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pro vyhledávání: '"C, Nakahara"'
Akademický článek
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Autor:
C. Nakahara, A. Tada
Publikováno v:
Journal of Investigative Dermatology. 141:S20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1cb0522bc505e3836da172fb8ef1a03
https://doi.org/10.1016/j.jid.2021.02.131
https://doi.org/10.1016/j.jid.2021.02.131
Publikováno v:
Journal of Investigative Dermatology. 139:S311
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7101658d50480dc062a1b000ce125572
https://doi.org/10.1016/j.jid.2019.07.475
https://doi.org/10.1016/j.jid.2019.07.475
Publikováno v:
Pediatric Nephrology. 20:657-661
We report the case of a 12- year-old Japanese boy who was receiving cyclosporine (Cs A) for steroid-dependent nephrotic syndrome despite a prior episode of Cs A-associated posterior encephalopathy. At the third relapsing of nephrotic syndrome, Cs A w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52f2a3a2b93ad6359e95e42eaf95a958
https://doi.org/10.1007/s00467-004-1752-1
https://doi.org/10.1007/s00467-004-1752-1
Autor:
Akira Matsui, Nobuaki Iwasaki, Satoko Nakahara, Yae Shimakura, Emiko Noguchi, Tadao Arinami, Kimiko Yamakawa-Kobayashi, Masayasu Ohta, Junko Nakayama, Yumi Horigome, C. Nakahara, Nao Yamamoto, Junko Shiono, Kenzo Hamano
Publikováno v:
Neuroscience Letters. 329:249-251
The voltage-gated sodium channel type II alpha polypeptide gene (SCN2A) R188W mutation with channel dysfunction was recently identified in a patient with febrile and afebrile seizures. A possible association between SCN2A R19K polymorphism and febril
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f1723b23f939fd32b72bf8aab7c80bb
https://doi.org/10.1016/s0304-3940(02)00651-1
https://doi.org/10.1016/s0304-3940(02)00651-1
Autor:
K. Kobayashi, N. Iwasaki, T. Arinami, C. Nakahara, Junko Nakayama, H. Hamaguchi, K. Hamano, N. Imoto, Y. Shimakura
Publikováno v:
Neuropediatrics. 28:335-337
We describe a Japanese boy with ring chromosome 18 in whom abnormal myelination was observed on magnetic resonance imaging. Cytogenetic investigation revealed 46, XY, r(18) (p11.2 q21.33). T 2- weighted magnetic resonance imaging scan of the brain de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5234807f5ef18d990a9c95228d22cc2
https://doi.org/10.1055/s-2007-973727
https://doi.org/10.1055/s-2007-973727
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
C, Nakahara, D, Hayashi, H, Kinugasa, H, Horigome, A, Matsui, A, Takagi, N, Kato, M, Kobayashi
Publikováno v:
Clinical nephrology. 56(4)
We report here on an 11-year-old Japanese girl who was found to have proteinuria by routine mass screening urinalysis for school children, and who developed systemic lupus erythematosus (SLE) 21 months later. The initial renal biopsy, performed 3 mon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ab9c91021791913642ac51fa6788654
https://pubmed.ncbi.nlm.nih.gov/11680664
https://pubmed.ncbi.nlm.nih.gov/11680664
Publikováno v:
Clinical nephrology. 55(5)
In recent reports, C-reactive protein (CRP) has emerged as a component that may play important roles in atherogenesis. Based on the analogies set out in a previous report between focal-segmental sclerosis and atherosclerosis, we hypothesized that CRP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::200010eca1706aed6c60c603c38e5768
https://pubmed.ncbi.nlm.nih.gov/11393381
https://pubmed.ncbi.nlm.nih.gov/11393381
Autor:
C. Nakahara, Akira Matsui, Tetsuro Wada, M. Sibasaki, Michio Nagata, K. Kanemoto, Hideyo Kinugasa, Jun Kusakari
Publikováno v:
Pediatric nephrology (Berlin, Germany). 14(6)
We report an 11-year-old Japanese boy with Kimura disease and associated nephrotic syndrome. Before the diagnosis of Kimura disease was established, the patient had three episodes of swelling on the left cheek with subsequent nephrotic syndrome. Ster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d997e8790c2b49e391b8c3585a631420
https://pubmed.ncbi.nlm.nih.gov/10872189
https://pubmed.ncbi.nlm.nih.gov/10872189