Kawanishi C - Search Results

1

Interventions to prevent suicidal behavior and ideation for patients with cancer: A systematic review.

Kawashima Y, Yonemoto N, Inagaki M, Inoue K, Kawanishi C, Yamada M. Kawashima Y, et al. Among authors: kawanishi c. Gen Hosp Psychiatry. 2019 Sep-Oct;60:98-110. doi: 10.1016/j.genhosppsych.2019.07.003. Epub 2019 Jul 11. Gen Hosp Psychiatry. 2019. PMID: 31377631

2

Novel nonsense proteolipid protein gene mutation as a cause of X-linked spastic paraplegia in twin males.

Osaka H, Kawanishi C, Inoue K, Uesugi H, Hiroshi K, Nishiyama K, Yamada Y, Suzuki K, Kimura S, Kosaka K. Osaka H, et al. Among authors: kawanishi c. Biochem Biophys Res Commun. 1995 Oct 24;215(3):835-41. doi: 10.1006/bbrc.1995.2539. Biochem Biophys Res Commun. 1995. PMID: 7488049

3

New point mutation (R301X) of the alpha-galactosidase A gene causing Fabry disease.

Kawanishi C, Osaka H, Inoue K, Onishi H, Yamada Y, Sugiyama N, Suzuki K, Hanihara T, Miyagawa T, Kimura S, et al. Kawanishi C, et al. Hum Mutat. 1995;6(2):186-7. doi: 10.1002/humu.1380060214. Hum Mutat. 1995. PMID: 7581405 No abstract available.

4

MvaI polymorphism in the proteolipid protein (PLP) gene.

Osaka H, Inoue K, Kawanishi C, Yamada Y, Onishi H, Sugiyama N, Suzuki K, Nezu A, Kimura S, Kosaka K. Osaka H, et al. Among authors: kawanishi c. Hum Genet. 1995 Apr;95(4):461. doi: 10.1007/BF00208978. Hum Genet. 1995. PMID: 7705847

5

A duplicated PLP gene causing Pelizaeus-Merzbacher disease detected by comparative multiplex PCR.

Inoue K, Osaka H, Sugiyama N, Kawanishi C, Onishi H, Nezu A, Kimura K, Yamada Y, Kosaka K. Inoue K, et al. Among authors: kawanishi c. Am J Hum Genet. 1996 Jul;59(1):32-9. Am J Hum Genet. 1996. PMID: 8659540 Free PMC article.

6

Pelizaeus-Merzbacher disease: a novel mutation in the 5'-untranslated region of the proteolipid protein gene.

Kawanishi C, Sugiyama N, Osaka H, Inoue K, Suzuki K, Onishi H, Yamada Y, Nezu A, Kimura S, Kosaka K. Kawanishi C, et al. Hum Mutat. 1996;7(4):355-7. doi: 10.1002/(SICI)1098-1004(1996)7:4<355::AID-HUMU10>3.0.CO;2-1. Hum Mutat. 1996. PMID: 8723686 No abstract available.

7

Pelizaeus-Merzbacher-like disease: female case report.

Nezu A, Kimura S, Uehara S, Osaka H, Kobayashi T, Haraguchi M, Inoue K, Kawanishi C. Nezu A, et al. Among authors: kawanishi c. Brain Dev. 1996 Mar-Apr;18(2):114-8. doi: 10.1016/0387-7604(95)00078-x. Brain Dev. 1996. PMID: 8733901

8

Mutations in the proteolipid protein gene in Japanese families with Pelizaeus-Merzbacher disease.

Inoue K, Osaka H, Kawanishi C, Sugiyama N, Ishii M, Sugita K, Yamada Y, Kosaka K. Inoue K, et al. Among authors: kawanishi c. Neurology. 1997 Jan;48(1):283-5. doi: 10.1212/wnl.48.1.283. Neurology. 1997. PMID: 9008538

9

A new restriction-site polymorphism in the human proteolipid protein gene.

Kawanishi C, Osaka H, Inoue K, Onishi H, Yamada Y, Kosaka K. Kawanishi C, et al. Clin Genet. 1997 Jan;51(1):75. Clin Genet. 1997. PMID: 9084942 No abstract available.

10

A new missense mutation in exon 6 of the proteolipid protein gene in a patient with Pelizaeus-Merzbacher disease.

Kawanishi C, Osaka H, Owa K, Inoue K, Miyakawa T, Onishi H, Yamada Y, Suzuki K, Kimura S, Kosaka K. Kawanishi C, et al. Hum Mutat. 1997;9(5):475-6. doi: 10.1002/(SICI)1098-1004(1997)9:5<475::AID-HUMU19>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9143933 No abstract available.

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