Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Piyawan, Wattanasoontornsakul"'
Autor:
Pharuhad Pongmee, Sanchawan Wittayakornrerk, Ramrada Lekwuttikarn, Sasikarn Pakdeeto, Piangor Watcharakuldilok, Chatchay Prempunpong, Thipwimol Tim-Aroon, Chawintee Puttanapitak, Piyawan Wattanasoontornsakul, Thitiporn Junhasavasdikul, Parith Wongkittichote, Saisuda Noojarern, Duangrurdee Wattanasirichaigoon
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Epidermolysis bullosa (EB) is a rare and genetically heterogeneous disorder characterized by skin fragility and blister formation occurring spontaneously or after minor trauma. EB is accompanied by congenital absence of skin (EB with CAS) in some pat
Externí odkaz:
https://doaj.org/article/f06f261dd0a940148bd0425b6f476bcd
Autor:
Issarapa, Chunsuwan, Nichara, Ruangdaraganon, Tasnawat, Sombuntham, Piyawan, Wattanasoontornsakul, Pranee, Amornchaichan
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 99
Siblings of children with autism spectrum disorders (ASD) have higher prevalence of ASD with a recurrence of 19%. Children with ASD demonstrate significant impairment in all types of imitative skills. Imitation is markedly developed in the first few
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2479bc00fad6ad6b5804fc5b23d1cc9b
https://pubmed.ncbi.nlm.nih.gov/29917347
https://pubmed.ncbi.nlm.nih.gov/29917347