Niiyama T - Search Results

1

Hermansky-Pudlak syndrome with a novel mutation.

Iwakawa J, Matsuyama W, Watanabe M, Yamamoto M, Oonakahara K, Machida K, Higashimoto I, Niiyama T, Osame M, Arimura K. Iwakawa J, et al. Among authors: niiyama t. Intern Med. 2005 Jul;44(7):733-8. doi: 10.2169/internalmedicine.44.733. Intern Med. 2005. PMID: 16093596 Free article.

2

An autopsy case of peripheral neuroepithelioma in posterior mediastinum with p53 point mutation.

Matsuyama W, Wakimoto J, Nakagawa M, Mizuno K, Kanazawa H, Niiyama T, Mizoguchi A, Iwami F, Yamanaka K, Kawabata M, Osame M. Matsuyama W, et al. Among authors: niiyama t. Intern Med. 1998 Mar;37(3):324-9. doi: 10.2169/internalmedicine.37.324. Intern Med. 1998. PMID: 9617873 Free article.

3

Statistically significant differences in the number of CD24 positive muscle fibers and satellite cells between sarcoglycanopathy and age-matched Becker muscular dystrophy patients.

Higuchi I, Kawai H, Kawajiri M, Fukunaga H, Horikiri T, Niiyama T, Nakagawa M, Arimura K, Osame M. Higuchi I, et al. Among authors: niiyama t. Intern Med. 1999 May;38(5):412-5. doi: 10.2169/internalmedicine.38.412. Intern Med. 1999. PMID: 10397078 Free article.

4

Frameshift mutation in the collagen VI gene causes Ullrich's disease.

Higuchi I, Shiraishi T, Hashiguchi T, Suehara M, Niiyama T, Nakagawa M, Arimura K, Maruyama I, Osame M. Higuchi I, et al. Among authors: niiyama t. Ann Neurol. 2001 Aug;50(2):261-5. doi: 10.1002/ana.1120. Ann Neurol. 2001. PMID: 11506412

5

Dystrophin-related protein in Becker muscular dystrophy.

Higuchi I, Niiyama T, Fukunaga H, Nakamura K, Nakagawa M, Osame M. Higuchi I, et al. Among authors: niiyama t. Intern Med. 1994 Jun;33(6):334-6. doi: 10.2169/internalmedicine.33.334. Intern Med. 1994. PMID: 7919618 Free article.

6

Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency.

Higashi K, Higuchi I, Niiyama T, Uchida Y, Shiraishi T, Hashiguchi A, Saito A, Horikiri T, Suehara M, Arimura K, Osame M. Higashi K, et al. Among authors: niiyama t. Muscle Nerve. 2006 Jan;33(1):120-6. doi: 10.1002/mus.20449. Muscle Nerve. 2006. PMID: 16258947

7

Skeletal muscle abnormalities in two patients with dystonia.

Niiyama T, Higuchi I, Uchida Y, Horikiri T, Arimura K, Osame M. Niiyama T, et al. Acta Neuropathol. 2002 Dec;104(6):670-3. doi: 10.1007/s00401-002-0603-z. Epub 2002 Sep 11. Acta Neuropathol. 2002. PMID: 12410389

8

Multiple episodes of thrombosis in a patient with Becker muscular dystrophy with marked expression of utrophin on the muscle cell membrane.

Higuchi I, Niiyama T, Uchida Y, Inose M, Nakagawa M, Arimura K, Osame M. Higuchi I, et al. Among authors: niiyama t. Acta Neuropathol. 1999 Sep;98(3):313-6. doi: 10.1007/s004010051086. Acta Neuropathol. 1999. PMID: 10483791

9

Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease.

Niiyama T, Higuchi I, Suehara M, Hashiguchi T, Shiraishi T, Nakagawa M, Arimura K, Maruyama I, Osame M. Niiyama T, et al. Acta Neuropathol. 2002 Jul;104(1):67-71. doi: 10.1007/s00401-002-0522-z. Epub 2002 Apr 30. Acta Neuropathol. 2002. PMID: 12070666

10

Expression of thrombomodulin, caveolin-3, and desmin on muscle fibers in neuromuscular diseases.

Niiyama T, Higuchi I, Maruyama I, Osame M. Niiyama T, et al. Muscle Nerve. 1999 Dec;22(12):1713-6. doi: 10.1002/(sici)1097-4598(199912)22:12<1713::aid-mus15>3.0.co;2-2. Muscle Nerve. 1999. PMID: 10567086

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