Fukuda T - Search Results

1

A 78-year-old Japanese male with late-onset PHKA1-associated distal myopathy: Case report and literature review.

Mori-Yoshimura M, Aizawa K, Oya Y, Saito Y, Fukuda T, Sugie H, Nishino I, Takahashi Y. Mori-Yoshimura M, et al. Among authors: fukuda t. Neuromuscul Disord. 2022 Sep;32(9):769-773. doi: 10.1016/j.nmd.2022.05.010. Epub 2022 May 24. Neuromuscul Disord. 2022. PMID: 35710611 Review.

2

[Serotonin 2A receptor gene polymorphism and clinical efficacy of fluvoxamine in children with autistic disorder].

Sugie Y, Sugie H, Fukuda T, Ito M, Ohzeki T. Sugie Y, et al. Among authors: fukuda t. No To Hattatsu. 2003 Jan;35(1):23-8. No To Hattatsu. 2003. PMID: 12607287 Clinical Trial. Japanese.

3

[Studies on the adverse effects of fluvoxamine treatment in children with autistic disorder: correlation with genetic polymorphism in serotonin related genes].

Sugie Y, Sugie H, Fukuda T, Ito M, Ohzeki T. Sugie Y, et al. Among authors: fukuda t. No To Hattatsu. 2003 May;35(3):233-7. No To Hattatsu. 2003. PMID: 12755054 Japanese.

4

A 1-year-old infant with McArdle disease associated with hyper-creatine kinase-emia during febrile episodes.

Ito Y, Saito K, Shishikura K, Suzuki H, Yazaki E, Hayashi K, Fukuda T, Ito M, Sugie H, Osawa M. Ito Y, et al. Among authors: fukuda t. Brain Dev. 2003 Sep;25(6):438-41. doi: 10.1016/s0387-7604(03)00037-8. Brain Dev. 2003. PMID: 12907279

5

[Nation-wide survey on muscle glycogen storage disease (MGSDs) and comparison with our experiences in diagnosis of MGSDs].

Fukuda T, Sugie H, Ito M, Sugie Y, Saito K, Nishino I, Shimizu T. Fukuda T, et al. Rinsho Shinkeigaku. 2003 May;43(5):243-8. Rinsho Shinkeigaku. 2003. PMID: 12931628 Japanese.

6

Congenital form of glycogen storage disease type IV: a case report and a review of the literature.

Maruyama K, Suzuki T, Koizumi T, Sugie H, Fukuda T, Ito M, Hirato J. Maruyama K, et al. Among authors: fukuda t. Pediatr Int. 2004 Aug;46(4):474-7. doi: 10.1111/j.1442-200x.2004.01916.x. Pediatr Int. 2004. PMID: 15310318 Review. No abstract available.

7

Clinical efficacy of fluvoxamine and functional polymorphism in a serotonin transporter gene on childhood autism.

Sugie Y, Sugie H, Fukuda T, Ito M, Sasada Y, Nakabayashi M, Fukashiro K, Ohzeki T. Sugie Y, et al. Among authors: fukuda t. J Autism Dev Disord. 2005 Jun;35(3):377-85. doi: 10.1007/s10803-005-3305-2. J Autism Dev Disord. 2005. PMID: 16119478 Clinical Trial.

8

Neonatal factors in infants with Autistic Disorder and typically developing infants.

Sugie Y, Sugie H, Fukuda T, Ito M. Sugie Y, et al. Among authors: fukuda t. Autism. 2005 Dec;9(5):487-94. doi: 10.1177/1362361305057877. Autism. 2005. PMID: 16287701

9

A novel PYGM mutation in a Korean patient with McArdle disease: the role of nonsense-mediated mRNA decay.

Sohn EH, Kim HS, Lee AY, Fukuda T, Sugie H, Kim DS. Sohn EH, et al. Among authors: fukuda t. Neuromuscul Disord. 2008 Nov;18(11):886-9. doi: 10.1016/j.nmd.2008.06.384. Epub 2008 Jul 29. Neuromuscul Disord. 2008. PMID: 18667317

10

Clinical and genetic analysis of lipid storage myopathies.

Ohkuma A, Noguchi S, Sugie H, Malicdan MC, Fukuda T, Shimazu K, López LC, Hirano M, Hayashi YK, Nonaka I, Nishino I. Ohkuma A, et al. Among authors: fukuda t. Muscle Nerve. 2009 Mar;39(3):333-42. doi: 10.1002/mus.21167. Muscle Nerve. 2009. PMID: 19208393 Free PMC article.

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