Phenotypic spectrum associated with de novo mutations in QRICH1 gene von Ververi, A., Splitt, M., Dean, J. C. S., Brady, A. F.

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The Serotonergic System: Its Role in Pathogenesis and Early Developmental Treatment of Autism von Zafeiriou, D I, Ververi, A, Vargiami, E

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l -2-Hydroxyglutaric aciduria presenting with severe autistic features von Zafeiriou, D.I, Ververi, A, Salomons, G.S, Vargiami, E, Haas, D, Papadopoulou, V, Kontopoulos, E, Jakobs, C

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Tyrosine hydroxylase deficiency with severe clinical course von Zafeiriou, D.I., Willemsen, M.A., Verbeek, M.M., Vargiami, E., Ververi, A., Wevers, R.

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Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability von Pérez Baca, María del Rocío, Jacobs, Eva Z., Vantomme, Lies, Leblanc, Pontus, Bogaert, Elke, Dheedene, Annelies, De Cock, Laurenz, Haghshenas, Sadegheh, Foroutan, Aidin, Levy, Michael A., Kerkhof, Jennifer, McConkey, Haley, Chen, Chun-An, Batzir, Nurit Assia, Wang, Xia, Carels, Marieke, Agrawal, Pankaj, Armstrong Scott, Daryl, Bellini, Melissa, Beneteau, Claire, Bjørgo, Kathrine, Brooks, Alice, Brown, Natasha, Castle, Alison, Castro, Diana, Chorin, Odelia, Cleghorn, Mark, Clement, Emma, Coman, David, Costin, Carrie, Devriendt, Koen, Dong, Dexin, Dries, Annika, Duelund Hjortshøj, Tina, Dyment, David, Eng, Christine, Genetti, Casie, Grano, Siera, Henneman, Peter, Heron, Delphine, Hoffmann, Katrin, Du, Haowei, Isidor, Bertrand, Järvelä, Irma E., Jones, Julie, Keren, Boris, Kohlhase, Jürgen, Lalani, Seema, Le Caignec, Cedric, Lewis, Andi, Lovgren, Alysia, Lupski, James R., Lyons, Mike, Lysy, Philippe, Manning, Melanie, Marcelis, Carlo, McLean, Scott Douglas, Mercie, Sandra, Mertens, Mareike, Molin, Arnaud, Nugent, Kimberly Margaret, Öhman, Susanna, O'Leary, Melanie, Okashah Littlejohn, Rebecca, Petit, Florence, Pfundt, Rolph, Pottocki, Lorraine, Raas-Rotschild, Annick, Ranguin, Kara, Revencu, Nicole, Rosenfeld, Jill, Rhodes, Lindsay, Sals, Karen, Schrauwen, Isabelle, Schuurs-Hoeijmakers, Janneke H.M., Seaby, Eleanor G., Sheffer, Ruth, Snijders Blok, Lot, Sørensen, Kristina P., Srivastava, Siddharth, Stark, Zornitza, Stoeva, Radka, Stutterd, Chloe, Tan, Natalie B., Mathiesen Torring, Pernille, Vanakker, Olivier, van der Laan, Liselot, Ververi, Athina, Vincent, Marie, Wand, Dorothea, Wessels, Marja, White, Sue, Wojcik, Monica H., Wu, Nan, Zhao, Sen, Dermaut, Bart, Sadikovic, Bekim, Yuan, Bo, Vergult, Sarah, Callewaert, Bert

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Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation von Zafeiriou, D.I, Lehmann-Horn, F, Vargiami, E, Teflioudi, E, Ververi, A, Jurkat-Rott, K

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Manifesto for a Post-critical Pedagogy von Hodgson, Naomi, Vlieghe, Joris, Zamojski, Piotr

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P066 Clinicoepidemiological findings and associated comorbidities in children with Pervasive Developmental Disorders von Zafeiriou, D.I, Ververi, A, Vargiami, E, Papadopoulou, V, Tryfonas, D, Tsikoulas, I, Kontopolupos, E

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P319 Gaucher disease type III with craniosynosteosis von Zafeiriou, D.I, Vargiami, E, Anastasiou, A, Ververi, A, Michelakaki, E, Gombakis, N

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CPO05 The prognostic role of flash visual evoked potentials in children with bilateral spastic cerebral palsy von Vargiami, E, Zafeiriou, D, Kozeis, N, Ververi, A, Kontopoulos, E, Mavromatis, I, Tsikoulas, I

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MLP05 L-2-hydroxyglutaric aciduria presenting with severe autism von Zafeiriou, D, Ververi, A, Salomons, G, Vargiami, E, Haas, D, Papadopoulou, V, Kontopoulos, E, Jacobs, C

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Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth von Ververi, Athina, Vargiami, Euthymia, Papadopoulou, Vassiliki, Tryfonas, Dimitrios, Zafeiriou, Dimitrios

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P11.14 Short-latency somatosensory evoked potentials and Sensory Profile Questionnaire in boys with autism von Ververi, A., Vargiami, E., Papadopoulou, V., Tryfonas, D., Zafeiriou, D.

