McGrath JA - Search Results

1

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: mcgrath ja. Br J Dermatol. 2004 Aug;151(2):413-23. doi: 10.1111/j.1365-2133.2004.06076.x. Br J Dermatol. 2004. PMID: 15327549

2

Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated cases.

Mellerio JE, Smith FJ, McMillan JR, McLean WH, McGrath JA, Morrison GA, Tierney P, Albert DM, Wiche G, Leigh IM, Geddes JF, Lane EB, Uitto J, Eady RA. Mellerio JE, et al. Among authors: mcgrath ja. Br J Dermatol. 1997 Dec;137(6):898-906. Br J Dermatol. 1997. PMID: 9470905

3

Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex.

Corden LD, Mellerio JE, Gratian MJ, Eady RA, