Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Harumi Ikenaka"'
Autor:
Makiko Osawa, Seigo Shirakawa, Harumi Ikenaka, Keiko Ishigaki, Masako Sakauchi, Terumi Murakami
Publikováno v:
Brain and Development. 34:293-297
Fukuyama congenital muscular dystrophy (FCMD), which is characterized by cortical migration defect and eye abnormalities, is the most common subtype of CMD in Japan. Fukutin (FKTN), the responsible gene for FCMD, encodes a protein involved in the gly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8de4f7144ddcfc1b265d27317b0a108
https://doi.org/10.1016/j.braindev.2011.06.002
https://doi.org/10.1016/j.braindev.2011.06.002
Autor:
Yumi Arai, Harumi Ikenaka, Haruko Suzuki, Noriko Suzuki, Makiko Osawa, Sawako Sumida, Yukio Fukuyama, Keiko Shishikura
Publikováno v:
Neuropathology. 13:259-268
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::916309d2a67896fe7d578b489706acd3
https://doi.org/10.1111/j.1440-1789.1993.tb00206.x
https://doi.org/10.1111/j.1440-1789.1993.tb00206.x
Autor:
Noriko Okada, Kyoko Hirasawa, Yukio Fukuyama, Sawako Sumida, Keiko Shishikura, Yoshito Hirayama, Makiko Osawa, Harumi Ikenaka, Hiroko Murasugi, Haruko Suzuki, Atsuko Tsutsumi, Yumi Arai, Nobuko Sugahara, Keiko Ito, Yukio Uchida
Publikováno v:
Pediatrics International. 33:261-269
Clincopathological features of Fukuyama type congenital muscular dystrophy (FCMD), a combination of brain malformation and muscular dystrophy with facial muscle and CNS involvement and high prevalence in Japan, are reviewed. Evidence of progressive d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0737d3b5d706f29688958b23ef835c
https://doi.org/10.1111/j.1442-200x.1991.tb01552.x
https://doi.org/10.1111/j.1442-200x.1991.tb01552.x