Saito Y - Search Results

1

Dermatomyositis: Muscle Pathology According to Antibody Subtypes.

Tanboon J, Inoue M, Saito Y, Tachimori H, Hayashi S, Noguchi S, Okiyama N, Fujimoto M, Nishino I. Tanboon J, et al. Among authors: saito y. Neurology. 2022 Feb 15;98(7):e739-e749. doi: 10.1212/WNL.0000000000013176. Epub 2021 Dec 6. Neurology. 2022. PMID: 34873015 Free PMC article.

2

Early onset of cardiomyopathy and intellectual disability in a girl with Danon disease associated with a de novo novel mutation of the LAMP2 gene.

Sugie K, Yoshizawa H, Onoue K, Nakanishi Y, Eura N, Ogawa M, Nakano T, Sakaguchi Y, Hayashi YK, Kishimoto T, Shima M, Saito Y, Nishino I, Ueno S. Sugie K, et al. Among authors: saito y. Neuropathology. 2016 Dec;36(6):561-565. doi: 10.1111/neup.12307. Epub 2016 May 5. Neuropathology. 2016. PMID: 27145725

3

A Nationwide Survey on Danon Disease in Japan.

Sugie K, Komaki H, Eura N, Shiota T, Onoue K, Tsukaguchi H, Minami N, Ogawa M, Kiriyama T, Kataoka H, Saito Y, Nonaka I, Nishino I. Sugie K, et al. Among authors: saito y. Int J Mol Sci. 2018 Nov 8;19(11):3507. doi: 10.3390/ijms19113507. Int J Mol Sci. 2018. PMID: 30413001 Free PMC article.

4

[A case of Emery-Dreifuss muscular dystrophy with slight joint contracture].

Fujii S, Eguchi K, Sato C, Saito Y, Indrawati LA, Shirai S, Nishino I, Yabe I. Fujii S, et al. Among authors: saito y. Rinsho Shinkeigaku. 2020 Aug 7;60(8):554-559. doi: 10.5692/clinicalneurol.60.cn-001431. Epub 2020 Jul 7. Rinsho Shinkeigaku. 2020. PMID: 32641626 Japanese.

5

ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features.

Saito Y, Nishikawa A, Iida A, Mori-Yoshimura M, Oya Y, Ishiyama A, Komaki H, Nakamura S, Fujikawa S, Kanda T, Yamadera M, Sakiyama H, Hayashi S, Nonaka I, Noguchi S, Nishino I. Saito Y, et al. Neurology. 2020 Sep 15;95(11):e1500-e1511. doi: 10.1212/WNL.0000000000010237. Epub 2020 Jul 9. Neurology. 2020. PMID: 32646962

6

Adult-onset Repeat Rhabdomyolysis with a Very Long-chain Acyl-CoA Dehydrogenase Deficiency Due to Compound Heterozygous ACADVL Mutations.

Fuseya Y, Sakurai T, Miyahara JI, Sato K, Kaji S, Saito Y, Takahashi M, Nishino I, Fukuda T, Sugie H, Yamashita H. Fuseya Y, et al. Among authors: saito y. Intern Med. 2020 Nov 1;59(21):2729-2732. doi: 10.2169/internalmedicine.4604-20. Epub 2020 Jul 14. Intern Med. 2020. PMID: 32669490 Free PMC article.

7

An adult nemaline myopathy patient with respiratory and heart failure harboring a novel NEB variant.

Ohara M, Saito Y, Watanabe M, Mizutani S, Kobayashi M, Iida A, Nishino I, Fujigasaki H. Ohara M, et al. Among authors: saito y. eNeurologicalSci. 2020 Aug 26;21:100268. doi: 10.1016/j.ensci.2020.100268. eCollection 2020 Dec. eNeurologicalSci. 2020. PMID: 32939402 Free PMC article.

8

[Clinicopathological Features of Myositis and Necrotizing Myopathy: How to Distinguish between Myositis and Muscular Dystrophy on Muscle Pathology].

Saito Y, Nishino I. Saito Y, et al. Brain Nerve. 2021 Feb;73(2):147-159. doi: 10.11477/mf.1416201727. Brain Nerve. 2021. PMID: 33561829 Japanese.

9

[A Japanese family with POMT2-related limb girdle muscular dystrophy].

Tomita Y, Matusya N, Narita T, Saito Y, Nishino I, Fukudome T. Tomita Y, et al. Among authors: saito y. Rinsho Shinkeigaku. 2021 Jun 29;61(6):378-384. doi: 10.5692/clinicalneurol.cn-001547. Epub 2021 May 20. Rinsho Shinkeigaku. 2021. PMID: 34011809 Japanese.

10

Causative variant profile of collagen VI-related dystrophy in Japan.

Inoue M, Saito Y, Yonekawa T, Ogawa M, Iida A, Nishino I, Noguchi S. Inoue M, et al. Among authors: saito y. Orphanet J Rare Dis. 2021 Jun 24;16(1):284. doi: 10.1186/s13023-021-01921-2. Orphanet J Rare Dis. 2021. PMID: 34167565 Free PMC article.

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