Morimatsu Y - Search Results

1

[An autopsy case with sequela of encephalopathy and fibromuscular dysplasia of the renal artery].

Nagata J, Oshima T, Ishizawa M, Tamagawa K, Hayashi M, Tominaga K, Kato S, Nakayama H, Koyanagi K, Mochizuki Y, Morimatsu Y, Mizutani T, Hayashi H. Nagata J, et al. Among authors: morimatsu y. No To Shinkei. 2003 Nov;55(11):997-1006. No To Shinkei. 2003. PMID: 14727543 Review. Japanese. No abstract available.

2

[Morphometry of the brainstem with transverse section of the upper pons].

Satoh J, Mizutani T, Morimatsu Y. Satoh J, et al. Among authors: morimatsu y. No To Shinkei. 1987 Feb;39(2):163-8. No To Shinkei. 1987. PMID: 3828152 Japanese.

3

Peculiar form of cerebral microdysgenesis characterized by white matter neurons with perineuronal and perivascular glial satellitosis: A study using a variety of human autopsied brains.

Arai N, Umitsu R, Komori T, Hayashi M, Kurata K, Nagata J, Tamagawa K, Mizutani T, Oda M, Morimatsu Y. Arai N, et al. Among authors: morimatsu y. Pathol Int. 2003 Jun;53(6):345-52. doi: 10.1046/j.1440-1827.2003.01480.x. Pathol Int. 2003. PMID: 12787308

4

Pathological study on sibling autopsy cases of the late infantile form of neuronal ceroid lipofuscinosis.

Kurata K, Hayashi M, Satoh J, Kojima H, Nagata J, Tamagawa K, Shinohara T, Morimatsu Y, Kominami E. Kurata K, et al. Among authors: morimatsu y. Brain Dev. 1999 Jan;21(1):63-7. doi: 10.1016/s0387-7604(98)00062-x. Brain Dev. 1999. PMID: 10082255

5

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: morimatsu y. Brain Dev. 2002 Dec;24(8):770-5. doi: 10.1016/s0387-7604(02)00103-1. Brain Dev. 2002. PMID: 12453601

6

Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndrome.

Hayashi M, Sakamoto K, Kurata K, Nagata J, Satoh J, Morimatsu Y. Hayashi M, et al. Among authors: morimatsu y. Acta Neuropathol. 1996 Dec;92(6):625-30. doi: 10.1007/s004010050571. Acta Neuropathol. 1996. PMID: 8960322

7

Neuropathology of the brainstem in age-dependent epileptic encephalopathy--especially of cases with infantile spasms.

Satoh J, Mizutani T, Morimatsu Y. Satoh J, et al. Among authors: morimatsu y. Brain Dev. 1986;8(4):443-9. doi: 10.1016/s0387-7604(86)80067-5. Brain Dev. 1986. PMID: 2432797

8

Megalencephaly, hydrocephalus and cortical dysplasia in severe dwarfism mimicking leprechaunism.

Hayashi M, Kurata K, Suzuki K, Hirasawa K, Nagata J, Morimatsu Y. Hayashi M, et al. Among authors: morimatsu y. Acta Neuropathol. 1998 Apr;95(4):431-6. doi: 10.1007/s004010050821. Acta Neuropathol. 1998. PMID: 9560023

9

A neuropathological study of a case of the Prader-Willi syndrome with an interstitial deletion of the proximal long arm of chromosome 15.

Hayashi M, Itoh M, Kabasawa Y, Hayashi H, Satoh J, Morimatsu Y. Hayashi M, et al. Among authors: morimatsu y. Brain Dev. 1992 Jan;14(1):58-62. doi: 10.1016/s0387-7604(12)80281-6. Brain Dev. 1992. PMID: 1590529

10

An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA.

Terauchi A, Tamagawa K, Morimatsu Y, Kobayashi M, Sano T, Yoda S. Terauchi A, et al. Among authors: morimatsu y. Brain Dev. 1996 May-Jun;18(3):224-9. doi: 10.1016/0387-7604(96)00015-0. Brain Dev. 1996. PMID: 8836506

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

117 results

Search Page

Filters