Growth hormone therapy in patients with Noonan syndrome von Seo, Go Hun, Yoo, Han-Wook

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Metabolic Impacts of Discontinuation and Resumption of Recombinant Human Growth Hormone Treatment during the Transition Period in Patients with Childhood-Onset Growth Hormone Defic... von Lee, Yun Jeong, Choi, Yunha, Yoo, Han-Wook, Lee, Young Ah, Shin, Choong Ho, Choi, Han Saem, Kim, Ho-Seong, Kim, Jae Hyun, Moon, Jung Eun, Ko, Cheol Woo, Ahn, Moon Bae, Suh, Byung-Kyu, Choi, Jin-Ho

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Management issues of congenital adrenal hyperplasia during the transition from pediatric to adult care von Choi, Jin-Ho, Yoo, Han-Wook

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Progressive Familial Intrahepatic Cholestasis in Korea: A Clinicopathological Study of Five Patients von Kang, Hyo Jeong, Hong, Soon Auck, Oh, Seak Hee, Kim, Kyung Mo, Yoo, Han-Wook, Kim, Gu-Hwan, Yu, Eunsil

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Pubertal outcomes and sex of rearing of patients with ovotesticular disorder of sex development and mixed gonadal dysgenesis von Kim, Yoon Myung, Oh, Arum, Kim, Kun-Suk, Yoo, Han-Wook, Choi, Jin-Ho

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Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report von Jung, Dai, Seo, Go Hun, Kim, Yoon-Myung, Choi, Jin-Ho, Yoo, Han-Wook

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Prevalence of Fabry Disease in Korean Men with Left Ventricular Hypertrophy von Kim, Woo-Shik, Kim, Hyun Soo, Shin, Jinho, Park, Jong Chun, Yoo, Han-Wook, Takenaka, Toshihiro, Tei, Chuwa

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Etiology and therapeutic outcomes of children with gonadotropin-independent precocious puberty von Kang, Eungu, Cho, Ja Hyang, Choi, Jin-Ho, Yoo, Han-Wook

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Complete Recovery of Oxysterol 7α-Hydroxylase Deficiency by Living Donor Transplantation in a 4-Month-Old Infant: the First Korean Case Report and Literature Review von Hong, Jeana, Oh, Seak Hee, Yoo, Han-Wook, Nittono, Hiroshi, Kimura, Akihiko, Kim, Kyung Mo

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Chronic intermittent form of isovaleric aciduria in a 2-year-old boy von Cho, Jin Min, Lee, Beom Hee, Kim, Gu-Hwan, Kim, Yoo-Mi, Choi, Jin-Ho, Yoo, Han-Wook

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Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea von Choi, Jin Ho, Jung, Chang Woo, Kang, Eungu, Kim, Yoon Myung, Heo, Sun Hee, Lee, Beom Hee, Kim, Gu Hwan, Yoo, Han Wook

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Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome von Kim, Eun Hee, Yum, Mi Sun, Lee, Beom Hee, Kim, Hyo Won, Lee, Hyun Jeoung, Kim, Gu Hwan, Lee, Yun Jeong, Yoo, Han Wook, Ko, Tae Sung

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Genotype-Phenotype Correlation of SMN1 and NAIP Deletions in Korean Patients with Spinal Muscular Atrophy von Ahn, Eun Ji, Yum, Mi Sun, Kim, Eun Hee, Yoo, Han Wook, Lee, Beom Hee, Kim, Gu Hwan, Ko, Tae Sung

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The first Korean case of HDR syndrome confirmed by clinical and molecular investigation von Cheon, Chong Kun, Kim, Gu Hwan, Yoo, Han Wook

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Osler-Weber-Rendu disease presenting with hepatocellular carcinoma: radiologic and genetic findings von Lee, Joo Ho, Lee, Yung Sang, Kim, Pyo Nyun, Lee, Beom Hee, Kim, Gu Whan, Yoo, Han Wook, Heo, Nae Yun, Lim, Young Suk, Lee, Han Chu, Chung, Young Hwa, Suh, Dong Jin

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A phase 2 multi-center, open-label, switch-over trial to evaluate the safety and efficacy of Abcertin® in patients with type 1 Gaucher disease von Choi, Jin-Ho, Lee, Beom Hee, Ko, Jung Min, Sohn, Young Bae, Lee, Jin-Sung, Kim, Gu-Hwan, Heo, Sun Hee, Park, June-Young, Kim, Yoo-Mi, Kim, Ja-Hye, Yoo, Han-Wook

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Magnetic resonance imaging and spectroscopic analysis in 5 cases of Pelizaeus-Merzbacher disease: metabolic abnormalities as diagnostic tools von Lee, Eun, Yum, Mi-Sun, Choi, Hae-Won, Yoo, Han-Wook, You, Su Jeong, Lee, Eun-Hye, Ko, Tae-Sung

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Efficacy of short-term growth hormone treatment in prepubertal children with idiopathic short stature von Kim, Ho-Seong, Yang, Sei Won, Yoo, Han-Wook, Suh, Byung Kyu, Ko, Cheol Woo, Chung, Woo Yeong, Lee, Kee Hyoung, Hwang, Jin Soon, Ji, Hyi-Jeong, Ahn, Hyunji, Kim, Duk Hee

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Lowe syndrome: a single center's experience in Korea von Kim, Hyun-Kyung, Kim, Ja Hye, Kim, Yoo-Mi, Kim, Gu-Hwan, Lee, Beom Hee, Choi, Jin-Ho, Yoo, Han-Wook

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A de novo microdeletion of ANKRD11 gene in a Korean patient with KBG syndrome von Lim, Ji-Hun, Seo, Eul-Ju, Kim, Yoo-Mi, Cho, Hyun-Ju, Lee, Jin-Ok, Cheon, Chong Kun, Yoo, Han-Wook

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