Výsledky vyhledávání - "Rikken Maruyama"

Akademický článek

Acute encephalopathy with biphasic seizures and late reduced diffusion associated with Streptococcus sanguinis sepsis

Autor: Hitoshi Awaguni, Jun Shinozuka, Shin-ichiro Tanaka, Sayaka Kadowaki, Shigeru Makino, Rikken Maruyama, Yosuke Shigematsu, Kenji Hamaoka, Shinsaku Imashuku

Publikováno v: Pediatric Reports, Vol 10, Iss 1 (2018)

Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) develops in association with systemic as well as central nervous system (CNS) viral or bacterial infections. AESD is most often noted with influenza or human herpesvirus 6

Externí odkaz: https://doaj.org/article/81955f8e6e4e4449a4e1262894b4b2d1

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Akademický článek

Mild encephalopathy with reversible lesions in the splenium of corpus callosum and bilateral cerebral deep white matter in identical twins

Autor: Junko Tahara, Jun Shinozuka, Hitoshi Awaguni, Shin-ichiro Tanaka, Shigeru Makino, Rikken Maruyama, Shinsaku Imashuku

Publikováno v: Pediatric Reports, Vol 8, Iss 3 (2016)

Identical twin brothers developed mild encephalopathy at the age of 7.0 and 9.7 years (Patient 1) and 10.7 years (Patient 2). Patient 1 had influenza A at the time of his second episode, but triggering agents were not evident at the first episode. Th

Externí odkaz: https://doaj.org/article/8f3b6e3e8a9041418e0692e773946930

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Akademický článek

Neonatal Sweet’s syndrome associated with rectovestibular fistula with normal anus

Autor: Jun Shinozuka, Hideki Tomiyama, Shin-ichiro Tanak, Junko Tahara, Hitoshi Awaguni, Shigeru Makino, Rikken Maruyama, Shinsaku Imashuku

Publikováno v: Pediatric Reports, Vol 7, Iss 2 (2015)

Sweet’s syndrome, characterized by fever and a painful erythematous rash with a dermal neutrophilic infiltrate, develops primarily due to paraneoplastic phenomena in adults. Sweet’s syndrome is very rare in neonates. We report a Japanese female n

Externí odkaz: https://doaj.org/article/40c48aee6c844dc68b110cf404db52a3

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Akademický článek

Corrigendum to 'Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642H/R642W Mutation in the SLC12A3 Gene'

Autor: Shigeru Makino, Toshihiro Tajima, Jun Shinozuka, Aki Ikumi, Hitoshi Awaguni, Shin-ichiro Tanaka, Rikken Maruyama, Shinsaku Imashuku

Publikováno v: Case Reports in Pediatrics, Vol 2015 (2015)

Externí odkaz: https://doaj.org/article/0b8f15008f974773b71ea3a9f46c2056

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Akademický článek

Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642H/R642W Mutation in the SLC12A3 Gene

Autor: Shigeru Makino, Toshihiro Tajima, Jun Shinozuka, Aki Ikumi, Hitoshi Awaguni, Shin-ichiro Tanaka, Rikken Maruyama, Shinsaku Imashuku

Publikováno v: Case Reports in Pediatrics, Vol 2014 (2014)

An 8-year-old Japanese boy presented with a generalized convulsion. He had hypokalemia (serum K 2.4 mEq/L), hypomagnesemia, and metabolic alkalosis (BE 5.7 mmol/L). In addition, his plasma renin activity was elevated. He was tentatively diagnosed wit

Externí odkaz: https://doaj.org/article/2bfba479c3324d64a2fac946ce6dbdc8

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Spontaneous Regression of Pulmonary Nodules Presenting as Epstein-Barr Virus-related Atypical Infectious Mononucleosis

Autor: Jun Shinozuka, Tohru Inaba, Rikken Maruyama, Shin-ichiro Tanaka, Shinsaku Imashuku, Shigeru Makino, Hitoshi Awaguni

Publikováno v: Journal of Pediatric Hematology/Oncology. 38:e162-e165

Background Pulmonary nodules associated with Epstein-Barr virus (EBV)-related atypical infectious mononucleosis have rarely been described. Observations A 12-year-old Japanese boy, upon admission, revealed multiple small round nodules (a total of 7 n

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6205158e73c1c0cd93a322b0dc7d1d54
https://doi.org/10.1097/mph.0000000000000562

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Acute encephalopathy with biphasic seizures and late reduced diffusion associated with Streptococcus sanguinis sepsis

Autor: Shinsaku Imashuku, Yosuke Shigematsu, Kenji Hamaoka, Rikken Maruyama, Shin-ichiro Tanaka, Hitoshi Awaguni, Jun Shinozuka, Sayaka Kadowaki, Shigeru Makino

Publikováno v: Pediatric Reports, Vol 10, Iss 1 (2018)
Pediatric Reports
Volume 10
Issue 1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c5ceebd2ca4ae84bb6e29e19db3b53d
http://www.pagepress.org/journals/index.php/pr/article/view/7424

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Sporadic Epstein syndrome with macrothrombocytopenia, sensorineural hearing loss and renal failure

Autor: Shin-ichiro Tanaka, Shinsaku Imashuku, Rikken Maruyama, Jun Shinozuka, Shigeru Makino, Hitoshi Awaguni, Shinji Kunishima, Aki Ikumi

Publikováno v: Pediatrics International. 57:977-981

We report here a sporadic case of Epstein syndrome, one of the MYH9 disorders. A Japanese boy was first noted to have thrombocytopenia at 3 years of age. Blood smear showed giant platelets but no Dohle-like bodies in the neutrophils. He had no family

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b7c1fb4e0244c9d2adc915cbf2803366
https://doi.org/10.1111/ped.12736

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