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11.

Braun D.A., Rao J., Mollet G., Schapiro D., Daugeron M.-C., Tan W., Gribouval O., Boyer O., Revy P., Jobst-Schwan T., Schmidt J.M., Lawson J.A., Schanze D., Ashraf S., Ullmann J.F.P., Hoogstraten C.A., Boddaert N., Collinet B., Martin G., Liger D., Lovric S., Furlano M., Guerrera I.C., Sanchez-Ferras O., Hu J.F., Boschat A.-C., Sanquer S., Menten B., Vergult S., De Rocker N., Airik M., Hermle T., Shril S., Widmeier E., Yung Gee H., Choi W.-I., Sadowski C.E., Pabst W.L., Warejko J.K., Daga A., Basta T., Matejas V., Scharmann K., Kienast S.D., Behnam B., Beeson B., Begtrup A., Bruce M., Ch'Ng G.-S., Lin S.-P., Chang J.-H., Chen C.-H., Cho M.T., Gaffney P.M., Gipson P.E., Hsu C.-H., Kari J.A., Ke Y.-Y., Kiraly-Borri C., Lai W.-M., Lemyre E., Littlejohn R.O., Masri A., Moghtaderi M., Nakamura K., Ozaltin F., Praet M., Prasad C., Topaloglu R., Vester U., Viskochil D.H., Vatanavicharn N., Kannu P., Chitayat D.

Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly
Nature Genetics. 2017. 49 (10): 1529-1538.

12.

Charuvanij S., Pattaragarn A., Wisuthsarewong W., Vatanavicharn N.

Juvenile gout in methylmalonic acidemia
Pediatrics International. 2016. 58 (6): 501-503.

13.

Thiboonboon K, Leelahavarong P, Wattanasirichaigoon D, Vatanavicharn N, Wasant P, Shotelersuk V, Pangkanon S, Kuptanon C, Chaisomchit S, Teerawattananon Y.

An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in Thailand
PLoS One. 2015. 10 (8):

14.

Sawangareetrakul P., Ketudat Cairns J.R., Vatanavicharn N., Liammongkolkul S., Wasant P., Svasti J., Champattanachai V.

Analysis of Novel Mutations and Methylmalonyl-CoA Mutase Levels in Thai Patients with Isolated Methylmalonic Acidemia
Biochem Genet. 2015. 53 (11): 310-318.

15.

Vatanavicharn N., Liammongkolkul S., Sakamoto O., Kamolsilp M., Sathienkijkanchai A., Wasant P.

Clinical characteristics and mutation analysis of propionic acidemia in Thailand
World Journal of Pediatrics. 2014. 10 (1): 64-68.

16.

Vatanavicharn N, Yamada K, Aoyama Y, Fukao T, Densupsoontorn N, Jirapinyo P, Sathienkijkanchai A, Yamaguchi S, Wasant P.

Carnitine-acylcarnitine translocase deficiency: Two neonatal cases with common splicing mutation and in vitro bezafibrate response.
Brain Dev. 2014.

17.

Vatanavicharn, N. Champattanachai, V. Liammongkolkul, S. Sawangareetrakul, P. Keeratichamroen, S. Ketudat Cairns, J. R. Srisomsap, C. Sathienkijkanchai, A. Shotelersuk, V. Kamolsilp, M. Wattanasirichaigoon, D. Svasti, J. Wasant, P.

Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia
MOLECULAR GENETICS AND METABOLISM. 2012. 106 (4): 424-429.

18.

Vatanavicharn, N; Ratanarak, P; Liammongkolkul, S; Sathienkijkanchai, A; Wasant, P

Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: An eight-year experience
CLINICA CHIMICA ACTA. 2012. 413 (13-14): 1141-1141 1144.

19.

Vatanavicharn N, Liammongkolkul S, Sakamoto O, Sathienkijkanchai A, Wasant P

Phenotypic and mutation spectrums of Thai patients with isovaleric acidemia
Pediatrics International. 2011. 53 (6): 990-994.

20.

Funari, V. A. Krakow, D. Nevarez, L. Chen, Z. Funari, T. L. Vatanavicharn, N. Wilcox, W. R. Rimoin, D. L. Nelson, S. F. Cohn, D. H.

BMPER mutation in diaphanospondylodysostosis identified by ancestral autozygosity mapping and targeted high-throughput sequencing
American Journal of Human Genetics. 2010. 87 (4): 532-537.

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