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A Critical Appraisal of Extracorporeal Photopheresis as a Treatment Modality for Acute and Chronic Graft-Versus-Host Disease.

Biomedicines

Rafei H, Kharfan-Dabaja MA, Nishihori T.
PMID: 29019937
Biomedicines. 2017 Oct 11;5(4). doi: 10.3390/biomedicines5040060.

Although significant advances have been made in the biologic understanding of graft-versus-host disease (GVHD) and its treatment options, GVHD remains the single most challenging obstacle to the success of allogeneic hematopoietic cell transplantation (HCT) due to high risk of...

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Rafei H, Kharfan-Dabaja MA, Nishihori T. A Critical Appraisal of Extracorporeal Photopheresis as a Treatment Modality for Acute and Chronic Graft-Versus-Host Disease. Biomedicines. 2017;5(4)doi: 10.3390/biomedicines5040060.
Rafei, H., Kharfan-Dabaja, M. A., & Nishihori, T. (2017). A Critical Appraisal of Extracorporeal Photopheresis as a Treatment Modality for Acute and Chronic Graft-Versus-Host Disease. Biomedicines, 5(4), . https://doi.org/10.3390/biomedicines5040060
Rafei, Hind, et al. "A Critical Appraisal of Extracorporeal Photopheresis as a Treatment Modality for Acute and Chronic Graft-Versus-Host Disease." Biomedicines vol. 5,4 (2017). doi: https://doi.org/10.3390/biomedicines5040060
Rafei H, Kharfan-Dabaja MA, Nishihori T. A Critical Appraisal of Extracorporeal Photopheresis as a Treatment Modality for Acute and Chronic Graft-Versus-Host Disease. Biomedicines. 2017 Oct 11;5(4). doi: 10.3390/biomedicines5040060. PMID: 29019937; PMCID: PMC5744084.
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Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts.

Molecular therapy. Nucleic acids

Noguchi S, Ogawa M, Kawahara G, Malicdan MC, Nishino I.
PMID: 24959844
Mol Ther Nucleic Acids. 2014 Jun 24;3:e171. doi: 10.1038/mtna.2014.22.

Ullrich congenital muscular dystrophy (UCMD) is an inherited muscle disorder characterized clinically by muscle weakness, distal joint hyperlaxity, and proximal joint contractures. Sporadic and recessive mutations in the three collagen VI genes, COL6A1, COL6A2, and COL6A3, are reported to...

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Noguchi S, Ogawa M, Kawahara G, et al. Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts. Mol Ther Nucleic Acids. 2014;3:e171doi: 10.1038/mtna.2014.22.
Noguchi, S., Ogawa, M., Kawahara, G., Malicdan, M. C., & Nishino, I. (2014). Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts. Molecular therapy. Nucleic acids, 3e171. https://doi.org/10.1038/mtna.2014.22
Noguchi, Satoru, et al. "Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts." Molecular therapy. Nucleic acids vol. 3 (2014): e171. doi: https://doi.org/10.1038/mtna.2014.22
Noguchi S, Ogawa M, Kawahara G, Malicdan MC, Nishino I. Allele-specific Gene Silencing of Mutant mRNA Restores Cellular Function in Ullrich Congenital Muscular Dystrophy Fibroblasts. Mol Ther Nucleic Acids. 2014 Jun 24;3:e171. doi: 10.1038/mtna.2014.22. PMID: 24959844; PMCID: PMC4078762.
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Preoperative embolization of meningiomas with low-concentration n-butyl cyanoacrylate.

Nagoya journal of medical science

Yamamoto T, Ohshima T, Nishihori M, Goto S, Nishizawa T, Shimato S, Kato K.
PMID: 26412880
Nagoya J Med Sci. 2015 Aug;77(3):347-53.

The aim of this study was to determine the clinical safety and efficacy of preoperative embolization of meningiomas with low-concentration n-butyl cyanoacrylate (NBCA). Nineteen cases of hypervascular intracranial meningiomas were treated by preoperative embolization with 14% NBCA, using a...

