Hamano K - Search Results

1

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.

Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondo-Iida E, Nomura Y, Segawa M, Yoshioka M, Saito K, Osawa M, Hamano K, Sakakihara Y, Nonaka I, Nakagome Y, Kanazawa I, Nakamura Y, Tokunaga K, Toda T. Kobayashi K, et al. Among authors: hamano k. Nature. 1998 Jul 23;394(6691):388-92. doi: 10.1038/28653. Nature. 1998. PMID: 9690476

2

Broader clinical spectrum of Fukuyama-type congenital muscular dystrophy manifested by haplotype analysis.

Yoshioka M, Toda T, Kuroki S, Hamano K. Yoshioka M, et al. Among authors: hamano k. J Child Neurol. 1999 Nov;14(11):711-5. doi: 10.1177/088307389901401105. J Child Neurol. 1999. PMID: 10593547 Review.

3

Sex identification by polymerase chain reaction using X-Y homologous primer.

Nakahori Y, Hamano K, Iwaya M, Nakagome Y. Nakahori Y, et al. Among authors: hamano k. Am J Med Genet. 1991 Jun 15;39(4):472-3. doi: 10.1002/ajmg.1320390420. Am J Med Genet. 1991. PMID: 1877627

4

Topographic pattern of the rearrangement of the dystrophin gene in Japanese Duchenne muscular dystrophy.

Imoto N, Arinami T, Hamano K, Matsumura K, Yamada H, Hamaguchi H, Takita H. Imoto N, et al. Among authors: hamano k. Hum Genet. 1993 Dec;92(6):533-6. doi: 10.1007/BF00420934. Hum Genet. 1993. PMID: 8262511

5

Abnormal myelination in a patient with ring chromosome 18.

Nakayama J, Hamano K, Shimakura Y, Iwasaki N, Nakahara C, Imoto N, Kobayashi K, Arinami T, Hamaguchi H. Nakayama J, et al. Among authors: hamano k. Neuropediatrics. 1997 Dec;28(6):335-7. doi: 10.1055/s-2007-973727. Neuropediatrics. 1997. PMID: 9453033

6

Muscle involvement in a case of oculocutaneous albinism.

Hamano K, Kawashima K, Joganoto M, Takita H, Nonaka I. Hamano K, et al. Neuropediatrics. 1986 Feb;17(1):53-6. doi: 10.1055/s-2008-1052500. Neuropediatrics. 1986. PMID: 2938023

7

Malignant hyperthermia in a patient with Becker muscular dystrophy: dystrophin analysis and caffeine contracture study.

Ohkoshi N, Yoshizawa T, Mizusawa H, Shoji S, Toyama M, Iida K, Sugishita Y, Hamano K, Takagi A, Goto K, et al. Ohkoshi N, et al. Among authors: hamano k. Neuromuscul Disord. 1995 Jan;5(1):53-8. doi: 10.1016/0960-8966(94)e0026-5. Neuromuscul Disord. 1995. PMID: 7719142

8

Molecular genetics of febrile seizures.

Iwasaki N, Nakayama J, Hamano K, Matsui A, Arinami T. Iwasaki N, et al. Among authors: hamano k. Epilepsia. 2002;43 Suppl 9:32-5. doi: 10.1046/j.1528-1157.43.s.9.8.x. Epilepsia. 2002. PMID: 12383277

9

Analysis of dystrophin in muscular diseases by two-dimensional gel electrophoresis using agarose gels in the first dimension.

Hamano K, Takeya T, Iwasaki N, Okoshi N, Fukubayashi T, Kirinoki M, Yao Y, Hirabayashi T, Takita H. Hamano K, et al. Acta Neurol Belg. 1996 Jun;96(2):102-7. Acta Neurol Belg. 1996. PMID: 8711982

10

A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures.

Nakayama J, Fu YH, Clark AM, Nakahara S, Hamano K, Iwasaki N, Matsui A, Arinami T, Ptácek LJ. Nakayama J, et al. Among authors: hamano k. Ann Neurol. 2002 Nov;52(5):654-7. doi: 10.1002/ana.10347. Ann Neurol. 2002. PMID: 12402266

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