Ausgabe Sonderheft 1/2013
7th Asia Pacific Paediatric Endocrine Society (APPES) Biennial Scientific Meeting
Inhalt (263 Artikel)
The molecular mechanisms underlying diabetic complications
Francesco Chiarelli, M Loredana Marcovecchio
New insights into disorders of gonad development using whole genome analysis
Andrew Sinclair
Factors involved in the development of the metabolic syndrome. We are what we eat and what we are eating
Hiroaki Masuzaki
Implementing evidence-based medicine practice in Indonesia: before, now, and the future
Sudigdo Sastroasmoro
The DICER1 familial cancer syndrome: clinical and molecular update
Cheri Deal
The growing controversy about growth charts: WHO or regional?
Vaman Khadilkar
Evidence based care of type 1 diabetes in the asia pacific region
Maria Craig
Chinese childrens’ diabetes status, trends and hardship
Junfen Fu, Li Liang, Chunxiu Gong, Feng Xiong, Feihong Luo, Geli Liu, Pin Li, Li Liu, Ying Xin, Hui Yao, Lanwei Cui, Xing Shi, Yu Yang, Linqi Chen, Haiyan Wei
How safe is growth hormone therapy? SAGhE and beyond
Jean-Claude Carel
DKA management and outcomes
Francesco Chiarelli, M Loredana Marcovecchio
Aromatase excess syndromeas a model for genomic disorder: identification of molecular bases and phenotypic determinants
Tsutomu Ogata, Makio Shozu, Maki Fukami
Chronic treatment with valproate protects INS1 cell from palmitate-induced ER stress and apoptosis by inhibiting GSK3β
Shan Huang, Wei Wu, Yan Liang, Qin Ning, Xiao-ping Luo
Early markers of the metabolic syndrome in children born post-term
Ahila Ayyavoo, Paul L Hofman, José GB Derraik, Sarah Mathai, Peter Stone, Lynn Sadler, Wayne S Cutfield
Neurodevelopmental outcomes are normal in congenital hypothyroid children diagnosed early and treated aggressively over the first three years
Ben Albert, Natasha Heather, Wayne Cutfield, Dianne Webster, Alistair Gunn, Craig Jefferies, Trecia Wouldes, Caitrin Roberts, Sheryl Tregurtha, Heather Stewart, Sarah Mathai, José Derraik, Paul Hofman
Serum aminoterminal proctype natriuretic peptide in girls with idiopathic central precocious puberty during GNRHA treatment
Qiu-li Chen, Hua-mei Ma, Zhe Su, Yan-hong Li, Hong-shan Chen, Min-lian Du
Molecular defects of the GNRH receptor gene in Chinese patients with idiopathic hypogonadotropic hypogonadism and the severity of hypogonadism
Aws K Fathi, Sicui Hu, Xi Fu, Shan Huang, Yan Liang, Xiaoping Luo
Polymorphism of exon 13 lgr8 gene as risk factors for cryptorchidism in children
I Wayan Bikin Suryawan, Soetjiningsih, Ketut Suastika, Joserizal Latief batubara
Analysis growth development of 153 disorders of sex development
Wu Di, Gong Chunxiu, Qin Miao
A study on sexual development of SD rats by using KiSS1RNA interference mediated bylentivirus-based vectors
Dong Hong, Li Pin
A pilot study on children with bone-age advancement without early sexual maturation; auxological and laboratory (GNRH stimulation) characteristics
Choi Byung Ho, Park Hyo Min, Lee Sang In, Ko Cheol Woo
Do patients with celiac disease patients differ from those with concurrent celiac disease with type 1 diabetes mellitus?
Ashu Rastogi, Sanjay Kumar, Bhadada Rakesh Kochhar
Autologous nonmyeloablative hematopoietic stem cell transplantion in newly diagnosed childhood type 1 diabetes mellitus: the first year report
Feihong Luo, Yijin Gao, Xiaowen Qian, Li Xi, Ruoqian Cheng
High unchanged incidence of diabetic ketoacidosis between 2000 and 2009 in Auckland children
SW Cutfield, J Derraik, C Jefferies, PL Hofman, WS Cutfield
The effect of eggplant (Solanum melongena L.) extract peroal against blood glucose level of white rat (Ratus novergicus) wistar strain diabetic model
Nanda Rela Qonita, Maimun Zulhaidah, Sudiarto, Harjoedi Adji Tjahjono
Olive leaf extract improves insulin sensitivity in overweight middle aged males; a randomized, double-blinded, placebo controlled, crossover trial
Martin de Bock, Jose Derraik, Christine Brennan, Eric Thorstensen, Wayne Cutfield
The role of activation of PERK in activating glycogen synthase kinase 3(GSK-3) by oleic acid(OA) in type 2 diabetes
Wei Wu, Shan Huang, Xiaoping Luo
Association between insulin resistance with UCP2 -866G/A, UCP2 45BP INS/DEL, UCP3 -55C/T, GHSR1A RS2922126, GHSR1A RS509035 and PRO12ALA PPARΓ2 gene polymorphisms in obese female adolescents in Yogyakarta, Indonesia
Rina Susilowati, Dian Eurike Septyaningtrias, Cut Gina Inggriyani, Harry Freitag Luglio Muhammad, Madarina Julia
Association of polymorphisms in the FOXO1 and UCP3 genes with nonalcoholic fatty liver disease in Chinese children
Yan-ping Xu, Li Liang, Chun-lin Wang
Genetic susceptibility of serum cholesterol and triglyceride in Chinese Han children and adolescents
Wei-fen Zhu, Li Liang, Chun-lin Wang
