Yuji Nakamura
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Explore the profile of Yuji Nakamura including associated specialties, affiliations and a list of published articles.
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Articles
143
Citations
702
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Recent Articles
1.
Takenoya T, Shimazu M, Wang W, Nakayama F, Mizuno S, Suzuki K, et al.
Gan To Kagaku Ryoho
. 2025 Feb;
51(13):1357-1359.
PMID: 39948855
A 72-year-old man visited our hospital for evaluation of a liver tumor documented on abdominal ultrasonography. Computed tomography revealed a liver tumor measuring 13 cm and a tumor thrombus in...
2.
Fujimoto M, Nakamura Y, Hosoki K, Iwaki T, Sato E, Ieda D, et al.
HGG Adv
. 2024 Aug;
5(4):100342.
PMID: 39169619
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by the loss of function of maternal UBE3A. The major cause of AS is a maternal deletion in 15q11.2-q13, and the...
3.
Nakamura Y, Shimada I, Maroofian R, Falabella M, Zaki M, Fujimoto M, et al.
Brain
. 2024 Jul;
147(11):3949-3967.
PMID: 39082157
Patatin-like phospholipase domain-containing lipase 8 (PNPLA8), one of the calcium-independent phospholipase A2 enzymes, is involved in various physiological processes through the maintenance of membrane phospholipids. Biallelic variants in PNPLA8 have...
4.
Hirose K, Ikai A, Ito H, Ishidou M, Toritsuka D, Nakamura Y, et al.
Interdiscip Cardiovasc Thorac Surg
. 2024 Feb;
38(2).
PMID: 38374222
Objectives: The 18- and 16-mm conduits in extracardiac total cavopulmonary connection (eTCPC) were reported to be optimal based on energy loss and flow stagnation at the relatively early phase. However,...
5.
Segawa M, Iizuka N, Ogihara H, Tanaka K, Nakae H, Usuku K, et al.
Front Med Technol
. 2023 Mar;
5:1050909.
PMID: 36993786
Background: In Kampo medicine, tongue examination is used to diagnose the pathological condition "Sho," but an objective evaluation method for its diagnostic ability has not been established. We constructed a...
6.
Fujimoto M, Nakamura Y, Iwaki T, Sato E, Ieda D, Hattori A, et al.
J Hum Genet
. 2022 Dec;
68(2):111-112.
PMID: 36456768
No abstract available.
7.
Fujimoto M, Nakamura Y, Iwaki T, Sato E, Ieda D, Hattori A, et al.
J Hum Genet
. 2022 Oct;
68(2):87-90.
PMID: 36224263
Angelman syndrome (AS) is caused by the functional absence of the maternal ubiquitin-protein ligase E3A (UBE3A) gene. Approximately 5% of AS is caused by paternal uniparental disomy of chromosome 15...
8.
Chatani T, Shikama T, Ueno Y, Kado S, Kawazome H, Minami T, et al.
Sci Rep
. 2022 Sep;
12(1):15567.
PMID: 36151115
For plasma spectroscopy, Stokes spectropolarimetry is used as a method to spatially invert the viewing-chord-integrated spectrum on the basis of the correspondence between the given magnetic field profile along the...
9.
Narita K, Muramatsu H, Narumi S, Nakamura Y, Okuno Y, Suzuki K, et al.
Sci Rep
. 2022 Aug;
12(1):14589.
PMID: 36028527
Recently, whole-exome sequencing (WES) has been used for genetic diagnoses of patients who remain otherwise undiagnosed. WES was performed in 177 Japanese patients with undiagnosed conditions who were referred to...
10.
Yamamoto K, Ohashi K, Fujimoto M, Ieda D, Nakamura Y, Hattori A, et al.
Brain Dev
. 2022 May;
44(8):578-582.
PMID: 35527075
Introduction: Bicaudal D homolog 2 (BICD2) is a causative gene of autosomal-dominant lower extremity-predominant spinal muscular atrophy-2 (SMA-LED2). The severity of SMA-LED2 varies widely, ranging from cases in which patients...