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Hea-soo Koo, MD

Affiliations: 
Ewha Womans University, Korea, Seoul, South Korea 
Area:
Neuropathology
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"Hea-soo Koo"
Bio:

http://jkms.org/index.php?main=previous_v9

http://jkms.org/Synapse/Data/PDFData/0063JKMS/jkms-4-55.pdf

Cross-listing: Neurotree

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Parents

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Pierluigi C. Gambetti post-doc Case Western
George Perry post-doc 1987-1987 Case Western

Children

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Publications

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Park HJ, Chang Y, Lee JE, et al. (2016) Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V. Journal of Clinical Neurology (Seoul, Korea)
Lee J, Jung SC, Hong YB, et al. (2016) Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1. Molecular Medicine Reports
Hong YB, Joo J, Hyun YS, et al. (2016) A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy. Plos Genetics. 12: e1005829
Hong YB, Kang J, Kim JH, et al. (2016) DGAT2 Mutation in a Family with Autosomal Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease. Human Mutation
Choi YR, Hong YB, Jung SC, et al. (2015) A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy. Bmc Neurology. 15: 179
Hyun YS, Lee J, Kim HJ, et al. (2015) Charcot-Marie-Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families. Annals of Human Genetics
Choi YJ, Hyun YS, Nam SH, et al. (2015) Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family. Journal of Clinical Neurology (Seoul, Korea). 11: 92-6
Hong YB, Lee JH, Park HJ, et al. (2015) A family with axonal sensorimotor polyneuropathy with TUBB3 mutation. Molecular Medicine Reports. 11: 2729-34
Park MH, Woo HM, Hong YB, et al. (2014) Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy. Neurogenetics. 15: 171-82
Hong YB, Lee JH, Park JM, et al. (2013) A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease. Bmc Medical Genetics. 14: 125
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