Ichizo Nishino
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Explore the profile of Ichizo Nishino including associated specialties, affiliations and a list of published articles.
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636
Citations
15603
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Recent Articles
1.
Ikeda S, Shimizu T, Adachi T, Suzuki S, Nishino I, Hanajima R
Rinsho Shinkeigaku
. 2025 Feb;
PMID: 40010716
A 68-year-old woman presented with a one-month history of polyarthritis and fever, followed by myalgia and muscle weakness involving the proximal limbs, neck, trunk, and distal upper extremities. Myositis was...
2.
Suzuki N, Mori-Yoshimura M, Nishino I, Aoki M
J Neuromuscul Dis
. 2025 Feb;
:22143602241296226.
PMID: 39973407
GNE myopathy is an autosomal recessive hereditary muscle disorder that has the following clinical characteristics: develops in early adulthood, gradually progresses from the distal muscles, and is relatively sparing of...
3.
Nishimori Y, Tanboon J, Oyama M, Motegi H, Tomo Y, Oba M, et al.
J Neurol
. 2025 Feb;
272(3):206.
PMID: 39954092
It is still unknown whether anti-mitochondrial M2 antibody (AM2A)-positive myositis is an independent subtype of autoimmune myositis (AIM). As such, the aim of this study is to better characterize the...
4.
Funaguma S, Iida A, Saito Y, Tanboon J, De Los Reyes F, Sonehara K, et al.
Nat Commun
. 2025 Feb;
16(1):1318.
PMID: 39920152
Transposon-like human element 1B (THE1B) originates from ancient retroviral sequences integrated into the primate genome approximately 50 million years ago, now accounting for at least 27,233 copies in the human...
5.
Sumi K, Masuda T, Kondo H, Obayashi K, Takeuchi Y, Harada T, et al.
J Neurol Sci
. 2025 Feb;
470:123414.
PMID: 39914165
Immune-mediated necrotizing myopathy (IMNM) is accompanied by extramuscular manifestations including cardiac complications, and such cardiac complications have a serious prognostic impact on these patients. This study aims to investigate cardiac...
6.
Baba Y, Maeda M, Muramatsu K, Tominaga K, Ueda K, Ueda N, et al.
Rinsho Shinkeigaku
. 2025 Jan;
65(2):139-145.
PMID: 39864868
The patient was a 33-year-old woman with no family history of a similar disorder. At one year of age, she exhibited scoliosis and respiratory failure, necessitating a tracheostomy performed at...
7.
Kim S, Choi Y, Oh E, Nishino I, Suzuki S, Suh B, et al.
J Clin Neurol
. 2025 Jan;
21(1):31-39.
PMID: 39778565
Background And Purpose: This study evaluated the diagnostic utility of an anti-signal-recognition particle 54 (anti-SRP54) antibody-based enzyme-linked immunosorbent assay (ELISA) as well as the clinical, serological, and pathological characteristics of...
8.
Shimazaki R, Saito Y, Awaya T, Minami N, Kurosawa R, Hosokawa M, et al.
Orphanet J Rare Dis
. 2025 Jan;
20(1):1.
PMID: 39755676
Background: Sarcoglycanopathies (SGPs) are limb-girdle muscular dystrophies (LGMDs) that can be classified into four types, LGMDR3, LGMDR4, LGMDR5, and LGMDR6, caused by mutations in the genes, SGCA, SGCB, SGCG, and...
9.
Umemoto D, Nishino I, Yamashita D, Ishimaru N, Nishioka H
BMC Rheumatol
. 2024 Dec;
8(1):66.
PMID: 39639413
Background: Cholesterol embolism causes various organ dysfunctions, including skin, kidney, and gastrointestinal tract dysfunction, as well as immunological abnormalities, such as hypocomplementemia and eosinophilia. However, only a few cases of...
10.
Imai K, Nastume T, Shirai M, Motobayashi M, Ishiyama A, Suzuki S, et al.
J Clin Neuromuscul Dis
. 2024 Nov;
26(2):102-105.
PMID: 39590929
No abstract available.