Triglyceride and non-HDL-C are better predictors of cardiovascular disease risk factors in Chinese Han children and adolescents than LDL-C
Wei-fen Zhu, Li Liang, Chun-lin Wang
Study of visfatin, asp level in obese children and their clinical significance
LI Rui-zhen, MA Xin-yu, LU Hui-ling, YAO Hui, CHEN Shou-kang, KANG Si-xiu, LIN Han-hua
Evaluation of bone mineral density and bone/muscle geometry using pQCT in children after spinal cord injury
CF Munns, A Biggin, A Middleton, KA Ramjan, JN Briody, MCA Waugh
Losartan improves clinical outcome in Camurati Engelmann Disease
Ahila Ayyavoo, Tim Cundy, José GB Derraik, Paul L Hofman
An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene
Kohji Miura, Noriyuki Namba, Keiko Yamamoto, Makoto Fujiwara, Yasuhisa Ohata, Taichi Kitaoka, Takuo Kubota, Toshimi Michigami, Keiichi Ozono
Genetic diagnosis of Beckwith Wiedemann syndrome and Silver-Russell syndrome
Yoo-Mi Kim, Gu-Hwan Kim, Beom Hee Lee, Jin-Joo Lee, Seong-Hoon Choi, Ju Yeon Lee, Han-Wook Yoo
Association of imprinting status of IGF2 with the pathophysiology of intrauterine growth retardation in rats
Xiuyun Zhou, Xiaoping Luo
Down-regulation of SOCS3 gene in hypothalamus attenuates diet-induced obesity in young rats
Jie Bian, li Zhang, xuemei Bai, Yongli Zhao, Zhengjuan Liu
Factors affecting the timing of adiposity rebound
Satomi Koyama, Katsura Kariya, Go Ichikawa, Naoto Shimura, Toshimi Sairenchi, Osamu Arisaka
Extracts giving of purple eggplant (Solanum melongena L.) orally can lower blood serum levels of malondialdehide of white rat (Rattus novergicus) wistar diabetes mellitus induced by aloxan
Ellisma Swandini Nugraheni, Harjoedi Adji Tjahjono
Futher increase of obesity prevalence in Chinese children and adolescents - cross-sectional data of two consecutive samples from the city of Shanghai from 2003 to 2008
Feihong Luo, Miaoying Zhang, Fengxia Guo, Yuezhen Tu, Shuixian Shen
Prevalence and risk factors of overweight and obesity in adolescents in Malang, East Java-Indonesia
Ariani Harijono, Anik Puryatni, Haryudi Adji Cahyono, Mardhani Yosoprawoto
Severe hyperemesis gravidarum affects offspring metabolism in childhood
Ahila Ayyavoo, Paul L Hofman, José GB Derraik, Sarah Mathai, Peter Stone, Frank Bloomfield, Wayne S Cutfield
Changes of calcium channel characteristics and its relationship with pancreatic islet β cell parasecretion in rat born small for gestational age
Yan-Yan Jin, Li Liang
First born children are taller, insulin resistant and have higher blood pressure
Tim Savage, Ahila Ayyavoo, Paul Hofman, Jose Derraik, Wayne Cutfield
Clinical and molecular characteristics of congenital hypothyroidism with DUOX2 mutations
Yoo-Mi Kim, Hye Young Jin, Beom Hee Lee, Sun-Hee Heo, Gu-Hwan Kim, Han-Wook Yoo
A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan
Keisuke Nagasaki, Satoshi Narumi, Kiyomi Abe, Tadashi Asami, Hidetoshi Sato, Yohei Ogawa, Toru Kikuchi, Tomonobu Hasegawa, Akihiko Saitoh
Mauriac syndrome and early cataract diabetic
Eka Agustia Rini, Kemala Sayuti, Amirah zatil Izzah, Elfitrimelly
Characteristics of ketoacidosis diabetic at Fatmawati Hospital
Bina Akura, Ibnu Sastrawigoena
Pediatrician level of knowledge on management of type 1 diabetes mellitus and diabetic ketoacidosis
Ratna Dewi Artati, Indah S Widyahening, Aman B Pulungan
Neonatal diabetes in Wolcott–Rallison syndrome: a case report
Can Thi Bich Ngoc, Vu Chi Dung, Sarah Flanagan, Sian Ellard
Analysis of clinical and genetic features among 12 neonatal diabetes mellitus
Cao Bingyan, Gong Chunxiu, Yang Jinkui, Cao Xi, Wu Di
Acute kidney injury as a severe complication of diabetic ketoacidosis in children: a case report
Faisal Bukkar, Novina Andriana, RM Ryadi Fadil, Ahmedz Widiasta
Development of a resource tool to assist children to adjust emotionally to the diagnosis of type 1 diabetes
Angie de Casanove, Surita Stipp
Indonesia national registry of children with type 2 diabetes mellitus
Annang Giri Moelyo, Indra W Himawan, Vivekenanda Pateda, Ryadi Fadil
A case of insulin allergy in a girl with type 1 diabetes
Annang Giri Moelyo, Nova Ardyanto
Trends and complications profile in childhood-onset type 1 diabetes from North India
Tushar Godbole, Veena Nair, SVB Reddy, Vijayalakshmi Bhatia, Preeti Dabadghao, Kumudini Sharma, Eesh Bhatia
Visual evoked potentials for the evaluation of CNS impairment in type 1 diabetes in children
Heon-Seok Han, Jae Hong Yu
Illustration of children's blood pressure in diabetes mellitus type 1 in Indonesia
Indra Himawan, GM Annang, Aman B Pulungan
Epidemiologic characteristics of diabetes in children aged 0–14 years in Busan and Gyeonnam Province, Korea (2001–2010)
Suyoung Hong, Hyunji Kim, Junghyun Lee, Jaeho Yoo
Diabetic mellitus type 1 in patient with beta major thalassemia (case report)
