The clinical characteristics of attention deficit hyperactivity von Mahajnah, M, Zelnik, N

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P173 – 2561: The clinical profile of ADHD in Israel – Impact of ethnic and social diversities von Mahajnah, M, Sharkia, R, Shorbaji, N, Terkel-Dawer, R, Zelnik, N

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A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family von Abu-Rashid, M, Mahajnah, M, Jaber, L, Kornreich, L, Bar-On, E, Basel-Vanagaite, L, Soffer, D, Koenig, M, Straussberg, R

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Cognition, psychosocial adjustment and coping in familial cases of velocardiofacial syndrome von Gothelf, D, Aviram-Goldring, A, Burg, M, Steinberg, T, Mahajnah, M, Frisch, A, Fennig, S, Zalsman, G, Weizman, A

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An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures von STRAUSSBERG, R, BASEL-VANAGAITE, L, LUPSKI, J. R, DELAGUE, V, MEGARBANE, A, RICHTER, A, LESHINSKY, E, BERKOVIC, S. F, KIVITY, S, DABBY, R, CIRAK, S, NURNBERG, P, VOIT, T, MAHAJNAH, M, INBAR, D, SAIFI, G. M

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A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an ArabaIsraeli family von Abu-Rashid, M, Mahajnah, M, Jaber, L, Kornreich, L, Bar-On, E, Basel-Vanagaite, L, Soffer, D, Koenig, M, Straussberg, R

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A Prospective Case Study of the Safety and Efficacy of Lysine-Restricted Diet and Arginine Supplementation Therapy in a Patient With Pyridoxine-Dependent Epilepsy Caused by Mutatio... von Mahajnah, Muhammad, MD, PhD, Corderio, Dawn, RN, Austin, Valerie, RD, Herd, Sarah, RD, Mutch, Carly, OT, Carter, Melissa, MD, Struys, Eduard, PhD, Mercimek-Mahmutoglu, Saadet, MD, PhD

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Phenotypic Heterogeneity in Consanguineous Patients With a Common CLN8 Mutation von Mahajnah, Muhammad, MD, Zelnik, Nathanel, MD

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VARIANT LATE INFANTILE NEURONAL CEROID LIPOFUSCINOSIS – A NOVEL C>G MISSENSE MUTATION AT THE CLN8 GENE – THE FIRST CASE OUTSIDE FINLAND OR TURKEY von Zelnik, N, Mahajnah, M, Iancu, TC, Ziegler, M

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THE HETEROGENEITY OF MUSCLE BIOPSY FINDINGS OF INFANTS WITH CONGENITAL MYOTONIC DYSTROPHY von Mahajnah, M, Shahar, E, Valdawsky, E, Zelnik, N

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The Influence of Excessive Chewing Gum Use on Headache Frequency and Severity Among Adolescents von Watemberg, Nathan, MD, Matar, Manar, MD, Har-Gil, Miki, MD, Mahajnah, Muhammad, MD

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Familial Cognitive Impairment With Ataxia With Oculomotor Apraxia von Mahajnah, Muhammad, Basel-Vanagaite, Lina, Inbar, Dov, Kornreich, Liora, Weitz, Raphael, Straussberg, Rachel

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ASSOCIATION OF PARIETO-OCCIPITAL POLYMICROGYRIA, CHIARI MALFORMATION TYPE 1 AND SYRINGOMYELIA von Mahajnah, M, Lev Lev, D, Blumkin, L, Watemberg, N, Lerman-Sagie, T

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Pediatric-Onset Gelastic Seizures: Clinical Data and Outcome von Shahar, Eli, MD, Kramer, Uri, MD, Mahajnah, Muhammad, MD, PhD, Lerman-Sagie, Tallie, MD, Goez, Rachel, MD, Gross, Varda, MD, Kutai, Miriam, MD, Genizi, Jacob, MD

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Childhood-Onset Idiopathic Intracranial Hypertension: Relation of Sex and Obesity von Genizi, Jacob, MD, Lahat, Eli, MD, Zelnik, Nathanel, MD, Mahajnah, Muhammad, MD, PhD, Ravid, Sarit, MD, Shahar, Eli, MD

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Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation von Yang, Yawei J., Baltus, Andrew E., Mathew, Rebecca S., Murphy, Elisabeth A., Evrony, Gilad D., Gonzalez, Dilenny M., Wang, Estee P., Marshall-Walker, Christine A., Barry, Brenda J., Murn, Jernej, Tatarakis, Antonis, Mahajan, Muktar A., Samuels, Herbert H., Shi, Yang, Golden, Jeffrey A., Mahajnah, Muhammad, Shenhav, Ruthie, Walsh, Christopher A.

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Clinical, radiological, and genetic characteristics of 16 patients with ACO2 gene defects: Delineation of an emerging neurometabolic syndrome von Sharkia, Rajech, Wierenga, Klaas J., Kessel, Amit, Azem, Abdussalam, Bertini, Enrico, Carrozzo, Rosalba, Torraco, Alessandra, Goffrini, Paola, Ceccatelli Berti, Camilla, McCormick, M. Eileen, Plecko, Barbara, Klein, Andrea, Abela, Lucia, Hengel, Holger, Schöls, Ludger, Shalev, Stavit, Khayat, Morad, Mahajnah, Muhammad, Spiegel, Ronen

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Multiplex families with epilepsy: Success of clinical and molecular genetic characterization von Afawi, Zaid, Oliver, Karen L, Kivity, Sara, Mazarib, Aziz, Blatt, Ilan, Neufeld, Miriam Y, Helbig, Katherine L, Goldberg-Stern, Hadassa, Misk, Adel J, Straussberg, Rachel, Walid, Simri, Mahajnah, Muhammad, Lerman-Sagie, Tally, Ben-Zeev, Bruria, Kahana, Esther, Masalha, Rafik, Kramer, Uri, Ekstein, Dana, Shorer, Zamir, Wallace, Robyn H, Mangelsdorf, Marie, MacPherson, James N, Carvill, Gemma L, Mefford, Heather C, Jackson, Graeme D, Scheffer, Ingrid E, Bahlo, Melanie, Gecz, Jozef, Heron, Sarah E, Corbett, Mark, Mulley, John C, Dibbens, Leanne M, Korczyn, Amos D, Berkovic, Samuel F

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