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Molecular Genetics & Genomic Medicine
|
August 24, 2021
Genetic and clinical heterogeneity in Korean patients with Rubinstein-Taybi syndrome
Naye Choi, Hwa Young Kim, Byung Chan Lim, et al.
Brain & Development
|
September 8, 2004
Clinical features of A3243G mitochondrial tRNA mutation
Jong Hee Chae, Hee Hwang, Byung Chan Lim, et al.
Journal of Clinical Medicine
|
December 8, 2020
Pediatric Miller Fisher Syndrome; Characteristic Presentation and Comparison with Adult Miller Fisher Syndrome
Yeonji Jang, Jae-Hwan Choi, Jong Hee Chae, et al.
Epilepsy Research
|
August 7, 2013
Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndrome
Dong Wook Kim, Byung Chan Lim, Ki Joong Kim, et al.
Journal of the Neurological Sciences
|
March 16, 2010
A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathy
Jong-Hee Chae, Byung Chan Lim, Hae Il Cheong, et al.
Brain & Development
|
March 1, 2023
A case of pediatric anti-leucine-rich glioma inactivated 1 encephalitis with faciobrachial dystonic seizure
Seoyun Jang, Soo Yeon Kim, Woo Joong Kim, et al.
Journal of Clinical Neurology (Seoul, Korea)
|
April 23, 2020
A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel <i>POLR1C</i> Mutations
Ji Yeon Han, Soo Yeon Kim, Jung Eun Cheon, et al.
Journal of Child Neurology
|
January 30, 2010
Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism
Se Hee Kim, Hee Hwang, Jong Hee Chae, et al.
Encephalitis (Seoul, Korea)
|
July 20, 2023
Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case report
Dayun Kang, Soo Yeon Kim, Jong Hee Chae, et al.
Journal of Human Genetics
|
November 6, 2015
Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients
Young Bae Sohn, Jung Min Ko, Choong Ho Shin, et al.
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of 28
Search research articles
Search
Showing results (31-40 of 272) with videos related to
Sort By:
Page
of 28
Molecular Genetics & Genomic Medicine
|
August 24, 2021
Genetic and clinical heterogeneity in Korean patients with Rubinstein-Taybi syndrome
Naye Choi, Hwa Young Kim, Byung Chan Lim, et al.
Brain & Development
|
September 8, 2004
Clinical features of A3243G mitochondrial tRNA mutation
Jong Hee Chae, Hee Hwang, Byung Chan Lim, et al.
Journal of Clinical Medicine
|
December 8, 2020
Pediatric Miller Fisher Syndrome; Characteristic Presentation and Comparison with Adult Miller Fisher Syndrome
Yeonji Jang, Jae-Hwan Choi, Jong Hee Chae, et al.
Epilepsy Research
|
August 7, 2013
Low incidence of SCN1A genetic mutation in patients with hemiconvulsion-hemiplegia-epilepsy syndrome
Dong Wook Kim, Byung Chan Lim, Ki Joong Kim, et al.
Journal of the Neurological Sciences
|
March 16, 2010
A single large-scale deletion of mtDNA in a child with recurrent encephalopathy and tubulopathy
Jong-Hee Chae, Byung Chan Lim, Hae Il Cheong, et al.
Brain & Development
|
March 1, 2023
A case of pediatric anti-leucine-rich glioma inactivated 1 encephalitis with faciobrachial dystonic seizure
Seoyun Jang, Soo Yeon Kim, Woo Joong Kim, et al.
Journal of Clinical Neurology (Seoul, Korea)
|
April 23, 2020
A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel <i>POLR1C</i> Mutations
Ji Yeon Han, Soo Yeon Kim, Jung Eun Cheon, et al.
Journal of Child Neurology
|
January 30, 2010
Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism
Se Hee Kim, Hee Hwang, Jong Hee Chae, et al.
Encephalitis (Seoul, Korea)
|
July 20, 2023
Angiography-negative childhood primary angiitis of the central nervous system diagnosed by open brain biopsy: a case report
Dayun Kang, Soo Yeon Kim, Jong Hee Chae, et al.
Journal of Human Genetics
|
November 6, 2015
Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients
Young Bae Sohn, Jung Min Ko, Choong Ho Shin, et al.
Page
of 28