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Yamamoto T, Ohshima T, Nishihori M, et al. Preoperative embolization of meningiomas with low-concentration n-butyl cyanoacrylate. Nagoya J Med Sci. 2015;77(3):347-53
Yamamoto, T., Ohshima, T., Nishihori, M., Goto, S., Nishizawa, T., Shimato, S., & Kato, K. (2015). Preoperative embolization of meningiomas with low-concentration n-butyl cyanoacrylate. Nagoya journal of medical science, 77(3), 347-53.
Yamamoto, Taiki, et al. "Preoperative embolization of meningiomas with low-concentration n-butyl cyanoacrylate." Nagoya journal of medical science vol. 77,3 (2015): 347-53.
Yamamoto T, Ohshima T, Nishihori M, Goto S, Nishizawa T, Shimato S, Kato K. Preoperative embolization of meningiomas with low-concentration n-butyl cyanoacrylate. Nagoya J Med Sci. 2015 Aug;77(3):347-53. PMID: 26412880; PMCID: PMC4574321.
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A Qualitative Study of Confusing Experiences among Japanese Adult Patients with Type 1 Diabetes.

Yonago acta medica

Nishio I, Chujo M, Kataoka H.
PMID: 27046954
Yonago Acta Med. 2016 Mar;59(1):81-8. Epub 2016 Apr 01.

BACKGROUND: In this study, we investigated the powerlessness of patients with type 1 diabetes (T1D), and described the structure of powerlessness that these individuals experienced. In order for patients to recover from this state, we recommend that they take...

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Nishio I, Chujo M, Kataoka H. A Qualitative Study of Confusing Experiences among Japanese Adult Patients with Type 1 Diabetes. Yonago Acta Med. 2016;59(1):81-8
Nishio, I., Chujo, M., & Kataoka, H. (2016). A Qualitative Study of Confusing Experiences among Japanese Adult Patients with Type 1 Diabetes. Yonago acta medica, 59(1), 81-8.
Nishio, Ikuko, et al. "A Qualitative Study of Confusing Experiences among Japanese Adult Patients with Type 1 Diabetes." Yonago acta medica vol. 59,1 (2016): 81-8.
Nishio I, Chujo M, Kataoka H. A Qualitative Study of Confusing Experiences among Japanese Adult Patients with Type 1 Diabetes. Yonago Acta Med. 2016 Mar;59(1):81-8. Epub 2016 Apr 01. PMID: 27046954; PMCID: PMC4816752.
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[Myopathy, myotubular].

Ryoikibetsu shokogun shirizu

Nishino I.
PMID: 11528724
Ryoikibetsu Shokogun Shirizu. 2001;(34):249-50.

No abstract available.

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Nishino I. [Myopathy, myotubular]. Ryoikibetsu Shokogun Shirizu. 2001;(34):249-50
Nishino, I. (2001). [Myopathy, myotubular]. Ryoikibetsu shokogun shirizu, (34), 249-50.
Nishino, I. "[Myopathy, myotubular]." Ryoikibetsu shokogun shirizu vol. ,34 (2001): 249-50.
Nishino I. [Myopathy, myotubular]. Ryoikibetsu Shokogun Shirizu. 2001;(34):249-50. Japanese. PMID: 11528724.
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Collapse of gels in an electric field.

Science (New York, N.Y.)

Tanaka T, Nishio I, Sun ST, Ueno-Nishio S.
PMID: 17808541
Science. 1982 Oct 29;218(4571):467-9. doi: 10.1126/science.218.4571.467.

An infinitesimal change in electric potential across a polyelectrolyte gel produces a discrete, reversible volume change. The volume of the collapsed gel can be several hundred times smaller than that of the swollen gel.

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Tanaka T, Nishio I, Sun ST, et al. Collapse of gels in an electric field. Science. 1982;218(4571):467-9doi: 10.1126/science.218.4571.467.
Tanaka, T., Nishio, I., Sun, S. T., & Ueno-Nishio, S. (1982). Collapse of gels in an electric field. Science (New York, N.Y.), 218(4571), 467-9. https://doi.org/10.1126/science.218.4571.467
Tanaka, T, et al. "Collapse of gels in an electric field." Science (New York, N.Y.) vol. 218,4571 (1982): 467-9. doi: https://doi.org/10.1126/science.218.4571.467
Tanaka T, Nishio I, Sun ST, Ueno-Nishio S. Collapse of gels in an electric field. Science. 1982 Oct 29;218(4571):467-9. doi: 10.1126/science.218.4571.467. PMID: 17808541.
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Intraoperative evaluation of local cerebral hemodynamic change by indocyanine green videoangiography: prediction of incidence and duration of postoperative transient neurological events in patients with moyamoya disease.

