Adachi M - Search Results

1

[Urological problems in Prader-Willi syndrome].

Sano K, Terashima K, Adachi M, Tachibana K. Sano K, et al. Among authors: adachi m. Nihon Hinyokika Gakkai Zasshi. 1994 Aug;85(8):1218-22. doi: 10.5980/jpnjurol1989.85.1218. Nihon Hinyokika Gakkai Zasshi. 1994. PMID: 7933754 Free article. Clinical Trial. Japanese.

2

[A case of aphallia].

Nakaigawa N, Terashima K, Adachi M, Tachibana K. Nakaigawa N, et al. Among authors: adachi m. Hinyokika Kiyo. 1996 Sep;42(9):695-7. Hinyokika Kiyo. 1996. PMID: 8918673 Free article. Review. Japanese.

3

Monthly urinary gonadotropin and ovarian hormone excretory patterns in normal girls and female patients with idiopathic precocious puberty.

Maesaka H, Tachibana K, Adachi M, Okada T. Maesaka H, et al. Among authors: adachi m. Pediatr Res. 1996 Dec;40(6):853-60. doi: 10.1203/00006450-199612000-00013. Pediatr Res. 1996. PMID: 8947962

4

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: adachi m. 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

5

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: adachi m. Eur J Pediatr. 1997 Aug;156(8):631-5. doi: 10.1007/s004310050680. Eur J Pediatr. 1997. PMID: 9266196

6

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. Eur J Pediatr. 1998 Jan;157(1):34-8. doi: 10.1007/s004310050762. Eur J Pediatr. 1998. PMID: 9461360

7

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: adachi m. 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

8

A male patient presenting with major clinical symptoms of glucocorticoid deficiency and skeletal dysplasia, showing a steroid pattern compatible with 17alpha-hydroxylase/17,20-lyase deficiency, but without obvious CYP17 gene mutations.

Adachi M, Tachibana K, Asakura Y, Suwa S, Nishimura G. Adachi M, et al. Endocr J. 1999 Apr;46(2):285-92. doi: 10.1507/endocrj.46.285. Endocr J. 1999. PMID: 10460013 Free article.

9

Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features.

Adachi M, Tachibana K, Asakura Y, Muroya K, Ogata T. Adachi M, et al. Hum Genet. 2000 Mar;106(3):306-10. doi: 10.1007/s004390051042. Hum Genet. 2000. PMID: 10798359

10

Shinkai M, Ohhama Y, Nishi T, Yamamoto H, Fujita S, Take H, Adachi M, Tachibana K, Aida N, Kato K, Tanaka Y, Takemiya S, Tanaka K. Shinkai M, et al. Among authors: adachi m. Transplant Proc. 2000 Nov;32(7):2184. doi: 10.1016/s0041-1345(00)01626-2. Transplant Proc. 2000. PMID: 11120124 No abstract available.

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