Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Sawako Yamazaki"'
Autor:
Rie Okumura, Sawako Yamazaki, Tsukasa Ohashi, Shinichi Magara, Jun Tohyama, Hiroshi Sakuma, Masaharu Hayashi, Akihiko Saitoh
Publikováno v:
Case Reports in Pediatrics, Vol 2018 (2018)
Immune-mediated central nervous system manifestations of group A β-hemolytic Streptococcus (GABHS) infection include Sydenham’s chorea, pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection (PANDAS)—which includ
Externí odkaz:
https://doaj.org/article/356f976dde4649c89af6d0111de1763f
Autor:
Takanori Yamagata, Masaya Kubota, Jun-ichi Takanashi, Akiko Shibata, Kenjiro Kikuchi, Ichiro Kuki, Masayasu Ohta, Ai Hoshino, Gaku Yamanaka, Akira Kumakura, Sawako Yamazaki, Takashi Shiihara, Akira Oka, Masashi Mizuguchi, Hiroshi Matsumoto, Taku Miyagawa, Mariko Kasai, Shinya Hara
Publikováno v:
Brain and Development. 41:862-869
Objectives Acute encephalopathy is an acute brain dysfunction after preceding infection, consisting of multiple syndromes. Some syndromes, such as acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), are severe with poor out
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ec4e2d3a0874943546b29c9dfb61e8
https://doi.org/10.1016/j.braindev.2019.07.008
https://doi.org/10.1016/j.braindev.2019.07.008
Publikováno v:
Pediatrics International. 58:1023-1026
Background Although Fanconi syndrome is rare in patients with epilepsy treated with sodium valproate (VPA), the prevalence might be higher in children with severe motor and intellectual disabilities (SMID). VPA-induced Fanconi syndrome usually has a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f456e216248a469a68e980eefeaa8281
https://doi.org/10.1111/ped.12956
https://doi.org/10.1111/ped.12956
Autor:
Hiroshi Sakuma, Tsukasa Ohashi, Shinichi Magara, Akihiko Saitoh, Jun Tohyama, Rie Okumura, Sawako Yamazaki, Masaharu Hayashi
Publikováno v:
Case Reports in Pediatrics, Vol 2018 (2018)
Case Reports in Pediatrics
Case Reports in Pediatrics
Immune-mediated central nervous system manifestations of group A β-hemolytic Streptococcus (GABHS) infection include Sydenham’s chorea, pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection (PANDAS)—which includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f80d94f895f7976be73598de5f68f4b
https://doaj.org/article/356f976dde4649c89af6d0111de1763f
https://doaj.org/article/356f976dde4649c89af6d0111de1763f
Autor:
Hideshi Kawashima, Sawako Yamazaki, Shinichi Magara, Noriyuki Akasaka, Yu Kobayashi, Jun Tohyama
Publikováno v:
Brain and Development. 37:725-728
We report a case of infantile refractory epilepsy associated with Turner syndrome (TS), showing very frequent, focal clonic seizures of the left upper extremity. Characteristically, in addition to spontaneous fits, her seizure was inducible by rubbin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08da1590553c0c296edf5e558d0057b2
https://doi.org/10.1016/j.braindev.2014.11.004
https://doi.org/10.1016/j.braindev.2014.11.004
Publikováno v:
Congenital Anomalies. 56:253-255
Interstitial deletions of the 16q centromeric region are rarely reported. A microdeletion of the 16q12.2q21 region was identified in a patient with intellectual disability, epilepsy, short stature, and distinctive features; including up-slanting palp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7816862bbd53e5b7ef1e1e7a78f91cec
https://doi.org/10.1111/cga.12172
https://doi.org/10.1111/cga.12172
Publikováno v:
Journal of the Japan Epilepsy Society. 26:9-15
Benign childhood epilepsy with centrotemporal spikes(BECT）は国際分類では特発性てんかんとして位置づけられている。今回、障害児にRolandic Discharge(RD）に類似した脳波所見を認めた11例を経験した。
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd2f37d223009038f385b008d49cc024
https://doi.org/10.3805/jjes.26.9
https://doi.org/10.3805/jjes.26.9
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 58(10)
Although Fanconi syndrome is rare in patients with epilepsy treated with sodium valproate (VPA), the prevalence might be higher in children with severe motor and intellectual disabilities (SMID). VPA-induced Fanconi syndrome usually has a favorable o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a78a24eb4fa98e850ce3a2ae32a2f191
https://pubmed.ncbi.nlm.nih.gov/26896192
https://pubmed.ncbi.nlm.nih.gov/26896192
Publikováno v:
Pediatric Nephrology. 20:814-817
Although renal Fanconi syndrome resulting from valproate (VPA) has occasionally been reported, the detailed clinical characteristics of this disease remain unclear. To clarify the clinical features of patients with VPA-induced Fanconi syndrome, we an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb86c0777881c5898675caf05b5a99da
https://doi.org/10.1007/s00467-005-1827-7
https://doi.org/10.1007/s00467-005-1827-7
Autor:
Sawako Yamazaki, Hideto Yoshikawa
Publikováno v:
Journal of the Japan Epilepsy Society. 22:180-185
1997年から2002年までの6年間に小児けいれん重積症に対してミダゾラム静注療法を施行した71例89機会の治療効果につき検討した。けいれんの原因はてんかん43機会、急性脳炎・脳症17機会
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc35a57db2c2440fec04084756170c7d
https://doi.org/10.3805/jjes.22.180
https://doi.org/10.3805/jjes.22.180