Phenotypic spectrum associated with de novo mutations in QRICH1 gene by 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 by Zafeiriou, D I, Ververi, A, Vargiami, E

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l -2-Hydroxyglutaric aciduria presenting with severe autistic features by 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 by 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 by 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 by Zafeiriou, D.I, Lehmann-Horn, F, Vargiami, E, Teflioudi, E, Ververi, A, Jurkat-Rott, K

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P066 Clinicoepidemiological findings and associated comorbidities in children with Pervasive Developmental Disorders by 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 by 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 by 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 by 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 by 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 by 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 by Vargiami, E, Hourmouzi, D, Psarra, N, Kyriazi, M, Dragoumi, P, Ververi, A, Bellou, A, Zafeiriou, DI

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

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

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

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Green ultrasound-assisted extraction of carotenoids from pomegranate wastes using vegetable oils by Goula, Athanasia M., Ververi, Maria, Adamopoulou, Anna, Kaderides, Kyriakos

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Type IV collagen-related nephropathy as a diagnosis in nephrotic syndrome by Dotis, John, Ververi, Athina, Printza, Nikoleta

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Recent advances in the detection of drugs of abuse by dried blood spots by Ververi, Christina, Vincenti, Marco, Salomone, Alberto

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The Council of Europe's citizenship conception in 'Education for Democratic Citizenship': a critical discourse analysis of two textbooks by Ververi, Olga

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