Takeshita K - Search Results

1

A case of Høyeraal-Hreidarsson syndrome: delayed myelination and hypoplasia of corpus callosum are other important signs.

Akaboshi S, Yoshimura M, Hara T, Kageyama H, Nishikwa K, Kawakami T, Ieshima A, Takeshita K. Akaboshi S, et al. Among authors: takeshita k. Neuropediatrics. 2000 Jun;31(3):141-4. doi: 10.1055/s-2000-7531. Neuropediatrics. 2000. PMID: 10963101 Review.

2

Neuroradiological findings in the carbohydrate-deficient glycoprotein syndrome.

Akaboshi S, Ohno K, Takeshita K. Akaboshi S, et al. Among authors: takeshita k. Neuroradiology. 1995 Aug;37(6):491-5. doi: 10.1007/BF00600103. Neuroradiology. 1995. PMID: 7477867

3

Elevated nerve growth factor levels in cerebrospinal fluid associated with progressive cortical atrophy.

Suzaki I, Hara T, Tanaka C, Dejima S, Takeshita K. Suzaki I, et al. Among authors: takeshita k. Neuropediatrics. 1997 Oct;28(5):268-71. doi: 10.1055/s-2007-973712. Neuropediatrics. 1997. PMID: 9413006

4

Unilateral involuntary movement associated with streptococcal infection: neurophysiological investigation.

Maegaki Y, Akaboshi S, Inagaki M, Takeshita K. Maegaki Y, et al. Among authors: takeshita k. Neuropediatrics. 2000 Apr;31(2):70-4. doi: 10.1055/s-2000-7476. Neuropediatrics. 2000. PMID: 10832580

5

A case of atypical absence seizures induced by leuprolide acetate.

Akaboshi S, Takeshita K. Akaboshi S, et al. Among authors: takeshita k. Pediatr Neurol. 2000 Sep;23(3):266-8. doi: 10.1016/s0887-8994(00)00181-8. Pediatr Neurol. 2000. PMID: 11033292

6

Neuroleptic malignant syndrome in striatonigral degeneration.

Itoh M, Nakano E, Ieshima A, Takeshita K. Itoh M, et al. Among authors: takeshita k. Pediatr Neurol. 1995 Oct;13(3):255-6. doi: 10.1016/0887-8994(95)00155-9. Pediatr Neurol. 1995. PMID: 8554665

7

Intracranial calcifications, epilepsy, and optic atrophy associated with metaphyseal dysplasia: a case report.

Ohtagaki A, Hara T, Maegaki Y, Takeshita K. Ohtagaki A, et al. Among authors: takeshita k. Brain Dev. 1997 Sep;19(6):414-7. doi: 10.1016/s0387-7604(97)00040-5. Brain Dev. 1997. PMID: 9339870

8

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: takeshita k. Am J Med Genet. 1998 Jan 13;75(2):141-4. Am J Med Genet. 1998. PMID: 9450874

9

Case of a mentally retarded child with non-24 hour sleep-wake syndrome caused by deficiency of melatonin secretion.

Akaboshi S, Inoue Y, Kubota N, Takeshita K. Akaboshi S, et al. Among authors: takeshita k. Psychiatry Clin Neurosci. 2000 Jun;54(3):379-80. doi: 10.1046/j.1440-1819.2000.00723.x. Psychiatry Clin Neurosci. 2000. PMID: 11186122 Free article.

10

A novel neurological disorder with progressive CNS calcification, deafness, renal tubular acidosis, and microcytic anemia.

Yoshimura M, Hara T, Maegaki Y, Koeda T, Okubo K, Hamasaki N, Sly WS, Takeshita K. Yoshimura M, et al. Among authors: takeshita k. Dev Med Child Neurol. 1997 Mar;39(3):198-201. doi: 10.1111/j.1469-8749.1997.tb07410.x. Dev Med Child Neurol. 1997. PMID: 9112970 Free article.

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

1,353 results

Search Page

Filters