Eka Intan, Fitriana Aditiawati
Clinical characteristics and laboratory findings of children and adolescents with diabetes
Se Young Kim, Eun Young Kim, Jin Soon Hwang
Clinical characteristics and laboratory findings of children and adolescents who were newly diagnosed with diabetes mellitus
You Jin Kim, Hae Sang Lee, Jin Soon Hwang
Hemichorea in 15-year-old patient with poorly controlled type 1 diabetes mellitus
Yong Hyuk Kim, Ho-Seong Kim
Factors associated with glycaemic control in Singapore children and young people with diabetes
Ngee Lek, Angela Hui, Bixia Ang, Christine Chua, Suzanne Goh, Pei Kwee Lim, Joyce Lim, Rashida Vasanwala, Fabian Yap
Case report and literature review: T2DM with DKA, HHS and rhabdomyolysis
Wenjing Li, Chunxiux Gong, Di Wu, Bing Sun
The obstacles in managing type 1 diabetes mellitus patients in H.Adam Malik Hospital, North Sumatera, Indonesia
Siska Mayasari Lubis, Melda Deliana, Hakimi
Diabetes ketoacidosis in L-asparaginase therapy
Marichu P Mabulac, Carol Boongaling, Lorna R Abad
Transient diabetes mellitus secondary to L-asparaginase
Lalaine Audrey G Matitu-Untalan
Misdiagnosis of type 1 diabetes mellitus
Noor Shafina Mohd Nor, Muhamad Yazid Jalaludin, Fatimah Harun
Vitamin D gene polymorphisms are associated with type 1 diabetes mellitus in Korean youth
Hyo-Kyoung Nam, Young Jun Rhie, Kee-Hyoung Lee
Quality of life in monogenic diabetes (a case report)
Nur Rochmah, Muhammad Faizi, Ahmad Yuniari, EP Netty
Early initiation of insulin in a child with T2DM and clinical course - a case report
S Ramkumar, AC Ammini
Time to peak postprandial glucose levels in childhood-onset diabetic patients analyzed with a continuous glucose monitoring system
Junichi Suzuki, Remi Kuwabara, Masako Habu, Misako Okuno, Ayako Yoshida, Tatsuhiko Urakami
Clinical picture of diabetic ketoasidosis in Saiful Anwar Hospital Malang, Indonesia, 2005-2009
Harjoedi Adji Tjahjono
Clinical picture and laboratory result of diabetes mellitus type-1
Harjoedi Adji Tjahjono
Correlation between glycemic control and quality of life of adolescents aged 13-18 years with type 1 diabetes mellitus
Elina Waiman, Bambang Tridjaja, Bambang Supriyatno
Trends in diabetes mellitus among Taiwanese adolescents and young adults during 2000-2009: a national population-based cohort study
Meng-Che Tsai, Chih-Ching Chang, Yen-Yin Chou, Shio-Jean Lin, Sheng-Hsiang Lin
Pharmacological therapies for children with type 2 diabetes mellitus should be individualized
T Urakami, M Okuno, A Yoshida, J Suzuki, H Mugisima
Medication adherence and economic problem among patients with type 1 diabetes in Central Java Province, Indonesia
Agustini Utari, Asri Purwanti, Rudy Susanto
The study of cognitive function in children with type 1 diabetes mellitus
NI Jia, XIN Ying
Frequency of dawn phenomenon and its associations with age, HbA1c and diabetes duration in Japanese type 1 diabetes mellitus (T1DM) using the continuous glucose monitoring system (CGMS)
Ayako Yoshida, Tatsuhiko Urakami, Junichi Suzuki, Misa Okuno, Masako Habu, Remi Kuwabara, Shouri Takahashi, Hideo Mugishima
Significance of the measurement of serum fructosamine in the management of childhood diabetes
Youn Shim Shin, Jiyun Park, Dong Soo Kang, Jeesuk Yu
Extra-hepatic portal vein obstruction and type 1 diabetes in a child: a co-incidence or causal association?
Rakesh Kumar, Devi Dayal
Childhood hypertension due to a rare cause
Sachin Mittal, Ameya Joshi, Anitha Ananthan, Jane David, Radha Ghildyal, Tejal lathia, Nikhil Bhagwat, Premlata Varthakavi, Manoj Chadha
Spectrum of MODY in the south of New Zealand – including two novel mutations
N Patterson, B Taylor, G Dainty, D Prosser, P Tomlinson, DR Love, B Wheeler
Classic Bartter syndrome complicated with profound growth hormone deficiency
Masanori Adachi, Toshihiro Tajima, Koji Muroya, Yumi Asakura
The growth patterns, hemoglobin pretransfusion, serum ferritin and bone age in thalassemia major patients
Made Arimbawa, Ketut Ariawati
A case of Shwachman–Diamond syndrome
Ji Hoon Kim, Won Kyoung Cho, Tai-sung Kim, Yun-Jung Choi, Byung-Kyu Suh
Growth after hematopoietic stem cell transplantation in children with acute myeloid leukemia
Seung Joon Chung, Jieun Lee, Min Jae Kang, Choong Ho Shin, Sei Won Yang
The clinical and molecular genetic study of 20 Silver Russell Syndrome cases
Chunxiu Gong, Ming-Qiang Zhu, Di Wu, Bingyan Cao
Quantifying adherence to growth hormone treatment: the easypod™ connect observational study (ECOS)
Peter Davies, Ho-Seong Kim, Martin Borkenstein, Minlian Du, Jeremy Kirk, Ludmila Kostalova, Jan Lebl, Sandro Loche, Andrea Luczay, Marc Nicolino, Svante Norgren, Dolores Rodriguez Arnao, John Vandermeulen, Christoph Gasteyger, Jürgen Zieschang, Monia Zignani
