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フルテキストURL fulltext.pdf
著者 Hiraki, Takahiro| Okai, Koichi| Bartokos, Michael| Beeks, Kjeld| Fujimoto, Hiroyuki| Fukunaga, Yuta| Haba, Hiromitsu| Kasamatsu, Yoshitaka| Kitao, Shinji| Leitner, Adrian| Masuda, Takahiko| Guan, Ming| Nagasawa, Nobumoto| Ogake, Ryoichiro| Pimon, Martin| Pressler, Martin| Sasao, Noboru| Schaden, Fabian| Schumm, Thorsten| Seto, Makoto| Shigekawa, Yudai| Shimizu, Kotaro| Sikorsky, Tomas| Tamasaku, Kenji| Takatori, Sayuri| Watanabe, Tsukasa| Yamaguchi, Atsushi| Yoda, Yoshitaka| Yoshimi, Akihiro| Yoshimura, Koji|
備考 The version of record of this article, first published in Nature Communications, is available online at Publisher’s website: http://dx.doi.org/10.1038/s41467-024-49631-0|
発行日 2024-07-16
出版物タイトル Nature Communications
15巻
1号
出版者 Nature Portfolio
開始ページ 5536
ISSN 2041-1723
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © The Author(s) 2024
論文のバージョン publisher
PubMed ID 39013899
DOI 10.1038/s41467-024-49631-0
Web of Science KeyUT 001270192000037
関連URL isVersionOf https://doi.org/10.1038/s41467-024-49631-0
フルテキストURL fulltext.pdf
著者 Oguma, Yukiko| Yamamoto, Masanori| Sunatsuki, Yukinari| Ota, Hiromi| Yamaji, Minoru| Okamoto, Hideki|
キーワード Cyclophane Azacyclophane Naphthalenophane Photocycloaddition [4 + 4] cycloaddition
備考 The version of record of this article, first published in Photochemical & Photobiological Sciences, is available online at Publisher’s website: http://dx.doi.org/10.1007/s43630-024-00610-w|
発行日 2024-07-10
出版物タイトル Photochemical & Photobiological Sciences
23巻
8号
出版者 Springer Science and Business Media LLC
開始ページ 1509
終了ページ 1519
ISSN 1474-905X
NCID AA11791060
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © The Author(s) 2024
論文のバージョン publisher
PubMed ID 38981991
DOI 10.1007/s43630-024-00610-w
Web of Science KeyUT 001268956300001
関連URL isVersionOf https://doi.org/10.1007/s43630-024-00610-w
フルテキストURL fulltext20240716-03.pdf
著者 Nakanishi, Kotaro| Kojima, Keiichi| Sowa, Yoshiyuki| Sudo, Yuki|
備考 This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Physical Chemistry B, copyright © 2024 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jpcb.4c03027.| This fulltext file will be available in Aug. 2025.|
発行日 2024-07-01
出版物タイトル The Journal of Physical Chemistry B
128巻
27号
出版者 American Chemical Society (ACS)
開始ページ 6509
終了ページ 6517
ISSN 1520-6106
NCID AA11114073
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2024 American Chemical Society
論文のバージョン author
PubMed ID 38949422
DOI 10.1021/acs.jpcb.4c03027
Web of Science KeyUT 001261316100001
関連URL isVersionOf https://doi.org/10.1021/acs.jpcb.4c03027
JaLCDOI 10.18926/AMO/67201
フルテキストURL 78_3_259.pdf
著者 Vural, Gonul| Demir, Esra| Gumusyayla, Sadiye| Eren, Funda| Barakli, Serdar| Neselioglu, Salim| Erel, Ozcan|
抄録 The aim of this study is to investigate the relationship of the lipid profile, dysfunctional high-density lipoprotein, ischaemia-modified albumin and thiol–disulfide homeostasis with cognitive impairment, fatigue and sleep disorders in patients with multiple sclerosis. The cognitive functions of patients were evaluated with the Brief International Cognitive Assessment for Multiple Sclerosis battery. Fatigue was evaluated with the Fatigue Severity Scale and the Fatigue Impact Scale. The Pittsburgh Sleep Quality Index and the Epworth Sleepiness Scale were used to assess patients’ sleep disturbance. Peripheral blood samples were collected, and lipid levels and myeloperoxidase and paraoxonase activity were measured. The myeloperoxidase/paraoxonase ratio, which indicates dysfunctional high-density lipoprotein, was calculated. Thiol–disulfide homeostasis and ischaemia-modified albumin were measured.
