Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Tokitsugi Hayashi"'
Autor:
Ken Nagaya, Fumikatsu Nohara, Toshio Okamoto, Gen Nishimura, Akiko Yamashita, Tokitsugi Hayashi, Hiroshi Azuma, Hiroko Asai, Etsushi Tsuchida
Publikováno v:
American journal of medical genetics. Part A. (8):1953-1956
Author
Heterozygous COL2A1 mutations create a group of skeletal dysplasias collectively termed type II collagenopathies. Sporadic cases of type II collagenopathies are almost exclusively caused by de novo mutations. Very few cases with intrafami
Heterozygous COL2A1 mutations create a group of skeletal dysplasias collectively termed type II collagenopathies. Sporadic cases of type II collagenopathies are almost exclusively caused by de novo mutations. Very few cases with intrafami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4735a66480c3b537a6141e5ff3c29a68
http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=22711552
http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=22711552
Publikováno v:
Pediatric and Developmental Pathology. 15:114-117
To investigate the correlation between maternal and fetal angiotensin-converting enzyme gene insertion or deletion polymorphism and birth size, angiotensin-converting enzyme gene insertion or deletion polymorphisms of 470 Japanese pairs of mothers an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73fbde4ca448d1236fd5e1769e22c2ee
https://doi.org/10.2350/11-09-1092-oa.1
https://doi.org/10.2350/11-09-1092-oa.1
Autor:
Masaru Shirai, Tokitsugi Hayashi, Eiki Nakamura, Toshio Okamoto, Ken Nagaya, Satoru Takahashi, Kenji Fujieda
Publikováno v:
Early Human Development. 86:251-254
In approximately 60% of infants with posthemorrhagic hydrocephalus (PHH), ventricular dilation resolves by unknown intrinsic mechanisms, without the need for a shunt operation. A pathological hallmark of PHH is extensive deposition of extracellular m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::610fe7a8b4307ac97a5862362e87edad
https://doi.org/10.1016/j.earlhumdev.2010.03.007
https://doi.org/10.1016/j.earlhumdev.2010.03.007
Autor:
Ken Nagaya, Toshio Okamoto, Satoru Takahashi, Kenji Fujieda, Tokitsugi Hayashi, Eiki Nakamura
Publikováno v:
Biochemical and Biophysical Research Communications. 383(4):475-479
http://dx.doi.org/10.1016/j.bbrc.2009.04.038
Transforming growth factor (TGF)-β1, a cytokine released into the cerebrospinal fluid (CSF) after intraventricular hemorrhage (IVH), stimulates the expression of the components of the extracellular m
Transforming growth factor (TGF)-β1, a cytokine released into the cerebrospinal fluid (CSF) after intraventricular hemorrhage (IVH), stimulates the expression of the components of the extracellular m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1a935840881b8d5bb35e06fad4321a4
http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=19371720
http://amcor.asahikawa-med.ac.jp/modules/xoonips/detail.php?id=19371720
Autor:
Hiroko Asai, Tokitsugi Hayashi, Etsushi Tsuchida, Fumikatsu Nohara, Hiroshi Sakata, Toshio Okamoto, Ken Nagaya, Hiroshi Azuma, Yutaka Terao
Publikováno v:
Pediatrics International. 55:519-521
Since the mid-1980s, there have been increasing reports of severe invasive group A streptococcal (GAS) disease in children and adults. There are few reports, however, of neonatal invasive disease, particularly neonatal pleural empyema caused by GAS.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17882692f04c7066d02008cab03b613a
https://doi.org/10.1111/ped.12061
https://doi.org/10.1111/ped.12061
Autor:
Yoko Asai, Kenichi Iseki, Toshio Okamoto, Shin Koyano, Tsunehisa Nagamori, Hiroshi Azuma, Yurika Miura, Fumikatsu Nohara, Naoya Tsuda, Tokitsugi Hayashi, Ken Nagaya
Publikováno v:
Journal of Clinical Virology. 53:265-267
Author
BACKGROUND: Disseminated neonatal herpes simplex virus (HSV) infection causes a typical systemic inflammatory response syndrome and has a high mortality rate. However, the validity of anti-inflammatory intervention against this condition
BACKGROUND: Disseminated neonatal herpes simplex virus (HSV) infection causes a typical systemic inflammatory response syndrome and has a high mortality rate. However, the validity of anti-inflammatory intervention against this condition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::927b5d020528bb801e85a415f1fd8bf6
https://doi.org/10.1016/j.jcv.2011.12.017
https://doi.org/10.1016/j.jcv.2011.12.017
Autor:
Kenji Fujieda, Tokitsugi Hayashi, Eiki Nakamura, Satoru Takahashi, Toshio Okamoto, Masaru Shirai, Ken Nagaya
Publikováno v:
Early Human Development. 84:137-139
The cerebrospinal fluid matrix metalloproteinase (MMP) activities were measured in infants with posthemorrhagic hydrocephalus to elucidate the intrinsic mechanism for the resolution of ventricular dilation. Increased MMP-9 activities were observed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30c0b2a56e53af6657fd6f4ac91d19bc
https://doi.org/10.1016/j.earlhumdev.2007.08.006
https://doi.org/10.1016/j.earlhumdev.2007.08.006
Autor:
Fumikatsu, Nohara, Ken, Nagaya, Hiroko, Asai, Etsushi, Tsuchida, Toshio, Okamoto, Tokitsugi, Hayashi, Hiroshi, Sakata, Yutaka, Terao, Hiroshi, Azuma
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 55(4)
Since the mid-1980s, there have been increasing reports of severe invasive group A streptococcal (GAS) disease in children and adults. There are few reports, however, of neonatal invasive disease, particularly neonatal pleural empyema caused by GAS.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82e7c473592d0e07347eea16322e909f
https://pubmed.ncbi.nlm.nih.gov/23910803
https://pubmed.ncbi.nlm.nih.gov/23910803
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 23(11)
Campomelic dysplasia (CD) is a rare and usually fatal congenital skeletal disorder with respiratory failure. The SOX9 gene has been cloned as a candidate gene for CD. Here, we report the cases of 2 Japanese patients with CD who have survived for over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d0cadf45cbe01474ba59726fe9a264a
https://pubmed.ncbi.nlm.nih.gov/21284335
https://pubmed.ncbi.nlm.nih.gov/21284335
Autor:
Hiromi Manabe, Yoshio Makita, Ken Nagaya, Toshio Okamoto, Masaya Sugimoto, Tokitsugi Hayashi, Eiki Nakamura, Kenji Fujieda, Genya Taketazu, Hiroki Kajino
Publikováno v:
European journal of medical genetics. 54(3)
All patients with terminal deletion of chromosome 15q have been reported to show intrauterine growth retardation, postnatal growth retardation, abnormal facial appearance and developmental delay. Haploinsufficiency of IGF1R was considered to be respo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a44870beeb4e3e6ecab1f1385ccfbf40
https://pubmed.ncbi.nlm.nih.gov/21172461
https://pubmed.ncbi.nlm.nih.gov/21172461