Akaboshi S - 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. 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. Neuroradiology. 1995 Aug;37(6):491-5. doi: 10.1007/BF00600103. Neuroradiology. 1995. PMID: 7477867

3

Unilateral involuntary movement associated with streptococcal infection: neurophysiological investigation.

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

4

A case of atypical absence seizures induced by leuprolide acetate.

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

5

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

6

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. 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.

7

The carbohydrate deficient glycoprotein syndrome in three Japanese children.

Ohno K, Yuasa I, Akaboshi S, Itoh M, Yoshida K, Ehara H, Ochiai Y, Takeshita K. Ohno K, et al. Among authors: akaboshi s. Brain Dev. 1992 Jan;14(1):30-5. doi: 10.1016/s0387-7604(12)80276-2. Brain Dev. 1992. PMID: 1590525

8

[Clinical studies of learning disability. Part II: A prospective study of children with risk factors for learning disability at three year-old screening].

Koeda T, Shiota M, Akaboshi S, Takeshita K. Koeda T, et al. Among authors: akaboshi s. No To Hattatsu. 1995 Nov;27(6):461-5. No To Hattatsu. 1995. PMID: 8534511 Japanese.

9

A C57BL/KsJ mouse model of Niemann-Pick disease (spm) belongs to the same complementation group as the major childhood type of Niemann-Pick disease type C.

Akaboshi S, Yano T, Miyawaki S, Ohno K, Takeshita K. Akaboshi S, et al. Hum Genet. 1997 Mar;99(3):350-3. doi: 10.1007/s004390050370. Hum Genet. 1997. PMID: 9050921

10

Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case.

Akaboshi S, Tomita Y, Suzuki Y, Une M, Sohma O, Takashima S, Takeshita K. Akaboshi S, et al. Brain Dev. 1997 Jun;19(4):295-9. doi: 10.1016/s0387-7604(97)00550-0. Brain Dev. 1997. PMID: 9187482 Review.

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