Search Results - "Mitsuhashi, Y."

Long-term Changes in Spleen Volume After Living Donor Liver Transplantation in Pediatric Recipients by Mitsuhashi, Y., Wakiya, T., Ishido, K., Kudo, D., Kimura, N., Sato, K., Amagasa, J., Shibazuka, T., Toyoki, Y., Hakamada, K.

“…Living donor liver transplantation (LDLT) is a definitive procedure for splenomegaly caused by liver cirrhosis and portal hypertension, but splenomegaly…”
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Living-Donor Liver Transplantation With the Use of a Left-Lobe Graft From a Donor With Anomalous Biliary Anatomy in Which B4 Joins the Right Anterior Sectional Duct: A Case Report by Wakasa, Y., Kudo, D., Ishido, K., Kimura, N., Wakiya, T., Mitsuhashi, Y., Hakamada, K.

“…When there is an anatomic anomaly in the biliary tract of the donor for living-donor liver transplantation, the risk of postoperative biliary tract…”
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Impact of Smoking Cessation in Donor Candidates for Living Donor Liver Transplantation by Wakiya, T., Ishido, K., Kudo, D., Kimura, N., Sato, K., Mitsuhashi, Y., Kagiya, T., Uchida, C., Umetsu, S., Yoshida, T., Wakasa, Y., Toyoki, Y., Hakamada, K.

“…The relationship between smoking cessation and weight gain is well recognized. Examining the link between smoking cessation and weight gain in donor candidates…”
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In vitro fermentation characteristics of novel fibers, coconut endosperm fiber and chicory pulp, using canine fecal inoculum by de Godoy, M R C, Mitsuhashi, Y, Bauer, L L, Fahey, Jr, G C, Buff, P R, Swanson, K S

“…The objective of this experiment was to determine the effects of in vitro fermentation of coconut endosperm fiber (CEF), chicory pulp (CHP), and selective…”
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Morphologic Evaluation of the Caudal End of the Inferior Petrosal Sinus Using 3D Rotational Venography by Mitsuhashi, Y, Nishio, A, Kawahara, S, Ichinose, T, Yamauchi, S, Naruse, H, Matsuoka, Y, Ohata, K, Hara, M

“…The inferior petrosal sinus (IPS) is the main transvenous access route used to examine or treat lesions involving the cavernous sinus. To carry out these…”
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Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation by Umegaki, N., Nakano, H., Tamai, K., Mitsuhashi, Y., Akasaka, E, Sawamura, D., Katayama, I.

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Overexpression of tumour necrosis factor-α-converting enzyme in psoriasis by Kawaguchi, M., Mitsuhashi, Y., Kondo, S.

“…Summary Background  Tumour necrosis factor (TNF)‐α‐converting enzyme (TACE) is a metalloproteinase‐disintegrin that releases soluble TNF‐α from cells by…”
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Self-Formation of Vascularized Hepatic Tissue From Human Adult Hepatocyte by Enomoto, Y, Enomura, M, Takebe, T, Mitsuhashi, Y, Kimura, M, Yoshizawa, E, Taniguchi, H

“…Abstract Background Recent study has demonstrated the important role of endothelial-mesenchymal interactions in 3-dimensional self-organization of immature…”
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Mutant ras oncogenes upregulate VEGF/VPF expression : implications for induction and inhibition of tumor angiogenesis by RAK, J, MITSUHASHI, Y, BAYKO, L, FILMUS, J, SHIRASAWA, S, SASAZUKI, T, KERBEL, R. S

“…The growth of solid tumors in vivo beyond 1-2 mm in diameter requires induction and maintenance of an angiogenic response. This can occur through the release…”
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Mycobacterium avium genotype is associated with the therapeutic response to lung infection by Kikuchi, T., Kobashi, Y., Hirano, T., Tode, N., Santoso, A., Tamada, T., Fujimura, S., Mitsuhashi, Y., Honda, Y., Nukiwa, T., Kaku, M., Watanabe, A., Ichinose, M.

