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Akademický článek

A Case of Drug-Induced Hypersensitivity Syndrome-Like Symptoms Following HHV-6 Encephalopathy

Autor: Satoshi Saida, Akira Yoshida, Rieko Tanaka, Junya Abe, Keigo Hamahata, Mitsuyoshi Okumura, Toru Momoi

Publikováno v: Allergology International, Vol 59, Iss 1, Pp 83-86 (2010)

Background: Drug-induced hypersensitivity syndrome (DIHS) is a rare but severe disorder due to a systemic hypersensitivity reaction. We report on a case with DIHS-like symptoms following human herpes virus 6 (HHV-6) infection complicated with encepha

Externí odkaz: https://doaj.org/article/caa33f2da4f0476e9fc274b651635cf0

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A Case of Drug-Induced Hypersensitivity Syndrome-Like Symptoms Following HHV-6 Encephalopathy

Autor: Mitsuyoshi Okumura, Rieko Tanaka, Akira Yoshida, Toru Momoi, Keigo Hamahata, Junya Abe, Satoshi Saida

Publikováno v: Allergology International, Vol 59, Iss 1, Pp 83-86 (2010)

Background Drug-induced hypersensitivity syndrome (DIHS) is a rare but severe disorder due to a systemic hypersensitivity reaction. We report on a case with DIHS-like symptoms following human herpes virus 6 (HHV-6) infection complicated with encephal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::171d6980212ee5ab8abef812dd84ac06
https://doi.org/10.2332/allergolint.09-cr-0090

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Lipoprotein profiles in children with two common cholesteryl ester transfer protein gene mutations, D442G and I14A, during the first year of life

Autor: Takashi Miida, Ken-ichi Hirano, Masaki Takayanagi, Yukiyasu Sato, Hirokazu Tsukahara, Junko Yorifuji, Kunihiko Kobayashi, Tomozumi Takatani, Akemi Ota, Hitoshi Chiba, Toru Momoi, Hironori Nagasaka, Tohru Yorifuji

Publikováno v: Clinica Chimica Acta. 406:52-56

Background Hyperalphalipoproteinemia is associated with cholesteryl ester transfer protein (CETP) deficiency in adults but has unclear associations in children. Methods We measured lipoproteins in 19 heterozygotes (D442G, n = 17; I14A, n = 2), one D4

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93db563c0e3fcb33934353e4bc3e36e4
https://doi.org/10.1016/j.cca.2009.05.007

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Leukocyte and plasma N-laurylsphingosine deacylase (ceramidase) in Farber disease

Autor: R. Gagne, M. R. Parvathy, Yoav Ben-Yoseph, Deborah A. Mitchell, Toru Momoi

Publikováno v: Clinical Genetics. 36:38-42

Severe deficiency of acid ceramidase activity (4-5% of normal) was demonstrated in cultured skin fibroblasts, leukocytes and plasma from a 1-year-old boy who was diagnosed as being affected with Farber disease. Determination of ceramidase activity in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cca11ee3fe204ae3f5aa4f28a8975047
https://doi.org/10.1111/j.1399-0004.1989.tb03364.x

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Earlier initiation of GH therapy does not influence adult height but enables earlier start of pubertal induction in children with multiple pituitary hormone deficiency

Autor: Tatsutoshi Nakahata, Masahiko Kawai, Toru Momoi, Mitsukazu Mamada, Tohru Yorifuji

Publikováno v: Clinical Endocrinology. 60:608-612

Summary objective For patients with GH and gonadotrophin deficiency, adult height and sexual maturation are important not only for their physical but also psychological status. GH therapy is usually initiated soon after diagnosis but the differences

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4194bd70b811b44c451e9f62a43ea73f
https://doi.org/10.1111/j.1365-2265.2004.02013.x

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Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: Implications for the mechanism leading to generation of a 45,X karyotype

Autor: Chutaro Yamanaka, Toru Momoi, Tatsutoshi Nakahata, Masahiko Kawai, Masayuki Kaji, Ayumi Uematsu, Junko Muroi, Tohru Yorifuji, Mitsukazu Mamada

Publikováno v: American Journal of Medical Genetics. 111:134-139

The parental origin of the X chromosome of 45,X females has been the subject of many studies, and most of them have shown that the majority (60-80%) of the X chromosomes are maternal in origin. However, studies on the parental origin of normal X chro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e7d2b4849beadb1e691d8be5f90e395
https://doi.org/10.1002/ajmg.10506

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Combination therapy with GH and cyproterone acetate does not improve final height in boys with non-GH-deficient short stature

Autor: Hiroshi Sasaki, Masahiko Kawai, Toru Momoi, Chutaro Yamanaka, Junko Muroi, Kenshi Furusho, Tohru Yorifuji

Publikováno v: Clinical Endocrinology. 48:53-57

BACKGROUND AND OBJECTIVE Recently, we reported that GH therapy without gonadal suppression (GS) decreased the final height of boys with non-GH- deficient short stature by decreasing the height standard deviation score (SDS) for bone age (BA) during p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1778b73f7f47c449c4d63b75900fcc56
https://doi.org/10.1046/j.1365-2265.1998.00348.x

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