Fukuda T - Search Results

1

Effects of enzyme replacement therapy on five patients with advanced late-onset glycogen storage disease type II: a 2-year follow-up study.

Furusawa Y, Mori-Yoshimura M, Yamamoto T, Sakamoto C, Wakita M, Kobayashi Y, Fukumoto Y, Oya Y, Fukuda T, Sugie H, Hayashi YK, Nishino I, Nonaka I, Murata M. Furusawa Y, et al. Among authors: fukuda t. J Inherit Metab Dis. 2012 Mar;35(2):301-10. doi: 10.1007/s10545-011-9393-6. Epub 2011 Oct 7. J Inherit Metab Dis. 2012. PMID: 21984055

2

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

3

[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.

4

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.

5

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

6

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

7

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.

8

Study of HOXD genes in autism particularly regarding the ratio of second to fourth digit length.

Sugie Y, Sugie H, Fukuda T, Osawa J. Sugie Y, et al. Among authors: fukuda t. Brain Dev. 2010 May;32(5):356-61. doi: 10.1016/j.braindev.2009.05.005. Epub 2009 Jun 18. Brain Dev. 2010. PMID: 19540081

9

Case of glycogen storage disease type VI (phosphorylase deficiency) complicated by focal nodular hyperplasia.

Ogawa A, Ogawa E, Yamamoto S, Fukuda T, Sugie H, Kohno Y. Ogawa A, et al. Among authors: fukuda t. Pediatr Int. 2010 Jun;52(3):e150-3. doi: 10.1111/j.1442-200X.2010.03073.x. Pediatr Int. 2010. PMID: 20723115 No abstract available.

10

Another promising treatment option for neuroblastoma-associated opsoclonus-myoclonus syndrome by oral high-dose dexamethasone pulse: lymphocyte markers as disease activity.

Oguma M, Morimoto A, Takada A, Kashii Y, Fukuda T, Mori M, Yamagata T, Sugie H, Momoi MY. Oguma M, et al. Among authors: fukuda t. Brain Dev. 2012 Mar;34(3):251-4. doi: 10.1016/j.braindev.2011.04.005. Epub 2011 Apr 29. Brain Dev. 2012. PMID: 21531096

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