Browsing by Author Piranit Nik Kantaputra

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Issue DateTitleAuthor(s)
1-Dec-2017Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutationPiranit Nik Kantaputra; Seema Kapoor; Prashant Verma; Massupa Kaewgahya; Katsushige Kawasaki; Atsushi Ohazama; James R. Ketudat Cairns
1-Jan-2016All enamel is not created equal: Supports from a novel FAM83H mutationPiranit Nik Kantaputra; Worrachet Intachai; Prim Auychai
1-Jan-2014BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cellsPiranit Nik Kantaputra
5-Apr-2013Clinical Correlate: CLCN7-Associated Autosomal Recessive OsteopetrosisPiranit Nik Kantaputra
1-Jan-2014Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutationsPiranit Nik Kantaputra; Hulya Kayserili; Yeliz Guven; Warissara Kantaputra; Mehmet C. Balci; Pranoot Tanpaiboon; Napaporn Tananuvat; Anusha Uttarilli; Ashwin Dalal
1-Mar-2020Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratodermaPiranit Nik Kantaputra; Worrachet Intachai; Bruce M. Carlson; Chulabhorn Pruksachatkunakorn
1-Feb-2022Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutationPiranit Nik Kantaputra; Nutsuchar Wangtiraumnuay; Chumpol Ngamphiw; Bjorn Olsen; Worrachet Intachai; Abigail S. Tucker; Sissades Tongsima
1-Sep-2012Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutationPiranit Nik Kantaputra; Wannapa Chinadet; Atsushi Ohazama; Michihiro Kono
1-Jan-2014Enamel-renal-gingival syndrome and FAM20A mutationsPiranit Nik Kantaputra; Massupa Kaewgahya; Udomrat Khemaleelakul; Prapai Dejkhamron; Suchitra Sutthimethakorn; Visith Thongboonkerd; Anak Iamaroon
1-Jan-2014Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutationPiranit Nik Kantaputra; Chotika Bongkochwilawan; Massupa Kaewgahya; Atsushi Ohazama; Hulya Kayserili; Arzu Pinar Erdem; Oya Aktoren; Yeliz Guven
1-Aug-2020Impaired dentin mineralization, supernumerary teeth, hypoplastic mandibular condyles with long condylar necks, and a TRPS1 mutationPiranit Nik Kantaputra; Stephanie A. Coury; Wen Hann Tan
1-Jan-2018Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutationPiranit Nik Kantaputra; Wannapa Chinadet; Worrachet Intachai; Chumpol Ngamphiw; James R. Ketudat Cairns; Sissades Tongsima
1-Nov-2020Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2Piranit Nik Kantaputra; Prapai Dejkhamron; Sissades Tongsima; Chumpol Ngamphiw; Worrachet Intachai; Lukana Ngiwsara; Phannee Sawangareetrakul; Jisnuson Svasti; Bjorn Olsen; James R.Ketudat Cairns; Kanokkan Bumroongkit
1-Jan-2017Making extra teeth: Lessons from a TRPS1 mutationWorawan Kunotai; Panjit Ananpornruedee; Mark Lubinsky; Apitchaya Pruksametanan; Piranit Nik Kantaputra
1-Jul-2012Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patientHülya Kayserili; Piranit Nik Kantaputra
1-Jan-2013A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creasesPiranit Nik Kantaputra; Rekwan Sittiwangkul; Nuntigar Sonsuwan; Valeria Romanelli; Jair Tenorio; Pablo Lapunzina
1-Jan-2014Oral manifestations of 17 patients affected with mucopolysaccharidosis type VIPiranit Nik Kantaputra; Hülya Kayserili; Yeliz Güven; Warissara Kantaputra; Mehmet C. Balci; Pranoot Tanpaiboon; Anusha Uttarilli; Ashwin Dalal
1-Jul-2018Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutationPiranit Nik Kantaputra; Yuddhasert Sirirungruangsarn; Worrachet Intachai; Chumpol Ngamphiw; Sissades Tongsima; Prapai Dejkhamron
1-Jul-2017Periodontal disease and FAM20A mutationsPiranit Nik Kantaputra; Chotika Bongkochwilawan; Mark Lubinsky; Supansa Pata; Massupa Kaewgahya; Huei Jinn Tong; James R. Ketudat Cairns; Yeliz Guven; Nipon Chaisrisookumporn
1-Jan-2016Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutationsOnnida Wattanarat; Piranit Nik Kantaputra