Nobuyuki Eura
Overview
Explore the profile of Nobuyuki Eura including associated specialties, affiliations and a list of published articles.
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Articles
36
Citations
162
Followers
0
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Recent Articles
1.
Komaki S, Kubota A, Katsuse K, Kitamura A, Maeda M, Matsukawa T, et al.
Intern Med
. 2024 May;
64(2):329.
PMID: 38811214
No abstract available.
2.
Takeuchi Y, Masuda T, Kimura N, Sumi K, Jikumaru M, Eura N, et al.
Intern Med
. 2024 Apr;
63(24):3371-3375.
PMID: 38631855
X-linked myotubular myopathy (XLMTM) is a rare genetic disorder caused by X-linked mutations in the MTM1 gene. Although heterozygous females are typically asymptomatic, affected cases have recently been reported. We...
3.
Komaki S, Kubota A, Katsuse K, Kitamura A, Maeda M, Matsukawa T, et al.
Intern Med
. 2024 Mar;
63(22):3083-3086.
PMID: 38494715
Calpainopathy is primarily an autosomal recessive inherited myopathy; however, dominantly inherited cases with a pathogenic variant of c.1333G>A have been reported. A 13-year-old Japanese girl presented with toe walking and...
4.
Mano T, Iguchi N, Eura N, Iwasa N, Yamada N, Horikawa H, et al.
Front Neurol
. 2024 Jan;
14:1295396.
PMID: 38249752
Introduction: Inclusion body myositis (IBM) is a chronic inflammatory muscle disease that is characterized by mixed myogenic and neurogenic electromyography (EMG) findings. We investigated the association between EMG findings and...
5.
Eura N, Noguchi S, Ogasawara M, Kumutpongpanich T, Hayashi S, Nishino I
J Neurol
. 2023 Aug;
270(12):5988-5998.
PMID: 37634163
Background And Objectives: Oculopharyngodistal myopathy (OPDM) is an autosomal dominant myopathy clinically characterized by distal muscle weakness. Even though the identification of four causative genes, LRP12, GIPC1, NOTCH2NLC and RILPL1,...
6.
Kume K, Kurashige T, Muguruma K, Morino H, Tada Y, Kikumoto M, et al.
Am J Hum Genet
. 2023 Jun;
110(7):1086-1097.
PMID: 37339631
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by the degeneration of motor neurons. Although repeat expansion in C9orf72 is its most common cause, the pathogenesis of ALS isn't...
7.
Takahashi Y, Morimoto N, Nada T, Morimoto M, Eura N, Minami N, et al.
J Neuromuscul Dis
. 2023 Feb;
10(3):459-463.
PMID: 36847015
Immediately after the initial methionine codon, the PABPN1 gene encodes a stretch of 10 alanines, 1 glycine, and 2 alanines. Oculopharyngeal muscular dystrophy (OPMD) is caused by the expansion of...
8.
Ogasawara M, Eura N, Iida A, Kumutpongpanich T, Minami N, Nonaka I, et al.
Acta Neuropathol Commun
. 2022 Dec;
10(1):176.
PMID: 36476314
Oculopharyngodistal myopathy (OPDM) and oculopharyngeal muscular dystrophy (OPMD) are similar and even believed to be indistinguishable in terms of their myopathological features. To address the diagnostic gap, we evaluated the...
9.
Eura N, Iida A, Ogasawara M, Hayashi S, Noguchi S, Nishino I
Am J Hum Genet
. 2022 Nov;
109(11):2088-2089.
PMID: 36332612
No abstract available.
10.
Shiota T, Eura N, Hasegawa A, Kiriyama T, Sugie K
Neuropathology
. 2022 May;
42(4):309-314.
PMID: 35508303
Chronic graft-versus-host disease (cGVHD) is the most important complication resulting in the death of bone marrow transplantation (BMT) survivors. It is also a relatively rare cause of inflammatory myopathy (IM)....