Hamada T - Search Results

1

Generalized dystonia and striatal calcifications with lipoid proteinosis.

Teive HA, Pereira ER, Zavala JA, Lange MC, de Paola L, Raskin S, Werneck LC, Hamada T, McGrath JA. Teive HA, et al. Among authors: hamada t. Neurology. 2004 Dec 14;63(11):2168-9. doi: 10.1212/01.wnl.0000145602.64073.c2. Neurology. 2004. PMID: 15596773

2

Molecular basis of lipoid proteinosis in a Libyan family.

Chan I, El-Zurghany A, Zendah B, Benghazil M, Oyama N, Hamada T, McGrath JA. Chan I, et al. Among authors: hamada t. Clin Exp Dermatol. 2003 Sep;28(5):545-8. doi: 10.1046/j.1365-2230.2003.01341.x. Clin Exp Dermatol. 2003. PMID: 12950350

3

Clinical and molecular characterization of lipoid proteinosis in Namaqualand, South Africa.

Van Hougenhouck-Tulleken W, Chan I, Hamada T, Thornton H, Jenkins T, McLean WH, McGrath JA, Ramsay M. Van Hougenhouck-Tulleken W, et al. Among authors: hamada t. Br J Dermatol. 2004 Aug;151(2):413-23. doi: 10.1111/j.1365-2133.2004.06076.x. Br J Dermatol. 2004. PMID: 15327549

4

Clinical and molecular abnormalities in lipoid proteinosis.

Desmet S, Devos SA, Chan I, Hamada T, Dhooge I, McGrath JA, Naeyaert JM. Desmet S, et al. Among authors: hamada t. Eur J Dermatol. 2005 Sep-Oct;15(5):344-6. Eur J Dermatol. 2005. PMID: 16172042

5

Lipoid proteinosis.

Hamada T. Hamada T. Clin Exp Dermatol. 2002 Nov;27(8):624-9. doi: 10.1046/j.1365-2230.2002.01143.x. Clin Exp Dermatol. 2002. PMID: 12472532 Review.

6

Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia.

Kantaputra PN, Hamada T, Kumchai T, McGrath JA. Kantaputra PN, et al. Among authors: hamada t. J Dent Res. 2003 Jun;82(6):433-7. doi: 10.1177/154405910308200606. J Dent Res. 2003. PMID: 12766194

7

Progressive osseous heteroplasia resulting from a new mutation in the GNAS1 gene.

Chan I, Hamada T, Hardman C, McGrath JA, Child FJ. Chan I, et al. Among authors: hamada t. Clin Exp Dermatol. 2004 Jan;29(1):77-80. doi: 10.1111/j.1365-2230.2004.01439.x. Clin Exp Dermatol. 2004. PMID: 14723729

8

Spinocerebellar ataxia type 1 and familial spontaneous pneumothorax.

Fukazawa T, Sasaki H, Kikuchi S, Hamada K, Hamada T, Tashiro K. Fukazawa T, et al. Among authors: hamada t, hamada k. Neurology. 1997 Nov;49(5):1460-2. doi: 10.1212/wnl.49.5.1460. Neurology. 1997. PMID: 9371943

9

Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation.

Hamada T, Yasumoto S, Karashima T, Ishii N, Shimada H, Kawano Y, Imayama S, McGrath JA, Hashimoto T. Hamada T, et al. Br J Dermatol. 2007 Sep;157(3):605-8. doi: 10.1111/j.1365-2133.2007.08086.x. Epub 2007 Jul 16. Br J Dermatol. 2007. PMID: 17635506 No abstract available.

10

Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1.

Hamada T, South AP, Mitsuhashi Y, Kinebuchi T, Bleck O, Ashton GH, Hozumi Y, Suzuki T, Hashimoto T, Eady RA, McGrath JA. Hamada T, et al. Exp Dermatol. 2002 Apr;11(2):107-14. doi: 10.1034/j.1600-0625.2002.110202.x. Exp Dermatol. 2002. PMID: 11994137

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