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Journal of Neurosurgery
|
October 3, 2015
Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease
Eun-Hee Kim, Mi-Sun Yum, Young-Shin Ra, et al.
Journal of Clinical Neurology (Seoul, Korea)
|
April 14, 2016
Erratum to: Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome
Eun Hee Kim, Mi Sun Yum, Beom Hee Lee, et al.
Brain & Development
|
September 11, 2007
Comparison of corpus callosotomy and vagus nerve stimulation in children with Lennox-Gastaut syndrome
Su Jeong You, Hoon-Chul Kang, Tae-Sung Ko, et al.
Neuroimage. Clinical
|
July 1, 2017
Large-scale structural alteration of brain in epileptic children with <i>SCN1A</i> mutation
Yun-Jeong Lee, Mi-Sun Yum, Min-Jee Kim, et al.
BMC Medical Genomics
|
September 29, 2022
Clinical and genetic analyses of patients with lateralized overgrowth
Yoon-Myung Kim, Yena Lee, Yunha Choi, et al.
Medicine
|
December 29, 2020
Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia
Hyunji Ahn, Go Hun Seo, Arum Oh, et al.
Clinical and Experimental Pediatrics
|
February 19, 2026
Long-term outcome in children with infantile epileptic spasms syndrome: a multicenter retrospective study in Korea
Sun Ah Choi, Minhye Kim, Hye Jin Kim, et al.
Journal of Epilepsy Research
|
January 28, 2022
The Role of Focal Epilepsy Features in Defining <i>SCN1A</i> Mutation-positive Dravet Syndrome as Generalized and Focal Epilepsy
Young Jun Ko, Il Han Yoo, Jiwon Lee, et al.
Journal of Medical Genetics
|
April 6, 2018
Biochemical and molecular characterisation of neurological Wilson disease
Go Hun Seo, Yoon-Myung Kim, Seak Hee Oh, et al.
Journal of Human Genetics
|
October 29, 2025
Expanding genetic and clinical spectra of β-tubulinopathies: A Korean study
Soojin Hwang, Hyunwoo Bae, Dohyung Kim, et al.
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of 12
Search research articles
Search
Showing results (101-110 of 119) with videos related to
Sort By:
Page
of 12
Journal of Neurosurgery
|
October 3, 2015
Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease
Eun-Hee Kim, Mi-Sun Yum, Young-Shin Ra, et al.
Journal of Clinical Neurology (Seoul, Korea)
|
April 14, 2016
Erratum to: Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome
Eun Hee Kim, Mi Sun Yum, Beom Hee Lee, et al.
Brain & Development
|
September 11, 2007
Comparison of corpus callosotomy and vagus nerve stimulation in children with Lennox-Gastaut syndrome
Su Jeong You, Hoon-Chul Kang, Tae-Sung Ko, et al.
Neuroimage. Clinical
|
July 1, 2017
Large-scale structural alteration of brain in epileptic children with <i>SCN1A</i> mutation
Yun-Jeong Lee, Mi-Sun Yum, Min-Jee Kim, et al.
BMC Medical Genomics
|
September 29, 2022
Clinical and genetic analyses of patients with lateralized overgrowth
Yoon-Myung Kim, Yena Lee, Yunha Choi, et al.
Medicine
|
December 29, 2020
Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia
Hyunji Ahn, Go Hun Seo, Arum Oh, et al.
Clinical and Experimental Pediatrics
|
February 19, 2026
Long-term outcome in children with infantile epileptic spasms syndrome: a multicenter retrospective study in Korea
Sun Ah Choi, Minhye Kim, Hye Jin Kim, et al.
Journal of Epilepsy Research
|
January 28, 2022
The Role of Focal Epilepsy Features in Defining <i>SCN1A</i> Mutation-positive Dravet Syndrome as Generalized and Focal Epilepsy
Young Jun Ko, Il Han Yoo, Jiwon Lee, et al.
Journal of Medical Genetics
|
April 6, 2018
Biochemical and molecular characterisation of neurological Wilson disease
Go Hun Seo, Yoon-Myung Kim, Seak Hee Oh, et al.
Journal of Human Genetics
|
October 29, 2025
Expanding genetic and clinical spectra of β-tubulinopathies: A Korean study
Soojin Hwang, Hyunwoo Bae, Dohyung Kim, et al.
Page
of 12