Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Hideto Akama"'
Autor:
Tomoo Fukuda, Keiko Yamagami, Kimito Kawahata, Yuzo Suzuki, Yoshihiro Sasaki, Takashi Miyagi, Iris Jacobs, John-Philip Lawo, Fiona Glassman, Hideto Akama, Michihiro Hide, Isao Ohsawa
Publikováno v:
Allergology International, Vol 72, Iss 3, Pp 451-457 (2023)
Background: Hereditary angioedema (HAE) is a rare and potentially life-threatening genetic disorder characterized by recurrent attacks of angioedema. HAE types I and II result from deficient or dysfunctional C1-esterase inhibitor (C1–INH). This Pha
Externí odkaz:
https://doaj.org/article/41fb99ae42094f549215fbbd33660195
Autor:
Fiona Glassman, Summer Goodson, Alex Bica, Anthony Roberts, Hideto Akama, Yumiko Asami, Meena Jain, Milin Acharya
Publikováno v:
Journal of Allergy and Clinical Immunology. 151:AB144
Autor:
Shunji Matsuki, Maiko Nomoto, Seiichiro Hojo, Hideto Akama, Kyoko Matsuguma, Fuminori Ohba, Shuhei Imayama
Publikováno v:
Journal of Dermatological Treatment. 27:467-472
Phosphodiesterase type 4 (PDE4) inhibition is a well-known anti-inflammatory mechanism. However, the clinical use of PDE4 inhibitors has been compromised by the occurrence of mechanism-associated adverse reactions, which often limit the maximum toler
Publikováno v:
Journal of Dermatological Treatment. 27:241-246
The purpose of the present studies was to assess the safety, tolerability and pharmacokinetics of topical application of a novel phosphodiesterase inhibitor, E6005, in healthy volunteers and in patients with atopic dermatitis (AD).In two randomized,
Autor:
Masutaka, Furue, Yasumi, Kitahara, Hideto, Akama, Seiichiro, Hojo, Nobukazu, Hayashi, Hidemi, Nakagawa, Satoshi, Takeuchi
Publikováno v:
The Journal of Dermatology. 41:577-585
The safety and efficacy of topical E6005, a novel phosphodiesterase 4 inhibitor, in Japanese adults with atopic dermatitis were evaluated. A total of 78 patients were randomized to receive either the 0.2% E6005 ointment or vehicle control (without E6
Autor:
Shoji Uchida, Hideto Akama, Vipin Arora, Hisashi Yamanaka, Yoshiya Tanaka, Tsutomu Takeuchi, Tsukasa Matsubara, Nobuyuki Miyasaka, Masaya Mukai, Naoki Ishiguro, Hartmut Kupper
Publikováno v:
Rheumatology (Oxford, England)
Objective. The aim of this study was to compare efficacy outcomes of initial treatment with adalimumab + MTX vs adalimumab addition following 26 weeks of MTX monotherapy in Japanese early RA patients naive to MTX with high disease activity. Methods.
Autor:
Shoji Uchida, Yoshiya Tanaka, Hartmut Kupper, Masaya Mukai, Nobuyuki Miyasaka, Hideto Akama, Hisashi Yamanaka, Tsukasa Matsubara, Vipin Arora, Tsutomu Takeuchi, Naoki Ishiguro
Publikováno v:
Annals of the Rheumatic Diseases
ObjectivesTo evaluate the efficacy and safety of adalimumab+methotrexate (MTX) in Japanese patients with early rheumatoid arthritis (RA) who had not previously received MTX or biologics.MethodsThis randomised, double-blind, placebo-controlled, multic
Autor:
Hideto Akama
Publikováno v:
Japanese Journal of Clinical Immunology. 34:464-475
Glucocorticoids (steroids) have been widely used for the treatment of patients with rheumatoid arthritis (RA) since Hench had attempted to administer cortisone (Kendall's compound E) to an active RA patient in 1948. Rheumatologists even in the 21st c
Autor:
Hideto Akama
Publikováno v:
Japanese Journal of Clinical Immunology. 30:404-407
RANK ligand (RANKL) is a key mediator of osteoclast formation, function, and survival. Therefore, RANKL is thought to be responsible for osteoclast-mediated bone resorption in a broad range of disorders such as postmenopausal osteoporosis and cancer-
Autor:
Mika Katagiri, Hatsue Tazaki, Masao Sasamata, Aishi Kimoto, Shun-ichi Harada, Toru Ogasawara, Hiroshi Kawaguchi, Tsuyoshi Takato, Kazuto Hoshi, Daichi Chikazu, Masahiro Noguchi, Kozo Nakamura, Ung-il Chung, Hideto Akama
Publikováno v:
Journal of Bone and Mineral Research. 21:219-227
In vitro assays revealed that COX-2 inhibitors with CA II inhibitory potency suppressed both differentiation and activity of osteoclasts, whereas that without the potency reduced only osteoclast differentiation. However, all COX-2 inhibitors similarl