Zobrazeno 1 - 10
of 153
pro vyhledávání: '"Itaru Toyoshima"'
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 1, Pp 211-217 (2021)
We report a long-lived patient with Lafora disease (LD). A 34-year-old woman experienced onset of seizures at the age of 11 years. She was bedridden in her early twenties due to frequent generalized tonic-clonic seizures, myoclonus, and progressive m
Externí odkaz:
https://doaj.org/article/243bc9730fcf426f818fa1d7712aa0dc
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 1, Pp 17-23 (2021)
In anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis, progressive cerebellar atrophy potentially leads to severe sequelae. We encountered a patient with anti-NMDAR antibody encephalitis who showed a decrease of blood flow in the cerebellum. A 1
Externí odkaz:
https://doaj.org/article/9ee4da4863b44994a41c6804a02e181a
Publikováno v:
Case Reports in Neurology, Vol 12, Iss 3, Pp 270-275 (2020)
Epileptic seizures are common in the elderly Down syndrome population. We encountered a patient with Down syndrome in whom karyotyping showed the rare isodicentric chromosome 21 and who suffered from myoclonic seizures. A 52-year-old woman with Down
Externí odkaz:
https://doaj.org/article/d2b439795b574b46b7198c3115a98aee
Publikováno v:
Molecular Syndromology. 14:51-58
Introduction: Cornelia de Lange syndrome (CdLS) is a rare congenital malformation characterized by distinctive facial features, short stature, and limb defects. In addition, half of the patients with CdLS exhibit repetitive self-injurious behaviors (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ff7c5838d21ab392623f0b1a0e81bf1
https://doi.org/10.1159/000525681
https://doi.org/10.1159/000525681
Publikováno v:
Journal of General and Family Medicine, Vol 21, Iss 4, Pp 146-147 (2020)
Abstract A 65‐year‐old woman with mutation of the ABCD1 gene for adrenoleukodystrophy (ALD) was admitted to our hospital with a urinary tract infection. Abdominal computed tomography showed dilation of the urinary tract. Although she had noticed
Externí odkaz:
https://doaj.org/article/c93286f42afc4d82a51a75247604664f
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::631fecc9eece41e9b0eea59ee1b49e47
https://doi.org/10.7759/cureus.33379
https://doi.org/10.7759/cureus.33379
Publikováno v:
Case Reports in Neurology
Case Reports in Neurology, Vol 13, Iss 1, Pp 211-217 (2021)
Case Reports in Neurology, Vol 13, Iss 1, Pp 211-217 (2021)
We report a long-lived patient with Lafora disease (LD). A 34-year-old woman experienced onset of seizures at the age of 11 years. She was bedridden in her early twenties due to frequent generalized tonic-clonic seizures, myoclonus, and progressive m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c07b8d49144324ff8b18b72c0e92d09
https://doi.org/10.1159/000514243
https://doi.org/10.1159/000514243
Publikováno v:
Mol Syndromol
Introduction: Dyggve-Melchior-Clausen syndrome (DMC) is a rare autosomal recessive spondyloepimetaphyseal dysplasia characterized by short stature, microcephaly, intellectual disability, and coarse face. This disorder is caused by pathogenic/likely p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd12b05423c07dd5a677906ebac9583f
https://europepmc.org/articles/PMC9421667/
https://europepmc.org/articles/PMC9421667/
Autor:
Masafumi Komatsu, Tsuyoshi Ono, Ko Nakajima, Itaru Toyoshima, Mitsuro Chiba, Osamu Masamune, Shunji Ohkubo, Tsukasa Yoshida, Hitoshi Yagisawa, Kanji Komatsu, Hideki Wakamatsu, Nobuo Yamada, Hiroyuki Watanabe, Tsuyoshi Mukojima, Mitsuo Goto
Publikováno v:
Canadian Journal of Gastroenterology, Vol 11, Iss 7, Pp 579-582 (1997)
Sixty-one chronic hepatitis C patients were randomly assigned to receive either 6x106 or 9x106 U of recombinant interferon-alpha-2a (IFNα-2a) six days a week for the first two weeks of treatment, followed in both cases by 6x106 U three days a week f
Externí odkaz:
https://doaj.org/article/df8e7ad5bcd94301af26af18cd67bada
Autor:
Masafumi Komatsu, Tohru Ishii, Tsuyoshi Ono, Takao Hoshino, Tomoyuki Kuramitsu, Takashi Goto, Tomoo Fujii, Itaru Toyoshima, Mitsuro Chiba, Osamu Masamune
Publikováno v:
Canadian Journal of Gastroenterology, Vol 11, Iss 6, Pp 507-511 (1997)
A controlled trial comparing combination therapy with ofloxacin (OFLX) and interferon (IFN) versus IFN monotherapy was conducted in patients with chronic hepatitis C who failed IFN therapy. Twenty patients were assigned randomly to two groups. Equal
Externí odkaz:
https://doaj.org/article/8fc69607af6c401b99aa73a26a62833a