Noroviruses: The Most Common Pediatric Viral Enteric Pathogen at a Large University Hospital After Introduction of Rotavirus Vaccination

Heasoo Koo, F. H. Neill, Mary K. Estes, +4

Journal of the Pediatric Infectious Diseases Society

Virus EpidemiologyViral PathogenesisGastroenterologyTraveler DiarrheaRotavirus Vaccine Introduction +15

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

Khriezhanuo Nakhro, Jin-Mo Park, Young Bin Hong, +11

Neurology

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

Yeon‐Lim Suh, Heasoo Koo, Tai Seung Kim, +12

Journal of Neuro-Oncology

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

Byung‐Ok Choi, Sung Hee Kang, Young Se Hyun, +12

Human Mutation

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

Minjin Lee, Woon Sup Han, Ok Kyoung Kim, +4

Pathology - Research and Practice

Tumor BiologyHuman Colon CancerMedicinePrognostic ValueColorectal Cancer +9

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

Young Bin Hong, Jaesoon Joo, Young Se Hyun, +13

PLoS Genetics

Pmp22 DuplicationCharcot-marie-tooth DiseaseNeurological DisorderPhysiologyDegenerative Disease +7

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

Khriezhanuo Nakhro, Jin-Mo Park, Ye Jin Kim, +5

Neuromuscular Disorders

Novel Lys141thr MutationGeneticsPathogenesisMolecular BiologyMolecular Genetics +2

Proximal Dominant Hereditary Motor and Sensory Neuropathy With Proximal Dominance Association With Mutation in the TRK-Fused Gene

Sang-Soo Lee, Hye Jin Lee, Jin-Mo Park, +12

JAMA Neurology

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

Ki Wha Chung, Il Nam Sunwoo, Seung Min Kim, +7

Neurogenetics

Gjb1 V136aGeneticsPathogenesisPathologyMolecular Genetics +5

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

Hyeon Jin Kim, Young Bin Hong, Jin-Mo Park, +9

Orphanet Journal of Rare Diseases