Berardinelli-Seip syndrome in a Chinese boy with Seipin gene mutation: a case study and literature review of genotype-phenotype
Shan Huang, Cai Zhang, Yan Liang, Qin Ning, Xiao-Ping Luo
Factors predicting the response to growth hormone therapy in Taiwanese patients with Turner syndrome
Ying-Hua Huang, Fu-Sung Lo, Yang-Hau Van, Hsun-Hui Sui
Hospital malnutrition at pediatric ward Dr. Wahidin Sudirohusodo Hospital Makassar
Aidah Juliaty Wahyudin, JS Lisal
Factors affecting growth and adult height in pediatric renal transplantation
Minjae Kang, Jieun Lee, Seung Joon Chung, Choong Ho Shin, Sei Won Yang
Response to growth hormone therapy in children with Noonan syndrome: correlation with or without PTPN11 Gene mutation
Yoo-Mi Kim, Jin-Ho Choi, Beom Hee Lee, Chang-Woo Jung, Hye Young Jin, Jae-Min Kim, Gu-Hwan Kim, Jin Soon Hwang, Sei Won Yang, Jin Lee, Han-Wook Yoo
Serum levels of FGF21 are reduced and negatively correlated with adiponectin in children with Prader-Willi syndrome
Su Jin Kim, Young Bae Sohn, Sung-Yoon Cho, Young Ok Choi, Chi Hwa Kim, Dong-Kyu Jin
Tall stature in children: differential diagnosis and management
Sanjay Kumar
EasypodTM adherence in children with growth disorders treated with r-hGH. A preliminary Italian experience
Sandro Loche, Piernicola Garofalo, Mariacarolina Salerno, Mohamed Maghnie, Maria Rosaria Licenziati, Giuliana Marcella Cardinale, Giuseppe Citro, Manuela Caruso Nicoletti, Salvatore Longobardi, Raffaella Perrone
Endocrine complications in patients with thalassaemia major
Zhe Meng, Liyang Liang, Lina Zhang, Liping Hou, Zulin Liu, Xiangyang Luo, Jianpei Fang, Zhanwen He, Dongfang Li
Molecular and cytogenetic analyses of a patient with Prader-Willi syndrome who also had the phenotype of Angelman syndrome
Kenichi Miyako, Atsuko Kawano, Yuichi Mushimoto
Clinical phenotype and karyotype finding of Turner syndrome in Jakarta
I Nyoman Arie Purwana, I Made Arimbawa, Frida Soesanti, Aman B Pulungan, Jose RL Batubara
Endocrinopathies in Thalassemia major patients in Thalassemia Center Jakarta, Indonesia
Frida Soesanti, Siti Ayu Putriasih, Aman Pulungan, Pustika Amalia Wahidiyat
Clinical, biochemical, and genetic analysis of two Korean patients with Trichorhinophalangeal syndrome type I and growth hormone deficiency
Young Bae Sohn, Chang-Seok Ki, Sung Won Park, Sung-Yoon Cho, Ah-Ra Ko, Min-Jung Kwon, Ji-Youn Kim, Hyung-Doo Park, Ok-Hwa Kim, Dong-Kyu Jin
Clinical and laboratory characteristics of Prader-Willi syndrome
Bui Phuong Thao, Vu Chi Dung, Nguyen Ngoc Khanh, Can Thi Bich Ngoc, Ngo Diem Ngoc, Dinh Thi Hong Nhung, An Thuy Lan, Nguyen Thi Mai, Nguyen Phu Dat, Nguyen Thi Hoan
Factors affecting height in children and adolescents with transfusion-dependent Thalassaemia – results from a Thalassaemia center in Malaysia
Tzer Hwu Ting, Bina Sharine Menon, Hishamshah Mohd Ibrahim
Association of change on insulin-like growth factor (IGF)-i and IGF-binding protein 3 with genetic markers after a month of growth hormone (GH) therapy on Chinese children born with GH deficiency
Wei Wang, Shuixian Shen, Xiaoping Luo, Chunxiu Gong, Xuefan Gu, Yun Li, Minlian Minlian, Minlian Jin, Bin Wu
Safety and effectiveness of recombinant human growth hormone replacement in postoperative craniopharyngioma children
Zhang-qian Zheng, Di-jing Zhi, Shui-xian Shen, Fei-hong Luo, Zhu-hui Zhao, Zhong Lu, Rong Ye, Ruo-qian Cheng, Xiao-jing Li
Pathological gynecomastia in children at Cipto Mangunkusumo hospital Jakarta
Novina Andriana, Frida Soesanti, Aman B Pulungan
Precocious puberty in children
Irum Atta, Taj Muhammad laghari, Yasir Naqi Khan, Saira Waqar Lone, Mohsina Ibrahim, Jamal Raza
Hyperandrogenism secondary to topical testosterone exposure
A Carroll, S Moloney, NP Murphy
Three cases of pediatric patients with testicular microlithiasis showing gynecomastia and testicular enlargement
Chong Kun Cheon, Su Yung Kim
Changes in pubertal hormones, neurotransmitters and sleep patterns during sleep in girls with precocious puberty
Ersoy Betul, Yazici Pinar, Yilmaz Hikmet, Onur Ece
Different clinical courses of central precocious pubertal girls according to the age at presentation and treatment
Heon-Seok Han, Jae Hong Yu
Central precocious puberty secondary to hypothalamic hamartoma
CG Tay, MY Jalaludin, F Harun
Serum bisphenol A levels in girls with central precocious puberty
Shin Hye Kim, Mi Jung Park, Duk Hee Kim
Basal luteinizing hormone and follicular stimulating hormone: is it sufficient for diagnosis of precocious puberty in Korean girls?
Sun Hee Lee, Woo Yeung Chung, Jae Hyun Kim
Gonadotropin-releasing hormone (GnRH) stimulation test before and after GnRH analogue treatment in central precocious puberty; can GnRH test simplify adequately?
