Effect of Iron Supplementation in Children with Attention-Deficit/Hyperactivity Disorder and Iron Deficiency: A Randomized Controlled Trial.

Autor: Pongpitakdamrong A; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.; Department of Pediatrics, Institute of Medicine Suranaree University of Technology, Nakhon Ratchasima, Thailand., Chirdkiatgumchai V; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Ruangdaraganon N; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Roongpraiwan R; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Sirachainan N; Division of Pediatric Hematology and Oncology, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Soongprasit M; Division of Child and Adolescent Psychiatry, Department of Psychiatry, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Udomsubpayakul U; Section for Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Publikováno v: Journal of developmental and behavioral pediatrics : JDBP [J Dev Behav Pediatr] 2022 Feb-Mar 01; Vol. 43 (2), pp. 80-86.

Prevalence of immunological aberrations and 22q11.2 deletion in children with conotruncal anomalies: A cross-sectional study.

Autor: Das, Souvik¹ (AUTHOR), Baranwal, Arun Kumar² (AUTHOR) baranwal1970@gmail.com, Rawat, Amit³ (AUTHOR), Nair, Ashwini³ (AUTHOR), Naganur, Sanjeev Hanumantacharya⁴ (AUTHOR), Kaur, Anupriya³ (AUTHOR), Mishra, Anand Kumar⁵ (AUTHOR), Jindal, Ankur³ (AUTHOR), Kaur, Anit³ (AUTHOR)

Publikováno v: Annals of Pediatric Cardiology. Sep/Oct2024, Vol. 17 Issue 5, p339-346. 8p.

A clinical checklist for fragile X syndrome: screening of Thai boys with developmental delay of unknown cause

Autor: Limprasert, P., Vasiknanonte, P., Jaruratanasirikul, S., Hutcha Sriplung, Ruangdaraganon, N., Sura, T., Sriwongpanich, N.

Publikováno v: Europe PubMed Central
Scopus-Elsevier

The aim of this study was to determine a cost-effective clinical checklist for fragile X syndrome (FXS) screening in a Thai male pediatric population with developmental delay of unknown cause. We studied 179 non-FXS male patients and 27 FXS patients

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a0b8cf3af4dfdec5928e8d36a5d51b0f
https://pubmed.ncbi.nlm.nih.gov/11143494

Effectiveness of neurofeedback versus medication for attention-deficit/hyperactivity disorder.

Autor: Sudnawa KK; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Chirdkiatgumchai V; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Ruangdaraganon N; Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Khongkhatithum C; Division of Pediatric Neurology, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Udomsubpayakul U; Section for Clinical Epidemiology and Biostatistics, Ramathibodi Hospital, Bangkok, Thailand., Jirayucharoensak S; National Electronics and Computer Technology Center, Pathumthani, Thailand., Israsena P; National Electronics and Computer Technology Center, Pathumthani, Thailand.

Publikováno v: Pediatrics international : official journal of the Japan Pediatric Society [Pediatr Int] 2018 Sep; Vol. 60 (9), pp. 828-834. Date of Electronic Publication: 2018 Sep 05.

Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.

Autor: Hnoonual A; Graduate Program in Biomedical Sciences, Prince of Songkla University, Songkhla, Thailand., Thammachote W; Program in Translational Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Tim-Aroon T; Division of Medical Genetics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Rojnueangnit K; Division of Medical Genetics, Department of Pediatrics, Faculty of Medicine, Thammasart University, Pathumthani, Thailand., Hansakunachai T; Division of Child Development, Department of Pediatrics, Faculty of Medicine, Thammasart University, Pathumthani, Thailand., Sombuntham T; Division of Developmental-Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Roongpraiwan R; Division of Developmental-Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Worachotekamjorn J; Division of Child Development, Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand., Chuthapisith J; Division of Developmental-Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Fucharoen S; Thalassemia Research Center, Institute of Molecular Biosciences, Mahidol University, Salaya, Nakhon Pathom, Thailand., Wattanasirichaigoon D; Division of Medical Genetics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Ruangdaraganon N; Division of Developmental-Behavioral Pediatrics, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand., Limprasert P; Division of Human Genetics, Department of Pathology, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand. lpornpro@yahoo.com., Jinawath N; Program in Translational Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand. jnatini@hotmail.com.; Integrative Computational Bioscience Center, Mahidol University, Salaya, Nakhon Pathom, Thailand. jnatini@hotmail.com.

Publikováno v: Scientific reports [Sci Rep] 2017 Sep 21; Vol. 7 (1), pp. 12096. Date of Electronic Publication: 2017 Sep 21.