Kazumaru Wada

Relationship between attention and activities of daily living among older people in long-term care health facility: A cross-sectional study

Maki Ogasawara, Toshimasa Sone, Kazumaru Wada, Takao Osanai

Objective: Attention decline affects the activities of daily living （ADL） of people with brain dysfunction. However, the association between attention and ADL in older people with Long-Term Care Insurance Certification （LTCIC） having ADL disabilities remains unexplored. This study aimed to determine the …

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Visual imagery imitation skills and cognitive functions in patients with Schizophrenia

Makoto Tanaka, Takao Osanai, Takuhiko Kato, Hisako Ogasawara et autres

Background/Objectives Visual demonstration by occupational therapists is very common in psychiatric treatment, however, some patients with schizophrenia could not imitate the actions despite the absence of any physical impairments. Therefore, the purpose of this study was to identify how cognitive functions such …

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The Effect of Cognitive Function on Imitation Skills in Patients with Schizophrenia.

Makoto Tanaka, Takao Osanai, Takuhiko Kato, Hisako Ogasawara et autres

The purpose of this study is to identify how cognitive functions such as attention and cognitive processes, such as the retention process to maintain an image needed in the learning by imitation process, are related to the ability to convert this into …

jp, us (code pays fourni par la source)

Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Akane Terasaki, Masayuki Nakamura, Yuka Urata, Hanae Hiwatashi et autres

jp (code pays fourni par la source)

DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Akane Terasaki, Masayuki Nakamura, Yuka Urata, Hanae Hiwatashi et autres

jp (code pays fourni par la source)

Anger Is a Distinctive Feature of Epilepsy Patients with Depression

Yasuhiro Mori, Kousuke Kanemoto, Teiichi Onuma, Masaki Tanaka et autres

Controversy exists regarding the similarity between depression as seen in patients with epilepsy and in those with idiopathic major depression. The objective of this study was to examine whether anger is a distinctive feature of depression in epilepsy. Participants included 487 adult …

jp, cn (code pays fourni par la source)

Detection of SCN1A mutations in patients with severe myoclonic epilepsy in infancy by custom resequence array

Takayuki Sugawara, Shuichi Yoshida, Naoko T. Onodera, Kazumaru Wada et autres

Sciendo provides publishing services and solutions to academic and professional organizations and individual authors. We publish journals, books, conference proceedings and a variety of other publications.

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P3046 The factors of drowsiness during duty for medical residents(Poster Presentation,Occupational Health in the Age of Decentralization Reform in Japan,The 79th Annual Meeting of Japan Society for Occupational Health)

Kazumaru Wada

Marital Status of Patients with Epilepsy with Special Reference to the Influence of Epileptic Seizures on the Patient's Married Life

Kazumaru Wada, Hiroto Iwasa, Motohiro Okada, Yuko Kawata et autres

PURPOSE: We investigated the marital status of the patients with epilepsy to clarify the clinical factors impeding improvement of the quality of life in adults with epilepsy. METHODS: We examined the marital status of adult patients with epilepsy who did not have …

jp, au (code pays fourni par la source)

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity

Kazuaki Kanai, Shinichi Hirose, Hirokazu Oguni, Goryu Fukuma et autres

BACKGROUND AND METHODS: Many missense mutations in the voltage-gated sodium channel subunit gene SCN1A were identified in patients with generalized epilepsy with febrile seizures plus (GEFS+) and severe myoclonic epilepsy of infancy (SMEI), although GEFS+ is distinct from SMEI in terms of …

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Impaired M‐Current and Neuronal Excitability

Motohiro Okada, Kazumaru Wada, Akihisa Kamata, Takuya Murakami et autres

PURPOSE: Benign familial neonatal convulsions (BFNC), a hereditary epilepsy, occurs specifically in newborns and remits spontaneously after this period. Several mutations of either KCNQ2 or KCNQ3, members of the KCNQ-related K+-channel (KCNQ-channel) family, were identified as a cause of BFNC. Such mutations …

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Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel α1 subunit gene, SCN1A

M. Ito, Hiroshi Nagafuji, Hidehiko Okazawa, Kazuhiro Yamakawa et autres

jp (code pays fourni par la source)