Ryosuke Miyamoto
Overview
Explore the profile of Ryosuke Miyamoto including associated specialties, affiliations and a list of published articles.
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Articles
98
Citations
529
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Recent Articles
1.
Shitara H, Hiroki T, Koda R, Sasaki T, Kamiyama M, Miyamoto R, et al.
Diagnostics (Basel)
. 2025 Feb;
15(3).
PMID: 39941223
: Non-invasive evaluations of muscle elasticity and tone are crucial in musculoskeletal medicine. Shear wave elastography (SWE) provides quantitative assessments of muscle elasticity, whereas train-of-four (TOF) monitoring measures muscle tone...
2.
Shitara H, Hamano N, Tajika T, Ichinose T, Sasaki T, Kamiyama M, et al.
Orthop J Sports Med
. 2025 Feb;
13(2):23259671241305607.
PMID: 39926584
Background: The Functional Movement Screen (FMS) is used to evaluate fundamental movement patterns in patients. It is unknown whether the FMS can be used as a predictive tool for the...
3.
Miyamoto R, Honma H, Masuda Y, Okumura A
ACG Case Rep J
. 2025 Feb;
12(2):e01603.
PMID: 39901882
No abstract available.
4.
Iwama K, Kato M, Uchiyama Y, Sakamoto M, Miyamoto R, Izumi Y, et al.
J Hum Genet
. 2025 Jan;
70(4):181-188.
PMID: 39843638
Interferon regulatory factor 2 binding protein-like (IRF2BPL) is a single-exon gene that is ubiquitously expressed in various tissues, including the brain. IRF2BPL encodes a transcription factor with two zinc-finger domains...
5.
Osaki Y, Nodera H, Sato R, Haji S, Fujita K, Miyamoto R, et al.
Clin Neurophysiol
. 2024 Dec;
170:156-167.
PMID: 39724790
Objective: Neuronal Intranuclear Inclusion Disease (NIID) is a neurodegenerative disease affecting the central and peripheral nerves. We aimed to assess the pathophysiological features of peripheral nerve dysfunction in NIID. Methods:...
6.
Shitara H, Ichinose T, Sasaki T, Hamano N, Kamiyama M, Miyamoto R, et al.
J Bone Joint Surg Am
. 2024 Aug;
PMID: 39213337
Background: A rotator cuff retear following arthroscopic rotator cuff repair (ARCR) is a concern in older patients. However, only a few of its risk factors are amenable to preoperative intervention....
7.
Yagi S, Miyamoto R, Tasaki M, Morino H, Otani R, Kadota M, et al.
Hum Genome Var
. 2024 Aug;
11(1):30.
PMID: 39152105
ApoA-I amyloidosis is an extremely rare form of systemic amyloidosis that commonly involves the heart, kidneys, and liver. ApoA-I amyloidosis is caused by amyloidogenic variants of APOA1 that are inherited...
8.
Miyamoto R, Honma H, Masuda Y, Ito Y, Okumura A
Cureus
. 2024 Aug;
16(7):e64637.
PMID: 39149675
Prostaglandin E-major urinary metabolite (PGE-MUM) is a valuable biomarker reflecting the cytokine profile. We encountered a case of a 14-year-old boy with pan-colitis-type ulcerative colitis who was unresponsive to steroids...
9.
Intermediate phenotype between CMT2Z and DIGFAN associated with a novel MORC2 variant: a case report
Hanada K, Osaki Y, Miyamoto R, Muto K, Haji S, Nazere K, et al.
Hum Genome Var
. 2024 Aug;
11(1):29.
PMID: 39143067
Charcot-Marie-Tooth disease type 2Z is caused by MORC2 mutations and presents with axonal neuropathy. MORC2 mutations can also manifest as developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy (DIGFAN)....
10.
Morigaki R, Miyamoto R, Miyake K, Omae H, Suzuki K, Matsuda T, et al.
Mov Disord Clin Pract
. 2024 Aug;
11(11):1462-1464.
PMID: 39132907
No abstract available.