Takashima H - Search Results

1

A new type of hereditary motor and sensory neuropathy linked to chromosome 3.

Takashima H, Nakagawa M, Nakahara K, Suehara M, Matsuzaki T, Higuchi I, Higa H, Arimura K, Iwamasa T, Izumo S, Osame M. Takashima H, et al. Ann Neurol. 1997 Jun;41(6):771-80. doi: 10.1002/ana.410410613. Ann Neurol. 1997. PMID: 9189038

2

Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neuroimaging and genetic studies.

Utatsu Y, Takashima H, Michizono K, Kanda N, Endou K, Mitsuyama Y, Fujimoto T, Nagai M, Umehara F, Higuchi I, Arimura K, Nakagawa M, Osame M. Utatsu Y, et al. Among authors: takashima h. J Neurol Sci. 1997 Mar 20;147(1):55-62. doi: 10.1016/s0022-510x(96)05310-5. J Neurol Sci. 1997. PMID: 9094061

3

A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths.

Nakagawa M, Suehara M, Saito A, Takashima H, Umehara F, Saito M, Kanzato N, Matsuzaki T, Takenaga S, Sakoda S, Izumo S, Osame M. Nakagawa M, et al. Among authors: takashima h. Neurology. 1999 Apr 12;52(6):1271-5. doi: 10.1212/wnl.52.6.1271. Neurology. 1999. PMID: 10214757

4

Germline mosaicism of MPZ gene in Dejerine-Sottas syndrome (HMSN III) associated with hereditary stomatocytosis.

Takashima H, Nakagawa M, Kanzaki A, Yawata Y, Horikiri T, Matsuzaki T, Suehara M, Izumo S, Osame M. Takashima H, et al. Neuromuscul Disord. 1999 Jun;9(4):232-8. doi: 10.1016/s0960-8966(99)00012-7. Neuromuscul Disord. 1999. PMID: 10399750

5

Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1.

Takashima H, Nakagawa M, Suehara M, Saito M, Saito A, Kanzato N, Matsuzaki T, Hirata K, Terwilliger JD, Osame M. Takashima H, et al. Neuromuscul Disord. 1999 Oct;9(6-7):368-71. doi: 10.1016/s0960-8966(99)00021-8. Neuromuscul Disord. 1999. PMID: 10545038

6

Hereditary motor and sensory neuropathy with proximal dominant involvement: clinical, pathological, and genetic features.

Nakagawa M, Takashima H, Suehara M, Saito M, Saito A, Kanzato N, Matsuzaki T, Hirata K, Izumo S, Terwilliger JD, Osame M. Nakagawa M, et al. Among authors: takashima h. Ann N Y Acad Sci. 1999 Sep 14;883:449-52. Ann N Y Acad Sci. 1999. PMID: 10586270 No abstract available.

7

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.

Shibasaki Y, Tanaka H, Iwabuchi K, Kawasaki S, Kondo H, Uekawa K, Ueda M, Kamiya T, Katayama Y, Nakamura A, Takashima H, Nakagawa M, Masuda M, Utsumi H, Nakamuro T, Tada K, Kurohara K, Inoue K, Koike F, Sakai T, Tsuji S, Kobayashi H. Shibasaki Y, et al. Among authors: takashima h. Ann Neurol. 2000 Jul;48(1):108-12. Ann Neurol. 2000. PMID: 10894224

8

Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma.

Kiwaki T, Umehara F, Takashima H, Nakagawa M, Kamimura K, Kashio N, Sakamoto Y, Unoki K, Nobuhara Y, Michizono K, Watanabe O, Arimura H, Osame M. Kiwaki T, et al. Among authors: takashima h. Neurology. 2000 Aug 8;55(3):392-7. doi: 10.1212/wnl.55.3.392. Neurology. 2000. PMID: 10932274

9

Identification of a novel mutation (Tyr1081Ter) in sisters with hereditary component C3 deficiency and SLE-like symptoms.

Matsuyama W, Nakagawa M, Takashima H, Muranaga F, Sano Y, Osame M. Matsuyama W, et al. Among authors: takashima h. Hum Mutat. 2001;17(1):79. doi: 10.1002/1098-1004(2001)17:1<79::AID-HUMU22>3.0.CO;2-5. Hum Mutat. 2001. PMID: 11139258 No abstract available.

10

Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene.

Nakagawa M, Matsuzaki T, Suehara M, Kanzato N, Takashima H, Higuchi I, Matsumura T, Goto K, Arahata K, Osame M. Nakagawa M, et al. Among authors: takashima h. J Neurol Sci. 2001 Feb 15;184(1):15-9. doi: 10.1016/s0022-510x(00)00484-6. J Neurol Sci. 2001. PMID: 11231027

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