Sakurai A - Search Results

1

Comprehensive genetics clinic for familial tumors: proposal for a suitable system in Japan.

Fukushima Y, Sakurai A. Fukushima Y, et al. Among authors: sakurai a. Int J Clin Oncol. 2004 Aug;9(4):304-7. doi: 10.1007/s10147-004-0405-5. Int J Clin Oncol. 2004. PMID: 15375707 Review.

2

Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1.

Sakurai A, Shirahama S, Fujimori M, Katai M, Itakura Y, Kobayashi S, Amano J, Fukushima Y, Hashizume K. Sakurai A, et al. J Hum Genet. 1998;43(3):199-201. doi: 10.1007/s100380050070. J Hum Genet. 1998. PMID: 9747036

3

Identification of two novel mutations in the OCRL1 gene in Japanese families with Lowe syndrome.

Kubota T, Sakurai A, Arakawa K, Shimazu M, Wakui K, Furihata K, Fukushima Y. Kubota T, et al. Among authors: sakurai a. Clin Genet. 1998 Sep;54(3):199-202. doi: 10.1111/j.1399-0004.1998.tb04284.x. Clin Genet. 1998. PMID: 9788721

4

Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidism.

Fujimori M, Shirahama S, Sakurai A, Hashizume K, Hama Y, Ito K, Shingu K, Kobayashi S, Amano J, Fukushima Y. Fujimori M, et al. Among authors: sakurai a. Am J Med Genet. 1998 Nov 16;80(3):221-2. doi: 10.1002/(sici)1096-8628(19981116)80:3<221::aid-ajmg8>3.0.co;2-1. Am J Med Genet. 1998. PMID: 9843042

5

Multiple endocrine neoplasia type 1 concomitant with Prader-Willi syndrome: case report and genetic diagnosis.

Nakajima K, Sakurai A, Kubota T, Katai M, Mori J, Aizawa T, Fukushima Y, Hashizume K. Nakajima K, et al. Among authors: sakurai a. Am J Med Sci. 1999 May;317(5):346-9. doi: 10.1097/00000441-199905000-00012. Am J Med Sci. 1999. PMID: 10334123

6

[Septo-optic dysplasia].

Sakurai A, Fukushima Y. Sakurai A, et al. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):625-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528932 Review. Japanese. No abstract available.

7

[SHORT syndrome].

Sakurai A, Fukushima Y. Sakurai A, et al. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):629-30. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528934 Review. Japanese. No abstract available.

8

[von Hippel-Lindau syndrome].

Sakurai A, Fukushima Y. Sakurai A, et al. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):799-801. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11529029 Review. Japanese. No abstract available.

9

[Genetic testing and counseling for familial tumor syndromes].

Katai M, Sakurai A, Fukushima Y. Katai M, et al. Among authors: sakurai a. Gan To Kagaku Ryoho. 2002 Apr;29(4):502-7. Gan To Kagaku Ryoho. 2002. PMID: 11977532 Japanese.

10

[Genetic test and genetic counseling of diabetes].

Sakurai A, Fukushima Y. Sakurai A, et al. Nihon Rinsho. 2002 Aug;60 Suppl 8:293-7. Nihon Rinsho. 2002. PMID: 12355762 Review. Japanese. No abstract available.

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