Sugawara T - Search Results

1

Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents.

Sugawara T, Tsurubuchi Y, Fujiwara T, Mazaki-Miyazaki E, Nagata K, Montal M, Inoue Y, Yamakawa K. Sugawara T, et al. Epilepsy Res. 2003 May;54(2-3):201-7. doi: 10.1016/s0920-1211(03)00084-6. Epilepsy Res. 2003. PMID: 12837571

2

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline.

Kamiya K, Kaneda M, Sugawara T, Mazaki E, Okamura N, Montal M, Makita N, Tanaka M, Fukushima K, Fujiwara T, Inoue Y, Yamakawa K. Kamiya K, et al. Among authors: sugawara t. J Neurosci. 2004 Mar 17;24(11):2690-8. doi: 10.1523/JNEUROSCI.3089-03.2004. J Neurosci. 2004. PMID: 15028761 Free PMC article.

3

Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.

Suzuki T, Morita R, Sugimoto Y, Sugawara T, Bai DS, Alonso ME, Medina MT, Bailey JN, Rasmussen A, Ramos-Peek J, Cordova S, Rubio-Donnadieu F, Ochoa A, Jara-Prado A, Inazawa J, Delgado-Escueta AV, Yamakawa K. Suzuki T, et al. Among authors: sugawara t. Epilepsy Res. 2002 Aug;50(3):265-75. doi: 10.1016/s0920-1211(02)00052-9. Epilepsy Res. 2002. PMID: 12200217

4

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.

Fujiwara T, Sugawara T, Mazaki-Miyazaki E, Takahashi Y, Fukushima K, Watanabe M, Hara K, Morikawa T, Yagi K, Yamakawa K, Inoue Y. Fujiwara T, et al. Among authors: sugawara t. Brain. 2003 Mar;126(Pt 3):531-46. doi: 10.1093/brain/awg053. Brain. 2003. PMID: 12566275

5

Seizure phenotypes of a family with missense mutations in SCN2A.

Ito M, Shirasaka Y, Hirose S, Sugawara T, Yamakawa K. Ito M, et al. Among authors: sugawara t. Pediatr Neurol. 2004 Aug;31(2):150-2. doi: 10.1016/j.pediatrneurol.2004.02.013. Pediatr Neurol. 2004. PMID: 15301839

6

A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures.

Kimura K, Sugawara T, Mazaki-Miyazaki E, Hoshino K, Nomura Y, Tateno A, Hachimori K, Yamakawa K, Segawa M. Kimura K, et al. Among authors: sugawara t. Brain Dev. 2005 Sep;27(6):424-30. doi: 10.1016/j.braindev.2004.11.005. Epub 2005 Jan 12. Brain Dev. 2005. PMID: 16122630

7

Genetic abnormalities underlying familial epilepsy syndromes.

Hirose S, Okada M, Yamakawa K, Sugawara T, Fukuma G, Ito M, Kaneko S, Mitsudome A. Hirose S, et al. Among authors: sugawara t. Brain Dev. 2002 Jun;24(4):211-22. doi: 10.1016/s0387-7604(02)00056-6. Brain Dev. 2002. PMID: 12015163 Review.

8

Usefulness of the Glove Finger Pad for Ultrasonography in Nasal Fracture Reduction.

Kashimura T, Sugawara T, Soejima K. Kashimura T, et al. Among authors: sugawara t. J Craniofac Surg. 2024 Apr 30. doi: 10.1097/SCS.0000000000010149. Online ahead of print. J Craniofac Surg. 2024. PMID: 38687083

9

ASO Visual Abstract: Adjuvant Chemotherapy with or Without Radiotherapy for Resected Pancreatic Cancer Following Multiagent Neoadjuvant Chemotherapy.

Franklin O, Sugawara T, Ross RB, Franco SR, Colborn K, Karam S, Schulick RD, Chiaro MD. Franklin O, et al. Among authors: sugawara t. Ann Surg Oncol. 2024 Apr 26. doi: 10.1245/s10434-024-15335-4. Online ahead of print. Ann Surg Oncol. 2024. PMID: 38671290 No abstract available.

10

The components of the AhR-molecular chaperone complex differ depending on whether the ligands are toxic or non-toxic.

Narita Y, Tamura A, Hatakeyama S, Uemura S, Miura A, Haga A, Tsuji N, Fujie N, Izumi Y, Sugawara T, Otaka M, Okamoto K, Lu P, Okuda S, Suzuki M, Nagata K, Shimizu H, Itoh H. Narita Y, et al. Among authors: sugawara t. FEBS Lett. 2024 Apr 11. doi: 10.1002/1873-3468.14871. Online ahead of print. FEBS Lett. 2024. PMID: 38605276

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