RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia
Daniella, Nishri, Hadassa, Goldberg-Stern, Iris, Noyman, Lubov, Blumkin, Sara, Kivity, Hirotomo, Saitsu, Mitsuko, Nakashima, Naomichi, Matsumoto, Esther, Leshinsky-Silver, Tally, Lerman- Sagie, Dorit, Lev
Published in European journal of paediatric neurology (01.05.2016)
Published in European journal of paediatric neurology (01.05.2016)
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Journal Article
Neurologic Manifestations of Influenza in Children
Pozailov, Shani, Elamour, Siham, Noyman, Iris, Ben-Shimol, Shalom
Published in The Pediatric infectious disease journal (01.06.2023)
Published in The Pediatric infectious disease journal (01.06.2023)
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Journal Article
Using nirmatrelvir/ritonavir in patients with epilepsy: An update from the Israeli chapter of the International League Against Epilepsy
Noyman, Iris, Ekstein, Dana, Fahoum, Firas, Herskovitz, Moshe, Linder, Ilan, Ben Zeev, Bruria, Eyal, Sara
Published in Epilepsia (Copenhagen) (01.05.2022)
Published in Epilepsia (Copenhagen) (01.05.2022)
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Journal Article
Adeno-associated virus serotype 9 antibody titers in patients with SMA pre-screened for treatment with onasemnogene abeparvovec -routine care evidence
Aharoni, Sharon, Bistritzer, Jacob, Levine, Hagit, Sagi, Liora, Fattal-Valevski, Aviva, Ginzberg, Mira, Noyman, Iris, Cohen, Rony, Nevo, Yoram
Published in Gene therapy (01.02.2023)
Published in Gene therapy (01.02.2023)
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Journal Article
Imaging blood-brain barrier dysfunction as a biomarker for epileptogenesis
Bar-Klein, Guy, Lublinsky, Svetlana, Kamintsky, Lyn, Noyman, Iris, Veksler, Ronel, Dalipaj, Hotjensa, Senatorov, Jr, Vladimir V, Swissa, Evyatar, Rosenbach, Dror, Elazary, Netta, Milikovsky, Dan Z, Milk, Nadav, Kassirer, Michael, Rosman, Yossi, Serlin, Yonatan, Eisenkraft, Arik, Chassidim, Yoash, Parmet, Yisrael, Kaufer, Daniela, Friedman, Alon
Published in Brain (London, England : 1878) (01.06.2017)
Published in Brain (London, England : 1878) (01.06.2017)
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Journal Article
Real-Life Outcome After Gene Replacement Therapy for Spinal Muscular Atrophy: A Multicenter Experience
Tokatly Latzer, Itay, Sagi, Liora, Lavi, Revital, Aharoni, Sharon, Bistritzer, Jacob, Noyman, Iris, Ginsburg, Mira, Lev-Or, Angela, Katzenellenbogen, Sharona, Nevo, Yoram, Fattal-Valevski, Aviva
Published in Pediatric neurology (01.07.2023)
Published in Pediatric neurology (01.07.2023)
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Journal Article
Treatment of seizures in the neonate: Guidelines and consensus‐based recommendations—Special report from the ILAE Task Force on Neonatal Seizures
Pressler, Ronit M., Abend, Nicholas S., Auvin, Stéphan, Boylan, Geraldine, Brigo, Francesco, Cilio, Maria Roberta, De Vries, Linda S., Elia, Maurizio, Espeche, Alberto, Hahn, Cecil D., Inder, Terrie, Jette, Nathalie, Kakooza‐Mwesige, Angelina, Mader, Silke, Mizrahi, Eli M., Moshé, Solomon L., Nagarajan, Lakshmi, Noyman, Iris, Nunes, Magda L., Samia, Pauline, Shany, Eilon, Shellhaas, Renée A., Subota, Ann, Triki, Chahnez Charfi, Tsuchida, Tammy, Vinayan, Kollencheri Puthenveettil, Wilmshurst, Jo M., Yozawitz, Elissa G., Hartmann, Hans
Published in Epilepsia (Copenhagen) (01.10.2023)
Published in Epilepsia (Copenhagen) (01.10.2023)
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Journal Article
UNC80 mutation causes a syndrome of hypotonia, severe intellectual disability, dyskinesia and dysmorphism, similar to that caused by mutations in its interacting cation channel NALCN
Perez, Yonatan, Kadir, Rotem, Volodarsky, Michael, Noyman, Iris, Flusser, Hagit, Shorer, Zamir, Gradstein, Libe, Birnbaum, Ramon Y, Birk, Ohad S
Published in Journal of medical genetics (01.06.2016)
Published in Journal of medical genetics (01.06.2016)
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Journal Article
Generic substitutions of antiseizure medications: recommendations issued by the Israeli Chapter of the International League Against Epilepsy
Fahoum, Firas, Linder, Ilan, Herskovitz, Moshe, Noyman, Iris, Ekstein, Dana, Ben Zeev, Bruria, Eyal, Sara
Published in Epileptic disorders (01.10.2022)
Published in Epileptic disorders (01.10.2022)
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Journal Article
New DSM-5 Criteria for ADHD- Does it Matter?
