Kurosawa K - Search Results

1

[An autopsy case of malignant histiocytosis (author's transl)].

Aozasa K, Uda H, Kurosawa K, Yoshihara W, Ha K, Tanaka S. Aozasa K, et al. Among authors: kurosawa k. Rinsho Ketsueki. 1979 Apr;20(4):424-30. Rinsho Ketsueki. 1979. PMID: 449059 Japanese. No abstract available.

2

Lymph node involvement in two cases of macroglobulinemia.

Aozasa K, Uda H, Kurosawa K, Yokoyama M, Tsuji M. Aozasa K, et al. Among authors: kurosawa k. Med J Osaka Univ. 1978 Dec;29(3-4):207-16. Med J Osaka Univ. 1978. PMID: 111012 No abstract available.

3

Segmental and full paternal isodisomy for chromosome 14 in three patients: narrowing the critical region and implication for the clinical features.

Kagami M, Nishimura G, Okuyama T, Hayashidani M, Takeuchi T, Tanaka S, Ishino F, Kurosawa K, Ogata T. Kagami M, et al. Among authors: kurosawa k. Am J Med Genet A. 2005 Oct 1;138A(2):127-32. doi: 10.1002/ajmg.a.30941. Am J Med Genet A. 2005. PMID: 16152632 Review.

4

Epilepsy in Christianson syndrome: Two cases of Lennox-Gastaut syndrome and a review of literature.

Ikeda A, Yamamoto A, Ichikawa K, Tsuyusaki Y, Tsuji M, Iai M, Enomoto Y, Murakami H, Kurosawa K, Miyatake S, Matsumoto N, Goto T. Ikeda A, et al. Among authors: kurosawa k. Epilepsy Behav Rep. 2019 Dec 5;13:100349. doi: 10.1016/j.ebr.2019.100349. eCollection 2020. Epilepsy Behav Rep. 2019. PMID: 31879735 Free PMC article.

5

5,10-Methylenetetrahydrofolate reductase deficiency with progressive polyneuropathy in an infant.

Tsuji M, Takagi A, Sameshima K, Iai M, Yamashita S, Shinbo H, Furuya N, Kurosawa K, Osaka H. Tsuji M, et al. Among authors: kurosawa k. Brain Dev. 2011 Jun;33(6):521-4. doi: 10.1016/j.braindev.2010.08.013. Epub 2010 Sep 20. Brain Dev. 2011. PMID: 20850942

6

Discordant phenotype caused by CASK mutation in siblings with NF1.

Murakami H, Kimura Y, Enomoto Y, Tsurusaki Y, Akahira-Azuma M, Kuroda Y, Tsuji M, Goto T, Kurosawa K. Murakami H, et al. Among authors: kurosawa k. Hum Genome Var. 2019 Apr 26;6:20. doi: 10.1038/s41439-019-0051-0. eCollection 2019. Hum Genome Var. 2019. PMID: 31044082 Free PMC article.

7

A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy.

Tsuji M, Aida N, Obata T, Tomiyasu M, Furuya N, Kurosawa K, Errami A, Gibson KM, Salomons GS, Jakobs C, Osaka H. Tsuji M, et al. Among authors: kurosawa k. J Inherit Metab Dis. 2010 Feb;33(1):85-90. doi: 10.1007/s10545-009-9022-9. Epub 2010 Jan 6. J Inherit Metab Dis. 2010. PMID: 20052547 Free PMC article.

8

Expanding the phenotype of COL4A1-related disorders-Four novel variants.

Nishimura N, Kumaki T, Murakami H, Enomoto Y, Tsurusaki Y, Tsuji M, Tsuyusaki Y, Goto T, Aida N, Kurosawa K. Nishimura N, et al. Among authors: kurosawa k. Brain Dev. 2020 Oct;42(9):639-645. doi: 10.1016/j.braindev.2020.05.009. Epub 2020 Jun 19. Brain Dev. 2020. PMID: 32565002

9

Paternal UPD14 is responsible for a distinctive malformation complex.

Kurosawa K, Sasaki H, Sato Y, Yamanaka M, Shimizu M, Ito Y, Okuyama T, Matsuo M, Imaizumi K, Kuroki Y, Nishimura G. Kurosawa K, et al. Am J Med Genet. 2002 Jul 1;110(3):268-72. doi: 10.1002/ajmg.10404. Am J Med Genet. 2002. PMID: 12116236

10

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

Kagami M, Sekita Y, Nishimura G, Irie M, Kato F, Okada M, Yamamori S, Kishimoto H, Nakayama M, Tanaka Y, Matsuoka K, Takahashi T, Noguchi M, Tanaka Y, Masumoto K, Utsunomiya T, Kouzan H, Komatsu Y, Ohashi H, Kurosawa K, Kosaki K, Ferguson-Smith AC, Ishino F, Ogata T. Kagami M, et al. Among authors: kurosawa k. Nat Genet. 2008 Feb;40(2):237-42. doi: 10.1038/ng.2007.56. Epub 2008 Jan 6. Nat Genet. 2008. PMID: 18176563

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