Vestibular Migraine in Children and Adolescents: Clinical Findings and Laboratory Tests

Por Langhagen, Thyra, Lehrer, Nicole, Borggraefe, Ingo, Heinen, Florian, Jahn, Klaus
Publicado no Front Neurol (2015)

Babesia microti Primarily Invades Mature Erythrocytes in Mice

Por Borggraefe, Ingo, Yuan, Jie, Telford, Sam R., Menon, Sanjay, Hunter, Rouette, Shah, Sohela, Spielman, Andrew, Gelfand, Jeffrey A., Wortis, Henry H., Vannier, Edouard
Publicado em 2006

Anisotropy of transcallosal motor fibers indicates functional impairment in children with periventricular leukomalacia

Por KOERTE, INGA, PELAVIN, PAULA, KIRMESS, BERIT, FUCHS, TERESA, BERWECK, STEFFEN, LAUBENDER, RUEDIGER PAUL, BORGGRAEFE, INGO, SCHROEDER, SEBASTIAN, DANEK, ADRIAN, RUMMENY, CLAUDIA, REISER, MAXIMILIAN, KUBICKI, MAREK, SHENTON, MARTHA E, ERTL-WAGNER, BIRGIT, HEINEN, FLORIAN
Publicado em 2010

Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia

Por Zech, Michael, Boesch, Sylvia, Maier, Esther M., Borggraefe, Ingo, Vill, Katharina, Laccone, Franco, Pilshofer, Veronika, Ceballos-Baumann, Andres, Alhaddad, Bader, Berutti, Riccardo, Poewe, Werner, Haack, Tobias B., Haslinger, Bernhard, Strom, Tim M., Winkelmann, Juliane
Publicado no Am J Hum Genet (2016)

Childhood Stroke: Awareness, Interest, and Knowledge Among the Pediatric Community

Por Bonfert, Michaela V., Badura, Katharina, Gerstl, Julia, Borggraefe, Ingo, Heinen, Florian, Schroeder, Sebastian, Olivieri, Martin, Weinberger, Raphael, Landgraf, Mirjam N., Vill, Katharina, Tacke, Moritz, Berweck, Steffen, Reiter, Karl, Hoffmann, Florian, Nicolai, Thomas, Gerstl, Lucia
Publicado no Front Pediatr (2018)

Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy

Por Kotlarz, Daniel, Marquardt, Benjamin, Barøy, Tuva, Lee, Way S., Konnikova, Liza, Hollizeck, Sebastian, Magg, Thomas, Lehle, Anna S., Walz, Christoph, Borggraefe, Ingo, Hauck, Fabian, Bufler, Philip, Conca, Raffaele, Wall, Sarah M., Schumacher, Eva M., Misceo, Doriana, Frengen, Eirik, Bentsen, Beint S., Uhlig, Holm H., Hopfner, Karl-Peter, Muise, Aleixo M., Snapper, Scott B., Strømme, Petter, Klein, Christoph
Publicado no Nat Genet (2018)

SYT1-associated neurodevelopmental disorder: a case series

Por Baker, Kate, Gordon, Sarah L, Melland, Holly, Bumbak, Fabian, Scott, Daniel J, Jiang, Tess J, Owen, David, Turner, Bradley J, Boyd, Stewart G, Rossi, Mari, Al-Raqad, Mohammed, Elpeleg, Orly, Peck, Dawn, Mancini, Grazia M S, Wilke, Martina, Zollino, Marcella, Marangi, Giuseppe, Weigand, Heike, Borggraefe, Ingo, Haack, Tobias, Stark, Zornitza, Sadedin, Simon, Tan, Tiong Yang, Jiang, Yunyun, Gibbs, Richard A, Ellingwood, Sara, Amaral, Michelle, Kelley, Whitley, Kurian, Manju A, Cousin, Michael A, Raymond, F Lucy
Publicado no Brain (2018)

Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes

Por de Kovel, Carolien G. F., Syrbe, Steffen, Brilstra, Eva H., Verbeek, Nienke, Kerr, Bronwyn, Dubbs, Holly, Bayat, Allan, Desai, Sonal, Naidu, Sakkubai, Srivastava, Siddharth, Cagaylan, Hande, Yis, Uluc, Saunders, Carol, Rook, Martin, Plugge, Susanna, Muhle, Hiltrud, Afawi, Zaid, Klein, Karl-Martin, Jayaraman, Vijayakumar, Rajagopalan, Ramakrishnan, Goldberg, Ethan, Marsh, Eric, Kessler, Sudha, Bergqvist, Christina, Conlin, Laura K., Krok, Bryan L., Thiffault, Isabelle, Pendziwiat, Manuela, Helbig, Ingo, Polster, Tilman, Borggraefe, Ingo, Lemke, Johannes R., van den Boogaardt, Marie-José, Møller, Rikke S., Koeleman, Bobby P. C.
Publicado no JAMA Neurol (2017)

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies

Por Møller, Rikke S., Wuttke, Thomas V., Helbig, Ingo, Marini, Carla, Johannesen, Katrine M., Brilstra, Eva H., Vaher, Ulvi, Borggraefe, Ingo, Talvik, Inga, Talvik, Tiina, Kluger, Gerhard, Francois, Laurence L., Lesca, Gaetan, de Bellescize, Julitta, Blichfeldt, Susanne, Chatron, Nicolas, Holert, Nils, Jacobs, Julia, Swinkels, Marielle, Betzler, Cornelia, Syrbe, Steffen, Nikanorova, Marina, Myers, Candace T., Larsen, Line H.G., Vejzovic, Sabina, Pendziwiat, Manuela, von Spiczak, Sarah, Hopkins, Sarah, Dubbs, Holly, Mang, Yuan, Mukhin, Konstantin, Holthausen, Hans, van Gassen, Koen L., Dahl, Hans A., Tommerup, Niels, Mefford, Heather C., Rubboli, Guido, Guerrini, Renzo, Lemke, Johannes R., Lerche, Holger, Muhle, Hiltrud, Maljevic, Snezana
Publicado no Neurology (2017)