Growth hormone therapy in patients with Noonan syndrome

od Seo, Go Hun, Yoo, Han-Wook
Izdano u Ann Pediatr Endocrinol Metab (2018)

Weiss-Kruszka Syndrome With Unreported Manifestations; Empty Sella Syndrome Associated With Growth Hormone Deficiency

od Park, Jisun, Kim, Su Jin, Seo, GoHun, Lee, Ji-Eun
Izdano u J Endocr Soc (2021)

Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report

od Jung, Dai, Seo, Go Hun, Kim, Yoon-Myung, Choi, Jin-Ho, Yoo, Han-Wook
Izdano u Ann Pediatr Endocrinol Metab (2018)

A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing

od Kim, Yoon-Myung, Seo, Go Hun, Kim, Gu-Hwan, Ko, Jung Min, Choi, Jin-Ho, Yoo, Han-Wook
Izdano u BMC Med Genet (2018)

Empty Sella Syndrome Associated with Growth Hormone Deficiency: the First Case Report of Weiss-Kruszka Syndrome

od Park, Jisun, Ha, Dong Jun, Seo, Go Hun, Maeng, Seri, Kang, Sung Mo, Kim, Sujin, Lee, Ji Eun
Izdano u J Korean Med Sci (2021)

Recent Advances in the Application of Antibacterial Complexes Using Essential Oils

od Cho, Tae Jin, Park, Sun Min, Yu, Hary, Seo, Go Hun, Kim, Hye Won, Kim, Sun Ae, Rhee, Min Suk
Izdano u Molecules (2020)

Clinical Application of Whole Exome Sequencing to Identify Rare but Remediable Neurologic Disorders

od Kim, Min-Jee, Yum, Mi-Sun, Seo, Go Hun, Lee, Yena, Jang, Han Na, Ko, Tae-Sung, Lee, Beom Hee
Izdano u J Clin Med (2020)

Turner syndrome presented with tall stature due to overdosage of the SHOX gene

od Seo, Go Hun, Kang, Eungu, Cho, Ja Hyang, Lee, Beom Hee, Choi, Jin-Ho, Kim, Gu-Hwan, Seo, Eul-Ju, Yoo, Han-Wook
Izdano u Ann Pediatr Endocrinol Metab (2015)

The phenotypic heterogeneity of patients with Marfan-related disorders and their variant spectrums

od Seo, Go Hun, Kim, Yoon-Myung, Kang, Eungu, Kim, Gu-Hwan, Seo, Eul-Ju, Lee, Beom Hee, Choi, Jin-Ho, Yoo, Han-Wook
Izdano u Medicine (Baltimore) (2018)

Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort

od Kim, Yoon-Jeon, Kim, You-Na, Yoon, Young-Hee, Seo, Eul-Ju, Seo, Go-Hun, Keum, Changwon, Lee, Beom-Hee, Lee, Joo-Yong
Izdano u Genes (Basel) (2021)

Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay

od Seo, Go Hun, Kim, Ja Hye, Cho, Ja Hyang, Kim, Gu-Hwan, Seo, Eul-Ju, Lee, Beom Hee, Choi, Jin-Ho, Yoo, Han-Wook
Izdano u Korean J Pediatr (2016)

An A627V-activating mutation in the thyroid-stimulating hormone receptor gene in familial non-autoimmune hyperthyroidism

od Shin, Jung Hyun, Seo, Go Hun, Oh, Seung Hwan, Chung, Woo Yeong, Kim, Hye Young, Kim, Young Mi, Bae, Mi Hye, Park, Kyung Hee, Kwak, Min Jung
Izdano u Ann Pediatr Endocrinol Metab (2020)

De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans

od Lee, Yeonmi, Kim, Taeho, Lee, Miju, So, Seongjun, Karagozlu, Mustafa Zafer, Seo, Go Hun, Choi, In Hee, Lee, Peter C. W., Kim, Chong-Jai, Kang, Eunju, Lee, Beom Hee
Izdano u Genes (Basel) (2021)

Clinical and genetic spectra in patients with dystrophinopathy in Korea: A single-center study

od Yun, UnKyu, Lee, Seung-Ah, Choi, Won Ah, Kang, Seong-Woong, Seo, Go Hun, Lee, Jung Hwan, Park, Goeun, Lee, Sujee, Choi, Young-Chul, Park, Hyung Jun
Izdano u PLoS One (2021)

Ultra-rare renal diseases diagnosed with whole-exome sequencing: Utility in diagnosis and management

od Jung, Jiwon, Lee, Joo Hoon, Park, Young Seo, Seo, Go Hun, Keum, Changwon, Kang, Hee Gyung, Lee, Hajeong, Lee, Sang Koo, Lee, Sang Taek, Cho, Heeyeon, Lee, Beom Hee
Izdano u BMC Med Genomics (2021)

Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia

od Ahn, Hyunji, Seo, Go Hun, Oh, Arum, Lee, Yena, Keum, Changwon, Heo, Sun Hee, Kim, Taeho, Choi, Jeongmin, Kim, Gu-Hwan, Ko, Tae-Sung, Yum, Mi-Sun, Lee, Beom Hee, Choi, In Hee
Izdano u Medicine (Baltimore) (2020)

Fatal outcome of autosomal recessive polycystic kidney disease in neonates with recessive PKHD1 mutations

od Jung, Jiwon, Seo, Go Hun, Kim, Yoo-Mi, Han, Young Mi, Park, Ji Kwon, Kim, Gu-Hwan, Lee, Joo Hoon, Park, Young Seo, Lee, Byong Sop, Kim, Ellen Ai-Rhan, Lee, Pil-Ryang, Lee, Beom Hee
Izdano u Medicine (Baltimore) (2020)

Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients

od Kim, You Na, Song, Joon Seon, Oh, Seak Hee, Kim, Yoon Jeon, Yoon, Young Hee, Seo, Eul-Ju, Seol, Chang Ahn, Lee, Sae-Mi, Choi, Jong-Moon, Seo, Go Hun, Keum, Changwon, Lee, Beom Hee, Lee, Joo Yong
Izdano u Sci Rep (2020)

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE

od Seo, Go Hun, Kim, Taeho, Choi, In Hee, Park, Jung‐young, Lee, Jungsul, Kim, Sehwan, Won, Dhong‐gun, Oh, Arum, Lee, Yena, Choi, Jeongmin, Lee, Hajeong, Kang, Hee Gyung, Cho, Hee Yeon, Cho, Min Hyun, Kim, Yoon Jeon, Yoon, Young Hee, Eun, Baik‐Lin, Desnick, Robert J., Keum, Changwon, Lee, Beom Hee
Izdano u Clin Genet (2020)

Pharmacologic properties of high-dose ambroxol in four patients with Gaucher disease and myoclonic epilepsy

od Kim, Yoon-Myung, Yum, Mi-Sun, Heo, Sun Hee, Kim, Taeho, Jin, Hee Kyung, Bae, Jae-sung, Seo, Go Hun, Oh, Arum, Yoon, Hee Mang, Lim, Hyun Taek, Kim, Hyo-Won, Ko, Tae-Sung, Lim, Hyeong‐Seok, Osborn, Mark J, Tolar, Jakub, Cozma, Claudia, Rolfs, Arndt, Zimran, Ari, Lee, Beom Hee, Yoo, Han-Wook
Izdano u J Med Genet (2020)