Tachibana K - Search Results

1

Idiopathic hypoparathyroidism in two patients with 22q11 microdeletion.

Makita Y, Masuno M, Maizumi K, Tachibana K, Kuroki Y, Kurahashi H. Makita Y, et al. Among authors: tachibana k. J Med Genet. 1995 Aug;32(8):669. doi: 10.1136/jmg.32.8.669. J Med Genet. 1995. PMID: 7473668 Free PMC article. No abstract available.

2

Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion.

Adachi M, Tachibana K, Masuno M, Makita Y, Maesaka H, Okada T, Hizukuri K, Imaizumi K, Kuroki Y, Kurahashi H, Suwa S. Adachi M, et al. Among authors: tachibana k. Eur J Pediatr. 1998 Jan;157(1):34-8. doi: 10.1007/s004310050762. Eur J Pediatr. 1998. PMID: 9461360

3

SPONASTRIME dysplasia: report on a female patient with severe skeletal changes.

Masuno M, Nishimura G, Adachi M, Hotsubo T, Tachibana K, Makita Y, Imaizumi K, Kuroki Y. Masuno M, et al. Among authors: tachibana k. Am J Med Genet. 1996 Dec 30;66(4):429-32. doi: 10.1002/(SICI)1096-8628(19961230)66:4<429::AID-AJMG8>3.0.CO;2-F. Am J Med Genet. 1996. PMID: 8989461

4

Young-Simpson syndrome: further delineation of a distinct syndrome with congenital hypothyroidism, congenital heart defects, facial dysmorphism, and mental retardation.

Masuno M, Imaizumi K, Okada T, Adachi M, Nishimura G, Ishii T, Tachibana K, Kuroki Y. Masuno M, et al. Among authors: tachibana k. Am J Med Genet. 1999 May 7;84(1):8-11. doi: 10.1002/(sici)1096-8628(19990507)84:1<8::aid-ajmg2>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10213038

5

Premature thelarche in Rubinstein-Taybi syndrome.

Kurosawa K, Masuno M, Imaizumi K, Matsuo M, Kuroki Y, Tachibana K. Kurosawa K, et al. Among authors: tachibana k. Am J Med Genet. 2002 Apr 15;109(1):72-3. doi: 10.1002/ajmg.10297. Am J Med Genet. 2002. PMID: 11932997 Review. No abstract available.

6

Cerebro-costo-mandibular syndrome. A case report and review of the literature.

Tachibana K, Yamamoto Y, Osaki E, Kuroki Y. Tachibana K, et al. Hum Genet. 1980;54(2):283-6. doi: 10.1007/BF00278987. Hum Genet. 1980. PMID: 7390499

7

Osteopathia striata, short stature, and characteristic facies: a previously unknown skeletal dysplasia.

Nishimura G, Okada T, Tachibana K, Adachi M, Masuno M, Imaizumi K, Aida N. Nishimura G, et al. Among authors: tachibana k. Eur J Pediatr. 1997 Aug;156(8):631-5. doi: 10.1007/s004310050680. Eur J Pediatr. 1997. PMID: 9266196

8

Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: molecular analysis in four patients.

Muroya K, Ishii T, Nakahori Y, Asakura Y, Tachibana K, Masuno M, Imaizumi K, Tanaka Y, Kawada Y, Yukizane S, Ogata T. Muroya K, et al. Among authors: tachibana k. Genes Chromosomes Cancer. 1999 May;25(1):40-5. doi: 10.1002/(sici)1098-2264(199905)25:1<40::aid-gcc6>3.0.co;2-8. Genes Chromosomes Cancer. 1999. PMID: 10221338

9

Longitudinal growth and height velocity of Japanese children with Down's syndrome.

Kimura J, Tachibana K, Imaizumi K, Kurosawa K, Kuroki Y. Kimura J, et al. Among authors: tachibana k. Acta Paediatr. 2003 Sep;92(9):1039-42. doi: 10.1080/08035250310004306. Acta Paediatr. 2003. PMID: 14599066

10

Generalized skeletal dysplasia in mother and daughter with 22q11 deletion syndrome.

Adachi M, Tachibana K, Asakura Y, Nishimura G, Fukushima Y, Sakazume S. Adachi M, et al. Among authors: tachibana k. Am J Med Genet A. 2003 Mar 15;117A(3):295-8. doi: 10.1002/ajmg.a.10915. Am J Med Genet A. 2003. PMID: 12599196 No abstract available.

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