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Seizure|February 5, 2011
The mystery of electroencephalography in acute lymphoblastic leukemiaHadassa Goldberg-Stern, Rony Cohen, Lea Pollak, et al.Harefuah|August 31, 2017
[ANTI-N-METHYL-D-ASPARTATE (NMDA) ENCEPHALITIS: THE ISRAELI PEDIATRIC MULTI-CENTER EXPERIENCE]Keren Politi, Dafna Marom, Shay Ashkenazi, et al.Cancer|December 14, 2007
Association between standard clinical and pathologic characteristics and the 21-gene recurrence score in breast cancer patients: a population-based studyIdo Wolf, Noa Ben-Baruch, Ronnie Shapira-Frommer, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|November 28, 2015
Normal human CD4(+) helper T cells express Kv1.1 voltage-gated K(+) channels, and selective Kv1.1 block in T cells induces by itself robust TNFα production and secretion and activation of the NFκB non-canonical pathwayBarbara Fellerhoff-Losch, Sergiy V Korol, Yonatan Ganor, et al.American Journal of Medical Genetics. Part A|January 4, 2021
Epilepsy and electroencephalogram evolution in YWHAG gene mutation: A new phenotype and review of the literatureTomer Stern, Naama Orenstein, Avi Fellner, et al.Plos Neglected Tropical Diseases|July 9, 2020
Protection or susceptibility to devastating childhood epilepsy: Nodding Syndrome associates with immunogenetic fingerprints in the HLA binding grooveGil Benedek, Mahmoud Abed El Latif, Keren Miller, et al.Plos Neglected Tropical Diseases|October 18, 2021
Macrophage migration inhibitory factor in Nodding syndromeGil Benedek, Mahmoud Abed El Latif, Keren Miller, et al.Pediatric Neurology|August 28, 2014
Thiamine deficiency in infancy: long-term follow-upAviva Mimouni-Bloch, Hadassa Goldberg-Stern, Rachel Strausberg, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 14, 2016
RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasiaDaniella Nishri, Hadassa Goldberg-Stern, Iris Noyman, et al.Journal of Child Neurology|November 22, 2013
Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plusHadassa Goldberg-Stern, Sharon Aharoni, Zaid Afawi, et al.Pageof 9