Yamamoto T - Search Results

1

[Taste disturbance as an initial manifestation of Guillain-Barré syndrome in a 14-year-old girl].

Dejima S, Yamamoto T, Maeoka Y, Maegaki Y, Hara T. Dejima S, et al. Among authors: yamamoto t. No To Hattatsu. 1995 Nov;27(6):492-5. No To Hattatsu. 1995. PMID: 8534516 Japanese.

2

Pontine hypoplasia in a child with sensorineural deafness.

Maeoka Y, Yamamoto T, Ohtani K, Takeshita K. Maeoka Y, et al. Among authors: yamamoto t. Brain Dev. 1997 Sep;19(6):436-9. doi: 10.1016/s0387-7604(97)00056-9. Brain Dev. 1997. PMID: 9339875

3

[Two cases of post-encephalitic epilepsy characterized by auditory cognitive dysfunction; comparison with "a peculiar type of post-encephalitic/encephalopathic epilepsy"].

Yamamoto T, Nanba Y, Kodani N, Maegaki Y, Shiota M, Koeda T, Ando Y. Yamamoto T, et al. No To Hattatsu. 1995 Jul;27(4):291-6. No To Hattatsu. 1995. PMID: 7612290 Japanese.

4

Plasticity of central motor and sensory pathways in a case of unilateral extensive cortical dysplasia: investigation of magnetic resonance imaging, transcranial magnetic stimulation, and short-latency somatosensory evoked potentials.

Maegaki Y, Yamamoto T, Takeshita K. Maegaki Y, et al. Among authors: yamamoto t. Neurology. 1995 Dec;45(12):2255-61. doi: 10.1212/wnl.45.12.2255. Neurology. 1995. PMID: 8848203

5

Facilitation of ipsilateral motor pathways during recovery from hemiplegia in two adolescent patients.

Maegaki Y, Maeoka Y, Seki A, Ueno M, Yamamoto T, Takeshita K. Maegaki Y, et al. Among authors: yamamoto t. Eur J Paediatr Neurol. 1997;1(2-3):79-84. doi: 10.1016/s1090-3798(97)80067-0. Eur J Paediatr Neurol. 1997. PMID: 10728200

6

Abnormal expansion of peripheral gamma delta T cells in patients with neurologic disorders.

Yamamoto T, Hara T, Nanba E, Ohashi S, Suzuki N, Yoshino K, Takeshita K. Yamamoto T, et al. Brain Behav Immun. 1997 Sep;11(3):157-66. doi: 10.1006/brbi.1997.0495. Brain Behav Immun. 1997. PMID: 9417802 Clinical Trial.

7

Multiple epiphyseal dysplasia with small head, congenital nystagmus, hypoplasia of corpus callosum, and leukonychia totalis: a variant of Lowry-Wood syndrome?

Yamamoto T, Tohyama J, Koeda T, Maegaki Y, Takahashi Y. Yamamoto T, et al. Am J Med Genet. 1995 Mar 13;56(1):6-9. doi: 10.1002/ajmg.1320560103. Am J Med Genet. 1995. PMID: 7747786 Review.

8

Bilateral opercular syndrome caused by perinatal difficulties.

Yamamoto T, Koeda T, Maegaki Y, Tanaka C, Takeshita K. Yamamoto T, et al. Eur J Paediatr Neurol. 1997;1(2-3):73-7. doi: 10.1016/s1090-3798(97)80066-9. Eur J Paediatr Neurol. 1997. PMID: 10728199

9

Ataxia-telangiectasia without immunodeficiency: novel point mutations within and adjacent to the phosphatidylinositol 3-kinase-like domain.

Toyoshima M, Hara T, Zhang H, Yamamoto T, Akaboshi S, Nanba E, Ohno K, Hori N, Sato K, Takeshita K. Toyoshima M, et al. Among authors: yamamoto t. Am J Med Genet. 1998 Jan 13;75(2):141-4. Am J Med Genet. 1998. PMID: 9450874

10

[A two-year-old clinically manifesting carrier of Duchenne muscular dystrophy].

Yamamoto T, Kawahara H, Inagaki M, Ohta S. Yamamoto T, et al. No To Hattatsu. 1991 Jul;23(4):384-8. No To Hattatsu. 1991. PMID: 1873056 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

17,377 results

Search Page

Filters