Kobayashi O - Search Results

1

A case of McLeod syndrome with unusually severe myopathy.

Kawakami T, Takiyama Y, Sakoe K, Ogawa T, Yoshioka T, Nishizawa M, Reid ME, Kobayashi O, Nonaka I, Nakano I. Kawakami T, et al. Among authors: kobayashi o. J Neurol Sci. 1999 Jun 15;166(1):36-9. doi: 10.1016/s0022-510x(99)00108-2. J Neurol Sci. 1999. PMID: 10465497

2

Nondystrophinopathic muscular dystrophies including myotonic dystrophy.

Nonaka I, Kobayashi O, Osari S. Nonaka I, et al. Among authors: kobayashi o. Semin Pediatr Neurol. 1996 Jun;3(2):110-21. doi: 10.1016/s1071-9091(96)80040-4. Semin Pediatr Neurol. 1996. PMID: 8795845 Review.

3

Mutations of calpain 3 gene in patients with sporadic limb-girdle muscular dystrophy in Japan.

Minami N, Nishino I, Kobayashi O, Ikezoe K, Goto Y, Nonaka I. Minami N, et al. Among authors: kobayashi o. J Neurol Sci. 1999 Dec 1;171(1):31-7. doi: 10.1016/s0022-510x(99)00245-2. J Neurol Sci. 1999. PMID: 10567047

4

Walker-Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy.

Chadani Y, Kondoh T, Kamimura N, Matsumoto T, Matsuzaka T, Kobayashi O, Kondo-Iida E, Kobayashi K, Nonaka I, Toda T. Chadani Y, et al. Among authors: kobayashi k, kobayashi o. J Neurol Sci. 2000 Aug 15;177(2):150-3. doi: 10.1016/s0022-510x(00)00328-2. J Neurol Sci. 2000. PMID: 10980312

5

Basement membrane abnormality in merosin-negative congenital muscular dystrophy.

Osari S, Kobayashi O, Yamashita Y, Matsuishi T, Goto M, Tanabe Y, Migita T, Nonaka I. Osari S, et al. Among authors: kobayashi o. Acta Neuropathol. 1996;91(4):332-6. doi: 10.1007/s004010050433. Acta Neuropathol. 1996. PMID: 8928608

6

[Non-Fukuyama type merosin-positive congenital muscular dystrophy with delayed muscle fiber type differentiation: a case report].

Korematsu S, Kobayashi O, Fukushima N, Sawaguchi H, Ishihara T, Izumi T, Ogawa T, Nonaka I. Korematsu S, et al. Among authors: kobayashi o. No To Hattatsu. 1995 Jul;27(4):309-14. No To Hattatsu. 1995. PMID: 7612293 Japanese.

7

Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive form.

Kobayashi O, Hayashi Y, Arahata K, Ozawa E, Nonaka I. Kobayashi O, et al. Neurology. 1996 Mar;46(3):815-8. doi: 10.1212/wnl.46.3.815. Neurology. 1996. PMID: 8618689

8

Merosin-negative non-Fukuyama-type congenital muscular dystrophy: a case report.

Yamashita Y, Ohtaka E, Matsuishi T, Osari S, Kobayashi O, Nonaka I. Yamashita Y, et al. Among authors: kobayashi o. Brain Dev. 1996 Mar-Apr;18(2):131-4. doi: 10.1016/0387-7604(95)00140-9. Brain Dev. 1996. PMID: 8733905

9

A case of Walker-Warburg syndrome.

Asano Y, Minagawa K, Okuda A, Matsui T, Ando K, Kondo-Iida E, Kobayashi O, Toda T, Nonaka I, Tanizawa T. Asano Y, et al. Among authors: kobayashi o. Brain Dev. 2000 Oct;22(7):454-7. doi: 10.1016/s0387-7604(00)00181-9. Brain Dev. 2000. PMID: 11102733

10

MTM1 gene mutations in Japanese patients with the severe infantile form of myotubular myopathy.

Nishino I, Minami N, Kobayashi O, Ikezawa M, Goto Y, Arahata K, Nonaka I. Nishino I, et al. Among authors: kobayashi o. Neuromuscul Disord. 1998 Oct;8(7):453-8. doi: 10.1016/s0960-8966(98)00075-3. Neuromuscul Disord. 1998. PMID: 9829274 Free article.

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