Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Juthamas Wirojanan"'
Autor:
Chariyawan Charalsawadi, Sasipong Trongnit, Kanoot Jaruthamsophon, Juthamas Wirojanan, Somchit Jaruratanasirikul, Anupong Nitiruangjaras, Pornprot Limprasert
Publikováno v:
International Journal of Pediatrics, Vol 2021 (2021)
Background. Little is currently known about the genetics of pilomatricoma. A number of studies have reported some evidence that this disease may have a genetic association with mutations of CTNNB1 gene or expression of the beta-catenin protein. In th
Externí odkaz:
https://doaj.org/article/ccb0545f17274e4cb6d3ed34a4ef6946
Autor:
Chariyawan Charalsawadi, Juthamas Wirojanan, Somchit Jaruratanasirikul, Nichara Ruangdaraganon, Alan Geater, Pornprot Limprasert
Publikováno v:
International Journal of Pediatrics, Vol 2017 (2017)
Background. Clinical characteristics of fragile X syndrome (FXS) have been well documented in Caucasians, whereas in Asians they have rarely been described. Those that have been conducted used small cohorts that utilized DNA for diagnosis and larger
Externí odkaz:
https://doaj.org/article/b89744f3aafa4b5e89581cedbef076a2
Autor:
Juthamas Wirojanan, Somchit Jaruratanasirikul, Chariyawan Charalsawadi, Nichara Ruangdaraganon, Pornprot Limprasert, Alan Geater
Publikováno v:
International Journal of Pediatrics, Vol 2017 (2017)
International Journal of Pediatrics
International Journal of Pediatrics
Background. Clinical characteristics of fragile X syndrome (FXS) have been well documented in Caucasians, whereas in Asians they have rarely been described. Those that have been conducted used small cohorts that utilized DNA for diagnosis and larger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83f06c1ea48471bf19776d9cd70c8ef0
https://doi.org/10.1155/2017/9318346
https://doi.org/10.1155/2017/9318346
Autor:
Susan Bacalman, Beth L. Goodlin-Jones, Randi J Hagerman, Juthamas Wirojanan, Thomas F. Anders, Rafael Diaz, Sébastien Jacquemont
Publikováno v:
Journal of Clinical Sleep Medicine. :145-150
Sleep disturbances are a common problem in childhood, with a prevalence of about 25% in typical preschool- and school-aged children.1 The problems have significant impact on not only children, but also their families. The association of sleep problem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32cb5625ce2e0bde2c6f51a062352f4b
https://doi.org/10.5664/jcsm.27443
https://doi.org/10.5664/jcsm.27443
Autor:
Supaporn Yangngam, Juthamas Wirojanan, Tippawan Hansakunachai, Rawiwan Roongpraiwan, Thanya Sripo, Tasnawat Sombuntham, Pornprot Limprasert, Nichara Ruangdaraganon, Oradawan Plong-On
Aim: Neurexin 1 has two major protein isoforms using alternative promoters, coding for the alpha-neurexin 1 (α-NRXN1) and beta-neurexin 1 (β-NRXN1) genes. This study is to explore the possibility that variants of the NRXN1 gene predispose to intell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c46930d818c71139b8fc5d793b72769
https://europepmc.org/articles/PMC4094023/
https://europepmc.org/articles/PMC4094023/
Autor:
Rawiwan Roongpraiwan, Chariyawan Charalsawadi, Tippawan Hansakunachai, Tasnawat Sombuntham, Pornprot Limprasert, Juthamas Wirojanan, Verayuth Praphanphoj, Worathai Maisrikhaw, Nichara Ruangdaraganon
Publikováno v:
Cytogenetic and genome research. 144(1)
Autistic spectrum disorder (ASD) is a group of neurodevelopmental disorders characterized by impairments of social interaction, communication and restricted, repetitive and stereotyped patterns of behavior, interests and activities. Frequencies of ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbc264071ad0166c6dfd50919c523aae
https://pubmed.ncbi.nlm.nih.gov/25171325
https://pubmed.ncbi.nlm.nih.gov/25171325
Autor:
Xiuqing Guo, Thanya Sripo, Nichara Ruangdaraganon, Pornprot Limprasert, Tasnawat Sombuntham, Juthamas Wirojanan, Rawiwan Roongpraiwan, Worathai Maisrikhaw, Tippawan Hansakunachai
Publikováno v:
Psychiatric Genetics. 24:230-231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa7238303562ca72dcd29f5a758904d5
https://doi.org/10.1097/ypg.0000000000000046
https://doi.org/10.1097/ypg.0000000000000046
Autor:
Juthamas, Wirojanan, Sebastien, Jacquemont, Rafael, Diaz, Susan, Bacalman, Thomas F, Anders, Randi J, Hagerman, Beth L, Goodlin-Jones
Publikováno v:
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine. 5(2)
To determine the efficacy of melatonin on sleep problems in children with autistic spectrum disorder (ASD) and fragile X syndrome (FXS).A 4-week, randomized, double blind, placebo-controlled, crossover design was conducted following a 1-week baseline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::57c0a06285bd31585d52060cd8b20bcd
https://pubmed.ncbi.nlm.nih.gov/19968048
https://pubmed.ncbi.nlm.nih.gov/19968048
Autor:
Juthamas Wirojanan, Flora Tassone, Kathleen Angkustsiri, Douglas S. Hawkins, Louise W. Gane, Charles D. Laird, Randi J Hagerman, Jeremy Kraff
Publikováno v:
Journal of pediatric hematology/oncology. 30(3)
Hepatic tumors are rare childhood neoplasms with uncertain etiology. We report the cooccurrence of hepatic tumors in 2 boys with fragile X syndrome, one with hepatoblastoma and another with desmoplastic nested spindle cell tumor of liver. The pathoge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::090fa618b079848090403eea68f28a8b
https://pubmed.ncbi.nlm.nih.gov/18376289
https://pubmed.ncbi.nlm.nih.gov/18376289
Publikováno v:
American journal of medical genetics. Part A. (7)
We present a girl with the fragile X premutation who obtained the premutation allele from donated sperm. Our patient has clinical characteristics of fragile X syndrome including emotional problems and neuropsychological difficulties presenting as lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53b6339743f218116d33b453eb98d710
https://pubmed.ncbi.nlm.nih.gov/18286596
https://pubmed.ncbi.nlm.nih.gov/18286596