Yasushi Oya
Overview
Explore the profile of Yasushi Oya including associated specialties, affiliations and a list of published articles.
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Articles
98
Citations
748
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0
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Recent Articles
1.
Okubo S, Naruse H, Ishiura H, Sudo A, Esaki K, Mitsui J, et al.
J Neurol
. 2024 Dec;
272(1):36.
PMID: 39666121
Introduction: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder of the motor system. Pathogenic variants in SPTLC1, encoding a subunit of serine palmitoyltransferase, cause hereditary sensory and autonomic neuropathy...
2.
Mori-Yoshimura M, Takizawa H, Unuma A, Oya Y, Yorimoto K, Katsuta W, et al.
Brain Dev
. 2024 Aug;
46(10):320-325.
PMID: 39142946
Background: There have been few descriptions in the literature on long-term enzyme replacement therapy (ERT) in patients with advanced late-onset Pompe disease (LOPD). Objectives: This study aimed to assess the...
3.
Suzuki N, Mori-Yoshimura M, Katsuno M, Takahashi M, Yamashita S, Oya Y, et al.
J Neurol Neurosurg Psychiatry
. 2024 Jun;
95(11):1093-1094.
PMID: 38839274
No abstract available.
4.
Esteller D, Schiava M, Verdu-Diaz J, Villar-Quiles R, Dibowski B, Venturelli N, et al.
J Neurol
. 2024 Feb;
271(4):2147-2148.
PMID: 38349561
No abstract available.
5.
Izumi R, Warita H, Niihori T, Furusawa Y, Nakano M, Oya Y, et al.
Cerebellum
. 2024 Feb;
23(4):1498-1508.
PMID: 38324175
Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS) is an autosomal recessive multisystem neurologic disorder caused by biallelic intronic repeats in RFC1. Although the phenotype of CANVAS has been expanding...
6.
Yamamoto T, Mori-Yoshimura M, Oya Y, Komaki H, Takahashi Y
Muscle Nerve
. 2023 Sep;
68(5):737-742.
PMID: 37688475
Introduction/aims: Nutritional management of adults with Duchenne muscular dystrophy (DMD) is an important clinical issue. However, it is not clear which dysphagia-related factors should prompt introduction of alternative nutrition (AN)....
7.
Esteller D, Schiava M, Verdu-Diaz J, Villar-Quiles R, Dibowski B, Venturelli N, et al.
J Neurol
. 2023 Aug;
270(12):5849-5865.
PMID: 37603075
Background: The diagnosis of patients with mutations in the VCP gene can be complicated due to their broad phenotypic spectrum including myopathy, motor neuron disease and peripheral neuropathy. Muscle MRI...
8.
Nagatomo Y, Yoshizawa S, Oya Y, Nishino I
Eur Heart J Case Rep
. 2023 Aug;
7(8):ytad348.
PMID: 37575533
No abstract available.
9.
Mori-Yoshimura M, Suzuki N, Katsuno M, Takahashi M, Yamashita S, Oya Y, et al.
Orphanet J Rare Dis
. 2023 Aug;
18(1):241.
PMID: 37568154
Background: A rare muscle disease, GNE myopathy is caused by mutations in the GNE gene involved in sialic acid biosynthesis. Our recent phase II/III study has indicated that oral administration...
10.
Ishiguro M, Nagatomo Y, Inoue K, Yoshikawa T, Yoshizawa S, Oya Y, et al.
Eur Heart J Case Rep
. 2023 Jun;
7(6):ytac158.
PMID: 37323533
Background: Anti-mitochondrial antibody (AMA)-associated myopathy is known to be concomitant with primary biliary cirrhosis and to cause both skeletal muscle disorders and arrhythmias, myocardium disorders, and respiratory muscle disorders. We...