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21篇 您的检索式:作者名="Isojima"
    题名 作者 年代 出处 被引量
1Vascular complications in dementia with Lewy bodies: a postmortem study显示文摘Isojima D Togo T Kosaka K 2006Neuropathoiogy2006,26,:1
2Screening for deletions in interval D16–22 of the Y chromosome in azoospermic and oligozoospermic Japanese men显示文摘H. Kato S. Komori Y. Nakata K. Sakata R. Kanazawa M. Handa S. Kobayashi K. Koyama S. Isojima 2001Journal of Human Genetics2001,,3:1
3ACS Nano显示文摘Isojima T Lattuada M Vander Sande JB Hatton T A 20082:1 7992008,2,:1
4Vascular complications in dementia with Lewy bodios:a postmortom study显示文摘Isojima D Togo T Kosaka K 2006Neuropathology2006,26,4:1
5Vascular complica-tions in dementia with Lewy bodies:a postmortem study显示文摘Isojima D Togo T Kosaka K 2006Neuropathology2006,26,4:1
6Screening for deletions in interval D16–22 of the Y chromosome in azoospermic and oligozoospermic Japanese men显示文摘H. Kato S. Komori Y. Nakata K. Sakata R. Kanazawa M. Handa S. Kobayashi K. Koyama S. Isojima 2001Journal of Human Genetics2001,,3:1
7New reference growth charts for Japanese girls with Turner syndrome显示文摘Isojima T Yokoya S Ito J 0,,05:1
8Standardized centile curves and reference intervals of serum insulin-like growth factor-I (IGF- I) levels in a normal Japanese population using the LMS method显示文摘Isojima T Shimatsu A Yokoya S 2012Endocr J2012,59,9:1
9Nonclassic steroid 21-hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Janpan显示文摘Shinagawa T Horikawa R Isojima T 2007Endocr J2007,54,:1
10LMXIB mutation with residual transcriptional activity as a cause of isolated glo- merulopathy显示文摘Isojima T Harita Y Furuyama M 2014Nephrol Dial Transplant2014,29,1:1
11Controlled assembly of nanoparticle structures: spherical and toroidal superlattices and nanoparticle-coated polymeric beads 显示文摘Tatsushi Isojima Su Kyung Suh 2009Langmuir2009,25,14:1
12Vascular complications in dementia with Lewy bodies:a postmortem study 显示文摘Isojima D Togo T Kosaka K 2006Neuropathology2006,26,4:1
13Nonclassic steroid 21-hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Japan显示文摘Shinagawa T Horikawa R Isojima T 2007Endocr J2007,54,6:1
14Verification tests of a 66 kV HTSC cable system for practical use (first cooling tests)显示文摘Masuda T Kato T Yumura H Watanabe M Ashibe Y Ohkura K Suzawa C Hirose M Isojima S Matsuo K 2002Physica C2002,,:1
15Uncoupling protein 2 influences dopamine secretion in PC12h cells显示文摘Yamada S Isojima Y Yamatodani A 2003J Neurochem2003,87,2:1
16Vascular complications in dementia with Lewy bodies:a postmortem study 显示文摘Isojima D Togo T Kosaka K 2006Neuropathology2006,26,4:1
17Vascular complications in dementia with Lewy bodies:a postmortem study 显示文摘Isojima D Togo T Kosaka K 2006Neuropathology2006,26,4:1
18PACAP-deficient mice exhibit light parameter-dependent abnormalities on nonvisual photoreception and early activity onset 显示文摘Kawaguchi C Isojima Y Shintani N 2010PLoS One2010,5,2:1
19Verification tests of a 66 kV HTSC cable system for practical use ( first cooling tests) 显示文摘Masuda T Kato T Yumura H Watanabe M Ashibe Y Ohkura K Suzawa C Hirose M Isojima S Matsuo K 2002Physica C2002,37,8381:1
20Nonclassie steroid 21- hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Japan 显示文摘Shinagawa T Horikawa R Isojima T 2007Endocr J2007,54,6:1
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