Sugie H - Search Results

1

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: sugie h. Brain Dev. 2003 Sep;25(6):438-41. doi: 10.1016/s0387-7604(03)00037-8. Brain Dev. 2003. PMID: 12907279

2

Computed tomography and magnetic resonance imaging of affected muscle in childhood acid alpha-glucosidase deficiency: a case report.

Arai Y, Osawa M, Shishikura K, Suzuki H, Saito K, Fukuyama Y, Sugie H. Arai Y, et al. Among authors: sugie h. Brain Dev. 1993 Mar-Apr;15(2):147-52. doi: 10.1016/0387-7604(93)90053-b. Brain Dev. 1993. PMID: 8214335

3

[Enzyme Replacement Therapy for Pompe Disease: The Long-Term Efficacy and Limitation].

Fukuda T, Sugie H. Fukuda T, et al. Among authors: sugie h. Brain Nerve. 2015 Sep;67(9):1091-8. doi: 10.11477/mf.1416200265. Brain Nerve. 2015. PMID: 26329149 Review. Japanese.

4

[Five cases of phosphorylase b kinase deficiency affecting muscle or liver: clinical symptoms and diagnosis].

Fukuda T, Sugie H, Sugie Y, Ito M, Tsurui S, Igarashi Y. Fukuda T, et al. Among authors: sugie h, sugie y. No To Hattatsu. 1994 Nov;26(6):493-7. No To Hattatsu. 1994. PMID: 7803079 Japanese.

5

[A biochemical study of an animal model with defective muscle glycolysis, induced by iodoacetate administration].

Furukawa N, Sugie H, Tsurui S, Ito M, Igarashi Y. Furukawa N, et al. Among authors: sugie h. No To Hattatsu. 1992 Jul;24(4):342-6. No To Hattatsu. 1992. PMID: 1520510 Japanese.

6

[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: sugie h. No To Hattatsu. 2003 Jan;35(1):23-8. No To Hattatsu. 2003. PMID: 12607287 Clinical Trial. Japanese.

7

[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: sugie h. No To Hattatsu. 2003 May;35(3):233-7. No To Hattatsu. 2003. PMID: 12755054 Japanese.

8

[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. Among authors: sugie h, sugie y. Rinsho Shinkeigaku. 2003 May;43(5):243-8. Rinsho Shinkeigaku. 2003. PMID: 12931628 Japanese.

9

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: sugie h. 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

10

A case of ADEM with atypical MRI findings of a centrally-located long spinal cord lesion.

Monden Y, Yamagata T, Kuroiwa Y, Takahashi T, Mori M, Fukuda T, Sugie H, Momoi MY. Monden Y, et al. Among authors: sugie h. Brain Dev. 2012 May;34(5):380-3. doi: 10.1016/j.braindev.2011.06.010. Epub 2011 Jul 23. Brain Dev. 2012. PMID: 21783334

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