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P204 – 1658 Ataxia, headshaking and hyperactive behavior in prenatally diagnosed rhombencephalosynapsis von Vargiami, E, Hourmouzi, D, Psarra, N, Kyriazi, M, Dragoumi, P, Ververi, A, Bellou, A, Zafeiriou, DI

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P233 – 1782 Mild phenotype and high-functioning autism in a boy with MECP2 duplication syndrome von Zafeiriou, DI, Ververi, A, Vargiami, E, Kalyva, E, Kyriazi, M, Gioula, G, Gerou, S, Al-Mutawa, H, Kambouris, M

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P11 – 1780 Dystonic cerebral palsy in monozygotic twins with 10p15.3 microdeletion syndrome von Vargiami, E, Ververi, A, Kyriazi, M, Papathanasiou, E, Gioula, G, Gerou, S, Al-Mutawa, H, Kambouris, M, Zafeiriou, DI

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P05.8 A case of galactosialidosis with renal failure and hippocampal sclerosis von Zafeiriou, D., Papachristou, F., Ververi, A., Printza, N., Vargiami, E., Giza, S., Michelakakis, H.

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Expanding the phenotype of TAB2 variants and literature review von Woods, E, Marson, I, Coci, E, Spiller, M, Kumar, A, Brady, A, Homfray, T, Fisher, R, Turnpenny, P, Rankin, J, Kanani, F, Platzer, K, Ververi, A, Emmanouilidou, E, Bourboun, N, Giannakoulas, G, Balasubramanian, M

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Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome von Salpietro, V, Maroofian, R, Zaki, MS, Wangen, J, Ciolfi, A, Barresi, S, Efthymiou, S, Lamaze, A, Aughey, GN, Al Mutairi, F, Rad, A, Rocca, C, Calì, E, Accogli, A, Zara, F, Striano, P, Mojarrad, M, Tariq, H, Giacopuzzi, E, Taylor, JC, Oprea, G, Skrahina, V, Rehman, KU, Abd Elmaksoud, M, Bassiony, M, El Said, HG, Abdel-Hamid, MS, Al Shalan, M, Seo, G, Kim, S, Lee, H, Khang, R, Issa, MY, Elbendary, HM, Rafat, K, Marinakis, NM, Traeger-Synodinos, J, Ververi, A, Sourmpi, M, Eslahi, A, Khadivi Zand, F, Beiraghi Toosi, M, Babaei, M, Jackson, A, Hannah, MG, Bugiardini, E, Bertini, E, Kriouile, Y, El-Khorassani, M, Aguennouz, M, Groppa, S, Karashova, BM, Goraya, JS, Sultan, T, Avdjieva, D, Kathom, H, Tincheva, R, Banu, S, Veggiotti, P, Verrotti, A, Lanari, M, Savasta, S, Macaya, A, Garavaglia, B, Borgione, E, Papacostas, S, Vikelis, M, Chelban, V, Kaiyrzhanov, R, Cortese, A, Sullivan, R, Papanicolaou, EZ, Dardiotis, E, Maqbool, S, Ibrahim, S, Kirmani, S, Rana, NN, Atawneh, O, Lim, SY, Zuccotti, GV, Marseglia, GL, Esposito, S, Shaikh, F, Cogo, P, Corsello, G, Mangano, S, Nardello, R, Mangano, D, Scardamaglia, A, Koutsis, G, Scuderi, C, Ferrara, P, Morello, G, Zollo, M, Berni-Canani, R, Terracciano, LM, Sisto, A, Di Fabio, S, Strano, F, Scorrano, G

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KIF1A‐related disorders in children: A wide spectrum of central and peripheral nervous system involvement von Nemani, T, Steel, D, Kaliakatsos, M, DeVile, C, Ververi, A, Scott, R, Getov, S, Sudhakar, S, Male, A, Mankad, K, Genomics England Research Consortium, Muntoni, F, Reilly, MM, Kurian, MA, Carr, L, Munot, P

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