Nagai T - Search Results

1

Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.

Hamabe J, Fukushima Y, Harada N, Abe K, Matsuo N, Nagai T, Yoshioka A, Tonoki H, Tsukino R, Niikawa N. Hamabe J, et al. Among authors: nagai t. Am J Med Genet. 1991 Oct 1;41(1):54-63. doi: 10.1002/ajmg.1320410116. Am J Med Genet. 1991. PMID: 1683159

2

Standard growth curves for Japanese patients with Prader-Willi syndrome.

Nagai T, Matsuo N, Kayanuma Y, Tonoki H, Fukushima Y, Ohashi H, Murai T, Hasegawa T, Kuroki Y, Niikawa N. Nagai T, et al. Am J Med Genet. 2000 Nov 13;95(2):130-4. doi: 10.1002/1096-8628(20001113)95:2<130::aid-ajmg7>3.0.co;2-r. Am J Med Genet. 2000. PMID: 11078562

3

Del(12)(p11.21p12.2) associated with an asphyxiating thoracic dystrophy or chondroectodermal dysplasia-like syndrome.

Nagai T, Nishimura G, Kato R, Hasegawa T, Ohashi H, Fukushima Y. Nagai T, et al. Am J Med Genet. 1995 Jan 2;55(1):16-8. doi: 10.1002/ajmg.1320550106. Am J Med Genet. 1995. PMID: 7702088

4

Japanese kindred with FG syndrome.

Kato R, Niikawa N, Nagai T, Fukushima Y. Kato R, et al. Among authors: nagai t. Am J Med Genet. 1994 Aug 15;52(2):242-3. doi: 10.1002/ajmg.1320520226. Am J Med Genet. 1994. PMID: 7802020 No abstract available.

5

The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

Ohta T, Tohma T, Soejima H, Fukushima Y, Nagai T, Yoshiura K, Jinno Y, Niikawa N. Ohta T, et al. Among authors: nagai t. Hum Genet. 1993 Aug;92(1):1-5. doi: 10.1007/BF00216136. Hum Genet. 1993. PMID: 8365720

6

Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locus.

Muroya K, Ogata T, Matsuo N, Nagai T, Franco B, Ballabio A, Rappold G, Sakura N, Fukushima Y. Muroya K, et al. Among authors: nagai t. Am J Med Genet. 1996 Sep 6;64(4):583-7. doi: 10.1002/(SICI)1096-8628(19960906)64:4<583::AID-AJMG11>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8870926

7

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: nagai t. 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.

8

No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients.

Kobayashi S, Uemura H, Kohda T, Nagai T, Chinen Y, Naritomi K, Kinoshita EI, Ohashi H, Imaizumi K, Tsukahara M, Sugio Y, Tonoki H, Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, Kaneko-Ishino T, Ishino F. Kobayashi S, et al. Among authors: nagai t. Am J Med Genet. 2001 Dec 1;104(3):225-31. Am J Med Genet. 2001. PMID: 11754049

9

Cause of sudden, unexpected death of Prader-Willi syndrome patients with or without growth hormone treatment.

Nagai T, Obata K, Tonoki H, Temma S, Murakami N, Katada Y, Yoshino A, Sakazume S, Takahashi E, Sakuta R, Niikawa N. Nagai T, et al. Am J Med Genet A. 2005 Jul 1;136(1):45-8. doi: 10.1002/ajmg.a.30777. Am J Med Genet A. 2005. PMID: 15937939

10

Growth hormone therapy and scoliosis in patients with Prader-Willi syndrome.

Nagai T, Obata K, Ogata T, Murakami N, Katada Y, Yoshino A, Sakazume S, Tomita Y, Sakuta R, Niikawa N. Nagai T, et al. Am J Med Genet A. 2006 Aug 1;140(15):1623-7. doi: 10.1002/ajmg.a.31295. Am J Med Genet A. 2006. PMID: 16770808

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

3,732 results

Search Page