Heasoo Koo

Mokdong, Republic of Korea

Last Updated: 09/26/2026

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Found 19 publications

Sleep Related Problems as a Nonmotor Symptom of Dentatorubropallidoluysian Atrophy.

Sleep Related Problems as a Nonmotor Symptom of Dentatorubropallidoluysian Atrophy.

Journal: Journal of Korean medical science

Published: February 22, 2017

Electron Microscopy Pathology of ADSSL1 Myopathy.

Electron Microscopy Pathology of ADSSL1 Myopathy.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: April 29, 2016

Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V.

Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: December 22, 2015

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.

Journal: PLoS genetics

Published: November 03, 2015

DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease.

DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease.

Journal: Human mutation

Published: October 28, 2015

Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1.

Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1.

Journal: Molecular medicine reports

Published: February 03, 2015

Charcot-Marie-Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families.

Charcot-Marie-Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families.

Journal: Annals of human genetics

Published: January 08, 2015

A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy.

A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy.

Journal: BMC neurology

Published: December 15, 2014

A family with axonal sensorimotor polyneuropathy with TUBB3 mutation.

A family with axonal sensorimotor polyneuropathy with TUBB3 mutation.

Journal: Molecular medicine reports

Published: February 18, 2014

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy.

Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy.

Journal: Neurogenetics

Published: December 19, 2013

Zonal difference and prognostic significance of foxp3 regulatory T cell infiltration in breast cancer.

Zonal difference and prognostic significance of foxp3 regulatory T cell infiltration in breast cancer.

Journal: Journal of breast cancer

Published: September 09, 2013

Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family.

Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: June 19, 2013

Showing 1-12 of 19

Last Updated: 09/26/2026