Zobrazeno 1 - 10 of 248 pro vyhledávání: '"Nobuhiko, Haga"'
1
Akademický článek
Histopathological Confirmation of Axonal Sprouting in Regenerative Peripheral Nerve Interface
Autor: Song Ho Chang, MD, PhD, Yuji Maenohara, MD, PhD, Jun Hirose, MD, PhD, Yasunori Omata, MD, PhD, Sayaka Fujiwara, MD, PhD, Nobuhiko Haga, MD, PhD, Masako Ikemura, MD, PhD, Taku Saito, MD, PhD, Sakae Tanaka, MD, PhD, Takumi Matsumoto, MD, PhD
Publikováno v: Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss 6, p e5878 (2024)
Summary:. Symptomatic neuroma represents a debilitating complication after major limb amputation. The regenerative peripheral nerve interface (RPNI) has emerged as a reproducible and practical surgery aimed at mitigating the formation of painful neur
Externí odkaz: https://doaj.org/article/79c2d87c09de445c945aecae54cd176f
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5
Akademický článek
Congenital limb deficiency in Japan: a cross-sectional nationwide survey on its epidemiology
Autor: Hiroshi Mano, Sayaka Fujiwara, Kazuyuki Takamura, Hiroshi Kitoh, Shinichiro Takayama, Tsutomu Ogata, Shuji Hashimoto, Nobuhiko Haga
Publikováno v: BMC Musculoskeletal Disorders, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background Congenital limb deficiency is a rare and intractable disease, which impairs both function and appearance of the limbs. To establish adequate medical care, it is necessary to reveal the actual conditions and problems associated wit
Externí odkaz: https://doaj.org/article/4c3f5dd9b46945eaaee8adbe715d6afe
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6
Akademický článek
Double non-contiguous fractures in a patient with spondylo-epiphyseal dysplasia with spinal ankylosis treated with open and percutaneous spinal fixation technique: a case report
Autor: Takahiro Ushijima, Kenichi Kawaguchi, Tadashi Matsumoto, Masaki Takagi, Tatsuro Kondoh, Gen Nishimura, Aritoshi Iida, Shiro Ikegawa, Nobuhiko Haga, Go Kato
Publikováno v: BMC Research Notes, Vol 11, Iss 1, Pp 1-5 (2018)
Abstract Background Patients with ankylosing spines are susceptible to developing spinal fractures even with minor trauma and can develop early or late neurological injuries. These fractures require early and aggressive surgical management to enable
Externí odkaz: https://doaj.org/article/dda90dcb55924290825e7ac3ece82936
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7
Akademický článek
International physician survey on management of FOP: a modified Delphi study
Autor: Maja Di Rocco, Genevieve Baujat, Marta Bertamino, Matthew Brown, Carmen L. De Cunto, Patricia L. R. Delai, Elisabeth M. W. Eekhoff, Nobuhiko Haga, Edward Hsiao, Richard Keen, Rolf Morhart, Robert J. Pignolo, Frederick S. Kaplan
Publikováno v: Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-5 (2017)
Abstract Fibrodysplasia ossificans progressiva (FOP), a disabling disorder of progressive heterotopic ossification (HEO), is caused by heterozygous gain-of- function mutations in Activin receptor A, type I (ACVR1, also known as ALK2), a bone morphoge
Externí odkaz: https://doaj.org/article/70121a696d704994a6d41ed65d4c72b6
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8
Gene Therapy for Fibrodysplasia Ossificans Progressiva
Autor: Elisabeth M.W. Eekhoff, Ruben D. de Ruiter, Bernard J. Smilde, Ton Schoenmaker, Teun J. de Vries, Coen Netelenbos, Edward C. Hsiao, Christiaan Scott, Nobuhiko Haga, Zvi Grunwald, Carmen L. De Cunto, Maja di Rocco, Patricia L. R. Delai, Robert J. Diecidue, Vrisha Madhuri, Tae-Joon Cho, Rolf Morhart, Clive S. Friedman, Michael Zasloff, Gerard Pals, Jae-Hyuck Shim, Guangping Gao, Frederick Kaplan, Robert J. Pignolo, Dimitra Micha
Publikováno v: Eekhoff, E M W, de Ruiter, R D, Smilde, B J, Schoenmaker, T, de Vries, T J, Netelenbos, C, Hsiao, E C, Scott, C, Haga, N, Grunwald, Z, De Cunto, C L, di Rocco, M, Delai, P L R, Diecidue, R J, Madhuri, V, Cho, T J, Morhart, R, Friedman, C S, Zasloff, M, Pals, G, Shim, J H, Gao, G, Kaplan, F, Pignolo, R J & Micha, D 2022, ' Gene Therapy for Fibrodysplasia Ossificans Progressiva : Feasibility and Obstacles ', Human gene therapy, vol. 33, no. 15-16, pp. 782-788 . https://doi.org/10.1089/hum.2022.023
Eekhoff, E M W, de Ruiter, R D, Smilde, B J, Schoenmaker, T, de Vries, T J, Netelenbos, C, Hsiao, E C, Scott, C, Haga, N, Grunwald, Z, de Cunto, C L, di Rocco, M, Delai, P L R, Diecidue, R J, Madhuri, V, Cho, T-J, Morhart, R, Friedman, C S, Zasloff, M, Pals, G, Shim, J-H, Gao, G, Kaplan, F, Pignolo, R J & Micha, D 2022, ' Gene Therapy for Fibrodysplasia Ossificans Progressiva : Feasibility and Obstacles ', Human Gene Therapy, vol. 33, no. 15-16, pp. 782-788 . https://doi.org/10.1089/hum.2022.023, https://doi.org/10.1089/hum.2022.023
Fibrodysplasia ossificans progressiva (FOP) is a rare and devastating genetic disease, in which soft connective tissue is converted into heterotopic bone through an endochondral ossification process. Patients succumb early as they gradually become tr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f624caf1588f9bd3b3300ebfe4d9333d
https://doi.org/10.1089/hum.2022.023
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10
Utility of side-lying posture in a patient with severe dysphagia secondary to oropharyngeal cancer surgery: A single case report
Autor: Asako Kaneoka, Haruhi Inokuchi, Akihito Yamauchi, Toshihiko Sakai, Yuki Saito, Nobuhiko Haga
Publikováno v: Advances in Communication and Swallowing. 25:29-36
INTRODUCTION: Few studies have documented the utility of side-lying in dysphagia management. We report on a patient who benefitted from the side-lying posture for safe and efficient oral intake. PATIENT: The patient underwent resections of the left t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ef2ce81fe7f098d531acc9eb6ff0f596
https://doi.org/10.3233/acs-210039
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