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Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle.
Inukai A, Doyu M, Kato T, Liang Y, Kuru S, Yamamoto M, Kobayashi Y, Sobue G. Inukai A, et al. Among authors: yamamoto m. Muscle Nerve. 2000 Sep;23(9):1421-6. doi: 10.1002/1097-4598(200009)23:9<1421::aid-mus14>3.0.co;2-y. Muscle Nerve. 2000. PMID: 10951446
An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val).
Misu K, Yoshihara T, Shikama Y, Awaki E, Yamamoto M, Hattori N, Hirayama M, Takegami T, Nakashima K, Sobue G. Misu K, et al. Among authors: yamamoto m. J Neurol Neurosurg Psychiatry. 2000 Dec;69(6):806-11. doi: 10.1136/jnnp.69.6.806. J Neurol Neurosurg Psychiatry. 2000. PMID: 11080237 Free PMC article.
[Inherited peripheral neuropathy].
Hattori N, Yamamoto M, Sobue G. Hattori N, et al. Among authors: yamamoto m. Nihon Rinsho. 2001 Dec;59 Suppl 8:597-603. Nihon Rinsho. 2001. PMID: 11808281 Review. Japanese. No abstract available.
Clinical and electrophysiologic correlates of IVIg responsiveness in CIDP.
Iijima M, Yamamoto M, Hirayama M, Tanaka F, Katsuno M, Mori K, Koike H, Hattori N, Arimura K, Nakagawa M, Yoshikawa H, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakazato M, Nakashima K, Kira J, Kaji R, Oka N, Sobue G. Iijima M, et al. Among authors: yamamoto m. Neurology. 2005 Apr 26;64(8):1471-5. doi: 10.1212/01.WNL.0000158680.89323.F8. Neurology. 2005. PMID: 15851750 Clinical Trial.
13,352 results
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