We did not identify any relationship between dysfunctional high-density lipoprotein and the physical disability, cognitive decline, fatigue and sleep problems of multiple sclerosis. Thiol–disulfide homeostasis was associated with cognitive scores. The shift of the balance towards disulfide was accompanied by a decrease in cognitive scores. On the other hand, we did not detect any relationship between fatigue and sleep disorders and thiol–disulfide homeostasis. Our findings revealed a possible correlation between cognitive dysfunction and thiol–disulfide homeostasis in multiple sclerosis patients.
キーワード multiple sclerosis dysfunctional HDL thiol–disulfide homeostasis cognitive decline
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2024-06
78巻
3号
出版者 Okayama University Medical School
開始ページ 259
終了ページ 270
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2024 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 38902214
Web of Science KeyUT 001267351000007
フルテキストURL fulltext20240527-01.pdf
著者 Nose, Keito| Yamaji, Minoru| Tani, Fumito| Goto, Kenta| Okamoto, Hideki|
キーワード Phenacene Imide Fluorescence Solvatofluorochromism Intramolecular charge transfer
備考 © 2024 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/| This fulltext file will be available in Mar. 2026.|
発行日 2024-07-01
出版物タイトル Journal of Photochemistry and Photobiology A: Chemistry
452巻
出版者 Elsevier BV
開始ページ 115613
ISSN 1010-6030
NCID AA10684407
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2024 Elsevier B.V.
論文のバージョン author
DOI 10.1016/j.jphotochem.2024.115613
Web of Science KeyUT 001222715400001
関連URL isVersionOf https://doi.org/10.1016/j.jphotochem.2024.115613
フルテキストURL fulltext20240501-01.pdf
著者 Zou, Yajuan| Shikano, Yutaka| Nishina, Yuta| Komatsu, Naoki| Kage-Nakadai, Eriko| Fujiwara, Masazumi|
キーワード iron oxide nanoparticles polyglycerol functionalization C. elegans accumulation distribution toxicity
発行日 2024-06
出版物タイトル Chemosphere
358巻
出版者 Elsevier BV
開始ページ 142060
ISSN 0045-6535
NCID AA00603442
資料タイプ プレプリント
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2024 Elsevier Ltd.
論文のバージョン author
PubMed ID 38648981
DOI 10.1016/j.chemosphere.2024.142060
関連URL isVersionOf https://doi.org/10.1016/j.chemosphere.2024.142060
JaLCDOI 10.18926/AMO/66924
フルテキストURL 78_2_151.pdf
著者 Komatsubara, Tadashi| Tazawa, Hiroshi| Hasei, Joe| Omori, Toshinori| Sugiu, Kazuhisa| Mochizuki, Yusuke| Demiya, Koji| Yoshida, Aki| Fujiwara, Tomohiro| Kunisada, Toshiyuki| Urata, Yasuo| Kagawa, Shunsuke| Ozaki, Toshifumi| Fujiwara, Toshiyoshi|
抄録 Soft-tissue sarcoma (STS) is a heterogeneous group of rare tumors originating predominantly from the embryonic mesoderm. Despite the development of combined modalities including radiotherapy, STSs are often refractory to antitumor modalities, and novel strategies that improve the prognosis of STS patients are needed. We previously demonstrated the therapeutic potential of two telomerase-specific replication-competent oncolytic adenoviruses, OBP-301 and tumor suppressor p53-armed OBP-702, in human STS cells. Here, we demonstrate in vitro and in vivo antitumor effects of OBP-702 in combination with ionizing radiation against human STS cells (HT1080, NMS-2, SYO-1). OBP-702 synergistically promoted the antitumor effect of ionizing radiation in the STS cells by suppressing the expression of B-cell lymphoma-X large (BCL-xL) and enhancing ionizing radiation-induced apoptosis. The in vivo experiments demonstrated that this combination therapy significantly suppressed STS tumors’ growth. Our results suggest that OBP-702 is a promising antitumor reagent for promoting the radiosensitivity of STS tumors.