Journal of neurosurgery

Uda K, Araki Y, Muraoka S, Ota S, Wada K, Yokoyama K, Nishihori M, Izumi T, Okamoto S, Wakabayashi T.
PMID: 29676693
J Neurosurg. 2018 Apr 01;1-9. doi: 10.3171/2017.10.JNS171523. Epub 2018 Apr 01.

OBJECTIVETransient neurological events (TNEs) occur frequently in the acute phase after direct bypass surgery for moyamoya disease (MMD), but there is currently no way to predict them. FlowInsight is a specialized software for analyzing indocyanine green (ICG) videoangiography taken...

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Uda K, Araki Y, Muraoka S, et al. Intraoperative evaluation of local cerebral hemodynamic change by indocyanine green videoangiography: prediction of incidence and duration of postoperative transient neurological events in patients with moyamoya disease. J Neurosurg. 2018;1-9doi: 10.3171/2017.10.JNS171523.
Uda, K., Araki, Y., Muraoka, S., Ota, S., Wada, K., Yokoyama, K., Nishihori, M., Izumi, T., Okamoto, S., & Wakabayashi, T. (2018). Intraoperative evaluation of local cerebral hemodynamic change by indocyanine green videoangiography: prediction of incidence and duration of postoperative transient neurological events in patients with moyamoya disease. Journal of neurosurgery, 1-9. https://doi.org/10.3171/2017.10.JNS171523
Uda, Kenji, et al. "Intraoperative evaluation of local cerebral hemodynamic change by indocyanine green videoangiography: prediction of incidence and duration of postoperative transient neurological events in patients with moyamoya disease." Journal of neurosurgery vol. (2018): 1-9. doi: https://doi.org/10.3171/2017.10.JNS171523
Uda K, Araki Y, Muraoka S, Ota S, Wada K, Yokoyama K, Nishihori M, Izumi T, Okamoto S, Wakabayashi T. Intraoperative evaluation of local cerebral hemodynamic change by indocyanine green videoangiography: prediction of incidence and duration of postoperative transient neurological events in patients with moyamoya disease. J Neurosurg. 2018 Apr 01;1-9. doi: 10.3171/2017.10.JNS171523. Epub 2018 Apr 01. PMID: 29676693.
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Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan.

PloS one

Liang WC, Tian X, Yuo CY, Chen WZ, Kan TM, Su YN, Nishino I, Wong LC, Jong YJ.
PMID: 28797072
PLoS One. 2017 Aug 10;12(8):e0183406. doi: 10.1371/journal.pone.0183406. eCollection 2017.

[This corrects the article DOI: 10.1371/journal.pone.0170517.].

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Liang WC, Tian X, Yuo CY, et al. Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan. PLoS One. 2017;12(8):e0183406doi: 10.1371/journal.pone.0183406.
Liang, W. C., Tian, X., Yuo, C. Y., Chen, W. Z., Kan, T. M., Su, Y. N., Nishino, I., Wong, L. C., & Jong, Y. J. (2017). Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan. PloS one, 12(8), e0183406. https://doi.org/10.1371/journal.pone.0183406
Liang, Wen-Chen, et al. "Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan." PloS one vol. 12,8 (2017): e0183406. doi: https://doi.org/10.1371/journal.pone.0183406
Liang WC, Tian X, Yuo CY, Chen WZ, Kan TM, Su YN, Nishino I, Wong LC, Jong YJ. Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan. PLoS One. 2017 Aug 10;12(8):e0183406. doi: 10.1371/journal.pone.0183406. eCollection 2017. PMID: 28797072; PMCID: PMC5552315.
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Two novel .

