Mutation screening of Beta-Neurexin 1 (β-NRXN1), Neuroligin 3 (NLGN3) and Neuroligin 4X (NLGN4X) genes in Thai Children with autism spectrum disorder

بواسطة Pornprot Limprasert, Vincent, John B
منشور في 2015

Unique AGG interruption in the CGG repeats of the FMR1 gene exclusively found in asians linked to a specific SNP haplotype

بواسطة Pornprot Limprasert, Janpen Thanakitgosate, Kanoot Jaruthamsophon, Thanya Sripo
منشور في 2018

Comparison of a new in-house and three published HLA-B∗15:02 screening methods for prevention of carbamazepine-induced severe drug reactions

بواسطة Kanoot Jaruthamsophon, Thanya Sripo, Chonlaphat Sukasem, Pornprot Limprasert
منشور في 2018

Molecular screening for fragile x syndrome in Thailand

بواسطة Pornprot Limprasert, Nichara Ruangdaraganon, thanyachai Sura, Punnee Vasiknanonte, Uraiwan Jinorose
منشور في 1999

A new structured interview for children with autism spectrum disorder based on the DSM-IV

بواسطة Tippawan Hansakunachai, Rawiwan Roongpraiwan, Tasnawat Sombuntham, Pornprot Limprasert, Nichara Ruangdaraganon
منشور في 2018

Molecular screening for fragile X syndrome in Thailand

بواسطة Pornprot Limprasert, Nichara Ruangdaraganon, Thanyachai Sura, Punnee Vasiknanonte, Uraiwan Jinorose
منشور في 2018

Prevalence and clinical characteristics of fragile X syndrome at Child Development Clinic, Ramathibodi Hospital

بواسطة Nichara Ruangdaraganon, Thanyachai Sura, Noppawan Sriwongpanich, Pornprot Limprasert, Tasanawat Sombuntham, Nittaya Kotchabhakdi
منشور في 2018

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

بواسطة Pornprot Limprasert, Punnee Vasiknanonte, Somchit Jaruratanasirikul, Hutcha Sriplung, Nichara Ruangdaraganon, Thanyachai Sura, Noppawon Sriwongpanich
منشور في 2018

Haplotype analysis at the FRAXA locus in Thai subjects

بواسطة Pornprot Limprasert, Vannarat Saechan, Nichara Ruangdaraganon, Thanyachai Sura, Punnee Vasiknanote, Somchit Jaruratanasirikul, W. Ted Brown
منشور في 2018

Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population

بواسطة Chuphong Thongnak, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Chonlaphat Sukasem, Wasun Chantratita
منشور في 2018

Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population

بواسطة Chuphong Thongnak, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Chonlaphat Sukasem, Wasun Chantratita
منشور في 2018

Whole-Exome Sequencing Identifies One de Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder

بواسطة Chuphong Thongnak, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Wasun Chantratita, Pornprot Limprasert, Chonlaphat Sukasem
منشور في 2019

Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorder

بواسطة Supaporn Yangngam, Oradawan Plong-On, Thanya Sripo, Rawiwan Roongpraiwan, Tippawan Hansakunachai, Juthamas Wirojanan, Tasnawat Sombuntham, Nichara Ruangdaraganon, Pornprot Limprasert
منشور في 2018

Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity

بواسطة Utcharee Intusoma, Fadell Hayeeduereh, Oradawan Plong-On, Thanya Sripo, Punnee Vasiknanonte, Supachai Janjindamai, Apasri Lusawat, Sasipa Thammongkol, Anannit Visudtibhan, Pornprot Limprasert
منشور في 2018

Screening of NLGN3 and NLGN4X genes in Thai children with autism spectrum disorder

بواسطة Anna Mikhailov, Alanna Fennell, Oradawan Plong-On, Thanya Sripo, Tippawan Hansakunachai, Rawiwan Roongpraiwan, Tasnawat Sombuntham, Nichara Ruangdaraganon, John B. Vincent, Pornprot Limprasert
منشور في 2018