Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Hiroko Asai"'
Publikováno v:
Pediatrics International. 64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::109d07100829c86bc91cf85bc4351351
https://doi.org/10.1111/ped.14984
https://doi.org/10.1111/ped.14984
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 63(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4734724a040c0109f563bdbb483ee8f6
https://pubmed.ncbi.nlm.nih.gov/34355466
https://pubmed.ncbi.nlm.nih.gov/34355466
Autor:
Hiroko Asai, Toshio Okamoto, Ken Nagaya, Ryuta Terao, Fumikatsu Nohara, Hiroshi Azuma, Mitsumaro Nii
Publikováno v:
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners. 27(3)
Introduction Although imatinib is the first-line of therapy for Philadelphia chromosome (Ph)-positive chronic myeloid leukemia (CML), in Japan, it is recommended by the manufacturer that lactating women treated with imatinib mesylate for CML should d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4994f19e6515be61e47a8e6aef03d2c
https://pubmed.ncbi.nlm.nih.gov/32787559
https://pubmed.ncbi.nlm.nih.gov/32787559
Publikováno v:
Journal of Neuroimaging. 24:603-606
BACKGROUND AND PURPOSE A thrombosed dural sinus malformation (DSM) is a rare condition, the clinical features of which have not yet been completely characterized. Here, we describe the clinical course of a patient with a thrombosed DSM and discuss th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::284dda201091e9cc2dc6f92c21b291ae
https://doi.org/10.1111/jon.12099
https://doi.org/10.1111/jon.12099
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
Autor:
Akiko Furuya, Masafumi Koga, Shigeru Suzuki, Hiroko Asai, Noriyasu Niizeki, Hiroshi Azuma, Yusuke Tanahashi, Yumi Kawata, Etsushi Tsuchida, Kumihiro Matsuo, Fumikatsu Nohara, Ken Nagaya, Hironori Takahashi, Toshio Okamoto
Publikováno v:
Pediatric Diabetes. 14:25-30
Background Glycated albumin (GA) reflects glycemic control in patients with neonatal diabetes mellitus (NDM). However, GA in NDM patients is apparently low in relation to glycemia. Objective To establish the reference intervals for GA in healthy infa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12f0469b533234f3d4d32d16f7852f8c
https://doi.org/10.1111/j.1399-5448.2012.00895.x
https://doi.org/10.1111/j.1399-5448.2012.00895.x
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:
Toshio, Okamoto, Ken, Nagaya, Yumi, Kawata, Hiroko, Asai, Etsushi, Tsuchida, Fumikatsu, Nohara, Kazuki, Okajima, Hiroshi, Azuma
Publikováno v:
Congenital anomalies. 55(3)
Short-rib polydactyly syndrome type III is an autosomal recessive lethal skeletal ciliopathy, which is phenotypically similar to nonlethal asphyxiating thoracic dystrophy. Mutations in DYNC2H1 have been identified in both of these disorders, indicati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7856843d3a96c4446a5032809b552fbe
https://pubmed.ncbi.nlm.nih.gov/25410398
https://pubmed.ncbi.nlm.nih.gov/25410398
Autor:
Hiroko, Asai, Toshio, Okamoto, Etsushi, Tsuchida, Fumikatsu, Nohara, Ken, Nagaya, Hiroshi, Azuma
Publikováno v:
Journal of neuroimaging : official journal of the American Society of Neuroimaging. 24(6)
A thrombosed dural sinus malformation (DSM) is a rare condition, the clinical features of which have not yet been completely characterized. Here, we describe the clinical course of a patient with a thrombosed DSM and discuss the outcomes in live birt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b4a87555ab30e14264471ed5c62ac1e0
https://pubmed.ncbi.nlm.nih.gov/24593318
https://pubmed.ncbi.nlm.nih.gov/24593318
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