Rigler, Tohar, Manor, Iris, Kalansky, Adie, Shorer, Zamir, Noyman, Iris, Sadaka, Yair
Published in Comprehensive psychiatry (01.07.2016)
Published in Comprehensive psychiatry (01.07.2016)
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Journal Article
Treating Epilepsy Patients with Investigational Anti-COVID-19 Drugs: Recommendations by the Israeli Chapter of the ILAE
Ekstein, Dana, Noyman, Iris, Fahoum, Firas, Herskovitz, Moshe, Linder, Ilan, Ben Zeev, Bruria, Eyal, Sara
Published in The Israel Medical Association journal (01.11.2020)
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Published in The Israel Medical Association journal (01.11.2020)
Journal Article
Seizures in Premature Infants Born at Less than 28 Weeks' Gestation
Meledin, Irina, Tzur-Sebton, Hilla, Noyman, Iris, Friger, Michael, Hazan, Guy, Shany, Eilon
Published in Neonatology (Basel, Switzerland) (01.04.2019)
Published in Neonatology (Basel, Switzerland) (01.04.2019)
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Journal Article
Temporal lobe surgery for intractable epilepsy in children: What to do with the hippocampus?
Benifla, Mony, Bennet-Back, Odeya, Shorer, Zamir, Noyman, Iris, Bar-Yosef, Rima, Ekstein, Dana
Published in Seizure (London, England) (01.11.2017)
Published in Seizure (London, England) (01.11.2017)
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Journal Article
Progressive hereditary spastic paraplegia caused by a homozygous KY mutation
Yogev, Yuval, Perez, Yonatan, Noyman, Iris, Madegem, Anwar Abu, Flusser, Hagit, Shorer, Zamir, Cohen, Eugene, Kachko, Leonid, Michaelovsky, Analia, Birk, Ruth, Koifman, Arie, Drabkin, Max, Wormser, Ohad, Halperin, Daniel, Kadir, Rotem, Birk, Ohad S
Published in European journal of human genetics : EJHG (01.08.2017)
Published in European journal of human genetics : EJHG (01.08.2017)
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Journal Article
Pelizaeus-Merzbacher-like Disease Caused by AIMP1/p43 Homozygous Mutation
Feinstein, Miora, Markus, Barak, Noyman, Iris, Shalev, Hannah, Flusser, Hagit, Shelef, Ilan, Liani-Leibson, Keren, Shorer, Zamir, Cohen, Idan, Khateeb, Shareef, Sivan, Sara, Birk, Ohad S.
Published in American journal of human genetics (10.12.2010)
Published in American journal of human genetics (10.12.2010)
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Journal Article
B4GALT1‐congenital disorders of glycosylation: Expansion of the phenotypic and molecular spectrum and review of the literature
Staretz‐Chacham, Orna, Noyman, Iris, Wormser, Ohad, Abu Quider, Abed, Hazan, Guy, Morag, Iris, Hadar, Noam, Raymond, Kimiyo, Birk, Ohad S., Ferreira, Carlos R., Koifman, Arie
Published in Clinical genetics (01.06.2020)
Published in Clinical genetics (01.06.2020)
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Journal Article
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN
Maydan, Gal, Noyman, Iris, Har-Zahav, Adi, Neriah, Ziva Ben, Pasmanik-Chor, Metsada, Yeheskel, Adva, Albin-Kaplanski, Adi, Maya, Idit, Magal, Nurit, Birk, Efrat, Simon, Amos J, Halevy, Ayelet, Rechavi, Gideon, Shohat, Mordechai, Straussberg, Rachel, Basel-Vanagaite, Lina
Published in Journal of medical genetics (01.06.2011)
Published in Journal of medical genetics (01.06.2011)
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Journal Article