Zobrazeno 1 - 10
of 582
pro vyhledávání: '"T, Nozoe"'
Autor:
Karen T. Nozoe, Ricardo T. Akamine, Diego R. Mazzotti, Daniel N. Polesel, Luís F. Grossklauss, Sergio Tufik, Monica L. Andersen, Gustavo A. Moreira
Publikováno v:
Sleep Science, Vol 9, Iss 3, Pp 129-133 (2016)
We discussed two cases of symptomatic female carriers to Duchenne Muscular Dystrophy. The first case is a 20 year-old girl with classical phenotypic manifestation of the disease, similar to the condition in boys. The case 2 is a 62 year-old woman wit
Externí odkaz:
https://doaj.org/article/78a1500e3b8a479786e03ca02e9665a4
Autor:
Karen T. Nozoe, Helena Hachul, MD, PhD, Camila Hirotsu, PhD, Daniel N. Polesel, MSc, Gustavo A. Moreira, MD, PhD, Sergio Tufik, MD, PhD, Monica L. Andersen, PhD
Publikováno v:
Sexual Medicine, Vol 2, Iss 3, Pp 133-140 (2014)
Introduction: The task of the caregiver, especially a caregiving mother of a son with a chronic and fatal disease, may interfere with their quality of sleep, sexuality, and some hormone levels. Aim: The aim of this study was to evaluate the sexual fu
Externí odkaz:
https://doaj.org/article/df5a1501e5f9408391e1dcf518fbde5b
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
T. Wakasa, J. Yasuda, M. Dozono, T. Fukunaga, S. Gotanda, K. Hatanaka, K. Ishibashi, Y. Kanaya, S. Kimura, Y. Maeda, Y. Nishio, T. Noro, T. Nozoe, K. Ohnaka, S. Sakaguchi, Y. Sakemi, K. Sekiguchi, T. Taguchi, Y. Wada
Publikováno v:
Physical Review C. 96
We report measurements of cross sections and analyzing powers for nucleon-knockout $(\stackrel{P\vec}{p},np)$ reactions of $^{2}\mathrm{H}, ^{6}\mathrm{Li}$, and $^{12}\mathrm{C}$ at 296 MeV using the RCNP NPOL3 neutron detector and large acceptance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad80bae432c76ad1f0d185b0e46ef328
https://doi.org/10.1103/physrevc.96.014604
https://doi.org/10.1103/physrevc.96.014604
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Kimio Shindo, T. Nozoe, Luo‐Chenz Zhang, Teruo Kurihara, Hideki Sakurai, Keisuke Ebata, Hidetugu Wakabayashi
Publikováno v:
Journal of the Chinese Chemical Society. 50:47-50
Treatment of benzo[b]cyclohepta[e] [1,4]oxazines (4) with 1.2 equiv. of tris(2-aminoethyl)amine (13) in methanol at 80 °C gave 1,4,12,15,18,26,31,39-octaazapentacyclo[13.13.13.0 5 , 1 1 .0 1 9 , 2 5 .0 2 5 .0 1 2 , 3 ]pentetraconta-4,6,8,10,18,20,22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8d7c4bc147505678f0d99d389cdf21d
https://doi.org/10.1002/jccs.200300006
https://doi.org/10.1002/jccs.200300006
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2129-2142
[2+4]-[6+4] Cycloadducts were obtained from the thermal cycloaddition reactions of azulenequinones with cyclic 4π systems such as 1,3-diphenylisobenzofuran and isobenzofuran while the reaction of cycloheptatriene and azulenequinones gave ene product
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::726c05020244af6c49f274c29b9b76af
https://doi.org/10.1039/a902493j
https://doi.org/10.1039/a902493j
Autor:
Masaaki Tsukada, Hidetsugu Wakabayashi, Paw-Wang Yang, T. Nozoe, Kimio Shindo, Teruo Kurihara, Masafumi Yasunami
Publikováno v:
Journal of the Chinese Chemical Society. 45:391-400
A very convenient, one-pot synthesis (over 80% yield) of 3-bromo-1,5- and −1,7-azulenequinones has been developed by bromination of azulene in aqueous tetrahydrofuran. Reduction of 3-bromo-1,5- and −1,7-azulenequinones with tin or zinc powder in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e948b14b75ba9695a4aaa8085708c0a7
https://doi.org/10.1002/jccs.199800062
https://doi.org/10.1002/jccs.199800062
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :3219-3224
The high-pressure Diels–Alder reaction of 3-bromo-1,5-azulenequinone and 3-bromo-1,7-azulenequinone with several dienophiles under 300 MPa pressure gave 1∶1 [4 + 2] cycloadducts in good yields. Bromoazulenequinones reacted with dienophiles on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73da2d3e0bd646fe0f9f464aaa3419db
https://doi.org/10.1039/a804846k
https://doi.org/10.1039/a804846k
Publikováno v:
Chest. 143(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7837a4a6917ae06df837e2c7f6343fc7
https://pubmed.ncbi.nlm.nih.gov/23546505
https://pubmed.ncbi.nlm.nih.gov/23546505