“…Factors that can interfere with the successful treatment of Mycobacterium avium lung infection have been inadequately studied. To identify a potent predictor…”
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Clinical and genetic features of 20 Japanese patients with vascular-type Ehlers-Danlos syndrome by Shimaoka, Y., Kosho, T., Wataya-Kaneda, M., Funakoshi, M., Suzuki, T., Hayashi, S., Mitsuhashi, Y., Isei, T., Aoki, Y., Yamazaki, K., Ono, M., Makino, K., Tanaka, T., Kunii, E., Hatamochi, A.

“…Summary Background  Vascular‐type Ehlers–Danlos syndrome (vEDS) is a severe autosomal dominant inherited disorder resulting from mutations within the α1 type…”
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Brunsting-Perry type pemphigoid with IgG autoantibodies to laminin-332, BP230 and desmoplakins I/II by Fukuda, S., Tsuruta, D., Uchiyama, M., Mitsuhashi, Y., Kobayashi, H., Ishikawa, T., Ohyama, B., Ishii, N., Hamada, T., Dainichi, T., Karashima, T., Nakama, T., Yasumoto, S., Hashimoto, T.

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Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation by Akasaka, E., Nakano, H., Nakano, A., Toyomaki, Y., Takiyoshi, N., Rokunohe, D., Nishikawa, Y., Korekawa, A., Matsuzaki, Y., Mitsuhashi, Y., Sawamura, D.

“…The palmoplantar keratodermas (PPKs) are a large group of genodermatoses comprising nearly 60 genetically distinct diseases. They are characterized by…”
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A Japanese piebald patient with auburn hair colour associated with a novel mutation p.P832L in the KIT gene and a homozygous variant p.I120T in the MC1R gene by Oiso, N., Kishida, K., Fukai, K., Motokawa, T., Hosomi, N., Suzuki, T., Mitsuhashi, Y., Tsuboi, R., Kawada, A.

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Re-induction of obese body weight occurs more rapidly and at lower caloric intake in beagles by Nagaoka, D, Mitsuhashi, Y, Angell, R, Bigley, K.E, Bauer, J.E

“…For the purpose of investigating the mechanism of obesity-induction/re-induction including weight-cycling in beagles, a study was conducted using commercially…”
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Novel and recurrent nonsense mutation of the SLC39A4 gene in Japanese patients with acrodermatitis enteropathica by Nakano, H., Nakamura, Y., Kawamura, T., Shibagaki, N., Matsue, H., Aizu, T., Rokunohe, D., Akasaka, E., Kimura, K., Nishizawa, A., Umegaki, N., Mitsuhashi, Y., Shimada, S., Sawamura, D.

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The association of latent Epstein-Barr virus infection with hydroa vacciniforme by IWATSUKI, K, XU, Z, KANEKO, F, TAKATA, M, IGUCHI, M, OHTSUKA, M, AKIBA, H, MITSUHASHI, Y, TAKENOSHITA, H, SUGIUCHI, R, TAGAMI, H

“…Patients with hydroa vacciniforme (HV)‐like eruptions and malignant potential have been reported from Asia and Mexico, and those patients frequently had an…”
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Novel COL7A1 mutations in a Japanese family with transient bullous dermolysis of the newborn associated with pseudosyndactyly by Nakano, H., Toyomaki, Y., Ohashi, S., Nakano, A., Jin, H., Munakata, T., Akita, N., Tamai, K., Mitsuhashi, Y.

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A novel H1 domain mutation in the keratin 2 gene in a Japanese family with ichthyosis bullosa of Siemens by Nishizawa, A., Toyomaki, Y., Nakano, A., Takeuchi, S., Matsuzaki, Y., Takeda, H., Kaneko, T., Mitsuhashi, Y., Nakano, H.

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Pregnancy complicated with Buerger's disease by Kikuchi, N., Kanai, M., Kita, N., Mitsuhashi, Y., Konishi, I.

“…Buerger's disease is an inflammatory occlusive vascular disorder involving small- and medium-sized arteries in the distal extremities and is usually…”
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