Ohnishi A - Search Results

1

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.

Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM. Othmane KB, et al. Among authors: ohnishi a. Genomics. 1999 Dec 15;62(3):344-9. doi: 10.1006/geno.1999.6028. Genomics. 1999. PMID: 10644431

2

De novo mutation (Arg98-->Cys) of the myelin P0 gene and uncompaction of the major dense line of the myelin sheath in a severe variant of Charcot-Marie-Tooth disease type 1B.

Komiyama A, Ohnishi A, Izawa K, Yamamori S, Ohashi H, Hasegawa O. Komiyama A, et al. Among authors: ohnishi a. J Neurol Sci. 1997 Jul;149(1):103-9. doi: 10.1016/s0022-510x(97)05400-2. J Neurol Sci. 1997. PMID: 9168174 Review.

3

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan. Hattori N, et al. Among authors: ohnishi a. Brain. 2003 Jan;126(Pt 1):134-51. doi: 10.1093/brain/awg012. Brain. 2003. PMID: 12477701 Review.

4

Small axons relative to number of myelin lamellae in Charcot-Marie-Tooth disease 1A with peripheral myelin protein 22 gene duplication.

Ohnishi A, Yamamoto T, Ikeda M. Ohnishi A, et al. J UOEH. 2000 Jun 1;22(2):107-17. doi: 10.7888/juoeh.22.107. J UOEH. 2000. PMID: 10862406

5

[A case of hereditary motor and sensory neuropathy (HMSN) with excessive myelin outfolding with autosomal recessive inheritance].

Ohnishi A, Narazaki O, Hanai T. Ohnishi A, et al. J UOEH. 1998 Dec 1;20(4):345-52. doi: 10.7888/juoeh.20.345. J UOEH. 1998. PMID: 9883484 Japanese.

6

Myelinated fibers in Charcot-Marie-Tooth disease type 1B with Arg98His mutation of Po protein.

Ohnishi A, Yamamoto T, Yamamori S, Sudo K, Fukushima Y, Ikeda M. Ohnishi A, et al. J Neurol Sci. 1999 Dec 15;171(2):97-109. doi: 10.1016/s0022-510x(99)00257-9. J Neurol Sci. 1999. PMID: 10581375

7

Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMT1A-REP repeat.

Yamamoto M, Keller MP, Yasuda T, Hayasaka K, Ohnishi A, Yoshikawa H, Yanagihara T, Mitsuma T, Chance PF, Sobue G. Yamamoto M, et al. Among authors: ohnishi a. Hum Mutat. 1998;11(2):109-13. doi: 10.1002/(SICI)1098-1004(1998)11:2<109::AID-HUMU2>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9482573

8

Mutations of connexin32 in Charcot-Marie-Tooth disease type X interfere with cell-to-cell communication but not cell proliferation and myelin-specific gene expression.

Yoshimura T, Satake M, Ohnishi A, Tsutsumi Y, Fujikura Y. Yoshimura T, et al. Among authors: ohnishi a. J Neurosci Res. 1998 Jan 15;51(2):154-61. doi: 10.1002/(SICI)1097-4547(19980115)51:2<154::AID-JNR4>3.0.CO;2-C. J Neurosci Res. 1998. PMID: 9469569

9

[A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation].

Ohnishi A, Yoshimura T, Kanehisa Y, Fukushima Y. Ohnishi A, et al. Rinsho Shinkeigaku. 1995 Jul;35(7):788-92. Rinsho Shinkeigaku. 1995. PMID: 8777804 Japanese.

10

Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP.

Yamamoto M, Yasuda T, Hayasaka K, Ohnishi A, Yoshikawa H, Yanagihara T, Ikegami T, Yamamoto T, Ohashi H, Nishimura T, Mitsuma T, Kiyosawa H, Chance PF, Sobue G. Yamamoto M, et al. Among authors: ohnishi a. Hum Genet. 1997 Feb;99(2):151-4. doi: 10.1007/s004390050330. Hum Genet. 1997. PMID: 9048912

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