Tatsumi K - Search Results

1

Analysis of the KAL1 gene in 19 Japanese patients with Kallmann syndrome.

Izumi Y, Tatsumi K, Okamoto S, Ogawa T, Hosokawa A, Matsuo T, Kato Y, Fukui H, Amino N. Izumi Y, et al. Among authors: tatsumi k. Endocr J. 2001 Apr;48(2):143-9. doi: 10.1507/endocrj.48.143. Endocr J. 2001. PMID: 11456260 Free article.

2

A novel mutation of the KAL1 gene in Kallmann syndrome.

Izumi Y, Tatsumi K, Okamoto S, Hosokawa A, Ueno S, Fukui H, Amino N. Izumi Y, et al. Among authors: tatsumi k. Endocr J. 1999 Oct;46(5):651-8. doi: 10.1507/endocrj.46.651. Endocr J. 1999. PMID: 10670750 Free article.

3

A novel mutation of the KAL1 gene in monozygotic twins with Kallmann syndrome.

Matsuo T, Okamoto S, Izumi Y, Hosokawa A, Takegawa T, Fukui H, Tun Z, Honda K, Matoba R, Tatsumi K, Amino N. Matsuo T, et al. Among authors: tatsumi k. Eur J Endocrinol. 2000 Dec;143(6):783-7. doi: 10.1530/eje.0.1430783. Eur J Endocrinol. 2000. PMID: 11124862

4

A novel E250X mutation of the PIT1 gene in a patient with combined pituitary hormone deficiency.

Irie Y, Tatsumi K, Ogawa M, Kamijo T, Preeyasombat C, Suprasongsin C, Amino N. Irie Y, et al. Among authors: tatsumi k. Endocr J. 1995 Jun;42(3):351-4. doi: 10.1507/endocrj.42.351. Endocr J. 1995. PMID: 7670563 Free article.

5

PIT1 abnormality.

Tatsumi K, Amino N. Tatsumi K, et al. Growth Horm IGF Res. 1999 Jun;9 Suppl B:18-22; discussion 23. doi: 10.1016/s1096-6374(99)80076-8. Growth Horm IGF Res. 1999. PMID: 10549301 Review.

6

A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect.

Fujiwara H, Tatsumi K, Tanaka S, Kimura M, Nose O, Amino N. Fujiwara H, et al. Among authors: tatsumi k. Thyroid. 2000 Jun;10(6):471-4. doi: 10.1089/thy.2000.10.471. Thyroid. 2000. PMID: 10907989

7

Nucleotide sequence of the complementary DNA for human Pit-1/GHF-1.

Tatsumi K, Notomi T, Amino N, Miyai K. Tatsumi K, et al. Biochim Biophys Acta. 1992 Jan 6;1129(2):231-4. doi: 10.1016/0167-4781(92)90494-k. Biochim Biophys Acta. 1992. PMID: 1370379

8

[Molecular pathology of congenital pituitary hypothyroidism--discovery of new clinical entities].

Tatsumi K, Amino N, Miyai K. Tatsumi K, et al. Rinsho Byori. 1993 May;41(5):533-40. Rinsho Byori. 1993. PMID: 8350517 Japanese.

9

[The pituitary specific transcription factor Pit-1/GHF-1 and PIT1 abnormality].

Tatsumi K, Amino N. Tatsumi K, et al. Rinsho Byori. 1997 Jul;45(7):656-9. Rinsho Byori. 1997. PMID: 9256012 Review. Japanese.

10

Recurrent T354P mutation of the Na+/I- symporter in patients with iodide transport defect.

Fujiwara H, Tatsumi K, Miki K, Harada T, Okada S, Nose O, Kodama S, Amino N. Fujiwara H, et al. Among authors: tatsumi k. J Clin Endocrinol Metab. 1998 Aug;83(8):2940-3. doi: 10.1210/jcem.83.8.5029. J Clin Endocrinol Metab. 1998. PMID: 9709973

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