Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mitsuaki Iwasa"'
Publikováno v:
Autism and Developmental Language Impairments, Vol 4 (2019)
Background and aims In many countries, early detection and diagnosis of autism spectrum disorder is largely dependent on parents’ initial concern with early symptoms of autism spectrum disorder. Previous research on parental perceptions of the auti
Externí odkaz:
https://doaj.org/article/7035fed14ef14caeaef0a660bc718296
Autor:
Mitsuaki Iwasa, Yasuo Shimizu, Daimei Sasayama, Miho Imai, Hiroko Ohzono, Miori Ueda, Ikuko Hara, Hideo Honda
Publikováno v:
Journal of Child Psychology and Psychiatry. 63:1563-1573
Previous longitudinal studies have demonstrated that psychosocial outcomes for autistic adults are very limited. However, most studies are clinic-based and liable to selection bias and major methodological problems.We conducted a long-term follow-up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c27adecdf6dd4fda42ae6f80fa2ebcf
https://doi.org/10.1111/jcpp.13614
https://doi.org/10.1111/jcpp.13614
Publikováno v:
Autism & Developmental Language Impairments, Vol 4 (2019)
Article
Autism & Developmental Language Impairments. 4: 1-12. (2019)
Autism & Developmental Language Impairments. 4: 1-12. (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e95471f58ae89971276393447bc29af
https://doi.org/10.1177/2396941519845201
https://doi.org/10.1177/2396941519845201
Autor:
Ayako Honda, Mitsuaki Iwasa, Ayumi Matsumoto, Mariko Y. Momoi, Takanori Yamagata, Mitsugu Hironaka, Nobuyuki Shimozawa, Masayuki Itoh, Masashi Mizuguchi
Publikováno v:
Neuropathology. 33:292-298
Contiguous ABCD1 DXS1357E deletion syndrome (CADDS) is a contiguous deletion syndrome involving the ABCD1 and DXS1357E/BAP31 genes on Xq28. Although ABCD1 is responsible for X-linked adrenoleukodystrophy (X-ALD), its phenotype differs from that of CA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9468c525344b0eaf28294427d2e1c76d
https://doi.org/10.1111/j.1440-1789.2012.01348.x
https://doi.org/10.1111/j.1440-1789.2012.01348.x
Autor:
Yukari Nitto, Yasuo Shimizu, Tomoko Hira, Hideo Honda, Takeshi Ozawa, Keiko Shiga, Miho Imai, Mitsuaki Iwasa
Publikováno v:
Journal of Child Psychology and Psychiatry. 50:972-981
For early detection of autism, it is difficult to maintain an efficient level of sensitivity and specificity based on observational data from a single screening. The Extraction and Refinement (ER) Strategy utilizes a public children's health surveill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e407f141cdda3194ece1c8d0838721b
https://doi.org/10.1111/j.1469-7610.2009.02055.x
https://doi.org/10.1111/j.1469-7610.2009.02055.x
Autor:
Mitsuaki, Iwasa, Takanori, Yamagata, Masashi, Mizuguchi, Masayuki, Itoh, Ayumi, Matsumoto, Mitsugu, Hironaka, Ayako, Honda, Mariko Y, Momoi, Nobuyuki, Shimozawa
Publikováno v:
Neuropathology : official journal of the Japanese Society of Neuropathology. 33(3)
Contiguous ABCD1 DXS1357E deletion syndrome (CADDS) is a contiguous deletion syndrome involving the ABCD1 and DXS1357E/BAP31 genes on Xq28. Although ABCD1 is responsible for X-linked adrenoleukodystrophy (X-ALD), its phenotype differs from that of CA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a67903c5f219b558b27f7227c629c99
https://pubmed.ncbi.nlm.nih.gov/22994209
https://pubmed.ncbi.nlm.nih.gov/22994209