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211 results

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Page 1
Pediatric necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies.
Liang WC, Uruha A, Suzuki S, Murakami N, Takeshita E, Chen WZ, Jong YJ, Endo Y, Komaki H, Fujii T, Kawano Y, Mori-Yoshimura M, Oya Y, Xi J, Zhu W, Zhao C, Watanabe Y, Ikemoto K, Nishikawa A, Hamanaka K, Mitsuhashi S, Suzuki N, Nishino I. Liang WC, et al. Among authors: hamanaka k. Rheumatology (Oxford). 2017 Feb;56(2):287-293. doi: 10.1093/rheumatology/kew386. Epub 2016 Nov 6. Rheumatology (Oxford). 2017. PMID: 27818386 Free PMC article.
Muscle from a 20-week-old myotubular myopathy fetus is not myotubular.
Hamanaka K, Inami I, Wada T, Mitsuhashi S, Noguchi S, Hayashi YK, Nishino I. Hamanaka K, et al. Neuromuscul Disord. 2016 Mar;26(3):234-5. doi: 10.1016/j.nmd.2015.11.010. Epub 2015 Dec 3. Neuromuscul Disord. 2016. PMID: 26898940 No abstract available.
Clinical features and prognosis in anti-SRP and anti-HMGCR necrotising myopathy.
Watanabe Y, Uruha A, Suzuki S, Nakahara J, Hamanaka K, Takayama K, Suzuki N, Nishino I. Watanabe Y, et al. Among authors: hamanaka k. J Neurol Neurosurg Psychiatry. 2016 Oct;87(10):1038-44. doi: 10.1136/jnnp-2016-313166. Epub 2016 May 4. J Neurol Neurosurg Psychiatry. 2016. PMID: 27147697
Corrigendum to "Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations": [Neuromuscular Disorders 26/4-5 (2016) 300-308].
Hamanaka K, Goto K, Arai M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Mitsuhashi S, Nishino I. Hamanaka K, et al. Neuromuscul Disord. 2016 Jul;26(7):472. doi: 10.1016/j.nmd.2016.05.015. Neuromuscul Disord. 2016. PMID: 27312129 No abstract available.
HLA-DRB1 alleles in immune-mediated necrotizing myopathy.
Ohnuki Y, Suzuki S, Shiina T, Uruha A, Watanabe Y, Suzuki S, Izumi S, Nakahara J, Hamanaka K, Takayama K, Suzuki N, Nishino I. Ohnuki Y, et al. Among authors: hamanaka k. Neurology. 2016 Nov 1;87(18):1954-1955. doi: 10.1212/WNL.0000000000003160. Epub 2016 Aug 31. Neurology. 2016. PMID: 27581220 No abstract available.
Sarcoplasmic MxA expression: A valuable marker of dermatomyositis.
Uruha A, Nishikawa A, Tsuburaya RS, Hamanaka K, Kuwana M, Watanabe Y, Suzuki S, Suzuki N, Nishino I. Uruha A, et al. Among authors: hamanaka k. Neurology. 2017 Jan 31;88(5):493-500. doi: 10.1212/WNL.0000000000003568. Epub 2016 Dec 30. Neurology. 2017. PMID: 28039312
Skeletal Muscle Involvement in Antisynthetase Syndrome.
Noguchi E, Uruha A, Suzuki S, Hamanaka K, Ohnuki Y, Tsugawa J, Watanabe Y, Nakahara J, Shiina T, Suzuki N, Nishino I. Noguchi E, et al. Among authors: hamanaka k. JAMA Neurol. 2017 Aug 1;74(8):992-999. doi: 10.1001/jamaneurol.2017.0934. JAMA Neurol. 2017. PMID: 28586844 Free PMC article.
Aberrant Myokine Signaling in Congenital Myotonic Dystrophy.
Nakamori M, Hamanaka K, Thomas JD, Wang ET, Hayashi YK, Takahashi MP, Swanson MS, Nishino I, Mochizuki H. Nakamori M, et al. Among authors: hamanaka k. Cell Rep. 2017 Oct 31;21(5):1240-1252. doi: 10.1016/j.celrep.2017.10.018. Cell Rep. 2017. PMID: 29091763 Free PMC article.
211 results