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Year Number of Results
2005 2
2006 1
2007 2
2008 1
2009 2
2011 1
2012 2
2014 2
2015 1
2017 1
2021 0
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13 results
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Page 1
Resolution of Primary Immune Defect in 22q11.2 Deletion Syndrome.
Suksawat Y, Sathienkijkanchai A, Veskitkul J, Jirapongsananuruk O, Visitsunthorn N, Vichyanond P, Pacharn P. Suksawat Y, et al. Among authors: sathienkijkanchai a. J Clin Immunol. 2017 May;37(4):375-382. doi: 10.1007/s10875-017-0394-6. Epub 2017 Apr 20. J Clin Immunol. 2017. PMID: 28429103
Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.
Messiaen L, Yao S, Brems H, Callens T, Sathienkijkanchai A, Denayer E, Spencer E, Arn P, Babovic-Vuksanovic D, Bay C, Bobele G, Cohen BH, Escobar L, Eunpu D, Grebe T, Greenstein R, Hachen R, Irons M, Kronn D, Lemire E, Leppig K, Lim C, McDonald M, Narayanan V, Pearn A, Pedersen R, Powell B, Shapiro LR, Skidmore D, Tegay D, Thiese H, Zackai EH, Vijzelaar R, Taniguchi K, Ayada T, Okamoto F, Yoshimura A, Parret A, Korf B, Legius E. Messiaen L, et al. Among authors: sathienkijkanchai a. JAMA. 2009 Nov 18;302(19):2111-8. doi: 10.1001/jama.2009.1663. JAMA. 2009. PMID: 19920235
Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia.
Vatanavicharn N, Champattanachai V, Liammongkolkul S, Sawangareetrakul P, Keeratichamroen S, Ketudat Cairns JR, Srisomsap C, Sathienkijkanchai A, Shotelersuk V, Kamolsilp M, Wattanasirichaigoon D, Svasti J, Wasant P. Vatanavicharn N, et al. Among authors: sathienkijkanchai a. Mol Genet Metab. 2012 Aug;106(4):424-9. doi: 10.1016/j.ymgme.2012.05.012. Epub 2012 May 29. Mol Genet Metab. 2012. PMID: 22695176
Fetal warfarin syndrome.
Sathienkijkanchai A, Wasant P. Sathienkijkanchai A, et al. J Med Assoc Thai. 2005 Nov;88 Suppl 8:S246-50. J Med Assoc Thai. 2005. PMID: 16856447
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