Nishino I - Search Results

1

Impact of muscle biopsy on diagnosis and management of children with neuromuscular diseases: A 10-year retrospective critical review.

Thavorntanaburt S, Tanboon J, Likasitwattanakul S, Sangruchi T, Nishino I, Ngerncham M, Tantemsapya N, Sanmaneechai O. Thavorntanaburt S, et al. Among authors: nishino i. J Pediatr Surg. 2018 Mar;53(3):489-492. doi: 10.1016/j.jpedsurg.2017.06.006. Epub 2017 Jun 16. J Pediatr Surg. 2018. PMID: 28651826

2

Floppy infant caused by MTM1 mutation: a first genetically-confirmed X-linked myotubular myopathy patient in Thailand.

Liewluck T, Raksadawan N, Limwongse C, Nishino I, Sangruchi T. Liewluck T, et al. Among authors: nishino i. J Med Assoc Thai. 2006 Jan;89(1):99-105. J Med Assoc Thai. 2006. PMID: 16583589

3

Mutation analysis of the GNE gene in distal myopathy with rimmed vacuoles (DMRV) patients in Thailand.

Liewluck T, Pho-Iam T, Limwongse C, Thongnoppakhun W, Boonyapisit K, Raksadawan N, Murayama K, Hayashi YK, Nishino I, Sangruchi T. Liewluck T, et al. Among authors: nishino i. Muscle Nerve. 2006 Dec;34(6):775-8. doi: 10.1002/mus.20583. Muscle Nerve. 2006. PMID: 16810679

4

Novel DYSF mutations in Thai patients with distal myopathy.

Liewluck T, Pongpakdee S, Witoonpanich R, Sangruchi T, Pho-Iam T, Limwongse C, Thongnoppakhun W, Boonyapisit K, Sopassathit V, Phudhichareonrat S, Suthiponpaisan U, Raksadawan N, Goto K, Hayashi YK, Nishino I. Liewluck T, et al. Among authors: nishino i. Clin Neurol Neurosurg. 2009 Sep;111(7):613-8. doi: 10.1016/j.clineuro.2009.05.001. Epub 2009 Jun 2. Clin Neurol Neurosurg. 2009. PMID: 19493611

5

Ophthalmoplegia in congenital neuromuscular disease with uniform type 1 fiber.

Sanmaneechai O, Likasitwattanakul S, Sangruchi T, Nishino I. Sanmaneechai O, et al. Among authors: nishino i. Brain Dev. 2015 Apr;37(4):459-62. doi: 10.1016/j.braindev.2014.07.009. Epub 2014 Aug 8. Brain Dev. 2015. PMID: 25112543

6

Kyphoscoliosis and easy fatigability in a 14-year-old boy.

Tanboon J, Hayashi YK, Nishino I, Sangruchi T. Tanboon J, et al. Among authors: nishino i. Neuropathology. 2015 Feb;35(1):91-3. doi: 10.1111/neup.12147. Epub 2014 Aug 28. Neuropathology. 2015. PMID: 25168271 No abstract available.

7

2 Month-Old Male with Hypotonia.

Tanboon J, Viravan S, Hayashi YK, Nishino I, Sangruchi T. Tanboon J, et al. Among authors: nishino i. Brain Pathol. 2015 Sep;25(5):651-2. doi: 10.1111/bpa.12284. Brain Pathol. 2015. PMID: 26276028 Free PMC article. No abstract available.

8

Targeted massively parallel sequencing and histological assessment of skeletal muscles for the molecular diagnosis of inherited muscle disorders.

Nishikawa A, Mitsuhashi S, Miyata N, Nishino I. Nishikawa A, et al. Among authors: nishino i. J Med Genet. 2017 Feb;54(2):104-110. doi: 10.1136/jmedgenet-2016-104073. Epub 2016 Sep 6. J Med Genet. 2017. PMID: 27600705

9

A 62-Year-Old Woman with A History of Muscle Pain and Skin Rash for 1 Month.

Tanboon J, Uruha A, Hamanaka K, Hasegawa J, Nishino I. Tanboon J, et al. Among authors: nishino i. Brain Pathol. 2018 Jan;28(1):121-122. doi: 10.1111/bpa.12574. Brain Pathol. 2018. PMID: 29265633 Free PMC article. No abstract available.

10

Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance (SLONM-MGUS): An alternative treatment using cyclophosphamide-thalidomide-dexamethasone (CTD) regimen.

Kumutpongpanich T, Owattanapanich W, Tanboon J, Nishino I, Boonyapisit K. Kumutpongpanich T, et al. Among authors: nishino i. Neuromuscul Disord. 2018 Jul;28(7):610-613. doi: 10.1016/j.nmd.2018.04.011. Epub 2018 May 16. Neuromuscul Disord. 2018. PMID: 29910095

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