Kobayashi K - Search Results

1

Clinical significance of apolipoprotein (a) deposition in kidney diseases of children.

Nakahara C, Nagata M, Watanabe T, Kobayashi K, Hamaguchi H, Kanemoto K, Kashiwagi R, Matsui A. Nakahara C, et al. Among authors: kobayashi k. Clin Nephrol. 1999 Sep;52(3):131-8. Clin Nephrol. 1999. PMID: 10499307

2

Plasma lipoprotein (a) levels in children with minimal lesion nephrotic syndrome.

Nakahara C, Kobayashi K, Hamaguchi H, Kanemoto K, Kashiwagi R, Matsui A. Nakahara C, et al. Among authors: kobayashi k. Pediatr Nephrol. 1999 Oct;13(8):657-61. doi: 10.1007/s004670050676. Pediatr Nephrol. 1999. PMID: 10502122

3

Pentanucleotide repeat and size polymorphisms in the apolipoprotein(a) gene are associated with the lipoprotein(a) concentration in chronic hemodialysis patients.

Tanaka M, Yanagi H, Ando R, Kurihara S, Hirano C, Kobayashi K, Kikuchi S, Hamaguchi H, Tsuchiya S, Tomura S. Tanaka M, et al. Among authors: kobayashi k. Nephron. 1999;81(4):414-20. doi: 10.1159/000045325. Nephron. 1999. PMID: 10095177 Clinical Trial.

4

High degree of genetic polymorphism in apolipoprotein(a) associated with plasma lipoprotein(a) levels in Japanese and Chinese populations.

Kikuchi S, Nakagawa A, Kobayashi K, Li L, Yanagi H, Arinami T, Kozu Y, Miyazaki R, Tsuchiya S, Hamaguchi H. Kikuchi S, et al. Among authors: kobayashi k. Hum Genet. 1993 Dec;92(6):537-44. doi: 10.1007/BF00420935. Hum Genet. 1993. PMID: 8262512

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: kobayashi k. Neuropediatrics. 1997 Dec;28(6):335-7. doi: 10.1055/s-2007-973727. Neuropediatrics. 1997. PMID: 9453033

6

Evidence for linkage between the development of asthma in childhood and the T-cell receptor beta chain gene in Japanese.

Noguchi E, Shibasaki M, Arinami T, Takeda K, Kobayashi K, Matsui A, Hamaguchi H. Noguchi E, et al. Among authors: kobayashi k. Genomics. 1998 Jan 1;47(1):121-4. doi: 10.1006/geno.1997.5054. Genomics. 1998. PMID: 9465304

7

Lack of association of atopy/asthma and the interleukin-4 receptor alpha gene in Japanese.

Noguchi E, Shibasaki M, Arinami T, Takeda K, Yokouchi Y, Kobayashi K, Imoto N, Nakahara S, Matsui A, Hamaguchi H. Noguchi E, et al. Among authors: kobayashi k. Clin Exp Allergy. 1999 Feb;29(2):228-33. doi: 10.1046/j.1365-2222.1999.00458.x. Clin Exp Allergy. 1999. PMID: 10051727

8

No association between atopy/asthma and the ILe50Val polymorphism of IL-4 receptor.

Noguchi E, Shibasaki M, Arinami T, Takeda K, Yokouchi Y, Kobayashi K, Imoto N, Nakahara S, Matsui A, Hamaguchi H. Noguchi E, et al. Among authors: kobayashi k. Am J Respir Crit Care Med. 1999 Jul;160(1):342-5. doi: 10.1164/ajrccm.160.1.9807130. Am J Respir Crit Care Med. 1999. PMID: 10390422

9

Plasminogen with type-I mutation in the Chinese Han population.

Li L, Kikuchi S, Arinami T, Kobayashi K, Tsuchiya S, Hamaguchi H. Li L, et al. Among authors: kobayashi k. Clin Genet. 1994 Jun;45(6):285-7. doi: 10.1111/j.1399-0004.1994.tb04031.x. Clin Genet. 1994. PMID: 7923856

10

Autosomal dominant hypoalphalipoproteinemia due to a completely defective apolipoprotein A-I gene.

Nakata K, Kobayashi K, Yanagi H, Shimakura Y, Tsuchiya S, Arinami T, Hamaguchi H. Nakata K, et al. Among authors: kobayashi k. Biochem Biophys Res Commun. 1993 Oct 29;196(2):950-5. doi: 10.1006/bbrc.1993.2341. Biochem Biophys Res Commun. 1993. PMID: 8240372

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