Molecular features of the CAG repeats and clinical manifestation of Machado—Joseph disease
…, T Sakai, M Doyu, G Sobue, M Seto… - Human molecular …, 1995 - academic.oup.com
Machado-Joseph disease (MJD) is an autosomal dominant spinocerebellar degeneration
mapped to chromosome 14q32.1. The CAG expansions of the MJD1 gene was identified as …
mapped to chromosome 14q32.1. The CAG expansions of the MJD1 gene was identified as …
Efficacy of upper extremity robotic therapy in subacute poststroke hemiplegia: an exploratory randomized trial
…, K Domen, T Sakamoto, M Toshima, Y Otaka, M Seto… - Stroke, 2016 - Am Heart Assoc
Background and Purpose— Our aim was to study the efficacy of robotic therapy as an
adjuvant to standard therapy during poststroke rehabilitation. Methods— Prospective, open, …
adjuvant to standard therapy during poststroke rehabilitation. Methods— Prospective, open, …
[PDF][PDF] Loss of 123I-MIBG uptake by the heart in Parkinson's disease: assessment of cardiac sympathetic denervation and diagnostic value
A Satoh, T Serita, M Seto, I Tomita… - Journal of Nuclear …, 1999 - Soc Nuclear Med
Methods: We studied35 patientswith Parkinson'sdisease and 24 control subjects with other
central nervous system diseases. The latter group consisted of 12 subjects with other …
central nervous system diseases. The latter group consisted of 12 subjects with other …
Bunina bodies in motor and non‐motor neurons revisited: a pathological study of an ALS patient after long‐term survival on a respirator
T Kimura, H Jiang, T Konno, M Seto… - …, 2014 - Wiley Online Library
Bunina bodies ( BBs ) are small eosinophilic neuronal cytoplasmic inclusions ( NCIs ) found
in the remaining lower motor neurons ( LMNs ) of patients with sporadic amyotrophic lateral …
in the remaining lower motor neurons ( LMNs ) of patients with sporadic amyotrophic lateral …
An outbreak of Legionnaires' pneumonia in a nursing home
…, H Matsuda, Y Higashiyama, K Hara, M Seto… - Internal …, 1992 - jstage.jst.go.jp
An outbreak of Legionnaires' pneumonia occurred at a nursing home in December 1990. A
79-year-old female and a 73-year-old male clerk who were staying at the nursing home …
79-year-old female and a 73-year-old male clerk who were staying at the nursing home …
Role of the macrophage in the pathogenesis of experimental autoimmune myasthenia gravis
…, T Nakamura, A Satoh, H Matsuo, M Seto… - Journal of the …, 1988 - Elsevier
To clarify the role of Ia antigen positive macrophages which invade motor end-plates in the
induction of the chronic phase, experimental autoimmune myasthenia gravis (EAMG) rats …
induction of the chronic phase, experimental autoimmune myasthenia gravis (EAMG) rats …
Treatment of myasthenia gravis: a comparison of the natural course and current therapies
M SETO, M MOTOMURA, GOU TAKEO… - The Tohoku Journal of …, 1993 - jstage.jst.go.jp
RESULTS Group 1 (Fig. l) consisted of 40 patients (12 men and 28 women, age range 15-61,
mean age 38.0±1.9, mean severity score 1.63±0.02). Most had been treated before 1975, …
mean age 38.0±1.9, mean severity score 1.63±0.02). Most had been treated before 1975, …
The effectiveness of pretreatment video-based psychoeducation for patients with breast cancer
T Sato, M Seto, T Sangai, S Norihiko… - Palliative & Supportive …, 2023 - cambridge.org
ObjectivesThis study confirms the effectiveness of pretreatment video-based psychoeducation
on stress management and relaxation in reducing depression, anxiety, and uncertainty …
on stress management and relaxation in reducing depression, anxiety, and uncertainty …
[HTML][HTML] Effect of Functional Electrical Stimulation in Convalescent Stroke Patients: A Multicenter, Randomized Controlled Trial
…, T Shigematsu, A Satone, H Okuma, M Seto… - Journal of Clinical …, 2023 - mdpi.com
Background: We evaluated whether the Walkaide ® device could effectively improve walking
ability and lower extremity function in post-stroke patients with foot drop. Patients aged 20–…
ability and lower extremity function in post-stroke patients with foot drop. Patients aged 20–…
A case of Creutzfeldt-Jakob disease with a point mutation at codon 232: correlation of MRI and neurologic findings
A Satoh, H Goto, H Satoh, I Tomita, M Seto… - Neurology, 1997 - AAN Enterprises
Discussion. This patient had atypical clinical CJD features: signs and symptoms of abnormal
cortical functions, particularly of the parietal cortex at the onset of illness, and the absence …
cortical functions, particularly of the parietal cortex at the onset of illness, and the absence …