Tachi N - Search Results

1

Resveratrol improves motor function in patients with muscular dystrophies: an open-label, single-arm, phase IIa study.

Kawamura K, Fukumura S, Nikaido K, Tachi N, Kozuka N, Seino T, Hatakeyama K, Mori M, Ito YM, Takami A, Hinotsu S, Kuno A, Kawasaki Y, Horio Y, Tsutsumi H. Kawamura K, et al. Among authors: tachi n. Sci Rep. 2020 Nov 25;10(1):20585. doi: 10.1038/s41598-020-77197-6. Sci Rep. 2020. PMID: 33239684 Free PMC article. Clinical Trial.

2

A new mutation of IGHMBP2 gene in spinal muscular atrophy with respiratory distress type 1.

Tachi N, Kikuchi S, Kozuka N, Nogami A. Tachi N, et al. Pediatr Neurol. 2005 Apr;32(4):288-90. doi: 10.1016/j.pediatrneurol.2004.11.003. Pediatr Neurol. 2005. PMID: 15797190

3

Expression of myotonic dystrophy protein kinase in biopsied muscles.

Tachi N, Kozuka N, Ohya K, Chiba S, Kikuchi K. Tachi N, et al. J Neurol Sci. 1995 Sep;132(1):61-4. doi: 10.1016/0022-510x(95)00123-j. J Neurol Sci. 1995. PMID: 8523032

4

Detection of the mutation in facioscapulohumeral muscular dystrophy patients.

Ohya K, Tachi N, Kozuka N, Kon S, Kikuchi K, Chiba S. Ohya K, et al. Among authors: tachi n. Acta Paediatr Jpn. 1997 Feb;39(1):92-6. doi: 10.1111/j.1442-200x.1997.tb03564.x. Acta Paediatr Jpn. 1997. PMID: 9124063

5

Immunocytochemical localization of myotonin protein kinase on muscle from patients with congenital myotonic dystrophy.

Tachi N, Kozuka N, Ohya K, Chiba S, Kikuchi K. Tachi N, et al. Histol Histopathol. 1996 Oct;11(4):869-71. Histol Histopathol. 1996. PMID: 8930628

6

De novo mutation of Charcot-Marie-Tooth disease type 1A.

Tachi N, Kozuka N, Ohya K, Chiba S. Tachi N, et al. Pediatr Neurol. 1997 Jul;17(1):67-9. doi: 10.1016/s0887-8994(97)80670-4. Pediatr Neurol. 1997. PMID: 9308980

7

Charcot-Marie-Tooth disease type 1A duplication by PCR analysis.

Tachi N, Kozuka N, Ohya K, Chiba S. Tachi N, et al. Pediatr Neurol. 1999 May;20(5):360-3. doi: 10.1016/s0887-8994(99)00016-8. Pediatr Neurol. 1999. PMID: 10371381

8

A double mutation in a patient with X-linked myotubular myopathy.

Tachi N, Kozuka N, Chiba S, Miyaji M, Watanabe I. Tachi N, et al. Pediatr Neurol. 2001 Apr;24(4):297-9. doi: 10.1016/s0887-8994(01)00244-2. Pediatr Neurol. 2001. PMID: 11377105

9

CTG repeat size and histologic findings of skeletal muscle from patients with congenital myotonic dystrophy.

Tachi N, Kozuka N, Ohya K, Chiba S, Kikuchi K. Tachi N, et al. J Child Neurol. 1996 Nov;11(6):430-2. doi: 10.1177/088307389601100602. J Child Neurol. 1996. PMID: 9120218

10

MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.

Tachi N, Kozuka N, Ohya K, Chiba S, Naganuma M. Tachi N, et al. Neuroradiology. 1995 Aug;37(6):496-9. doi: 10.1007/BF00600104. Neuroradiology. 1995. PMID: 7477868

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