Detection of copy number variations in epilepsy using exome data
Tsuchida, N., Nakashima, M., Kato, M., Heyman, E., Inui, T., Haginoya, K., Watanabe, S., Chiyonobu, T., Morimoto, M., Ohta, M., Kumakura, A., Kubota, M., Kumagai, Y., Hamano, S.‐I., Lourenco, C.M., Yahaya, N.A., Ch'ng, G.‐S., Ngu, L.‐H., Fattal‐Valevski, A., Weisz Hubshman, M., Orenstein, N., Marom, D., Cohen, L., Goldberg‐Stern, H., Uchiyama, Y., Imagawa, E., Mizuguchi, T., Takata, A., Miyake, N., Nakajima, H., Saitsu, H., Miyatake, S., Matsumoto, N.
Published in Clinical genetics (01.03.2018)
Published in Clinical genetics (01.03.2018)
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Multicenter long-term follow-up of children with idiopathic West syndrome: ACTH versus vigabatrin
Cohen-Sadan, S., Kramer, U., Ben-Zeev, B., Lahat, E., Sahar, E., Nevo, Y., Eidlitz, T., Zeharia, A., Kivity, S., Goldberg-Stern, H.
Published in European journal of neurology (01.04.2009)
Published in European journal of neurology (01.04.2009)
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Multicenter long-term follow-up of children with idiopathic West syndrome: ACTH versus vigabatrin - CME questions
Cohen-Sadan, S., Kramer, U., Ben-Zeev, B., Lahat, E., Sahar, E., Nevo, Y., Eidlitz, T., Zeharia, A., Kivity, S., Goldberg-Stern, H.
Published in European journal of neurology (01.05.2009)
Published in European journal of neurology (01.05.2009)
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Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes
Goldberg-Stern, H, Gonen, O.M, Sadeh, M, Kivity, S, Shuper, A, Inbar, D
Published in Seizure (London, England) (01.01.2010)
Published in Seizure (London, England) (01.01.2010)
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P757: Hyperventilation during routine EEG recording: are “3 minutes” really necessary?
Watemberg, N, Farkash, M, Har-Gil, M, Alehan, F, Goldberg-Stern, H
Published in Clinical neurophysiology (01.06.2014)
Published in Clinical neurophysiology (01.06.2014)
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Epilepsy in children with infantile thiamine deficiency
Fattal-Valevski, A, Bloch-Mimouni, A, Kivity, S, Heyman, E, Brezner, A, Strausberg, R, Inbar, D, Kramer, U, Goldberg-Stern, H
Published in Neurology (15.09.2009)
Published in Neurology (15.09.2009)
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OP14 – 2647: RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia
Nishri, D, Goldberg-Stern, H, Noyman, I, Blumkin, L, Kivity, S, Saitsu, H, Nakashima, M, Matsumoto, N, Leshinsky-Silver, E, Lev, D, Lerman-Sagie, T
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Erratum to: “Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes” [Seizure: European Journal of Epilepsy 19 (2010) 12–16]
Goldberg-Stern, H, Gonen, O.M, Sadeh, M, Kivity, S, Shuper, A, Inbar, D
Published in Seizure (London, England) (01.04.2010)
Published in Seizure (London, England) (01.04.2010)
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Journal Article
Antibodies to glutamate receptor subtype 3 (GluR3) are found in some patients suffering from epilepsy as the main disease, but not in patients whose epilepsy accompanies antiphospholipid syndrome or Sneddon's syndrome
Ganor, Y., Goldberg-Stern, H., Blank, M., Shoenfeld, Y., Dobrynina, L. A., Kalashnikova, L., Levite, M.
Published in Autoimmunity (Chur, Switzerland) (01.09.2005)
Published in Autoimmunity (Chur, Switzerland) (01.09.2005)
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Antibodies from ALS patients inhibit dopamine release mediated by L-type calcium channels
Offen, D, Halevi, S, Orion, D, Mosberg, R, Stern-Goldberg, H, Melamed, E, Atlas, D
Published in Neurology (01.10.1998)
Published in Neurology (01.10.1998)
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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
Heron, Sarah E., Grinton, Bronwyn E., Kivity, Sara, Afawi, Zaid, Zuberi, Sameer M., Hughes, James N., Pridmore, Clair, Hodgson, Bree L., Iona, Xenia, Sadleir, Lynette G., Pelekanos, James, Herlenius, Eric, Goldberg-Stern, Hadassa, Bassan, Haim, Haan, Eric, Korczyn, Amos D., Gardner, Alison E., Corbett, Mark A., Gécz, Jozef, Thomas, Paul Q., Mulley, John C., Berkovic, Samuel F., Scheffer, Ingrid E., Dibbens, Leanne M.
Published in American journal of human genetics (13.01.2012)
Published in American journal of human genetics (13.01.2012)
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PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures
Scheffer, Ingrid E, Grinton, Bronwyn E, Heron, Sarah E, Kivity, Sara, Afawi, Zaid, Iona, Xenia, Goldberg-Stern, Hadassa, Kinali, Maria, Andrews, Ian, Guerrini, Renzo, Marini, Carla, Sadleir, Lynette G, Berkovic, Samuel F, Dibbens, Leanne M
Published in Neurology (20.11.2012)
Published in Neurology (20.11.2012)
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Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes
Piao, Xianhua, Chang, Bernard S., Bodell, Adria, Woods, Katelyn, BenZeev, Bruria, Topcu, Meral, Guerrini, Renzo, Goldberg-Stern, Hadassa, Sztriha, Laszlo, Dobyns, William B., Barkovich, A. James, Walsh, Christopher A.
Published in Annals of neurology (01.11.2005)
Published in Annals of neurology (01.11.2005)
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Detection and measurement of an endogenous clonidine-displacing substance in human cerebrospinal fluid
Goldberg-Stern, H., Atlas, D., Schwartz, L., Achiron, A., Ziv, I., Djaldetti, R., Zoldan, Y., Melamed, E.
Published in Brain research (22.01.1993)
Published in Brain research (22.01.1993)
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