You Jean Yang, Min Sun Kim, Pyoung Han Hwang, Dae-Yeol Lee
Use of aromatase inhibitor in a girl with peripheral precocious puberty
CY Lee, SW Cheng, LK Lee
Final height outcome of boys with idiopathic central precocious puberty treated with gonadotropin-releasing hormone analogue
Hua-mei Ma, Zhe Su, Qiu-li Chen, Yan-hong Li, Hong-shan Chen, Min-lian Du
A clinical study of relationship between obesity and pubertal development in girls
Phil Soo Oh, Hui Kwon Kim, Jeh Hoon Shin
The age of onset of pubertal development in healthy Thai girls in Khon Kaen, Thailand
Nongnapat Jirawutthinan, Ouyporn Panamonta, Sumittra Jirawutthinan, Chatchai Suesirisawat, Manat Panamonta
Pseudo-precocious puberty in a 3-year old girl
Catherine Anne G Pangilinan-Vazquez, Sioksoan C Cua, Lorna R Abad, Carmelita F Domingo, Sylvia C Estrada, Caridad M Santos
Serum osteocalcin levels in girls with central precocious puberty
Young Jun Rhie, Hyo Kyoung Nam, Kee Hyoung Lee
Precocious puberty and ovarian tumors – 2 case reports
S Ramkumar, Shivprakash, AC Ammini
Two sporadic patients of Perrault syndrome with ovarian dysgenesis and sensorineural deafness
Young-Lim Shin
Central precocious puberty in girls aged 6 to 8 years and magnetic resonance imaging of the pituitary: 11-year experience in a single centre
Joanna Yuet-ling Tung, Pik-to Cheung
Correlation nitric oxide level and homeostatic model assessment insulin resistance in obese adolescent
Julinar, Eka Agustia Rini, Hafni Bachtiar, Fadil Oenzil
The effect of Vitamin C supplementation toward high sensitivity c-reactive protein (hsC-RP) level on male adolescent obesity in Padang
Nedi Hidayat, Eka Agustia Rini, Rizanda Machmud
The effect of vitamin c supplementation on intercellular adhesion molecule-1 (ICAM-1) concentration on male adolescent obesity in Padang
Hernofialdi, Eka Agustia Rini, Rizanda Machmud
Correlation between lipid profiles and body mass index of adolescents obesity in Padang
ES Zul Febrianti, Asviandri, Lita Farlina, Rahmi Lestari, Susetyo Cahyohadi, Eka Agustia Rini
Association between lipid profile and blood pressure in obese adolescents in Padang
Asviandri, Lita Farlina, Eka Agustia Rini, Rahmi Lestari, Susetyo Cahyohadi, ES Zul Febrianti
Prevalence of Non Alcoholic Steatohepatitis (NASH) and association with body mass index in obese adolescents in Padang
Lita Farlina, Eka Agustia Rini, Rahmi Lestari, Susetyo Cahyohadi, Asviandri, ES Zul Febrianti
University screening test at State University of Jakarta
Bina Akura, Lanny C Gultom
Prediabetic risk factors among adolescents with obesity
Satriono, Ratna Dewi Artati, Dasril Daud, Ufy Trisnawati
Variants of 11β-hydroxysteroid dehydrogenase (HSD11B) gene type 1 and 2 in Chinese obese adolescents
Zou Chao Chun
Microalbuminuria and obesity in children
Byung Ok Kwak, Hye Won Park, Hyung Jung Kim, Sochung Chung, Kyo Sun Kim
Association between overweight-obese girls and age of menarche
Annang Giri Moelyo, Ema Nur Fitriana
Correlation between acanthosis nigricans and insulin resistance in obese children in Manado
Arief Gunadi, Vivekenanda Pateda, Adrian Umboh, Kristellina Sangirta Tirtamulia
25-Hydroxyvitamin D status, metabolic syndrome and insulin resistance in preadolescent child in Korea
Hae Soon Kim, Hye Ah Lee, Young Ju Kim, Eun Ae Park, Hyesook Park
Correlation of leptin, neuropeptide Y and amylin in childhood obesity
Eun Young Kim, Sei Young Kim, Min Seon Choi, Kyung Hee Yi
Risk factors of impaired glucose tolerance in obese children aged 12-15 years old
Francisca Yohanna Maria Kristiani
Reference of serum insulin level and prevalence of insulin resistance of Korean children and adolescents
Jung Sub Lim, Ju Hee Seo, Jun Ah Lee, Dong Ho Kim
Profile of fasting blood glucose in obese children with insulin resistance
Yuri, Yose M Pangestu, Vivekenanda Pateda, Kristellina Tirtamulya, Sarah M Salendu Warouw
Screening tool for diagnosis childhood obesity: percent weight for height vs body mass index
Voraluck Phatarakijnirund, Taninee Sahakitrungruang, Vichit Supornsilchai, Suttipong Wacharasindhu
Prevalence of insulin resistance in obese adolescence
Ardita Puspitadewi, Rini Sekartini, Aman B Pulungan
Factors on educational outcome for obesity prevention in female adolesecents in Korea
Hyejung Shin, Seolhyang Baek
Metabolic abnormalities in obese children attending a tertiary care centre in South India
SM Zechariah, L Priyambada, A Simon
UCP2 and UCP3 polymorphisms as risk factors of insulin resistance for Indonesian obese adolescents
M Mexitalia, Agustini Utari, Suci Romadhona, Taro Yamauchi, Takafumi Ishida
The polymorphism of EGFL6 D535N is not associated with obesity in Chinese children
Chun Lin Wang, Yi Dong Wu, Li Liang, Chao Chun Zou, Jun Fen Fu
Aspartate aminotransferase-platelet ratio index, adiponectin and body mass index in children with fatty liver
Ninung RD Kusumawati, Maria Mexitalia, Suci Romadhona, Agustini Utari
Sleep and physical activity pattern of obese children
Madarina Julia, Emy Huriyati
Comprehensive genetic analyses of primary adrenal failure without enzymatic defects
Naoko Amano, Mie Hayashi, Satoshi Narumi, Koji Muroya, Rika Kizu, Hiroshi Mochizuki, Yuko Taniguchi, Hiroki Matsuura, Keiko Homma, Tomonobu Hasegawa
Adrenal cortex tumors: clinical features and laboratory finding
Can Thi Bich Ngoc, Vu Chi Dung, Bui Phuong Thao, Nguyen Ngoc Khanh, Tran Ngoc Son, Nguyen Thanh Liem, Nguyen Phu Dat, Nguyen Thi Hoan
Diagnosis and prevalence of Congenital Adrenal Hyperplasia (CAH) in Austrian children screened or not screened for CAH
Katharina Luxenberger, David Kasper, Elke Fröhlich-Reiterer, Elisabeth Suppan, Gudrun Weinhandl, Martin Borkenstein
Malignant paragangliomas with succinate dehydrogenase subunit B mutation in a 13-year old child treated successfully with surgery and 131-I-MIBG
Chi Kwan Jasmine Chow, PW Yau, CP Wong, Angel Chan, WM But
Congenital lipoid adrenal hyperplasia in twin sisters
Hye Won Park, Byung Ok Kwak, Han-Wook Yoo, Sochung Chung