キーワード soft-tissue sarcoma radiotherapy oncolytic adenovirus p53 BCL-xL
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2024-04
78巻
2号
出版者 Okayama University Medical School
開始ページ 151
終了ページ 161
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2024 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 38688833
Web of Science KeyUT 001229151800007
JaLCDOI 10.18926/AMO/66152
フルテキストURL 77_6_607.pdf
著者 Tani, Yasunari| Kashima, Saori| Mitsuhashi, Toshiharu| Suzuki, Etsuji| Takao, Soshi| Yorifuji, Takashi|
抄録 Many studies have shown an association between long-term exposure to particulate matter having an aerodynamic diameter of 2.5 μm or less (PM2.5) and diabetes mellitus (DM), but few studies have focused on Asian subjects. We thus examined the association between long-term exposure to PM2.5 and DM prevalence in Okayama City, Japan. We included 76,591 participants who had received basic health checkups in 2006 and 2007. We assigned the census-level modeled PM2.5 data from 2006 and 2007 to each participant and defined DM using treatment status and the blood testing. PM2.5 was associated with DM prevalence, and the prevalence ratio (95% confidence interval) was 1.10 (1.00-1.20) following each interquartile range increase (2.1 μg/m3) in PM2.5. This finding is consistent with previous results and suggests that long-term exposure to PM2.5 is associated with an increased prevalence of DM in Okayama City, Japan, where the PM2.5 level is lower than in other cities in Asian countries.
キーワード air pollution diabetes mellitus epidemiology glycosylated hemoglobin particulate matter
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2023-12
77巻
6号
出版者 Okayama University Medical School
開始ページ 607
終了ページ 612
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2023 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 38145934
Web of Science KeyUT 001164631200005
フルテキストURL fulltext20231101-01.pdf
著者 Ren, Jianchao| Danchana, Kaewta| Sasaki, Keiko| Kaneta, Takashi|
キーワード Laccase Mushroom Fluorometry 2,2'-Azinobis(3-ethylbenzthiazolin-6-sulfonic acid) N-Benzoyl leucomethylene blue
備考 © 2023 Elsevier Inc. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/| This fulltext file will be available in Aug. 2024.|
発行日 2023-10
出版物タイトル Journal of Food Composition and Analysis
123巻
出版者 Elsevier BV
開始ページ 105627
ISSN 0889-1575
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2023 Elsevier Inc.
論文のバージョン author
DOI 10.1016/j.jfca.2023.105627
Web of Science KeyUT 001068657200001
関連URL isVersionOf https://doi.org/10.1016/j.jfca.2023.105627
JaLCDOI 10.18926/AMO/65974
フルテキストURL 77_5_517.pdf
著者 Horiguchi, Shigeru| Matsumoto, Kazuyuki| Morimoto, Kosaku| Matsumi, Akihiro| Terasawa, Hiroyuki| Fujii, Yuki| Yamazaki, Tatsuhiro| Tsutsumi, Koichiro| Kato, Hironari|
抄録 We investigated the effect of modified FOLFIRINOX (mFFX) in unresectable pancreatic cancer by retrospectively analyzing the cases of 43 patients who underwent BRCA testing (germline, n=11; somatic, n=26; both germline and somatic, n=6). The association between BRCA mutations and therapeutic effect was clarified. Six patients tested positive for germline pathogenic variants. Familial pancreatic cancer (33% vs. 3%, p=0.006) and peritoneal disseminated lesions (66% vs. 8%, p<0.001) were significantly more common in patients with germline pathogenic variants. The partial response (PR) rate was 100% in the germline BRCA-positive patients, and 27% in the germline BRCA-negative patients (p<0.001). The median progression-free survival (PFS) was not reached for any germline BRCA-positive patients but was 9.0 months for the germline BRCA-negative patients (p=0.042). Patients with stage IV BRCA-associated pancreatic cancer had better overall survival than those with non-BRCA-associated pancreatic cancer, although the difference was nonsignificant (not reached vs. 655 days, p=0.061). Our results demonstrate that a PR and prolonged PFS can be expected in germline BRCA-positive patients after treatment with mFFX. Our findings also suggest that germline BRCA pathogenic variants may be useful as biomarkers for the therapeutic effect of mFFX in patients with pancreatic cancer.
