Nithiwat Vatanavicharn

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 5

Top Topics

Duchenne Muscular Dystrophy

Polycyclic Aromatic Hydrocarbons

Prognostic Factors

Top Venues

International journal of molecular sciences

Molecular biology reports

Pediatrics international : official journal of the Japan Pediatric Society

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

This page only lists publications with an associated author ORCID identifier.

Publications

Piranit Nik Kantaputra, Teerada Klaisuwan, Kantapong Kitiyamas, Panat Piyakhunakorn, Katsushige Kawasaki, Achara Sathienkijkanchai, Pornswan Wasant, Nithiwat Vatanavicharn, Thippawan Yasanga, Massupa Kaewgahya, Sissades Tongsima, Timothy C Cox, Stefan T Arold, Atsushi Ohazama, Chumpol Ngamphiw
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain. International journal of molecular sciences 25 (12) (2024)
Piranit Nik Kantaputra, Teerada Klaisuwan, Kantapong Kitiyamas, Panat Piyakhunakorn, Katsushige Kawasaki, Achara Sathienkijkanchai, Pornswan Wasant, Nithiwat Vatanavicharn, Thippawan Yasanga, Massupa Kaewgahya, Sissades Tongsima, Timothy C Cox, Stefan T Arold, Atsushi Ohazama, Chumpol Ngamphiw
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain. International journal of molecular sciences 25 (12) (2024)
Somporn Liammongkolkul, Boonchai Boonyawat, Chodchanok Vijarnsorn, Thipwimol Tim-Aroon, Pornswan Wasant, Nithiwat Vatanavicharn
Phenotypic and molecular features of Thai patients with primary carnitine deficiency. Pediatrics international : official journal of the Japan Pediatric Society (2022)
Sarut Chaisrisawadisuk, Nithiwat Vatanavicharn, Inthira Khumpalikit, Mark H Moore
Multisuture craniosynostosis: a case report of unusual presentation of chromosome 14q32 deletion. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2022)
Lukana Ngiwsara, Nithiwat Vatanavicharn, Phannee Sawangareetrakul, Somporn Liammongkolkul, Pisanu Ratanarak, Boonchai Boonyawat, Chantragan Srisomsap, Voraratt Champattanachai, James Ketudat-Cairns, Pornswan Wasant, Jisnuson Svasti
Molecular characterization of Thai patients with phenylalanine hydroxylase deficiency and in vitro functional study of two novel PAH variants. Molecular biology reports 48 (3) (2021)