Cushing’s Syndrome due to a non-adrenal ectopic adrenocorticotropin-secreting ewing sarcoma in a child
Nancy G Honor
Results from 28 years of newborn screening for congenital adrenal hyperplasia in Sapporo City
Katsura Ishizu, Akie Nakamura, Kaori Fujikura, Masaru Fukushi, Tomoyuki Hotsubo, Taiko Sasaki, Toshihiro Tajima
Giant bilateral symptomatic adrenal myelolipomas manifested in an adult with congetnial adrenal hyperplasia
Yoo-Mi Kim, Jin-Ho Choi, Beom-Hee Lee, Gu-Hwan Kim, Beom-Sik Hong, Yong-Joon Ryu, Han-Wook Yoo
Pheochromocytoma presenting as hypotension in a 12 year old female
Marichu P Mabulac, Lorna R Abad
Congenital adrenal hyperplasia- presenting as central precocious puberty
Vimal Mavila Veetil, MC Naseerali
Evaluation of a psychosocial education program for families with congenital adrenal hyperplasia
I Mitchelhill, G Betts, J King, F Murray, J Crisp, C Briggs
Treatment outcome and some affecting factors of congenital adrenalhyperplasia
Nguyen Phu Dat, Nguyen Thuy Giang, Vu Chi Dung, Bui Phuong Thao, Nguyen Ngoc Khanh, Can Thi Bich Ngoc, Nguyen Thi Hoan
Long-term treatment of a child with congenital adrenal hyperplasia
Rogatianus Bagus Pratignyo, Aditiawati
Psychosocial problems in children with congenital adrenal hyperplasia in Cipto Mangunkusumo Hospital, Jakarta, Indonesia
I Nyoman Arie Purwana, Frida Soesanti, Aman B Pulungan, Jose RL Batubara
A pilot study on the effect of three hydrocortisone dosing regimen on 17 hydroxyprogesterone levels in patients with congenital adrenal hyperplasia
Josephine Leiya Marie F Salud, Lorna Ramos-Abad
Study relationship between the value of 17-OHP and the value of testosterone in monitoring for congenital adrenal hyperplasia
Ngo Thi Thu Huong, Nguyen Phu Dat, Nguyen Thi Hoan, Bui Phuong Thao, Nguyen Ngoc Khanh, Can Thi Bich Ngoc, Vu Chi Dung
Congenital adrenal hyperplasia in Surabaya: retrospective analysis of paediatric endocrinology private practice (1997-2011)
Connie Untario
Congenital adrenal hypoplasia, glycerol kinase deficiency and myopathy: condition requiring prompt identification. Clinical and biochemical findings in two cases
Rashida Vasanwala, Fabian Yap
Mutations of ABCD1 gene and phenotype of Vietnamese patients with X-linked adrenoleukodystrophy (X-ALD)
Vu Chi Dung, Nobuyuki Shimozawa, Nguyen Ngoc Khanh, Bui Phuong Thao, Can Thi Bich Ngoc, Nguyen Phu Dat, Nguyen Thi Hoan
Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency
Vu Chi Dung, Tran Van Khanh, Maki Fukami, Le Thi Phuong, Nguyen Thi Ha, Nguyen Thanh Liem, Ta Thanh Van
A clinical follow-up study of premature thelarche in infants under the age of two
Yingmin Wang, Li Liang, Yanlan Fang, Junfen Fu, Guanping Dong, Chunlin Wang
A girl with primary pigmented adrenocortical disease (PPNAD): challenges in diagnosis and management
Karn Wejaphikul, Vichit Supornsilchai, Suttipong Washarasindhu, Taninee Sahakitrungruang
A case of virilzing adrenocortical carcinoma diagnosed by urine steroid profiling
Joanna Yuet-ling Tung, Angel OK Chan, Elim Man, Pik-to Cheung
Improving patient access to educational resources: the development of an educational resource for congenital adrenal hyperplasia
Irene Mitchelhill, Jennie King, Nat Jackson, Pamela Dawes
Translation of a psychosocial education program for congenital adrenal hyperplasia in DVD format
Irene Mitchell, Tran Trieu Phuong Dong, Nguyen Bich Phuong, Nat Jackson, Pamela Dawes, Tien Nguyen
Effectiveness of diabetes and congenital adrenal hyperplasia meeting clubs
Quynh TV Huynh, HTD Thuy, Kate Armstrong, Maria Craig
Functional ovarian cysts in a neonate with classical 21-hydroxylase deficiency: case report and review of the literature
Hideyuki Iwayama, Haruo Mizuno, Yutaro Hayashi, Tomonobu Hasegawa, Takeshi Usui
Tackling “pillar 5” – exploring options to help families of children who are living with congenital adrenal hyperplasia (CAH) in Vietnam to achieve financial independence
KL Armstrong, D Vu Chi, Nguyen Thanh Liem, S Ditchfield, C Cole, J Willett
Plasma renin activity profile of patients with congenital adrenal hyperplasia in Semarang, Indonesia: a preliminary study
Mahayu Dewi Ariani, Nani Maharani, Udin Bahrudin, Agustini Utari, Sultana MH Faradz
Phaeochromocytoma in a teenage girl with Cushing’s Syndrome
Suryono Yudha Patria, P Bagaswoto, Suripto
Adverse events related with propylthiouracil therapy of Graves’ Disease in children at Cipto Mangunkusumo Hospital Jakarta
Novina Andriana, Aman B Pulungan, Bambang Tridjaja
Profile of Congenital Hypothyroidism patients at Hasan Sadikin General Hospital, Bandung, Indonesia 2010-2012
Faisal Bukkar, RM Ryadi Fadil
Thyroid dysfunction after hematopoietic stem cell transplantation in children: older age and acute GVHD might be risk factors of thyroid dysfunction during 3 months after HSCT
Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Seung Hoon Hahn, Byung-Kyu Suh
Hashimoto’s Thyroiditis in children and adolescents: at presentation and during long-term follow up
You Jin Kim, Hae Sang Lee, Jin Soon Hwang
Effect of the pregnant mice with Graves’ disease on thyroid function in the offspring
Qianqi Liu, Yue Yu, Shu Wang, Chunrong Chen, Xing Shi, Shining Ni, Wei Gu, Ziyang Zhu
Thyrotoxic periodic paralysis and chorea: two uncommon neuromuscular complications in an adolescent with newly diagnosed Graves disease
Pairunyar Nakavachara, Montira Suppakrucha, Surachai Likasitwattanakul
Profile of Congenital Hypothyroidism in DR. Cipto Mangunkusumo Hospital
Dana Nur Prihadi, Frida Soesanti, Aman B Pulungan, Bambang Tridjaja, Jose RL Batubara
Factors affecting on the mental development in children with Congenital Hypothyroidism
Nguyen Phu Dat, Van Lam Tra, Vu Chi Dung, Bui Phuong Thao, Can Thi Bich Ngoc, Nguyen Ngoc Khanh, Nguyen Thi Hoan
The effects of stimulation intervention on speech development of children 1-3 years old in Iodine Deficiency Disorders (IDD) area
Asri Purwanti, Saldi Fitra, Agustini Utari, Rudy Susanto
Iodine deficiency profile of Central Java province Indonesia during the year 2011
