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Moesin is a possible target molecule for cytomegalovirus-related Guillain-Barré syndrome.
Sawai S, Satoh M, Mori M, Misawa S, Sogawa K, Kazami T, Ishibashi M, Beppu M, Shibuya K, Ishige T, Sekiguchi Y, Noda K, Sato K, Matsushita K, Kodera Y, Nomura F, Kuwabara S. Sawai S, et al. Among authors: sato k. Neurology. 2014 Jul 8;83(2):113-7. doi: 10.1212/WNL.0000000000000566. Epub 2014 Jun 11. Neurology. 2014. PMID: 24920858
High-throughput screening of extended RAS mutations based on high-resolution melting analysis for prediction of anti-EGFR treatment efficacy in colorectal carcinoma.
Ishige T, Itoga S, Sato K, Kitamura K, Nishimura M, Sawai S, Matsushita K, Suzuki K, Ota S, Miyauchi H, Matsubara H, Nakatani Y, Nomura F. Ishige T, et al. Among authors: sato k. Clin Biochem. 2014 Dec;47(18):340-3. doi: 10.1016/j.clinbiochem.2014.09.013. Epub 2014 Sep 28. Clin Biochem. 2014. PMID: 25262986
Monoamine oxidase B rs1799836 G allele polymorphism is a risk factor for early development of levodopa-induced dyskinesia in Parkinson's disease.
Kakinuma S, Beppu M, Sawai S, Nakayama A, Hirano S, Yamanaka Y, Yamamoto T, Masafumi C, Aisihaer X, Aersilan A, Gao Y, Sato K, Sakae I, Ishige T, Nishimura M, Matsushita K, Satoh M, Nomura F, Kuwabara S, Tanaka T. Kakinuma S, et al. Among authors: sato k. eNeurologicalSci. 2020 Apr 6;19:100239. doi: 10.1016/j.ensci.2020.100239. eCollection 2020 Jun. eNeurologicalSci. 2020. PMID: 32346620 Free PMC article.
Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B).
Takatani R, Minagawa M, Molinaro A, Reyes M, Kinoshita K, Takatani T, Kazukawa I, Nagatsuma M, Kashimada K, Sato K, Matsushita K, Nomura F, Shimojo N, Jüppner H. Takatani R, et al. Among authors: sato k. Bone. 2015 Oct;79:15-20. doi: 10.1016/j.bone.2015.05.011. Epub 2015 May 19. Bone. 2015. PMID: 25997889 Free PMC article.
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