Sugie K - Search Results

1

Two novel CAV3 gene mutations in Japanese families.

Sugie K, Murayama K, Noguchi S, Murakami N, Mochizuki M, Hayashi YK, Nonaka I, Nishino I. Sugie K, et al. Neuromuscul Disord. 2004 Dec;14(12):810-4. doi: 10.1016/j.nmd.2004.08.008. Neuromuscul Disord. 2004. PMID: 15564037

2

[Complex IV(cytochrome c oxidase)].

Sugie K, Nishino I. Sugie K, et al. Nihon Rinsho. 2002 Apr;60 Suppl 4:490-4. Nihon Rinsho. 2002. PMID: 12013921 Review. Japanese. No abstract available.

3

Clinicopathological features of genetically confirmed Danon disease.

Sugie K, Yamamoto A, Murayama K, Oh SJ, Takahashi M, Mora M, Riggs JE, Colomer J, Iturriaga C, Meloni A, Lamperti C, Saitoh S, Byrne E, DiMauro S, Nonaka I, Hirano M, Nishino I. Sugie K, et al. Neurology. 2002 Jun 25;58(12):1773-8. doi: 10.1212/wnl.58.12.1773. Neurology. 2002. PMID: 12084876 Review.

4

Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness.

Ishikawa H, Sugie K, Murayama K, Ito M, Minami N, Nishino I, Nonaka I. Ishikawa H, et al. Among authors: sugie k. Neurology. 2002 Sep 24;59(6):920-3. doi: 10.1212/wnl.59.6.920. Neurology. 2002. PMID: 12297580

5

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.

Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I. Nishino I, et al. Among authors: sugie k. Neurology. 2002 Dec 10;59(11):1689-93. doi: 10.1212/01.wnl.0000041631.28557.c6. Neurology. 2002. PMID: 12473753

6

[Merosin-positive congenital muscular dystrophy with early orthopaedic problems in relation to Ullrich's disease].

Chang S, Ishikawa T, Nonaka I, Tsukamoto H, Saito M, Ban K, Wada I, Sugie K, Nishino I. Chang S, et al. Among authors: sugie k. No To Hattatsu. 2003 Mar;35(2):159-64. No To Hattatsu. 2003. PMID: 12661101 Japanese.

7

Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I.

Driss A, Noguchi S, Amouri R, Kefi M, Sasaki T, Sugie K, Souilem S, Hayashi YK, Shimizu N, Minoshima S, Kudoh J, Hentati F, Nishino I. Driss A, et al. Among authors: sugie k. Neurology. 2003 Apr 22;60(8):1341-4. doi: 10.1212/01.wnl.0000065886.82930.c5. Neurology. 2003. PMID: 12707439

8

A novel form of autophagic vacuolar myopathy with late-onset and multiorgan involvement.

Kaneda D, Sugie K, Yamamoto A, Matsumoto H, Kato T, Nonaka I, Nishino I. Kaneda D, et al. Among authors: sugie k. Neurology. 2003 Jul 8;61(1):128-31. doi: 10.1212/01.wnl.0000069605.00498.bd. Neurology. 2003. PMID: 12847175

9

Characterization of Danon disease in a male patient and his affected mother.

Sugie K, Koori T, Yamamoto A, Ogawa M, Hirano M, Inoue K, Nonaka I, Nishino I. Sugie K, et al. Neuromuscul Disord. 2003 Nov;13(9):708-11. doi: 10.1016/s0960-8966(03)00105-6. Neuromuscul Disord. 2003. PMID: 14561493

10

[Immunohistochemical studies of a variant of congenital muscular dystrophy].

Yoshioka M, Sugie K, Nishino I, Toda T. Yoshioka M, et al. Among authors: sugie k. No To Hattatsu. 2004 Jan;36(1):55-9. No To Hattatsu. 2004. PMID: 14737865 Japanese.

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