Saldi Fitra, Rudy Susanto, Asri Purwanti, Agustini Utari
The cognitive and language abilities after stimulation in children aged less than 3 years iodine deficiency area
Asri Purwanti, Fitri Hartanto, Inikke
Neonatal screening for congenital hypothyroidism: primary thryotropin screening: comparison of false positive rate using radioimmunossay (RIA) Vs fluorometric assay (FIA)
Diet S Rustama, Elly Rosilawati, Vidi Permatagalih
A clinical profile of pediatric patients admitted for thryotoxicosis in a tertiary hospital using the 1992 Burch and Wartofsky criteria
Josephine Leiya Marie F Salud, Sylvia C Estrada
Effect of iodine supplementation during pregnancy on neonatal thyroid stimulating hormone
Dabuswinee Sukkhojaiwaratkul, Pat Mahachoklertwattana, Preamrudee Poomthavorn
Iodine status as indited by neonatal thyroid stimulating hormone screening in Mitre Keluarga Hospital in Surabaya at 2005-2010
Connie Untario, I Wayan Bikin Suryawan
Three cases report of resistance to thyroid hormone and the genetic mutation of these patients and their family members
Yi Gu, Chun-xiu Gong, Qian Dong, Chang Su
Factors related to decreased bone mineral density in childhood cancer survivors
Yun Jung Choi, Moon Hee Lee, Won Kyoung Cho, Kyoung Soon Cho, So Hyun Park, Min Ho Jung, Byung Kyu Suh, Byung Churl Lee
The first reported case of pseudoparathryoidism type IB in Hong Kong: hypocalcemia in an adolescent boy with recurrent seizures
Antony CC Fu, Kwok-lap Chan, Luke Chi-tak Tong
Alendronate treatment for osteogenesis imperfecta type III in twin babies: a case report
Annang Giri Moelyo, Septin Widiretnani, Ani Suryandari
Age and seasonal variation of serum vitamin D levels in healthy school children and adolescents
Min Sun Kim, You Jean Yang, Pyoung Han Hwang, Dae-Yeol Lee
Adequate vitamin D status and adiposity contribute to bone health in peripubertal nonobese children
Jieun Lee, Young Ah Lee, Choong Ho Shin, Sei Won Yang
An atypical 7Q11.2-Q21.11 deletion in a Williams-Beuren syndome patient
Wei Lu, Yi Yang, Xiao-hong Guo, Lin Yang, Hui-jun Wang, Ren-chao Liu, Yu An, Fei-hong Luo
Challenges in managing osteogenesis imperfecta patients in H. Adam Malik hospital, North Sumatera, Indonesia
Siska Mayasari Lubis, Melda Deliana, Hakimi
Solitary parathyroid adenoma presenting with spine fracture in a paediatric patient
Marichu P Mabulac, Carol Boongaling, Sioksoan Chan-Cua
Six monthly intravenous zoledronic acid in childhood osteoporosis
CF Munns, HL Ooi, JN Briody, CT Cowell
Non-transfusion dependent hemoglobin E/β thalassemia had high prevalence of vitamin D deficiency than more severe patients who received regular blood transfusion and iron chelation therapy
Pairunyar Nakavachara, Katharee Chaichanwattanakul, Vip Viprakasit
Osteogenesis imperfecta in children: Indosesian experiences
Nur Rochmah, Nanis S Marzuki, Eka Agustiarini, Aman B Pulungan
Vitamin D profile in healthy children aged 7-12 years old in Indonesia
Frida Soesanti, Aman Pulungan, Bambang Tridjaja, Jose RL Batubara
The Effect of Cumulative Dose of Glucocorticoids on Bone in Children with Inflammatory Bowel Disease (3-year Follow- up study)
S Tomková, E Majorová, P Vanuga, J Payer
Effect of osteogenesis imperfecta on children and their families
Vu Chi Dung, Kate Armstrong, Can Thi Bich Ngoc, Bui Phuong Thao, Nguyen Ngoc Khanh, Nguyen Thu Trang, Nguyen Thi Hoan, Nguyen Phu Dat, Craig Munns
A rare cause of primary hypoparathyroidism due to a novel mutation in the GATA3 gene – the Barakat syndrome
SMY Wong, WM But, Angel Chan, W Chan
Waist to height ratio; a simple and valid index for metabolic syndrome in Korean adolescents
In-Hyuk Chung, Sang Shin Park, Eun-Gyong Yoo
Targeted suppression of glutaryl-CoA dehydrogenase by lentivirus-mediated SHRNA and excessive intake of lysine induce the apoptosis of rat striatal neurons
Gao Jinzhi, Fu Xi, Zhang Cai, Gao Hongjie, Luo Xiaoping
A Chinese boy with episodic ataxia and low CSF glucose
Kwai-fun Huen
A case of sitosterolaemia with stomatocyticanaemia and thrombocytopenia treated with Ezetimibe with good response
Ching-ngar Hung, Ching-yin Lee
Geneotype and phenotype in 20 patients with glycogen storage disease type Ia
Cuili Liang, Li Liu, Huiying Sheng, Minyan Jiang, Xi Yin
Short term outcome of congenital hyperinsulinism: case series
Song Hai Lim, Janet YH Hong, MZ Fuziah, S Flanagan, S Ellard, K Hussain
21 hypoglycemia cases with hyperinsulinemia
Yusuke Mizuno, Satsuki Nishigaki, Kengo Miyashita, Akiko Yamamoto, Yasuhiro Naiki, Reiko Horikawa
A discordant of blood glucose analysed by Glucometer and the Central lab method in an infant with Galactosemia
Sukumarn Siripunthana, Taninee Sahakitrungruang, Suttipong Washarasindhu, Kanya Suphapeetiporn, Vichit Supornsilchai
Molecular genetics and phenotype of 26 Vietnamese patients with congenital hyperinsulinism
Vu Chi Dung, Nguyen Thanh Liem, Bui Phuong Thao, Nguyen Ngoc Khanh, Can Thi Bich Ngoc, Nguyen Thi Hoan, Khu Thi Khanh Dung, Le To Nhu, Dang Anh Duong, Nguyen Phu Dat, Sarah Flanagan, Sian Ellard
Detection of inborn error of metabolisms by urine organic acid GC-MS in Southern China
MinYan Jiang, Li Liu, HuiFen Mei, XiuZhen Li, Jing Cheng, YanNa Cai, Wen Zhang, XiaoJian Mao, ZhiKun Lu
First case report of short-chain acyl-CoA dehydrogenase deficiency in China
MinYan Jiang, Li Liu, MinZhi Peng, CuiLi Liang, HuiYing Sheng, YanNa Cai
Long-term outcome of a child with hyperinsulinism- hyperammonaemia syndrome
HC Yau, GWK Wong
A new celll model of glutaric acidemia type I and the toxicity research
Cai Zhang, Xiaoping Luo
Clinical, hormonal and chromosomal analysis of undervirilized male/46XY DSD – a 3years experience of national institute of child health
Irum Atta, Saira Lone, Yasir Naqi Khan, Mohsina Ibrahim, Jamal Raza
Etiologies of 46,XY disorders of sex development (DSD): a collaborative study in Hong Kong
WM But, Angel Chan, CY Lee, Almen Lam, YY Lam, PY Loung, KL Ng, MY Wong, KT Chan, WY Tse, CC Shek
Diagnosis of 5α–reductase 2 deficiency: is measurement of dihydrotestosterone essential?
