Intelligent Lead: A Novel HRI Sensor for Guide Robots

od Cho, Keum-Bae, Lee, Beom-Hee
Izdano 2012

Neurofibromatosis type I: points to be considered by general pediatricians

od Kang, Eungu, Yoon, Hee Mang, Lee, Beom Hee
izdano v Clin Exp Pediatr (2020)

Translational Read-Through of a Nonsense Mutation Causing Bartter Syndrome

od Cho, Hee Yeon, Lee, Beom Hee, Cheong, Hae Il
Izdano 2013

An Efficient Rescue System with Online Multi-Agent SLAM Framework

od Lee, SeungHwan, Kim, HanJun, Lee, BeomHee
izdano v Sensors (Basel) (2019)

Chylous Manifestations and Management of Gorham-Stout Syndrome

od Cho, Sungbin, Kang, Seung Ri, Lee, Beom Hee, Choi, Sehoon
izdano v Korean J Thorac Cardiovasc Surg (2019)

Ehlers–Danlos syndrome presenting as cystic lung disease with recurrent pneumothorax: a case report

od Kim, Min Jee, Choe, Jooae, Lee, Beom Hee, Song, Jin Woo
izdano v Respirol Case Rep (2021)

Clinical course and endocrinological characteristics of prolactinoma in children and adolescents

od Kim, Yoo-Mi, Choi, Jin-Ho, Lee, Beom Hee, Yoo, Han-Wook
Izdano 2013

Life-threatening bleeding from gastric mucosal angiokeratomas during anticoagulation: A case report of Fabry disease

od Kang, Eungu, Kim, Yoon-Myung, Kim, Dae-Hee, Yoo, Han-Wook, Lee, Beom Hee
izdano v Medicine (Baltimore) (2017)

Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome

od Kim, Eun Na, Song, Dong Eun, Yoon, Hee Mang, Lee, Beom Hee, Kim, Chong Jai
izdano v J Pathol Transl Med (2019)

Long-Term Follow-Up of Peripheral Pigmentary Retinopathy in Asian Patients with Danon Disease

od Yang, Jee Myung, Lee, Beom Hee, Nam, Gi-Byoung, Kim, June-Gone, Lee, Joo Yong
izdano v Genes (Basel) (2020)

Two cases of chronic pancreatitis associated with anomalous pancreaticobiliary ductal union and SPINK1 mutation

od Rho, Eun Sam, Kim, Earl, Koh, Hong, Yoo, Han-Wook, Lee, Beom Hee, Kim, Gu-Hwan
Izdano 2013

Hematopoietic stem cell transplantation in an infant with dedicator of cytokinesis 8 (DOCK8) deficiency associated with systemic lupus erythematosus: A case report

od Seo, Euri, Lee, Beom Hee, Lee, Joo Hoon, Park, Young Seo, Im, Ho Joon, Lee, Jina
izdano v Medicine (Baltimore) (2021)

Long-term clinical outcome and the identification of homozygous CYP27B1 gene mutations in a patient with vitamin D hydroxylation-deficient rickets type 1A

od Cho, Ja Hyang, Kang, Eungu, Kim, Gu-Hwan, Lee, Beom Hee, Choi, Jin-Ho, Yoo, Han-Wook
izdano v Ann Pediatr Endocrinol Metab (2016)

Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemia

od Kim, Hyun Jin, Kim, Yoon-Myung, Kang, Eungu, Lee, Beom Hee, Choi, Jin-Ho, Yoo, Han-Wook
izdano v Ann Pediatr Endocrinol Metab (2017)

DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea

od Cho, Ja Hyang, Kang, Eungu, Lee, Beom Hee, Kim, Gu-Hwan, Choi, Jin-Ho, Yoo, Han-Wook
izdano v J Korean Med Sci (2017)

Mutation Spectrum of STAR and the Founder Effect of p.Q258* in Korean Patients with Congenital Lipoid Adrenal Hyperplasia

od Kang, Eungu, Kim, Yoon-Myung, Kim, Gu-Hwan, Lee, Beom Hee, Yoo, Han-Wook, Choi, Jin-Ho
izdano v Mol Med (2017)

Clinical characteristics and treatment outcomes in Camurati–Engelmann disease: A case series

od Kim, Yoon-Myung, Kang, Eungu, Choi, Jin-Ho, Kim, Gu-Hwan, Yoo, Han-Wook, Lee, Beom Hee
izdano v Medicine (Baltimore) (2018)

Proteomic analysis of sera of asymptomatic, early-stage patients with Wilson's disease

od Park, Jung-Young, Mun, Joo Hee, Lee, Beom Hee, Heo, Sun Hee, Kim, Gu-Hwan, Yoo, Han-Wook
Izdano 2009

Chronic intermittent form of isovaleric aciduria in a 2-year-old boy

od Cho, Jin Min, Lee, Beom Hee, Kim, Gu-Hwan, Kim, Yoo-Mi, Choi, Jin-Ho, Yoo, Han-Wook
Izdano 2013

Clinical and molecular characteristics of congenital hypothyroidism with DUOX2 mutations

od Kim, Yoo-Mi, Jin, Hye Young, Lee, Beom Hee, Heo, Sun-Hee, Kim, Gu-Hwan, Yoo, Han-Wook
Izdano 2013