キーワード BRCA FOLFIRINOX pancreatic cancer progression-free survival pathogenic variant
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2023-10
77巻
5号
出版者 Okayama University Medical School
開始ページ 517
終了ページ 525
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2023 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 37899263
Web of Science KeyUT 001108661600009
フルテキストURL fulltext20231011-03.pdf
著者 Kurihara, Marie| Thiel, Vera| Takahashi, Hirona| Kojima, Keiichi| Ward, David M.| Bryant, Donald A.| Sakai, Makoto| Yoshizawa, Susumu| Sudo, Yuki|
キーワード rhodopsin ion transport retinal isomerization optogenetics
発行日 2023-02-01
出版物タイトル Chemical and Pharmaceutical Bulletin
71巻
2号
出版者 Pharmaceutical Society of Japan
開始ページ 154
終了ページ 164
ISSN 0009-2363
NCID AA00602100
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2023 The Pharmaceutical Society of Japan
論文のバージョン publisher
PubMed ID 36724978
DOI 10.1248/cpb.c22-00774
Web of Science KeyUT 000964953300013
関連URL isVersionOf https://doi.org/10.1248/cpb.c22-00774
フルテキストURL fulltext20231004-01.pdf
著者 Shimooka, So| Kawanaka, Miku| Gofuku, Akio|
キーワード Soft rotary actuator Extension soft actuator Flexible shaft Pneumatic drive
備考 © 2023 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/| This fulltext file will be available in Oct. 2025.|
発行日 2023-10-16
出版物タイトル Sensors and Actuators A: Physical
361巻
出版者 Elsevier BV
開始ページ 114603
ISSN 0924-4247
NCID AA10781039
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2023 Elsevier B.V.
論文のバージョン author
DOI 10.1016/j.sna.2023.114603
Web of Science KeyUT 001067606600001
関連URL isVersionOf https://doi.org/10.1016/j.sna.2023.114603
フルテキストURL fulltext20230828-02.pdf
著者 Ono, Ryota| Saeki, Nozomu| Kojima, Keiichi| Moriya, Hisao| Sudo, Yuki|
キーワード UVA Saccharomyces cerevisiae Iodide Growth inhibition Suppressive molecule
備考 © 2023 Elsevier Inc. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/| This fulltext file will be available in Oct. 2024.|
発行日 2023-10-15
出版物タイトル Biochemical and Biophysical Research Communications
677巻
出版者 Elsevier BV
開始ページ 1
終了ページ 5
ISSN 0006-291X
NCID AA00564395
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2023 Elsevier Inc.
論文のバージョン author
PubMed ID 37523893
DOI 10.1016/j.bbrc.2023.07.048
Web of Science KeyUT 001047346900001
関連URL isVersionOf https://doi.org/10.1016/j.bbrc.2023.07.048
JaLCDOI 10.18926/AMO/65746
フルテキストURL 77_4_371.pdf
著者 Iwamoto, Yosuke| Kaya, Mitsunori| Kijima, Hiroaki| Fujii, Masashi| Nagahata, Itsuki| Miyakoshi, Naohisa|
抄録 In recent publications on greater trochanteric pain syndrome (GTPS), the pathology receiving the most attention has been gluteus medius muscle tendinous injury, and surgical techniques such as gluteus medius tendon repair and their outcomes for GTPS have been reported. In our department-related facilities, arthroscopic surgeries are routinely performed for the patients with recalcitrant GTPS. A total of 51 patients were diagnosed with GTPS. Surgical treatment was carried out 22 patients (24 joints; 4 males and 18 females; mean age at surgery of 52.0 years). Arthroscopic findings confirmed bursitis in all 24 joints. In all cases, debridement of the greater trochanter bursa provided rapid relief of greater trochanter pain. The Numerical Rating Scale showed significant improvement, from the preoperative mean of 7.8 (range, 6-10) to the postoperative day 7 mean of 1.6 (range, 0-3). The modified Harris Hip Score was significantly improved from the preoperative mean of 65.5 (range, 52.5-78.3) to the final follow-up (average 2.9 months) mean of 96.0 (range, 85.2-100). Fascial damage of the gluteus medius muscle was observed in 21 joints while only 2 patients had a gluteus medius tendinous injury. Greater trochanteric bursitis and fascia or muscle-fiber injury of the gluteus medius muscle are the most common pathologies in patients with lateral hip pain.
