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Family Medicine and Community Health
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May 18, 2024
Harnessing innovation to help meet the needs of elders: field testing an electronic tool to streamline geriatric assessments across healthcare settings
Limor Adler, Zorian Radomyslsky, Miri Mizrahi Reuveni, et al.
Journal of Child Neurology
|
May 23, 2003
Clinical experience with open-label topiramate use in infants younger than 2 years of age
Nathan Watemberg, Hadassah Goldberg-Stern, Bruria Ben-Zeev, et al.
Epilepsia
|
January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrum
John A Damiano, Rosemary Burgess, Sara Kivity, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2012
Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative region
Marina Michelson, Anat Ben-Sasson, Chana Vinkler, et al.
Epilepsia
|
January 6, 2011
Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency
Zaid Afawi, Arvid Suls, Dana Ekstein, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 16, 2011
Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation
Lubov Blumkin, Arvid Suls, Tine Deconinck, et al.
Frontiers in Public Health
|
October 18, 2023
Association between COVID-19 vaccination and critical outcomes among older adults with dementia: a comparative cohort study
Zorian Radomyslsky, Sara Kivity, Shira Lidar, et al.
Pediatric Neurology
|
August 28, 2014
Thiamine deficiency in infancy: long-term follow-up
Aviva 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 hypoplasia
Daniella Nishri, Hadassa Goldberg-Stern, Iris Noyman, et al.
Epilepsy Research
|
March 23, 2013
TBC1D24 mutation associated with focal epilepsy, cognitive impairment and a distinctive cerebro-cerebellar malformation
Zaid Afawi, Simone Mandelstam, Amos D Korczyn, et al.
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of 7
Search research articles
Search
Showing results (31-40 of 62) with videos related to
Sort By:
Page
of 7
Family Medicine and Community Health
|
May 18, 2024
Harnessing innovation to help meet the needs of elders: field testing an electronic tool to streamline geriatric assessments across healthcare settings
Limor Adler, Zorian Radomyslsky, Miri Mizrahi Reuveni, et al.
Journal of Child Neurology
|
May 23, 2003
Clinical experience with open-label topiramate use in infants younger than 2 years of age
Nathan Watemberg, Hadassah Goldberg-Stern, Bruria Ben-Zeev, et al.
Epilepsia
|
January 19, 2017
Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrum
John A Damiano, Rosemary Burgess, Sara Kivity, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2012
Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative region
Marina Michelson, Anat Ben-Sasson, Chana Vinkler, et al.
Epilepsia
|
January 6, 2011
Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency
Zaid Afawi, Arvid Suls, Dana Ekstein, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 16, 2011
Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation
Lubov Blumkin, Arvid Suls, Tine Deconinck, et al.
Frontiers in Public Health
|
October 18, 2023
Association between COVID-19 vaccination and critical outcomes among older adults with dementia: a comparative cohort study
Zorian Radomyslsky, Sara Kivity, Shira Lidar, et al.
Pediatric Neurology
|
August 28, 2014
Thiamine deficiency in infancy: long-term follow-up
Aviva 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 hypoplasia
Daniella Nishri, Hadassa Goldberg-Stern, Iris Noyman, et al.
Epilepsy Research
|
March 23, 2013
TBC1D24 mutation associated with focal epilepsy, cognitive impairment and a distinctive cerebro-cerebellar malformation
Zaid Afawi, Simone Mandelstam, Amos D Korczyn, et al.
Page
of 7