All Stories

  1. A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome

    Article • Case Reports in Neurological Medicine, September 2019, Hindawi Publishing Corporation

    Boonchai Boonyawat

  2. X-Linked Chronic Granulomatous Disease: Initial Presentation with Intracranial Hemorrhage from Vitamin K Deficiency in Infant

    Article • Case Reports in Pediatrics, June 2018, Hindawi Publishing Corporation

    Boonchai Boonyawat, Chanchai Traivaree

  3. Clinical and molecular genetic features of Hb H and AE Bart’s diseases in central Thai children

    Article • The Application of Clinical Genetics, April 2018, Dove Medical Press

    Boonchai Boonyawat, Chanchai Traivaree

  4. Genotype–phenotype correlation among beta-thalassemia and beta-thalassemia/HbE disease in Thai children: predictable clinical spectrum using genotypic analysis

    Article • Journal of Blood Medicine, April 2018, Dove Medical Press

    Boonchai Boonyawat, Chanchai Traivaree

  5. Factor VII genotype Thailand

    Article • The Application of Clinical Genetics, June 2017, Dove Medical Press

    Boonchai Boonyawat, Arunotai Meekaewkunchorn , Chanchai Traivaree

  6. Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study

    Article • The Application of Clinical Genetics, December 2014, Taylor & Francis

    Boonchai Boonyawat, Chanchai Traivaree