キーワード greater trochanteric pain syndrome endoscopic findings bursitis
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2023-08
77巻
4号
出版者 Okayama University Medical School
開始ページ 371
終了ページ 375
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2023 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 37635137
Web of Science KeyUT 001163659800005
フルテキストURL fulltext.pdf
著者 Kojima, Keiichi| Kawanishi, Shiho| Nishimura, Yosuke| Hasegawa, Masumi| Nakao, Shin| Nagata, Yuya| Yoshizawa, Susumu| Sudo, Yuki|
備考 The version of record of this article, first published in Scientific Reports, is available online at Publisher’s website: http://dx.doi.org/10.1038/s41598-023-34125-8|
発行日 2023-04-28
出版物タイトル Scientific Reports
13巻
1号
出版者 nature portfolio
開始ページ 6974
ISSN 2045-2322
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © The Author(s) 2023
論文のバージョン publisher
PubMed ID 37117398
DOI 10.1038/s41598-023-34125-8
Web of Science KeyUT 000985908500047
関連URL isVersionOf https://doi.org/10.1038/s41598-023-34125-8
フルテキストURL fulltext20230413-01.pdf
著者 Kumano, Shota| Takaki, Tomoyasu| Uchida, Tetsuya|
発行日 2023-2-17
出版物タイトル Polymer Journal
出版者 Springer Science and Business Media LLC
ISSN 0032-3896
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © The Author(s) 2023.
論文のバージョン publisher
DOI 10.1038/s41428-023-00765-w
Web of Science KeyUT 000934721800001
関連URL isVersionOf https://doi.org/10.1038/s41428-023-00765-w
フルテキストURL fulltext.pdf
著者 Tanaka, Hiroyoshi Y.| Nakazawa, Takuya| Enomoto, Atsushi| Masamune, Atsushi| Kano, Mitsunobu R.|
キーワード pancreatic cancer tumor microenvironment nanomedicine fibrosis extracellular matrix fibroblast
発行日 2023-01-24
出版物タイトル Cancers
15巻
3号
出版者 MDPI
開始ページ 724
ISSN 2072-6694
資料タイプ 学術雑誌論文
言語 英語
OAI-PMH Set 岡山大学
著作権者 © 2023 by the authors.
論文のバージョン publisher
PubMed ID 36765684
DOI 10.3390/cancers15030724
Web of Science KeyUT 000929314700001
関連URL isVersionOf https://doi.org/10.3390/cancers15030724
JaLCDOI 10.18926/AMO/64355
フルテキストURL 77_1_1.pdf
著者 Nahar, Lutfun| Hagiya, Hideharu| Nada, Takahiro| Iio, Koji| Gotoh, Kazuyoshi| Matsushita, Osamu| Otsuka, Fumio|
抄録 Inducible resistance to the macrolide, lincosamide, and streptogramin B (iMLSB) antibiotic family is a latent mechanism for antimicrobial resistance in Staphylococcus aureus. We here investigated the frequency and genotypic profiles of iMLSB resistance in clindamycin (CLDM)-susceptible S. aureus isolated in Okayama University Hospital from June 2020 to June 2021. We phenotypically screened the iMLSB resistance via D-zone test and performed PCR testing for the erythromycin ribosomal methylase (erm) genes: ermA and ermC. Among 432 CLDM-susceptible S. aureus isolates, 138 (31.9%) exhibited an iMLSB-resistance phenotype, with methicillinresistant S. aureus isolates (MRSA; 61 isolates: 58.6%) exhibiting higher positivity than methicillin-sensitive S. aureus isolates (MSSA; 77 isolates: 23.5%) (p<0.001). Male patients had a higher frequency of iMLSB resistance than females (OR [95%CI]: 1.8 [1.2-2.8]; p=0.007). Genotypically, ermA predominated in both MSSA (70.1%) and MRSA (86.9%) compared to ermC (14.3% in MSSA and 11.5% in MRSA). A single strain of MRSA possessed both ermA and ermC, while 12 (15.6%) MSSA isolates were negative for both ermA and ermC, suggesting the presence of other genetic mechanisms. Collectively, these results show that approximately 33% of CLDM-susceptible S. aureus isolates at our university hospital exhibited iMLSB resistance, predominantly caused by ermA in both MSSA and MRSA.
