Hayasaka K - Search Results

1

Microcephaly, cerebellar atrophy, and focal segmental glomerulosclerosis in two brothers: a possible mild form of Galloway-Mowat syndrome.

Shiihara T, Kato M, Kimura T, Matsunaga A, Joh K, Hayasaka K. Shiihara T, et al. Among authors: hayasaka k. J Child Neurol. 2003 Feb;18(2):147-9. doi: 10.1177/08830738030180021801. J Child Neurol. 2003. PMID: 12693786

2

Progressive sliding hiatal hernia as a complication of Menkes' syndrome.

Shiihara T, Kato M, Honma T, Kimura T, Matsunaga A, Kodama H, Hayasaka K. Shiihara T, et al. Among authors: hayasaka k. J Child Neurol. 2002 May;17(5):401-2. doi: 10.1177/088307380201700521. J Child Neurol. 2002. PMID: 12150594

3

Congenital dysplastic microcephaly and hypoplasia of the brainstem and cerebellum with diffuse intracranial calcification.

Nakamura K, Kato M, Sasaki A, Kanai M, Hayasaka K. Nakamura K, et al. Among authors: hayasaka k. J Child Neurol. 2012 Feb;27(2):218-21. doi: 10.1177/0883073811416239. Epub 2011 Sep 21. J Child Neurol. 2012. PMID: 21940696

4

Fluctuation of computed tomographic findings in white matter in Alexander's disease.

Shiihara T, Kato M, Honma T, Ohtaki S, Sawaishi Y, Hayasaka K. Shiihara T, et al. Among authors: hayasaka k. J Child Neurol. 2002 Mar;17(3):227-30. doi: 10.1177/088307380201700316. J Child Neurol. 2002. PMID: 12026242

5

Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAP.

Shiihara T, Sawaishi Y, Adachi M, Kato M, Hayasaka K. Shiihara T, et al. Among authors: hayasaka k. J Neurol Sci. 2004 Oct 15;225(1-2):125-7. doi: 10.1016/j.jns.2004.07.008. J Neurol Sci. 2004. PMID: 15465095

6

Costello syndrome showing moyamoya-like vasculopathy.

Shiihara T, Kato M, Mitsuhashi Y, Hayasaka K. Shiihara T, et al. Among authors: hayasaka k. Pediatr Neurol. 2005 May;32(5):361-3. doi: 10.1016/j.pediatrneurol.2004.12.010. Pediatr Neurol. 2005. PMID: 15866441

7

Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor delta2 autoantibody.

Shiihara T, Kato M, Konno A, Takahashi Y, Hayasaka K. Shiihara T, et al. Among authors: hayasaka k. Brain Dev. 2007 May;29(4):254-6. doi: 10.1016/j.braindev.2006.09.004. Epub 2006 Oct 16. Brain Dev. 2007. PMID: 17049194

8

Diffuse pachygyria with cerebellar hypoplasia: a milder form of microlissencephaly or a new genetic syndrome?

Kato M, Takizawa N, Yamada S, Ito A, Honma T, Hashimoto M, Saito E, Ohta T, Chikaoka H, Hayasaka K. Kato M, et al. Among authors: hayasaka k. Ann Neurol. 1999 Oct;46(4):660-3. doi: 10.1002/1531-8249(199910)46:4<660::aid-ana17>3.0.co;2-q. Ann Neurol. 1999. PMID: 10514106

9

Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly.

Kato M, Nanba E, Akaboshi S, Shiihara T, Ito A, Honma T, Tsuburaya K, Hayasaka K. Kato M, et al. Among authors: hayasaka k. Ann Neurol. 2000 Apr;47(4):514-6. Ann Neurol. 2000. PMID: 10762164

10

Mild immunoglobulin A nephropathy in a patient with a marked increase in serum immunoglobulin A.

Matsunaga A, Mitsui T, Kobayashi K, Hayasaka K. Matsunaga A, et al. Among authors: hayasaka k. Pediatr Int. 2004 Jun;46(3):371-3. doi: 10.1111/j.1442-200x.2004.01899.x. Pediatr Int. 2004. PMID: 15151562 No abstract available.

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