| 113 |
Clinical characteristics in Japanese children with nonobese type 2 diabetesClinical characteristics in Japanese children with nonobese type 2 diabetes
Tatsuhiko UrakamiTatsuhiko Urakami
KMSID: 1516085344 Ann Pediatr Endocrinol Metab. 2018;23(3):113-118. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.113 |
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| 119 |
Type 2 diabetes mellitus in children and adolescent: an Indonesian perspectiveType 2 diabetes mellitus in children and adolescent: an Indonesian perspective
Aman Bhakti Pulungan, Ireska Tsaniya Afifa, Diadra AnnisaAman Bhakti Pulungan, Ireska Tsaniya Afifa, Diadra Annisa
KMSID: 1516085348 Ann Pediatr Endocrinol Metab. 2018;23(3):119-125. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.119 |
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| 126 |
Childhood diabetes in IndiaChildhood diabetes in India
Sanjay Kalra, Mudita DhingraSanjay Kalra, Mudita Dhingra
KMSID: 1516085346 Ann Pediatr Endocrinol Metab. 2018;23(3):126-130. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.126 |
|
| 131 |
Therapeutic potential of alpha-1 antitrypsin in human diseaseTherapeutic potential of alpha-1 antitrypsin in human disease
Minsun Kim, Qing Cai, Youngman OhMinsun Kim, Qing Cai, Youngman Oh
KMSID: 1516085345 Ann Pediatr Endocrinol Metab. 2018;23(3):131-135. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.131 |
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| 136 |
Evaluation of bone mineral status in prepuberal children with newly diagnosed type 1 diabetesEvaluation of bone mineral status in prepuberal children with newly diagnosed type 1 diabetes
Jung Gi Roh, Jong Seo Yoon, Kyu Jung Park, Jung Sub Lim, Hae Sang Lee, Jin Soon HwangJung Gi Roh, Jong Seo Yoon, Kyu Jung Park, Jung Sub Lim, Hae Sang Lee, Jin Soon Hwang
KMSID: 1516085353 Ann Pediatr Endocrinol Metab. 2018;23(3):136-140. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.136 |
|
| 141 |
Thyroid function in obese Korean children and adolescents: Korea National Health and Nutrition Examination Survey 2013–2015Thyroid function in obese Korean children and adolescents: Korea National Health and Nutrition Examination Survey 2013–2015
Young Min An, Soon Jeong Moon, Soon Ki Kim, Young Ju Suh, Ji Eun LeeYoung Min An, Soon Jeong Moon, Soon Ki Kim, Young Ju Suh, Ji Eun Lee
KMSID: 1516085349 Ann Pediatr Endocrinol Metab. 2018;23(3):141-147. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.141 |
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| 148 |
Factors affecting height velocity in normal prepubertal childrenFactors affecting height velocity in normal prepubertal children
Jun Hui Lee, Seul Ki Kim, Eun Kyoung Lee, Moon Bae Ahn, Shin Hee Kim, Won Kyoung Cho, Kyoung Soon Cho, Min Ho Jung, Byung Kyu SuhJun Hui Lee, Seul Ki Kim, Eun Kyoung Lee, Moon Bae Ahn, Shin Hee Kim, Won Kyoung Cho, Kyoung Soon Cho, Min Ho Jung, Byung Kyu Suh
KMSID: 1516085351 Ann Pediatr Endocrinol Metab. 2018;23(3):148-153. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.148 |
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| 154 |
Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11
Jong Seo Yoon, Kyu Jung Park, Young Bae Sohn, Hae Sang Lee, Jin Soon HwangJong Seo Yoon, Kyu Jung Park, Young Bae Sohn, Hae Sang Lee, Jin Soon Hwang
KMSID: 1516085352 Ann Pediatr Endocrinol Metab. 2018;23(3):154-157. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.154 |
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| 158 |
Compound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasiaCompound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasia
Hamza Nasir, Syed Ibaad Ali, Naeem Haque, Stefan K. Grebe, Salman KirmaniHamza Nasir, Syed Ibaad Ali, Naeem Haque, Stefan K. Grebe, Salman Kirmani
KMSID: 1516085347 Ann Pediatr Endocrinol Metab. 2018;23(3):158-161. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.158 |
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| 162 |
Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenitaTesticular microlithiasis in a boy with X-linked adrenal hypoplasia congenita
Anastasios Serbis, Vassiliki Regina Tsinopoulou, Konstantina Mouzaki, Eleni P. Kotanidou, Styliani Giza, Assimina Galli-TsinopoulouAnastasios Serbis, Vassiliki Regina Tsinopoulou, Konstantina Mouzaki, Eleni P. Kotanidou, Styliani Giza, Assimina Galli-Tsinopoulou
KMSID: 1516085350 Ann Pediatr Endocrinol Metab. 2018;23(3):162-165. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.162 |
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| 166 |
A case of Wolfram syndrome with chronic renal failureA case of Wolfram syndrome with chronic renal failure
Hüseyin Anıl KorkmazHüseyin Anıl Korkmaz
KMSID: 1516085354 Ann Pediatr Endocrinol Metab. 2018;23(3):166-167. Published online 2018 September 28 DOI: http://dx.doi.org/10.6065/apem.2018.23.3.166 |
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