Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Yuri Miyanomae"'
Autor:
Yuri Miyanomae, Takenori Tozawa, Hajime Hosoi, Tomohiro Chiyonobu, Daisuke Kaneda, Masafumi Morimoto, Tamaki Ueno, Akira Nishimura
Publikováno v:
Neuropediatrics. 49:200-203
Seronegative myasthenia gravis (MG) is a generalized form of MG that is diagnosed on the basis of clinical symptoms, electrophysiological testing, and pharmacological responses, in the absence of a seropositive status for anti-acetylcholine receptor
Autor:
Takenori Tozawa, Nishimura, Akira, Tamaki Ueno, Daisuke Kaneda, Yuri Miyanomae, Tomohiro Chiyonobu, Masafumi Morimoto, Hajime Hosoi
Publikováno v:
Neuropediatrics; 2018, Vol. 49 Issue 3, p200-203, 4p
Autor:
Tatsushi Toda, Masafumi Morimoto, Yuri Miyanomae, Akemi Nishimoto, Zhengping Jia, Shin Hayashi, Akira Nishimura, Issei Imoto, Kazuhiro Kobayashi, Johji Inazawa, Chiyomi Ito, Tomohiro Chiyonobu, Tohru Sugimoto
Publikováno v:
American journal of medical genetics. Part A. (13)
The genetic factors underlying mental retardation (MR) are very heterogeneous. Recent studies have identified a number of genes involved in MR, several of which lie on the X-chromosome, but the current understanding of the monogenic causes of MR is f
Publikováno v:
Pediatric neurology. 19(1)
A 12-year-old boy rapidly developed Guillain-Barre syndrome (GBS) after Campylobacter jejuni enteritis. Electrophysiologic studies suggested that demyelination was dominant, and serum anti-C. jejuni and both IgG and IgM anti-GM1 antibodies were signi
Autor:
Yoshihiro Takeuchi, Masaharu Ochi, Kiyoshi Hirai, Akira Nishimura, Tadashi Sawada, Syouji Kawase, Yuri Miyanomae
Publikováno v:
Acta paediatrica Japonica : Overseas edition. 38(6)
Median and posterior tibial motor nerve conduction studies were performed on 10 children with spinal muscular atrophy (SMA). Three patients with SMA type I, in whom rapid deterioration occurred, showed reduced motor nerve conduction velocity and a re
Autor:
Hiroshi Komatsu, Yuri Miyanomae, Tadashi Sawada, Kay E. Davies, Rachael J. Daniels, Yoshihiro Takeuchi, Hiroshi Yoshioka
Publikováno v:
Acta paediatrica Japonica : Overseas edition. 36(5)
The clinical, electrophysiological, pathological and genetic findings in trizygotic triplets with spinal muscular atrophy (SMA) are reported. The first child was clinically affected shortly after birth and the third one first showed symptoms at 1 mon
Autor:
Yoshihiro Takeuchi, Akira Nishimura, Tadashi Sawada, Yuri Miyanomae, Hiroshi Komatsu, Tetuo Nishiki, Sozo Okano, Yoshikazu Oomizono
Publikováno v:
Journal of child neurology. 9(3)
Children with spinal muscular atrophy were treated by the administration of thyrotropin-releasing hormone. In three infants with spinal muscular atrophy type I, thyrotropin-releasing hormone showed little efficacy, but in children with types II and I
Autor:
Hiroko Matsushita, Yoshihiro Takeuchi, Ichiro Yamazoe, Kazushi Takaya, Tadashi Sawada, Hisakazu Uehara, Yuri Miyanomae
Publikováno v:
Epilepsia. 39:82-82
Purpose: Despite rapid advances in the treatment of epilepsy with the introduction of new drugs, the seizures in a number of children with epilepsy remain uncontrollable. Thus a more potent, yet safer therapy is needed. Adrenocorticotropic hormone (A
Autor:
Takuro Kidowaki, Kozo Fujiwara, Tomoichi Kusunoki, Noriko Esumi, Takafumi Matsumura, Tadashi Sawada, Yuri Miyanomae, Akira Yoshioka
Publikováno v:
Japanese Journal of Clinical Oncology.
Metastasis to the brain or spinal cord parenchyma is extremely rare in cases of neuroblastoma. We present a 3-year-7-month-old boy with neuroblastoma, stage IV, with intraspinal metastasis. He had no neurologic manifestation except incontinentia urin