Iida S - Search Results

1

A heterozygous frameshift mutation of the PTEN/MMAC1 gene in a patient with Lhermitte-Duclos disease - only the mutated allele was expressed in the cerebellar tumor.

Iida S, Tanaka Y, Fujii H, Hayashi S, Kimura M, Nagareda T, Moriwaki K. Iida S, et al. Int J Mol Med. 1998 Jun;1(6):925-9. doi: 10.3892/ijmm.1.6.925. Int J Mol Med. 1998. PMID: 9852626

2

A somatic mutation of the p21(Waf1/Cip1) gene in a human adrenocortical adenoma.

Iida S, Fujii H, Moriwaki K. Iida S, et al. Anticancer Res. 1997 Jan-Feb;17(1B):633-6. Anticancer Res. 1997. PMID: 9066592

3

A heterozygous germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease.

Iida S, Nakamura Y, Fujii H, Kimura M, Moriwaki K. Iida S, et al. Int J Mol Med. 1998 Mar;1(3):565-8. doi: 10.3892/ijmm.1.3.565. Int J Mol Med. 1998. PMID: 9852263

4

Familial neurohypophyseal diabetes insipidus associated with a novel mutation in the vasopressin-neurophysin II gene.

Fujii H, Iida S, Moriwaki K. Fujii H, et al. Among authors: iida s. Int J Mol Med. 2000 Mar;5(3):229-34. doi: 10.3892/ijmm.5.3.229. Int J Mol Med. 2000. PMID: 10677561

5

Accelerated decline of blood glucose after intravenous glucose injection in a patient with Cowden disease having a heterozygous germline mutation of the PTEN/MMAC1 gene.

Iida S, Ono A, Sayama K, Hamaguchi T, Fujii H, Nakajima H, Namba M, Hanafusa T, Matsuzawa Y, Moriwaki K. Iida S, et al. Anticancer Res. 2000 May-Jun;20(3B):1901-4. Anticancer Res. 2000. PMID: 10928124

6

An intrasellar cystic mass and hypopituitarism.

Iida S, Fujii H, Tanaka Y, Hayashi S, Nagareda T, Moriwaki K. Iida S, et al. Postgrad Med J. 1996 Jul;72(849):441-2. doi: 10.1136/pgmj.72.849.441. Postgrad Med J. 1996. PMID: 8935611 Free PMC article. No abstract available.

7

[Familial cortisol resistance and mutations of the glucocorticoid receptor gene].

Iida S, Fujii H, Moriwaki K. Iida S, et al. Nihon Rinsho. 1998 Jul;56(7):1887-91. Nihon Rinsho. 1998. PMID: 9702071 Review. Japanese.

8

[Disorders caused by abnormalities of glucocorticoid receptors].

Iida S, Fujii H, Moriwaki K. Iida S, et al. Nihon Rinsho. 2002 Feb;60(2):356-60. Nihon Rinsho. 2002. PMID: 11857926 Review. Japanese.

9

[Cortisol hyperreactive syndrome].

Iida S, Fujii H, Moriwaki K. Iida S, et al. Ryoikibetsu Shokogun Shirizu. 1993;(1):463-5. Ryoikibetsu Shokogun Shirizu. 1993. PMID: 7757642 Review. Japanese. No abstract available.

10

Mutations of human butyrylcholinesterase gene in a family with hypocholinesterasemia.

Iida S, Kinoshita M, Fujii H, Moriyama Y, Nakamura Y, Yura N, Moriwaki K. Iida S, et al. Hum Mutat. 1995;6(4):349-51. doi: 10.1002/humu.1380060411. Hum Mutat. 1995. PMID: 8680411 No abstract available.

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