Fujieda K - Search Results

1

Ueda O, Fujieda K. Ueda O, et al. Among authors: fujieda k. Nihon Rinsho. 2006 Sep 28;Suppl 3:119-21. Nihon Rinsho. 2006. PMID: 17022513 Review. Japanese. No abstract available.

2

Molecular basis of neonatal diabetes in Japanese patients.

Suzuki S, Makita Y, Mukai T, Matsuo K, Ueda O, Fujieda K. Suzuki S, et al. Among authors: fujieda k. J Clin Endocrinol Metab. 2007 Oct;92(10):3979-85. doi: 10.1210/jc.2007-0486. Epub 2007 Jul 17. J Clin Endocrinol Metab. 2007. PMID: 17635943

3

A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variation.

Suzuki S, Kokumai T, Furuya A, Nagamori T, Matsuo K, Ueda O, Mukai T, Ito Y, Yano K, Fujieda K, Okuno A, Tanahashi Y, Azuma H. Suzuki S, et al. Among authors: fujieda k. Eur J Med Genet. 2020 Nov;63(11):104039. doi: 10.1016/j.ejmg.2020.104039. Epub 2020 Aug 14. Eur J Med Genet. 2020. PMID: 32805445

4

A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expression.

Suzuki S, Matsuo K, Ito Y, Kobayashi A, Kokumai T, Furuya A, Ueda O, Mukai T, Yano K, Fujieda K, Okuno A, Tanahashi Y, Azuma H. Suzuki S, et al. Among authors: fujieda k. Eur J Endocrinol. 2021 May 21;185(1):1-12. doi: 10.1530/EJE-20-1313. Eur J Endocrinol. 2021. PMID: 33886498

5

[Kallmann syndrome].

Fujieda K, Mukai T. Fujieda K, et al. Nihon Rinsho. 2006 Apr;64 Suppl 4:47-53. Nihon Rinsho. 2006. PMID: 16689283 Review. Japanese. No abstract available.

6

[Klinefelter syndrome].

Fujieda K. Fujieda K. Nihon Rinsho. 2006 Jun 28;Suppl 2:487-90. Nihon Rinsho. 2006. PMID: 16817447 Review. Japanese. No abstract available.

7

[Adrenogenital syndrome].

Fujieda K. Fujieda K. Nihon Rinsho. 2006 Jun 28;Suppl 2:643-6. Nihon Rinsho. 2006. PMID: 16817483 Review. Japanese. No abstract available.

8

[Leprechaunism (Donohue syndrome)].

Fujieda K. Fujieda K. Nihon Rinsho. 2006 Sep 28;Suppl 3:94-9. Nihon Rinsho. 2006. PMID: 17022508 Review. Japanese. No abstract available.

9

[Prader-Willi syndrome].

Fujieda K. Fujieda K. Nihon Rinsho. 2006 Jun 28;Suppl 2:229-33. Nihon Rinsho. 2006. PMID: 16817390 Review. Japanese. No abstract available.

10

[Leprechaunism caused by mutations in the insulin receptor gene].

Murashita M, Tajima T, Nakae J, Fujieda K. Murashita M, et al. Among authors: fujieda k. Nihon Rinsho. 2002 Feb;60(2):344-9. Nihon Rinsho. 2002. PMID: 11857924 Review. Japanese.

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