キーワード antimicrobial resistance clindamycin erm D-zone test inducible MLSB
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2023-02
77巻
1号
出版者 Okayama University Medical School
開始ページ 1
終了ページ 9
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2023 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 36849140
Web of Science KeyUT 000953663800001
JaLCDOI 10.18926/AMO/64124
フルテキストURL 76_6_731.pdf
著者 Kamamura, Maho| Higaki, Fumiyo| Sasada, Susumu| Matsushita, Toshi| Yasuhara, Takao| Date, Isao| Hiraki, Takao|
抄録 We report a rare case of idiopathic spinal cord herniation (ISCH) with a history of cerebrospinal fluid (CSF) leakage. ISCH is a protrusion of the spinal cord through a dural defect. Thin constructive interference in steady-state (CISS) images clearly demonstrated the herniated cord in the present case. The myelopathy worsened and the patient underwent surgery for reduction of herniated spinal cord; the dural defect was filled by placing collagen matrix graft (DuraGen®) between the inner and outer dural layers. The patient’s symptoms have improved without relapse for 8 months since surgery. This method may be a good surgical option for cases of spinal cord herniation.
キーワード cerebrospinal fluid leakage constructive interference in steady state collagen matrix graft magnetic resonance image spinal cord herniation
Amo Type Case Report
出版物タイトル Acta Medica Okayama
発行日 2022-12
76巻
6号
出版者 Okayama University Medical School
開始ページ 731
終了ページ 736
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2022 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 36549776
Web of Science KeyUT 000905195100014
JaLCDOI 10.18926/AMO/64117
フルテキストURL 76_6_673.pdf
著者 Okazawa-Sakai, Mika| Yamamoto, Yasuko| Futagawa, Mashu| Okamura, Miki| Miyawaki, Satoko| Nishina, Tomohiro| Takehara, Kazuhiro| Kozuki, Toshiyuki| Tomida, Shuta| Hyodo, Ichinosuke| Ohsumi, Shozo| Hirasawa, Akira|
抄録 Patients found to have presumed germline pathogenic variants (PGPVs) during comprehensive genomic profiling (CGP) require genetic counseling (GC) referrals. We retrospectively investigated the outcomes of patients with PGPVs. Among 159 patients who underwent CGP, we recommended GC for the 16 patients with PGPVs (3 with [FG group] and 13 without [G Group] a family/personal history of hereditary cancer) as well as for the 8 patients with no PGPVs, but a history (F group); 2 (67%), 5 (38%), and 3 (38%) patients received GC in the FG, G, and F groups, respectively. Germline testing results were positive in 1 and 2 patients of the FG and G groups, respectively. Among the patients recommended for GC, 58% did not receive GC due to lack of interest, poor performance status, or death. CGP contributes to the identification of germline variants in patients without a history of hereditary cancer. However, the proportion of patients who undergo GC should be improved.
キーワード comprehensive genomic profiling hereditary cancer germline findings presumed germline pathogenic variant(s) genetic counseling
Amo Type Original Article
出版物タイトル Acta Medica Okayama
発行日 2022-12
76巻
6号
出版者 Okayama University Medical School
開始ページ 673
終了ページ 678
ISSN 0386-300X
NCID AA00508441
資料タイプ 学術雑誌論文
言語 英語
著作権者 Copyright Ⓒ 2022 by Okayama University Medical School
論文のバージョン publisher
査読 有り
PubMed ID 36549769
Web of Science KeyUT 000905195100007