Sang-Heun Lee

发表

Perspective of functional magnetic resonance imaging in middle ear research

Yongmin Chang, Sang-Heun Lee, 2013, Hearing Research.

Effect of bimodal hearing in Korean children with profound hearing loss

Sang-Heun Lee, Kyu-yup Lee, M. Huh, 2008, Acta oto-laryngologica.

The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss

G. Vriend, H. Venselaar, J. Bok, 2014, Open Biology.

Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss.

U. Kim, Jeong-In Baek, Kyu-Yup Lee, 2013, Gene.

A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.

U. Kim, Kyu-Yup Lee, Sang-Heun Lee, 2012, Gene.

Identification of causative mutation in a Korean family with Crouzon syndrome using whole exome sequencing.

Jaetae Lee, U. Kim, Min-A Kim, 2014, Annals of clinical and laboratory science.

Construction of a DNA Chip for Screening of Genetic Hearing Loss

Young-Eun Kim, U. Kim, Sang-Heun Lee, 2009, Clinical and experimental otorhinolaryngology.

A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population

U. Kim, Jeong-In Baek, Kyu-Yup Lee, 2013, PloS one.

Comparison of auditory responses determined by acoustic stimulation and by mechanical round window stimulation at equivalent stapes velocities

Jin-Ho Cho, Jin-Ho Cho, Kyu-Yup Lee, 2014, Hearing Research.

Cochlear Implant in Patients with Incomplete Partition Type III

Sang-Heun Lee, Kyu-yup Lee, E. Lim, 2009 .

Evaluation of white matter structures in patients with tinnitus using diffusion tensor imaging

Jae-Jun Lee, Myoung-Nam Kim, Yongmin Chang, 2007, Journal of Clinical Neuroscience.

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

U. Kim, Sang-Heun Lee, S. Choi, 2012, Orphanet Journal of Rare Diseases.

Genetic characteristics of 32 autosomal STR loci and its application for identifying a locus in hereditary hearing loss in the Korean population

U. Kim, Sang-Heun Lee, S. Choi, 2009, Genes & Genomics.

Reversible Sensorineural Hearing Loss due to Pachymeningitis Associated with Elevated Serum MPO-ANCA

SungHee Kim, Sang-Heun Lee, Kyu-yup Lee, 2011, Clinical and experimental otorhinolaryngology.

A Case of Cochlear Implantation in a Postligual Deaf Patient with Osteogenesis Imperfecta

Sang-Heun Lee, Kyu-yup Lee, Ji-Hyun Park, 2009 .

Application of allele-specific primer extension-based microarray for simultaneous multi-gene mutation screening in patients with non-syndromic hearing loss.

Young-Eun Kim, U. Kim, J. Bae, 2010, International journal of molecular medicine.

Auditory neural pathway evaluation on sensorineural hearing loss using diffusion tensor imaging

Myoung-Nam Kim, Yongmin Chang, Yongmin Chang, 2004, Neuroreport.

Clinical study Evaluation of white matter structures in patients with tinnitus using diffusion tensor imaging

Yongmin Chang, Jae-Jun Lee, S. Baik, 2007 .

Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.

U. Kim, Sang-Heun Lee, Hyun-joo Cho, 2010, Annals of clinical and laboratory science.

Language Development in Profoundly Prelingually Deaf Children with Cochlear Implantation: Long-Term Outcomes

D. J. Jung, Sang-Heun Lee, Kyu-yup Lee, 2016 .

Effect of Bimodal Hearing in Speech Perception Under Noisy Environment According to Residual Hearing

Eun-Jung Lim, Kyu-Yup Lee, Yee-Hyuk Kim, 2009 .

Voxel-Wise Analysis of Diffusion Tensor Imaging for Clinical Outcome of Cochlear Implantation: Retrospective Study

Yongmin Chang, Sang-Heun Lee, Kyu-yup Lee, 2012, Clinical and experimental otorhinolaryngology.

A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine

G. Vriend, T. Friedrich, H. Venselaar, 2014, European Journal of Human Genetics.

Manganese-enhanced auditory tract-tracing MRI with cochlear injection.

Jae-Chang Jung, Jae-Jun Lee, Myoung-Nam Kim, 2007, Magnetic resonance imaging.

Molecular analysis of TMC1 gene in the Korean patients with nonsyndromic hearing loss

U. Kim, Sang-Heun Lee, Tae-Jun Kwon, 2011, Genes & Genomics.

Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.

U. Kim, D. Drayna, S. Choi, 2008, International journal of pediatric otorhinolaryngology.

Functional mapping of the auditory tract in rodent tinnitus model using manganese-enhanced magnetic resonance imaging

Sang-Heun Lee, Jin-Ho Cho, Hyun-Ju Cho, 2014, NeuroImage.