Bengt Hagberg (1923-2015), Swedish father of child neurology von Kyllerman, Mårten

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Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI von Poretti, Andrea, Vitiello, Giuseppina, Hennekam, Raoul C M, Arrigoni, Filippo, Bertini, Enrico, Borgatti, Renato, Brancati, Francesco, D'Arrigo, Stefano, Faravelli, Francesca, Giordano, Lucio, Huisman, Thierry A G M, Iannicelli, Miriam, Kluger, Gerhard, Kyllerman, Marten, Landgren, Magnus, Lees, Melissa M, Pinelli, Lorenzo, Romaniello, Romina, Scheer, Ianina, Schwarz, Christoph E, Spiegel, Ronen, Tibussek, Daniel, Valente, Enza Maria, Boltshauser, Eugen

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In Memoriam: Bengt Arthur Hagberg, MD, PhD—August 9, 1923–April 12, 2015 von Percy, Alan, Kyllerman, Mårten

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Diagnosis and management of glutaric aciduria type I – revised recommendations von Kölker, Stefan, Christensen, Ernst, Leonard, James V., Greenberg, Cheryl R., Boneh, Avihu, Burlina, Alberto B., Burlina, Alessandro P., Dixon, Marjorie, Duran, Marinus, García Cazorla, Angels, Goodman, Stephen I., Koeller, David M., Kyllerman, Mårten, Mühlhausen, Chris, Müller, Edith, Okun, Jürgen G., Wilcken, Bridget, Hoffmann, Georg F., Burgard, Peter

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Autosomal Dominant Myopathy: Missense Mutation (Gly-706 → Lys) in the Myosin Heavy Chain IIa Gene von Martinsson, T, Oldfors, A, Darin, N, Berg, K, Tajsharghi, H, Kyllerman, M, Wahlstrom, J

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Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children von Lundvall, Mikael, Rajaei, Saideh, Erlandson, Anna, Kyllerman, Mårten

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Pain, balance, activity, and participation in children with hypermobility syndrome von Schubert-Hjalmarsson, Elke, Öhman, Anna, Kyllerman, Mårten, Beckung, Eva

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In Memoriam: Bengt Arthur Hagberg, MD, PhD August 9, 1923-April 12, 2015 von Percy, Alan, MD, Kyllerman, Mårten, MD, PhD

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Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations von Brockmann, Knut, Dreha-Kulaczewski, Steffi, Dechent, Peter, Bönnemann, Carsten, Helms, Gunther, Kyllerman, Marten, Brück, Wolfgang, Frahm, Jens, Huehne, Kathrin, Gärtner, Jutta, Rautenstrauss, Bernd

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SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration von Örlén, Hanna, Melberg, Atle, Raininko, Raili, Kumlien, Eva, Entesarian, Miriam, Söderberg, Per, Påhlman, Magnus, Darin, Niklas, Kyllerman, Mårten, Holmberg, Eva, Engler, Henry, Eriksson, Urban, Dahl, Niklas

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Intractable Epilepsy in a Population‐Based Series of Mentally Retarded Children von Steffenburg, Ulf, Hedström, Anders, Lindroth, Anne, Wiklund, Lars‐Martin, Hagberg, Gudrun, Kyllerman, Mårten

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Early Infantile Onset ‘‘Congenital’’ Rett Syndrome Variants: Swedish Experience Through Four Decades and Mutation Analysis von Rajaei, Saideh, Erlandson, Anna, Kyllerman, Marten, Albage, Margareta, Lundstrom, Isa, Karrstedt, Ewa-Lotta, Hagberg, Bengt

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Speech, language, and cognitive dysfunction in children with focal epileptiform activity: A follow-up study von Rejnö-Habte Selassie, Gunilla, Hedström, Anders, Viggedal, Gerd, Jennische, Margareta, Kyllerman, Mårten

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Motor impairments, neurological signs, and developmental level in individuals with Angelman syndrome von Beckung, Eva, Steffenburg, Suzanne, Kyllerman, Mårten

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Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance von Barth, Peter G., Majoie, Charles B., Caan, Matthan W.A., Weterman, Marian A.J., Kyllerman, Marten, Smit, Leo M.E., Kaplan, Richard A., Haas, Richard H., Baas, Frank, Cobben, Jan-Maarten, Poll-The, Bwee Tien

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Welcome address von Kyllerman, Marten

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Mutations and sequence variation in the human myosin heavy chain IIa gene ( ) von TAJSHARGHI, Homa, DARIN, Niklas, REKABDAR, Elham, KYLLERMAN, Marten, WAHLSTRÖM, Jan, MARTINSSON, Tommy, OLDFORS, Anders

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Juvenile galactosialidosis with attacks of neuropathic pain and absence of sialyloligosacchariduria von Darin, Niklas, Kyllerman, Mårten, Hård, Anna-Lena, Nordborg, Claes, Månsson, Jan-Eric

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In Memoriam von Percy, Alan, Kyllerman, Mårten

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Angelman syndrome 2005: Updated consensus for diagnostic criteria von Williams, Charles A., Beaudet, Arthur L., Clayton-Smith, Jill, Knoll, Joan H., Kyllerman, Martin, Laan, Laura A., Magenis, R. Ellen, Moncla, Ann, Schinzel, Albert A., Summers, Jane A., Wagstaff, Joseph

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