Human genome variation

Inoue M, Iida A, Hayashi S, Mori-Yoshimura M, Nagaoka A, Yoshimura S, Shiraishi H, Tsujino A, Takahashi Y, Nonaka I, Hayashi YK, Noguchi S, Nishino I.
PMID: 29899994
Hum Genome Var. 2018 May 30;5:9. doi: 10.1038/s41439-018-0009-7. eCollection 2018.

No abstract available.

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Inoue M, Iida A, Hayashi S, et al. Two novel . Hum Genome Var. 2018;5:9doi: 10.1038/s41439-018-0009-7.
Inoue, M., Iida, A., Hayashi, S., Mori-Yoshimura, M., Nagaoka, A., Yoshimura, S., Shiraishi, H., Tsujino, A., Takahashi, Y., Nonaka, I., Hayashi, Y. K., Noguchi, S., & Nishino, I. (2018). Two novel . Human genome variation, 59. https://doi.org/10.1038/s41439-018-0009-7
Inoue, Michio, et al. "Two novel ." Human genome variation vol. 5 (2018): 9. doi: https://doi.org/10.1038/s41439-018-0009-7
Inoue M, Iida A, Hayashi S, Mori-Yoshimura M, Nagaoka A, Yoshimura S, Shiraishi H, Tsujino A, Takahashi Y, Nonaka I, Hayashi YK, Noguchi S, Nishino I. Two novel . Hum Genome Var. 2018 May 30;5:9. doi: 10.1038/s41439-018-0009-7. eCollection 2018. PMID: 29899994; PMCID: PMC5976715.
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A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy.

Journal of human genetics

Inoue-Shibui A, Niihori T, Kobayashi M, Suzuki N, Izumi R, Warita H, Hara K, Shirota M, Funayama R, Nakayama K, Nishino I, Aoki M, Aoki Y.
PMID: 33744911
J Hum Genet. 2021 Oct;66(10):965-972. doi: 10.1038/s10038-021-00916-y. Epub 2021 Mar 20.

Heat shock protein family B member 8, encoded by HSPB8, is an essential component of the chaperone-assisted selective autophagy complex, which maintains muscle function by degrading damaged proteins in the cells. Mutations in HSPB8 have been reported to cause...

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Inoue-Shibui A, Niihori T, Kobayashi M, et al. A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy. J Hum Genet. 2021;66(10):965-972doi: 10.1038/s10038-021-00916-y.
Inoue-Shibui, A., Niihori, T., Kobayashi, M., Suzuki, N., Izumi, R., Warita, H., Hara, K., Shirota, M., Funayama, R., Nakayama, K., Nishino, I., Aoki, M., & Aoki, Y. (2021). A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy. Journal of human genetics, 66(10), 965-972. https://doi.org/10.1038/s10038-021-00916-y
Inoue-Shibui, Aya, et al. "A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy." Journal of human genetics vol. 66,10 (2021): 965-972. doi: https://doi.org/10.1038/s10038-021-00916-y
Inoue-Shibui A, Niihori T, Kobayashi M, Suzuki N, Izumi R, Warita H, Hara K, Shirota M, Funayama R, Nakayama K, Nishino I, Aoki M, Aoki Y. A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy. J Hum Genet. 2021 Oct;66(10):965-972. doi: 10.1038/s10038-021-00916-y. Epub 2021 Mar 20. PMID: 33744911.
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Outcomes Following Intolerance to Tacrolimus/Sirolimus Graft-Versus-Host Disease Prophylaxis for Allogeneic Hematopoietic Cell Transplantation.

Transplantation and cellular therapy

Mirza AS, Tandon A, Jenneman D, Cao S, Brimer T, Kumar A, Kidd M, Khimani F, Faramand R, Mishra A, Liu H, Nishihori T, Perez L, Lazaryan A, Bejanyan N, Nieder M, Pidala J, Elmariah H.
PMID: 35017119
Transplant Cell Ther. 2022 Jan 08; doi: 10.1016/j.jtct.2022.01.003. Epub 2022 Jan 08.

BACKGROUND: Although tacrolimus and sirolimus (TAC/SIR) is an accepted graft-versus-host disease (GVHD) prophylaxis following allogeneic hematopoietic cell transplant (HCT), toxicity from this regimen can lead to premature discontinuation of immunosuppression. There are limited studies reporting outcomes and subsequent treatment...