Angel OK Chan, WM But, CY Lee, YY Lam, KL Ng, Joanna Tung, PT Cheung, Doris Chan, WY Tse, CC Shek
Penile length of newborns and children in Surakarta, Indonesia
Annang Giri Moelyo, Melita Widyastuti
The incidence of cryptorchidism among boys in some provinces in Indonesia
Siska Mayasari Lubis, Vivekenanda Pateda, Aditya Suryansyah, I Made Arimbawa, Wayan Bikin Suryawan
A novel mutation in the SRY gene causing 46 XY complete gonadal dysgenesis in a Chinese patient
Elim Man, Yuet-Ling Tung, Ho-Ming Luk, Fai-Man Ivan Lo, Tak-Sum Stephen Lam, Pik-To Cheung
A 45 X male patient with 7Q distal deletion and rearragement with SRY gene translocation; a case report
Ayşenur Ökten, Mevlit İkbal, Yakup Aslan
Clinical presentations and molecular characterization of Indonesian children with 5 alpha-reductase deficiency
Nanis S Marzuki, Lita P Suciati, Firman P Idris, Bambang Tridjaja
Sex rearing in individuals with 46,XY disorders of sex development prior to diagnosis
Nanis S Marzuki, Lita P Suciati, Chrysantine Paramayuda, Hannie D Kartapradja, Bambang Tridaja
Characteristic of patients with disorders of sex development (DSD) in Cipto Mangunkusumo Hospital, Jakarta
Agustini Utari, Aman B Pulungan, Bambang Tridjaja
Genotype and phenotype of Vietnamese patients with androgen insensitivity syndrome
Vu Chi Dung, Maki Fukami, Can Thi Bich Ngoc, Bui Phuong Thao, Nguyen Ngoc Khanh, Nguyen Thi Hoan, Nguyen Thanh Liem, Ngo Diem Ngoc, Nguyen Thi Phuong Mai, Pham Thu Nga, Nguyen Phu Dat, Tsutomu Ogata
Etiology and clinical profile of children and adolescents with disorders of sex development (DSD) presenting with ambiguous external genitalia
Sachin Mittal, Premlata Varthakavi, Manoj Chadha, Nikhil Bhagwat, Tejal Lathia, Ameya Joshi, Pratibha Pawal, Bharat Sharma
Hypothalamic hamartoma with pubertas precox and gelastic seizure in a boy (Case Report)
Iman Hendarman, Aditiawati, Msy Rita Dewi Arifin
Clinical course and endocrinological characteristics of prolactinoma in children and adolescents
Yoo-Mi Kim, Jin-Ho Choi, Beom Hee Lee, Han-Wook Yoo
Multiple pituitary hormone deficiency: beware of combined hormones deficiency
Nur Rochmah, Muhammad Faizi, Achmad Yuniari, Netty Harjantien
Relapse in pituitary adenoma after resection
Nur Rochmah, Frida Soesanti, Aman B Pulungan, Bambang Tridjaja, Jose RL Batubara
Sexual precocity with pituitary macroadenoma and bilateral multicystic ovaries - a case report
S Ramkumar, Parjeet Kaur, Ansu Joshi, AC Ammini,
Fluid and electrolyte imbalance related to intracranial abnormality
Frida Soesanti, Bambang Tridjaja, Jose RL Batubara, Aman Pulungan
Vitamin D serum levels and vitamin D receptor FokI polymorphism on tuberculosis children in Palembang, Indonesia
Ariesti Karmila, Aditiawati, Muhammad Nazir, Kiagus Yangtjik, Yuwono
An unusual presentation of girl with down syndrome: Van-Wyk Grumbach syndrome
Han Hyuk Lim, Hong Ryang Kil, Jae Young Kim
Blood spots screening for identification of Fragile X Syndrome among intellectual disability students in Flores Island, INDONESIA
Agustini Utari, Joyce Lo, Tzuhan Tong, Tri Indah Winarni, Sultana MH Faradz, Flora Tassone
The neuro-cardio-facial-cutaneous syndrome – unity in diversity
Carmen Vulpoi, Mihaela Anton, Ion Poeata, Jeanina Idriceanu, Cristina Rusu
Effect of intrauterine bodily development and nutritional status on the later body-length development of children. The MDN system
Péter Berkő, Kálmán Joubert, Gyula Gyenis
Association between exon-3 polymorphism of the GH Receptor(GHR) gene with catch growth in children born small for gestational age
Il Tae Hwang, Shim Young Shim
Uteroplacental insufficiency decreases forkhead box protein O1A (foxO1a) hepatic levels in perinatal and postnatal IUGR rats
Z Shen, CC Zou, SQ Shang, LZ Du