H. Koo

发表

Prognostic value of p16INK4a and p14ARF gene hypermethylation in human colon cancer.

Minjin Lee, Woon Sup Han, Ok Kyoung Kim, 2006, Pathology, research and practice.

J. Yun, H. Koo, Kyoung-Gyu Choi, 2018, Journal of Korean medical science.

Tumors of the Central Nervous System in Korea A Multicenter Study of 3221 Cases.

Y. Suh, J. Chi, H. Koo, 2002, Journal of Neuro-Oncology.

Microvessel and Lymphatic Vessel Density and VEGFR-3 Expression of Papillary Thyroid Carcinoma with Comparative Analysis of Clinicopathological Characteristics

H. Koo, M. Cho, D. Song, 2010 .

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

Deok‐Ho Kim, H. Koo, H. Kim, 2015, Annals of human genetics.

Wide phenotypic variations in Charcot-Marie-Tooth 1A neuropathy with rare copy number variations on 17p12

H. Koo, Byung-Ok Choi, Y. S. Hyun, 2011 .

Bimodal upregulation of glial cell line-derived neurotrophic factor (GDNF) in the neonatal rat brain following ischemic/hypoxic injury

T. Ikeda, H. Koo, T. Ikenoue, 2002, International Journal of Developmental Neuroscience.

Frequency of Intrahepatic FoxP3+ Regulatory T cells during the Natural Course of Chronic Hepatitis B: An Immunohistochemical Study Using Needle-Biopsied Liver Tissue

H. Koo, M. Cho, Jeong Kyong Lee, 2010 .

Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Orphanet Journal of Rare Diseases.

A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot–Marie–Tooth disease type 2L

H. Koo, Byung-Ok Choi, J. Yoo, 2013, Neuromuscular Disorders.

Two recessive intermediate Charcot‐Marie‐Tooth patients with GDAP1 mutations

H. Koo, Byung-Ok Choi, J. Yoo, 2011, Journal of the peripheral nervous system : JPNS.

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

H. Koo, G. Kwak, Won Min Mo, 2016, PLoS genetics.

A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease

H. Koo, Byung-Ok Choi, Y. Hong, 2013, BMC Medical Genetics.

Type and Incidence of Soft Tissue Sarcomas in Korea: 2001-2007

K. Jang, S. Kim, Dong-Hoon Kim, 2011 .

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

J. Kim, Ji Eun Lee, H. Koo, 2016, Human mutation.

Myotonic dystrophy type I combined with X-linked dominant Charcot–Marie–Tooth neuropathy

H. Koo, Byung-Ok Choi, K. Chung, 2010, neurogenetics.

Jejunal Mass Presented by Anemia

H. Koo, R. Lee, Gyoung Tae Noh, 2011 .

A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14

S. Züchner, Jong-Won Kim, H. Koo, 2011, Human mutation.

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

H. Koo, Byung-Ok Choi, Y. Hong, 2016, Molecular medicine reports.

Immunoglobulin G4-associated inflammatory pseudotumor of urinary bladder: a case report.

H. Koo, Sanghui Park, J. Ro, 2013, Annals of diagnostic pathology.

Myopathy due to chronic clevudine therapy - A case report

H. Koo, Youngshin Yoon, K. Park, 2009 .

Histopathological Evaluation of Pediatric Intestinal Pseudo-Obstruction: Quantitative Morphometric Analysis of Pathological Changes in the Enteric Nervous System

H. Koo, M. Cho, D. Song, 2010 .

Two de novo mutations of MFN2 associated with early-onset Charcot-Marie-Tooth disease type 2A neuropathy

H. Koo, Byung-Ok Choi, K. Chung, 2012, Genes & Genomics.

Retrorectal Teratoma with Ovarian Teratoma

H. Koo, B. Oh, R. Lee, 2012 .

Loss of PTEN Expression in Breast Cancers

Shi-Nae Lee, H. Koo, B. Moon, 2005 .

MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis.

H. Koo, Byung-Ok Choi, Jae-Won Hyun, 2011, International journal of molecular medicine.

Zonal Difference and Prognostic Significance of Foxp3 Regulatory T Cell Infiltration in Breast Cancer

H. Koo, Sanghui Park, Anbok Lee, 2014, Journal of breast cancer.

A Case of Disseminated Multidrug-Resistant Tuberculosis involving the Brain

H. Koo, Ji-Young Chang, E. Seo, 2016, Infection & chemotherapy.

Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot–Marie–Tooth disease family

H. Koo, K. Chung, J. Lee, 2005, Neurogenetics.

Expression of glial cell line-derived neurotrophic factor (GDNF) in the developing human fetal brain

H. Koo, B. H. Choi, 2001, International Journal of Developmental Neuroscience.

A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Neuromuscular Disorders.

Erratum to: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Orphanet Journal of Rare Diseases.

Ectopic hamartomatous thymoma: a case report showing CD99+ lymphocytes and a low proliferation index.

Shi-Nae Lee, H. Koo, M. Cho, 2009, Archives of pathology & laboratory medicine.

Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene.

Min Goo Lee, J. Lee, H. Koo, 2013, JAMA neurology.

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

H. Koo, Byung-Ok Choi, Y. Hong, 2014, Journal of clinical neurology.

Microscopic Colitis: The Pathologic Features of 24 Korean Patients

H. Koo, S. Jung, Min-Jung Kang, 2009 .

The Radioprotective Effect and Mechanism of Captopril on Radiation Induced-Heart Damage in Rats

H. Koo, K. Lee, Seung Hee Chang, 2004 .

Significance of Foxp3 Positive Regulatory T Cell and Tumor Infiltrating T Lymphocyte in Triple Negative Breast Cancer

H. Koo, B. Moon, M. Cho, 2011 .

A family with axonal sensorimotor polyneuropathy with TUBB3 mutation.

Ji Hoon Park, H. Koo, Byung-Ok Choi, 2015, Molecular medicine reports.

A Case of Ileal Lipoma Misdiagnosed as Colonic Lipoma

H. Koo, R. Lee, G. T. Noh, 2012 .

Unusual Intracranial Parasagittal Meningioma Extending into the Internal Jugular Vein through the Sinuses.

H. Koo, S. Lim, E. Seo, 2008, Journal of Korean Neurosurgical Society.

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

H. Koo, Byung-Ok Choi, Y. Hong, 2015, BMC Neurology.

A case of nonsystemic vasculitic neuropathy presenting with multiple cranial neuropathies.

Dongho Kim, H. Koo, Bon D. Ku, 2012, Neurology India.

Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2

H. Koo, H. Chung, Y. S. Hyun, 2013, neurogenetics.

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

H. Koo, K. Park, H. Park, 2016, Journal of clinical neurology.

An Adrenocorticotropic Hormone-secreting Malignant Pancreatic Neuroendocrine Tumor

H. Koo, C. Seong, K. Lee, 2011 .

Electron Microscopy Pathology of ADSSL1 Myopathy

S. Han, H. Koo, J. Yoo, 2016, Journal of Clinical Neurology.

SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

H. Koo, Byung-Ok Choi, Y. Hong, 2013, Neurology.

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

H. Koo, Byung-Ok Choi, Y. Hong, 2014, neurogenetics.

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

H. Koo, Y. Hong, K. Chung, 2014, neurogenetics.

Myofibrillar Myopathy - A Case Report -

Eun Hae Jeong, H. Koo, K. Park, 2010 .

Congenital hydrocephalus--analysis of 49 cases.

H. Koo, J. Chi, 1991, Journal of Korean medical science.

Middle mediastinal lesions: imaging findings and pathologic correlation.

K. S. Lee, H. Koo, Y. Kim, 2000, European journal of radiology.