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Mirza AS, Tandon A, Jenneman D, et al. Outcomes Following Intolerance to Tacrolimus/Sirolimus Graft-Versus-Host Disease Prophylaxis for Allogeneic Hematopoietic Cell Transplantation. Transplant Cell Ther. 2022;doi: 10.1016/j.jtct.2022.01.003.
Mirza, A. S., Tandon, A., Jenneman, D., Cao, S., Brimer, T., Kumar, A., Kidd, M., Khimani, F., Faramand, R., Mishra, A., Liu, H., Nishihori, T., Perez, L., Lazaryan, A., Bejanyan, N., Nieder, M., Pidala, J., & Elmariah, H. (2022). Outcomes Following Intolerance to Tacrolimus/Sirolimus Graft-Versus-Host Disease Prophylaxis for Allogeneic Hematopoietic Cell Transplantation. Transplantation and cellular therapy, . https://doi.org/10.1016/j.jtct.2022.01.003
Mirza, Abu-Sayeef, et al. "Outcomes Following Intolerance to Tacrolimus/Sirolimus Graft-Versus-Host Disease Prophylaxis for Allogeneic Hematopoietic Cell Transplantation." Transplantation and cellular therapy vol. (2022). doi: https://doi.org/10.1016/j.jtct.2022.01.003
Mirza AS, Tandon A, Jenneman D, Cao S, Brimer T, Kumar A, Kidd M, Khimani F, Faramand R, Mishra A, Liu H, Nishihori T, Perez L, Lazaryan A, Bejanyan N, Nieder M, Pidala J, Elmariah H. Outcomes Following Intolerance to Tacrolimus/Sirolimus Graft-Versus-Host Disease Prophylaxis for Allogeneic Hematopoietic Cell Transplantation. Transplant Cell Ther. 2022 Jan 08; doi: 10.1016/j.jtct.2022.01.003. Epub 2022 Jan 08. PMID: 35017119.
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Open penetrating external laryngotracheal injury and abdominal trauma by suicide attempt successfully treated with immediate intervention: A case report.

Trauma case reports

Kamidani R, Okada H, Kato R, Nishihori T, Kuze B, Yoshida T, Yoshida S, Ogura S.
PMID: 33718566
Trauma Case Rep. 2021 Feb 23;32:100435. doi: 10.1016/j.tcr.2021.100435. eCollection 2021 Apr.

An open penetrating external laryngotracheal injury (PE-LTI) is a rare life-threatening injury requiring immediate intervention. Penetrating injuries may cause tissue loss, which makes wound closure difficult sometimes. Here, we report the case of an open PE-LTI and abdominal trauma...

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Kamidani R, Okada H, Kato R, et al. Open penetrating external laryngotracheal injury and abdominal trauma by suicide attempt successfully treated with immediate intervention: A case report. Trauma Case Rep. 2021;32:100435doi: 10.1016/j.tcr.2021.100435.
Kamidani, R., Okada, H., Kato, R., Nishihori, T., Kuze, B., Yoshida, T., Yoshida, S., & Ogura, S. (2021). Open penetrating external laryngotracheal injury and abdominal trauma by suicide attempt successfully treated with immediate intervention: A case report. Trauma case reports, 32100435. https://doi.org/10.1016/j.tcr.2021.100435
Kamidani, Ryo, et al. "Open penetrating external laryngotracheal injury and abdominal trauma by suicide attempt successfully treated with immediate intervention: A case report." Trauma case reports vol. 32 (2021): 100435. doi: https://doi.org/10.1016/j.tcr.2021.100435
Kamidani R, Okada H, Kato R, Nishihori T, Kuze B, Yoshida T, Yoshida S, Ogura S. Open penetrating external laryngotracheal injury and abdominal trauma by suicide attempt successfully treated with immediate intervention: A case report. Trauma Case Rep. 2021 Feb 23;32:100435. doi: 10.1016/j.tcr.2021.100435. eCollection 2021 Apr. PMID: 33718566; PMCID: PMC7921001.
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Showing 1 to 12 of 203 entries