Kuwajima K - Search Results

1

Hyper-response of serum IgG1 to Staphylococcus aureus peptidoglycan in patients with hyper-IgE syndrome.

Ishizaka A, Kojima K, Sakiyama Y, Matsumoto S, Kuwajima K, Wagatsuma Y, Shibata R, Joh K. Ishizaka A, et al. Among authors: kuwajima k. Clin Exp Immunol. 1992 Jan;87(1):53-7. doi: 10.1111/j.1365-2249.1992.tb06412.x. Clin Exp Immunol. 1992. PMID: 1733637 Free PMC article.

2

Insulin binding to circulating monocytes in children with insulin-dependent and non-insulin-dependent diabetes mellitus.

Kida K, Goto Y, Watanabe N, Kaino Y, Miyagawa T, Inoue T, Ikeuchi M, Matsuda H, Kuwajima K. Kida K, et al. Among authors: kuwajima k. Diabetes Res Clin Pract. 1988 Feb 19;4(3):161-6. doi: 10.1016/s0168-8227(88)80013-5. Diabetes Res Clin Pract. 1988. PMID: 3282856

3

Familial occurrence of ring chromosome 15.

Horigome Y, Kondo I, Kuwajima K, Suzuki T. Horigome Y, et al. Among authors: kuwajima k. Clin Genet. 1992 Apr;41(4):178-80. doi: 10.1111/j.1399-0004.1992.tb03659.x. Clin Genet. 1992. PMID: 1576754

4

Limitations of urinary telomerase activity measurement in urothelial cancer.

Arai Y, Yajima T, Yagihashi A, Kobayashi D, Kameshima H, Sasaki M, Tanaka K, Kuwajima K, Miyao N, Tsukamoto T, Watanabe N. Arai Y, et al. Among authors: kuwajima k. Clin Chim Acta. 2000 Jun;296(1-2):35-44. doi: 10.1016/s0009-8981(00)00202-3. Clin Chim Acta. 2000. PMID: 10807969

5

Identification of a single cytosine base insertion mutation at Arg-597 of the beta subunit of the human epithelial sodium channel in a family with Liddle's disease.

Inoue T, Okauchi Y, Matsuzaki Y, Kuwajima K, Kondo H, Horiuchi N, Nakao K, Iwata M, Yokogoshi Y, Shintani Y, Bando H, Saito S. Inoue T, et al. Among authors: kuwajima k. Eur J Endocrinol. 1998 Jun;138(6):691-7. doi: 10.1530/eje.0.1380691. Eur J Endocrinol. 1998. PMID: 9678538 Review.

6

Weaver syndrome in two Japanese children.

Kondo I, Mori Y, Kuwajima K. Kondo I, et al. Among authors: kuwajima k. Am J Med Genet. 1991 Nov 1;41(2):221-4. doi: 10.1002/ajmg.1320410218. Am J Med Genet. 1991. PMID: 1785638 Review.

7

Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.

Mizugishi K, Yamanaka K, Kuwajima K, Kondo I. Mizugishi K, et al. Among authors: kuwajima k. J Hum Genet. 1998;43(3):178-81. doi: 10.1007/s100380050064. J Hum Genet. 1998. PMID: 9747030

8

Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2).

Kondo I, Matsuura S, Kuwajima K, Tokashiki M, Izumikawa Y, Naritomi K, Niikawa N, Kajii T. Kondo I, et al. Among authors: kuwajima k. Am J Med Genet. 1991 Nov 1;41(2):225-9. doi: 10.1002/ajmg.1320410219. Am J Med Genet. 1991. PMID: 1785639

9

A Japanese male infant with the Weaver syndrome.

Kondo I, Mori Y, Kuwajima K. Kondo I, et al. Among authors: kuwajima k. Jinrui Idengaku Zasshi. 1990 Sep;35(3):257-62. doi: 10.1007/BF01876855. Jinrui Idengaku Zasshi. 1990. PMID: 2266602

10

A Japanese patient with the Dubowitz syndrome.

Kondo I, Takeda K, Kuwajima K, Hirano T. Kondo I, et al. Among authors: kuwajima k. Clin Genet. 1987 Jun;31(6):389-92. doi: 10.1111/j.1399-0004.1987.tb02830.x. Clin Genet. 1987. PMID: 3621642

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