Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mayu Ohtsu"'
Publikováno v:
Neuropediatrics. 39:14-19
Purpose: We have studied the clinical differences between early-onset benign epilepsy with centro-temporal spikes (early-onset BECT) and Panayiotopoulos syndrome (PS) to investigate the hypothesis that BECT and PS nosologically constitute age-depende
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::851f8475801e938c4affef3b47180ce1
https://doi.org/10.1055/s-2008-1077087
https://doi.org/10.1055/s-2008-1077087
Publikováno v:
Brain and Development. 24:231-238
This study investigated the clinical and EEG characteristics of initial status epilepticus (SE) during infancy in patients with mesial temporal lobe epilepsy (MTLE). The subjects were six patients who had been brought to our emergency clinic and trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19dbfe233405d6803d7a5c0d88ee28e7
https://doi.org/10.1016/s0387-7604(02)00035-9
https://doi.org/10.1016/s0387-7604(02)00035-9
Autor:
Yukio Fukuyama, Kimiko Yasuda, Satoru Hirano, Hiroshi Yoshioka, Shinji Fujimoto, Hodaka Ohta, Ritsuko Tawa, Akashi Ishikawa, Shin-ichiroh Hamano, Naoya Itokazu, Atsushi Ogawa, Mayu Ohtsu, Kenji Sugai, Tohru Seki
Publikováno v:
Brain and Development. 23:558-564
Nationwide survey on familial cases of West syndrome (WS) in first- and second-degree relatives was conducted by mailing a questionnaire to 64 major university hospitals, children's hospitals, and epilepsy centers in Japan, and by review of the Japan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1aa484dabad3c9538c5a26ea5c79073f
https://doi.org/10.1016/s0387-7604(01)00262-5
https://doi.org/10.1016/s0387-7604(01)00262-5
Publikováno v:
Epilepsia. 44(3)
Summary: Purpose: We analyzed sequential changes in the localization of EEG foci along with age to identify a specific EEG pattern, and the relation between the clinical manifestations and the EEG pattern in patients with Panayiotopoulos syndrome (PS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a293d2f2f4eff0451449331a6cb13595
https://pubmed.ncbi.nlm.nih.gov/12614400
https://pubmed.ncbi.nlm.nih.gov/12614400
Publikováno v:
No to hattatsu = Brain and development. 34(3)
We report a 12-year-old boy with idiopathic torsion dystonia. Blepharospasm appeared at the age of 10, followed by truncal hypertonia and progressive scoliosis after 1 year. He had bizarre involuntary movement of his limbs upon waking, which was init
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6552bf48724bc525de711dca6e58bd4f
https://pubmed.ncbi.nlm.nih.gov/12030016
https://pubmed.ncbi.nlm.nih.gov/12030016
Autor:
Toru Higashinakagawa, Mayu Ohtsu, Yu-ichi Goto, Hirokazu Oguni, Toshiyuki Yamamoto, Kousaku Ohno, Eiji Nakagawa, Keiko Shimojima, Yuta Komoike, Jun Tohyama, Sonoko Takahashi, Makiko Osawa, Marco T. Páez
Publikováno v:
Genomics. (6):414-422
A novel microdeletion of 14q13.1q13.3 was identified in a patient with developmental delay and intractable epilepsy. The 2.2-Mb deletion included 15 genes, of which TULIP1 (approved gene symbol: RALGAPA1)was the only gene highly expressed in the brai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6823f29d133293f5799704f0e7741f4c