Hydrocephalus and Hirschsprung's disease in a patient with a mutation of L1CAM.

Por Okamoto, N, Wada, Y, Goto, M
Publicado em 1997

Novel nonsense mutation (Tyr44stop) of the Norrie disease gene in a Japanese family

Por Hatsukawa, Y, Nakao, T, Yamagishi, T, Okamoto, N, Isashiki, Y
Publicado em 2002

Observations on time course changes of the cherry red spot in a patient with Tay-Sachs disease

Por NAKAYA-ONISHI, M, SUZUKI, A, OKAMOTO, N, FUKUDA, M
Publicado em 2000

Severe post-laser suprachoroidal haemorrhaging in a diabetic patient receiving anticoagulants

Por Mikawa, A, Honda, S, Sugita, I, Okamoto, N, Toda, H
Publicado em 2004

Neuroradiological criteria of human L1CAM syndrome – report of 24 human L1CAM mutations including 17 noble mutations and clinical evaluation

Por Sakamoto H, Okamoto N, Kanemura Y, Yamasaki M, Kamiguchi H
Publicado em 2004-12-01

Three year follow up study of national influenza vaccination practices in Japan.

Por Morio, S, Okamoto, N, Kawamoto, A, Suyama, A, Okamoto, M, Nakayama, H
Publicado em 1994

MRI T1ρ and T2 mapping for the assessment of articular cartilage changes in patients with medial knee osteoarthritis after hemicallotasis osteotomy

Por Nishioka, H., Nakamura, E., Hirose, J., Okamoto, N., Yamabe, S., Mizuta, H.
Publicado no Bone Joint Res (2016)

Neuroradiologic Features of CASK Mutations

Por Takanashi, J., Arai, H., Nabatame, S., Hirai, S., Hayashi, S., Inazawa, J., Okamoto, N., Barkovich, A.J.
Publicado em 2010

A unique downregulation of h2-calponin gene expression in Down syndrome: a possible attenuation mechanism for fetal survival by methylation at the CpG island in the trisomic chromo...

Por Kuromitsu, J, Yamashita, H, Kataoka, H, Takahara, T, Muramatsu, M, Sekine, T, Okamoto, N, Furuichi, Y, Hayashizaki, Y
Publicado em 1997

Transgenic mice with increased expression of vascular endothelial growth factor in the retina: a new model of intraretinal and subretinal neovascularization.

Por Okamoto, N., Tobe, T., Hackett, S. F., Ozaki, H., Vinores, M. A., LaRochelle, W., Zack, D. J., Campochiaro, P. A.
Publicado em 1997

Local expression of immunoregulatory IL-12p40 gene prolonged syngeneic islet graft survival in diabetic NOD mice.

Por Yasuda, H, Nagata, M, Arisawa, K, Yoshida, R, Fujihira, K, Okamoto, N, Moriyama, H, Miki, M, Saito, I, Hamada, H, Yokono, K, Kasuga, M
Publicado em 1998

A microsatellite linkage map of rainbow trout (Oncorhynchus mykiss) characterized by large sex-specific differences in recombination rates.

Por Sakamoto, T, Danzmann, R G, Gharbi, K, Howard, P, Ozaki, A, Khoo, S K, Woram, R A, Okamoto, N, Ferguson, M M, Holm, L E, Guyomard, R, Hoyheim, B
Publicado em 2000

Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation

Por Harada, N, Hatchwell, E, Okamoto, N, Tsukahara, M, Kurosawa, K, Kawame, H, Kondoh, T, Ohashi, H, Tsukino, R, Kondoh, Y, Shimokawa, O, Ida, T, Nagai, T, Fukushima, Y, Yoshiura, K, Niikawa, N, Matsumoto, N
Publicado em 2004

Identification of eight novel NSD1 mutations in Sotos syndrome

Por Kamimura, J, Endo, Y, Kurotaki, N, Kinoshita, A, Miyake, N, Shimokawa, O, Harada, N, Visser, R, Ohashi, H, Miyakawa, K, Gerritsen, J, Innes, A, Lagace, L, Frydman, M, Okamoto, N, Puttinger, R, Raskin, S, Resic, B, Culic, V, Yoshiura, K, Ohta, T, Kishino, T, Ishikawa, M, Niikawa, N, Matsumoto, N
Publicado em 2003