Kumada S - Search Results

1

Thalamic lesions in a long-surviving child with spinal muscular atrophy type I: MRI and EEG findings.

Ito Y, Kumada S, Uchiyama A, Saito K, Osawa M, Yagishita A, Kurata K, Hayashi M. Ito Y, et al. Among authors: kumada s. Brain Dev. 2004 Jan;26(1):53-6. doi: 10.1016/s0387-7604(03)00075-5. Brain Dev. 2004. PMID: 14729416

2

Oxidative stress and disturbed glutamate transport in spinal muscular atrophy.

Hayashi M, Araki S, Arai N, Kumada S, Itoh M, Tamagawa K, Oda M, Morimatsu Y. Hayashi M, et al. Among authors: kumada s. Brain Dev. 2002 Dec;24(8):770-5. doi: 10.1016/s0387-7604(02)00103-1. Brain Dev. 2002. PMID: 12453601

3

Laryngeal dystonia in a case of severe motor and intellectual disabilities due to Japanese encephalitis sequelae.

Hamano K, Kumada S, Hayashi M, Naito R, Hayashida T, Uchiyama A, Kurata K. Hamano K, et al. Among authors: kumada s. Brain Dev. 2004 Aug;26(5):335-8. doi: 10.1016/S0387-7604(03)00194-3. Brain Dev. 2004. PMID: 15165675

4

Pathological study of bronchospasms/tracheomalasia in patients with severe motor and intellectual disabilities.

Ohtsuka E, Hayashi M, Hamano K, Kumada S, Uchiyama A, Kurata K, Osawa M. Ohtsuka E, et al. Among authors: kumada s. Brain Dev. 2005 Jan;27(1):70-2. doi: 10.1016/j.braindev.2004.04.003. Brain Dev. 2005. PMID: 15626546

5

Autonomic dysfunction in cases of spinal muscular atrophy type 1 with long survival.

Hachiya Y, Arai H, Hayashi M, Kumada S, Furushima W, Ohtsuka E, Ito Y, Uchiyama A, Kurata K. Hachiya Y, et al. Among authors: kumada s. Brain Dev. 2005 Dec;27(8):574-8. doi: 10.1016/j.braindev.2005.02.009. Brain Dev. 2005. PMID: 15876504

6

An autopsy case of caudate nucleus lobulation accompanied with diaphragmatic eventration.

Hamano K, Kumada S, Hayashi M, Kurano N, Uchiyama A, Kurata K. Hamano K, et al. Among authors: kumada s. Brain Dev. 2006 Jul;28(6):401-4. doi: 10.1016/j.braindev.2005.11.006. Epub 2005 Dec 20. Brain Dev. 2006. PMID: 16376044

7

Neuropathological analysis of the brainstem and cerebral cortex lesions on epileptogenesis in hereditary dentatorubral-pallidoluysian atrophy.

Hayashi M, Kumada S, Shioda K, Fukatsu R. Hayashi M, et al. Among authors: kumada s. Brain Dev. 2007 Sep;29(8):473-81. doi: 10.1016/j.braindev.2006.12.008. Epub 2007 Feb 20. Brain Dev. 2007. PMID: 17307319

8

The axonal damage marker tau protein in the cerebrospinal fluid is increased in patients with acute encephalopathy with biphasic seizures and late reduced diffusion.

Tanuma N, Miyata R, Kumada S, Kubota M, Takanashi J, Okumura A, Hamano S, Hayashi M. Tanuma N, et al. Among authors: kumada s. Brain Dev. 2010 Jun;32(6):435-9. doi: 10.1016/j.braindev.2009.07.004. Epub 2009 Aug 12. Brain Dev. 2010. PMID: 19679415

9

[Clinical symptoms and characteristic MR spectroscopic findings in Pelizaeus-Merzbacher disease].

Kurata K, Itoh M, Uchiyama A, Kurano N, Kumada S, Komine M, Tanuma N, Tomita S, Matsui R. Kurata K, et al. Among authors: kumada s. No To Hattatsu. 2000 Nov;32(6):503-8. No To Hattatsu. 2000. PMID: 11144164 Japanese.

10

Autopsy case of multiple anomalies with hypoplastic cerebrum, eyes, and endocrine organs, mimicking Micro syndrome.

Hamano K, Kumada S, Nagata J, Kurata K, Hayashi M, Kojima H. Hamano K, et al. Among authors: kumada s. J Child Neurol. 2003 Jan;18(1):54-7. doi: 10.1177/08830738030180010301. J Child Neurol. 2003. PMID: 12661939

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