Yamamoto T - Search Results

1

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

2

A patient with cerebral palsy whose mother had a traffic accident during pregnancy: a diffuse axonal injury?

Yamamoto T, Koeda T, Ishii S, Takeshita K. Yamamoto T, et al. Brain Dev. 1999 Jul;21(5):334-6. doi: 10.1016/s0387-7604(99)00026-1. Brain Dev. 1999. PMID: 10413021

3

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

4

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

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

[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.

7

Prenatal diagnosis of congenital myotonic dystrophy in two Japanese families: direct mutation analysis by a non-radioisotope PCR method and haplotype analysis with flanking DNA markers.

Nanba E, Ito T, Kadowaki K, Makio A, Nakagawa M, Yamamoto T, Yuasa I, Takeshita K. Nanba E, et al. Among authors: yamamoto t. Brain Dev. 1996 Mar-Apr;18(2):122-6. doi: 10.1016/0387-7604(95)00111-5. Brain Dev. 1996. PMID: 8733903

8

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.

9

Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis: lack of loss of heterozygosity in a lung cyst.

Zhang H, Yamamoto T, Nanba E, Kitamura Y, Terada T, Akaboshi S, Yuasa I, Ohtani K, Nakamoto S, Takeshita K, Ohno K. Zhang H, et al. Among authors: yamamoto t. Am J Med Genet. 1999 Feb 19;82(5):368-70. doi: 10.1002/(sici)1096-8628(19990219)82:5<368::aid-ajmg2>3.0.co;2-i. Am J Med Genet. 1999. PMID: 10069705

10

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

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