Fujii T - Search Results

1

Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophy.

Yoshioka M, Higuchi Y, Fujii T, Aiba H, Toda T. Yoshioka M, et al. Among authors: fujii t. Brain Dev. 2008 Jan;30(1):59-67. doi: 10.1016/j.braindev.2007.05.012. Epub 2007 Jun 26. Brain Dev. 2008. PMID: 17597323

2

Leigh syndrome associated with West syndrome.

Tsuji M, Kuroki S, Maeda H, Yoshioka M, Maihara T, Fujii T, Ito M. Tsuji M, et al. Among authors: fujii t. Brain Dev. 2003 Jun;25(4):245-50. doi: 10.1016/s0387-7604(02)00220-6. Brain Dev. 2003. PMID: 12767455

3

Multi-institutional study on the correlation between chromosomal abnormalities and epilepsy.

Kumada T, Ito M, Miyajima T, Fujii T, Okuno T, Go T, Hattori H, Yoshioka M, Kobayashi K, Kanazawa O, Tohyama J, Akasaka N, Kamimura T, Sasagawa M, Amagane H, Mutoh K, Yamori Y, Kanda T, Yoshida N, Hirota H, Tanaka R, Hamada Y. Kumada T, et al. Among authors: fujii t. Brain Dev. 2005 Mar;27(2):127-34. doi: 10.1016/j.braindev.2003.12.010. Brain Dev. 2005. PMID: 15668053

4

Prenatal diagnosis of Fukuyama-type congenital muscular dystrophy by microsatellite analysis.

Takai Y, Tsutsumi O, Harada I, Fujii T, Kashima T, Kobayashi K, Toda T, Taketani Y. Takai Y, et al. Among authors: fujii t. Hum Reprod. 1998 Feb;13(2):320-3. doi: 10.1093/humrep/13.2.320. Hum Reprod. 1998. PMID: 9557830

5

Co-segregation of benign infantile convulsions and paroxysmal kinesigenic choreoathetosis.

Hattori H, Fujii T, Nigami H, Higuchi Y, Tsuji M, Hamada Y. Hattori H, et al. Among authors: fujii t. Brain Dev. 2000 Oct;22(7):432-5. doi: 10.1016/s0387-7604(00)00178-9. Brain Dev. 2000. PMID: 11102728

6

Epilepsy in children with trisomy 18.

Kumada T, Maihara T, Higuchi Y, Nishida Y, Taniguchi Y, Fujii T. Kumada T, et al. Among authors: fujii t. Am J Med Genet A. 2013 Apr;161A(4):696-701. doi: 10.1002/ajmg.a.35763. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23494888

7

Low-dose ACTH therapy for West syndrome: initial effects and long-term outcome.

Ito M, Aiba H, Hashimoto K, Kuroki S, Tomiwa K, Okuno T, Hattori H, Go T, Sejima H, Dejima S, Ikeda H, Yoshioka M, Kanazawa O, Kawamitsu T, Ochi J, Miki N, Noma H, Oguro K, Ozaki N, Tamamoto A, Matsubara T, Miyajima T, Fujii T, Konishi Y, Okuno T, Hojo H. Ito M, et al. Among authors: fujii t. Neurology. 2002 Jan 8;58(1):110-4. doi: 10.1212/wnl.58.1.110. Neurology. 2002. PMID: 11781414

8

Phenotypic differences between T-->C and T-->G mutations at nt 8993 of mitochondrial DNA in Leigh syndrome.

Fujii T, Hattori H, Higuchi Y, Tsuji M, Mitsuyoshi I. Fujii T, et al. Pediatr Neurol. 1998 Mar;18(3):275-7. doi: 10.1016/s0887-8994(97)00187-2. Pediatr Neurol. 1998. PMID: 9568930

9

Epilepsy in pervasive developmental disorder without brain MRI abnormalities.

Miyajima T, Kimura N, Kumada T, Oda N, Shimomura H, Fujii T. Miyajima T, et al. Among authors: fujii t. Brain Dev. 2011 Jun;33(6):504-7. doi: 10.1016/j.braindev.2010.08.014. Epub 2010 Sep 21. Brain Dev. 2011. PMID: 20863637

10

[Sulthiame treatment for patients with intractable epilepsy].

Miyajima T, Kumada T, Kimura N, Mikuni T, Fujii T. Miyajima T, et al. Among authors: fujii t. No To Hattatsu. 2009 Jan;41(1):17-20. No To Hattatsu. 2009. PMID: 19172811 Japanese.

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

6,544 results

Search Page

Filters