Imai K - Search Results

1

Interstitial deletion of 14q, 46, XY, del (14) (q24.3q32.1) associated with status nonepileptic myoclonia and delayed myelination.

Ono J, Kurahashi H, Okinaga T, Mano T, Imai K, Inui K, Okada S. Ono J, et al. Among authors: imai k. J Child Neurol. 1999 Nov;14(11):756-8. doi: 10.1177/088307389901401116. J Child Neurol. 1999. PMID: 10593558 Review.

2

Ring chromosome 14 complicated with complex partial seizures and hypoplastic corpus callosum.

Ono J, Nishiike K, Imai K, Otani K, Okada S. Ono J, et al. Among authors: imai k. Pediatr Neurol. 1999 Jan;20(1):70-2. doi: 10.1016/s0887-8994(98)00099-x. Pediatr Neurol. 1999. PMID: 10029266

3

Intracranial lipoma of the quadrigeminal region associated with complex partial seizures.

Ono J, Ikeda T, Imai K, Mano T, Matsuoka T, Nagai T, Okada S. Ono J, et al. Among authors: imai k. Pediatr Radiol. 1998 Sep;28(9):729-31. doi: 10.1007/s002470050453. Pediatr Radiol. 1998. PMID: 9732507

4

[Connatal type of Pelizaeus-Merzbacher disease: a case report].

Kagitani K, Fukunishi M, Mano T, Matsuoka T, Imai K, Ono J, Okada S. Kagitani K, et al. Among authors: imai k. No To Hattatsu. 1999 Mar;31(2):171-6. No To Hattatsu. 1999. PMID: 10191641 Japanese.

5

Proton MR spectroscopy of Sjögren-Larsson's syndrome.

Mano T, Ono J, Kaminaga T, Imai K, Sakurai K, Harada K, Nagai T, Rizzo WB, Okada S. Mano T, et al. Among authors: imai k. AJNR Am J Neuroradiol. 1999 Oct;20(9):1671-3. AJNR Am J Neuroradiol. 1999. PMID: 10543638 Free PMC article.

6

Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome.

Inui K, Akagi M, Ono J, Tsukamoto H, Shimono K, Mano T, Imai K, Yamada M, Muramatsu T, Sakai N, Okada S. Inui K, et al. Among authors: imai k. Brain Dev. 2001 Jul;23(4):212-5. doi: 10.1016/s0387-7604(01)00197-8. Brain Dev. 2001. PMID: 11376998

7

Long-term response to zonisamide in patients with West syndrome.

Suzuki Y, Imai K, Toribe Y, Ueda H, Yanagihara K, Shimono K, Okinaga T, Ono J, Nagai T, Matsuoka T, Tagawa T, Abe J, Morita Y, Fujikawa Y, Arai H, Mano T, Okada S. Suzuki Y, et al. Among authors: imai k. Neurology. 2002 May 28;58(10):1556-9. doi: 10.1212/wnl.58.10.1556. Neurology. 2002. PMID: 12034801 Clinical Trial.

8

Neuronal intranuclear hyaline inclusion disease with rapidly progressive neurological symptoms.

Mano T, Takizawa S, Mohri I, Okinaga T, Shimono K, Imai K, Taniike M, Ozono K, Fujimura H. Mano T, et al. Among authors: imai k. J Child Neurol. 2007 Jan;22(1):60-6. doi: 10.1177/0883073807299952. J Child Neurol. 2007. PMID: 17608307

9

Isolated lissencephaly sequence with balanced chromosome translocation involving 17p13.3.

Honda A, Ono J, Kurahashi H, Mano T, Imai K, Okada S. Honda A, et al. Among authors: imai k. Brain Dev. 1998 Apr;20(3):190-2. doi: 10.1016/s0387-7604(98)00018-7. Brain Dev. 1998. PMID: 9628198

10

Evaluation of myelination by means of the T2 value on magnetic resonance imaging.

Ono J, Kodaka R, Imai K, Itagaki Y, Tanaka J, Inui K, Nagai T, Sakurai K, Harada K, Okada S. Ono J, et al. Among authors: imai k. Brain Dev. 1993 Nov-Dec;15(6):433-8. doi: 10.1016/0387-7604(93)90083-k. Brain Dev. 1993. PMID: 8147502

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