☰

Hea-soo Koo, MD

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

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

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

Mean distance: 16.34 (cluster 28)
 		SNBCP
Cross-listing: Neuropathology Tree

Tree Publications Grants Similar researchers PubMed Report error

Parents

Sign in to add mentor
Pierluigi C. Gambetti post-doc Case Western
George Perry post-doc 1987-1987 Case Western

Children

Sign in to add trainee

Collaborators

Sign in to add collaborator
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...