Kurosawa K - Search Results

1

A morphometric study to establish criteria for fetal and neonatal cerebellar hypoplasia: A special emphasis on trisomy 18.

Murakami A, Tanaka M, Ijiri R, Kato K, Yamashita S, Kurosawa K, Arai N, Aoki I, Tanaka Y. Murakami A, et al. Among authors: kurosawa k. Pathol Int. 2016 Jan;66(1):15-22. doi: 10.1111/pin.12371. Epub 2015 Dec 16. Pathol Int. 2016. PMID: 26669480

2

[Cerebellar agenesis].

Kurosawa K. Kurosawa K. Ryoikibetsu Shokogun Shirizu. 2001;(33):348. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462469 Review. Japanese. No abstract available.

3

Dissecting pulmonary arterial aneurysm associated with chromosome 22q11 deletion.

Tanaka Y, Kato Y, Kato K, Miyake T, Ijiri R, Miyamoto T, Matsuda S, Kurosawa K. Tanaka Y, et al. Among authors: kurosawa k. Am J Med Genet. 2001 Dec 1;104(3):260-1. Am J Med Genet. 2001. PMID: 11754055 No abstract available.

4

Congenital neuroblastoma in a patient with partial trisomy of 2p.

Dowa Y, Yamamoto T, Abe Y, Kobayashi M, Hoshino R, Tanaka K, Aida N, Take H, Kato K, Tanaka Y, Ariyama J, Harada N, Matsumoto N, Kurosawa K. Dowa Y, et al. Among authors: kurosawa k. J Pediatr Hematol Oncol. 2006 Jun;28(6):379-82. doi: 10.1097/00043426-200606000-00011. J Pediatr Hematol Oncol. 2006. PMID: 16794507

5

Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.

Osaka H, Ogiwara I, Mazaki E, Okamura N, Yamashita S, Iai M, Yamada M, Kurosawa K, Iwamoto H, Yasui-Furukori N, Kaneko S, Fujiwara T, Inoue Y, Yamakawa K. Osaka H, et al. Among authors: kurosawa k. Epilepsy Res. 2007 Jun;75(1):46-51. doi: 10.1016/j.eplepsyres.2007.03.018. Epub 2007 May 15. Epilepsy Res. 2007. PMID: 17507202

6

Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: report of two cases and review of the literature.

Yamamoto K, Yoshihashi H, Furuya N, Adachi M, Ito S, Tanaka Y, Masuno M, Chiyo H, Kurosawa K. Yamamoto K, et al. Among authors: kurosawa k. Congenit Anom (Kyoto). 2009 Mar;49(1):8-14. doi: 10.1111/j.1741-4520.2008.00212.x. Congenit Anom (Kyoto). 2009. PMID: 19243411

7

Clinical features of microdeletion 9q22.3 (pat).

Shimojima K, Adachi M, Tanaka M, Tanaka Y, Kurosawa K, Yamamoto T. Shimojima K, et al. Among authors: kurosawa k. Clin Genet. 2009 Apr;75(4):384-93. doi: 10.1111/j.1399-0004.2008.01141.x. Clin Genet. 2009. PMID: 19320658

8

Mild phenotype in Pelizaeus-Merzbacher disease caused by a PLP1-specific mutation.

Osaka H, Koizume S, Aoyama H, Iwamoto H, Kimura S, Nagai J, Kurosawa K, Yamashita S. Osaka H, et al. Among authors: kurosawa k. Brain Dev. 2010 Oct;32(9):703-7. doi: 10.1016/j.braindev.2009.11.004. Epub 2009 Dec 21. Brain Dev. 2010. PMID: 20022439

9

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

10

Heterozygous C-propeptide mutations in COL1A1: osteogenesis imperfecta type IIC and dense bone variant.

Takagi M, Hori N, Chinen Y, Kurosawa K, Tanaka Y, Oku K, Sakata H, Fukuzawa R, Nishimura G, Spranger J, Hasegawa T. Takagi M, et al. Among authors: kurosawa k. Am J Med Genet A. 2011 Sep;155A(9):2269-73. doi: 10.1002/ajmg.a.34152. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834035

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