Hasegawa Y - Search Results

1

Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata.

Hasegawa T, Ogata T, Hasegawa Y, Honda M, Nagai T, Fukushima Y, Nakahori Y, Matsuo N. Hasegawa T, et al. Among authors: hasegawa y. Hum Genet. 1996 May;97(5):564-7. doi: 10.1007/BF02281861. Hum Genet. 1996. PMID: 8655131

2

EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generations.

Hasegawa T, Hasegawa Y, Asamura S, Nagai T, Tsuchiya Y, Ninomiya M, Fukushima Y. Hasegawa T, et al. Among authors: hasegawa y. Clin Genet. 1991 Sep;40(3):202-6. doi: 10.1111/j.1399-0004.1991.tb03077.x. Clin Genet. 1991. PMID: 1773535

3

Proximal renal tubular acidosis associated with glycogen storage disease, type 9.

Nagai T, Matsuo N, Tsuchiya Y, Cho H, Hasegawa Y, Igarashi Y. Nagai T, et al. Among authors: hasegawa y. Acta Paediatr Scand. 1988 May;77(3):460-3. doi: 10.1111/j.1651-2227.1988.tb10681.x. Acta Paediatr Scand. 1988. PMID: 3164568

4

HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia) associated with del(10)(p13).

Hasegawa T, Hasegawa Y, Aso T, Koto S, Nagai T, Tsuchiya Y, Kim KC, Ohashi H, Wakui K, Fukushima Y. Hasegawa T, et al. Among authors: hasegawa y. Am J Med Genet. 1997 Dec 31;73(4):416-8. doi: 10.1002/(sici)1096-8628(19971231)73:4<416::aid-ajmg9>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9415468 Review.

5

GATA3 abnormalities and the phenotypic spectrum of HDR syndrome.

Muroya K, Hasegawa T, Ito Y, Nagai T, Isotani H, Iwata Y, Yamamoto K, Fujimoto S, Seishu S, Fukushima Y, Hasegawa Y, Ogata T. Muroya K, et al. Among authors: hasegawa t, hasegawa y. J Med Genet. 2001 Jun;38(6):374-80. doi: 10.1136/jmg.38.6.374. J Med Genet. 2001. PMID: 11389161 Free PMC article.

6

Turner syndrome and Xp deletions: clinical and molecular studies in 47 patients.

Ogata T, Muroya K, Matsuo N, Shinohara O, Yorifuji T, Nishi Y, Hasegawa Y, Horikawa R, Tachibana K. Ogata T, et al. Among authors: hasegawa y. J Clin Endocrinol Metab. 2001 Nov;86(11):5498-508. doi: 10.1210/jcem.86.11.8058. J Clin Endocrinol Metab. 2001. PMID: 11701728 Clinical Trial.

7

Increase in free insulin-like growth factor-I levels in precocious and normal puberty.

Yamada M, Hasegawa T, Hasegawa Y. Yamada M, et al. Among authors: hasegawa t, hasegawa y. Endocr J. 1998 Jun;45(3):407-12. doi: 10.1507/endocrj.45.407. Endocr J. 1998. PMID: 9790277 Free article.

8

Absence of proteolysis of insulin-like growth factor binding protein-3 in serum from patients with growth hormone deficiency.

Yamada M, Hasegawa T, Hasegawa Y. Yamada M, et al. Among authors: hasegawa t, hasegawa y. Endocr J. 1999 Oct;46(5):717-22. doi: 10.1507/endocrj.46.717. Endocr J. 1999. PMID: 10670759 Free article.

9

Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns.

Matsuo M, Muroya K, Nanao K, Hasegawa Y, Terasaki H, Kosaki K, Ogata T. Matsuo M, et al. Among authors: hasegawa y. Am J Med Genet. 2000 Apr 10;91(4):267-72. Am J Med Genet. 2000. PMID: 10766981 Review.

10

Partial growth hormone deficiency with pituitary stalk transection.

Hasegawa T, Hasegawa Y, Yokoyama T, Koto S, Tsuchiya Y. Hasegawa T, et al. Among authors: hasegawa y. Endocrinol Jpn. 1991 Oct;38(5):573-5. doi: 10.1507/endocrj1954.38.573. Endocrinol Jpn. 1991. PMID: 1668835 Free article.

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