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Browsing by Author Chulaluck Kuptanon

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Issue Date	Title	Author(s)
1-Dec-2021	Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients	Tim Phetthong; Thipwimol Tim-Aroon; Arthaporn Khongkraparn; Saisuda Noojarern; Chulaluck Kuptanon; Khunton Wichajarn; Achara Sathienkijkanchai; Kanya Suphapeetiporn; Pimlak Charoenkwan; Adisak Tantiworawit; Naruwan Noentong; Duangrurdee Wattanasirichaigoon
16-Jul-2018	The most 5' truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: A case report	Chulaluck Kuptanon; Chalurmpon Srichomthong; Apiruk Sangsin; Dool Kovitvanitcha; Kanya Suphapeetiporn; Vorasuk Shotelersuk
1-Mar-2019	Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII	Piranit N. Kantaputra; Lachlan J. Smith; Margret L. Casal; Chulaluck Kuptanon; Yu Cheng Chang; Sheela Nampoothiri; Apichai Paiyarom; Thanat Veerasakulwong; Objoon Trachoo; James R. Ketudat Cairns; Wannapa Chinadet; Pranoot Tanpaiboon
4-Mar-2017	Two novel compound heterozygous BMP1 mutations in a patient with osteogenesis imperfecta: A case report	Apiruk Sangsin; Chulaluck Kuptanon; Chalurmpon Srichomthong; Monnat Pongpanich; Kanya Suphapeetiporn; Vorasuk Shotelersuk

Showing results 1 to 4 of 4