Kida M - Search Results

1

The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency.

Kida M, Fujioka H, Kosaka Y, Hayashi K, Sakiyama Y, Ariga T. Kida M, et al. Blood Cells Mol Dis. 2008 May-Jun;40(3):410-3. doi: 10.1016/j.bcmd.2007.11.002. Epub 2008 Jan 16. Blood Cells Mol Dis. 2008. PMID: 18201916

2

Novel compound heterozygous mutations in the C3 gene: hereditary C3 deficiency.

Okura Y, Yamada M, Takezaki S, Nawate M, Takahashi Y, Kida M, Kawamura N, Ariga T. Okura Y, et al. Among authors: kida m. Pediatr Int. 2011 Apr;53(2):e16-9. doi: 10.1111/j.1442-200X.2010.03259.x. Pediatr Int. 2011. PMID: 21501302 No abstract available.

3

Analysis of the COL17A1 in non-Herlitz junctional epidermolysis bullosa and amelogenesis imperfecta.

Nakamura H, Sawamura D, Goto M, Nakamura H, Kida M, Ariga T, Sakiyama Y, Tomizawa K, Mitsui H, Tamaki K, Shimizu H. Nakamura H, et al. Among authors: kida m. Int J Mol Med. 2006 Aug;18(2):333-7. Int J Mol Med. 2006. PMID: 16820943

4

De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family.

Kida M, Tsutsumi T, Shindoh M, Ikeda H, Ariga T. Kida M, et al. Eur J Oral Sci. 2009 Dec;117(6):691-4. doi: 10.1111/j.1600-0722.2009.00683.x. Eur J Oral Sci. 2009. PMID: 20121932

5

Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.

Kida M, Ariga T, Shirakawa T, Oguchi H, Sakiyama Y. Kida M, et al. J Dent Res. 2002 Nov;81(11):738-42. doi: 10.1177/0810738. J Dent Res. 2002. PMID: 12407086

6

A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.

Kida M, Sakiyama Y, Matsuda A, Takabayashi S, Ochi H, Sekiguchi H, Minamitake S, Ariga T. Kida M, et al. J Dent Res. 2007 Jan;86(1):69-72. doi: 10.1177/154405910708600111. J Dent Res. 2007. PMID: 17189466

7

Outcomes in two Japanese adenosine deaminase-deficiency patients treated by stem cell gene therapy with no cytoreductive conditioning.

Otsu M, Yamada M, Nakajima S, Kida M, Maeyama Y, Hatano N, Toita N, Takezaki S, Okura Y, Kobayashi R, Matsumoto Y, Tatsuzawa O, Tsuchida F, Kato S, Kitagawa M, Mineno J, Hershfield MS, Bali P, Candotti F, Onodera M, Kawamura N, Sakiyama Y, Ariga T. Otsu M, et al. Among authors: kida m. J Clin Immunol. 2015 May;35(4):384-98. doi: 10.1007/s10875-015-0157-1. Epub 2015 Apr 15. J Clin Immunol. 2015. PMID: 25875699

8

Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation.

Lee SK, Lee KE, Hwang YH, Kida M, Tsutsumi T, Ariga T, Park JC, Kim JW. Lee SK, et al. Among authors: kida m. Oral Dis. 2011 Apr;17(3):314-9. doi: 10.1111/j.1601-0825.2010.01760.x. Epub 2010 Oct 28. Oral Dis. 2011. PMID: 21029264

9

A case of needle tract seeding of pancreatic adenosquamous carcinoma after a single endoscopic ultrasound-guided tissue acquisition.

Hanaoka T, Okuwaki K, Nishizawa N, Watanabe M, Adachi K, Tamaki A, Iwai T, Kida M, Kumamoto Y, Kusano C. Hanaoka T, et al. Among authors: kida m. Clin J Gastroenterol. 2024 Nov 21. doi: 10.1007/s12328-024-02068-w. Online ahead of print. Clin J Gastroenterol. 2024. PMID: 39570504

10

Incidence of Cholecystitis After Endoscopic Biliary Drainage Using a Low Axial Force Covered Self-Expandable Metallic Stent in Patients With Malignant Distal Biliary Obstruction: A Multicenter Prospective Study.

Minato N, Okuwaki K, Watanabe M, Woo J, Matsumoto T, Tadehara M, Kaneko T, Ishizaki J, Iwai T, Imaizumi H, Kida M, Haradome H, Kusano C. Minato N, et al. Among authors: kida m. J Gastroenterol Hepatol. 2024 Nov 20. doi: 10.1111/jgh.16824. Online ahead of print. J Gastroenterol Hepatol. 2024. PMID: 39567461

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