Maha S, Northrup, Hope, McNamara, Hanna K, Aldinger, Kimberly A, Phelps, Ian G, Deng, Mei, Glass, Ian A, Morrow, Bernice, McDonald-McGinn, Donna M, Sanna-Cherchi, Simone, Lamb, Dolores J, Gleeson, Joseph G

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The expanding clinical and genetic spectrum of DYNC1H1-related disorders von Möller, Birk, Becker, Lena-Luise, Saffari, Afshin, Afenjar, Alexandra, Coci, Emanuele G, Williamson, Rachel, Ward-Melver, Catherine, Gibaud, Marc, Sedláčková, Lucie, Laššuthová, Petra, Libá, Zuzana, Vlčková, Markéta, William, Nancy, Klee, Eric W, Gavrilova, Ralitza H, Lévy, Jonathan, Capri, Yline, Scavina, Mena, Körner, Robert Walter, Valuvullah, Zaheer, Weiß, Claudia, Möller, Greta Marit, Thiel, Moritz, Sinnema, Margje, Kamsteeg, Erik-Jan, Donkervoort, Sandra, Duboc, Veronique, Zaafrane-Khachnaoui, Khaoula, Elkhateeb, Nour, Selim, Laila, Margot, Henri, Marin, Victor, Beneteau, Claire, Isidor, Bertrand, Cogne, Benjamin, Keren, Boris, Küsters, Benno, Beggs, Alan H, Genetti, Casie A, Nicolai, Joost, Dötsch, Jörg, Koy, Anne, Bönnemann, Carsten G, von der Hagen, Maja, von Kleist-Retzow, Jürgen-Christoph, Voermans, Nicol, Jungbluth, Heinz, Dafsari, Hormos Salimi

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Goldberg-Shprintzen megacolon syndrome with associated sensory motor axonal neuropathy von Dafsari, Hormos Salimi, Byrne, Susan, Lin, Jean-Pierre, Pitt, Matthew, Jongbloed, Jan DH, Flinter, Frances, Jungbluth, Heinz

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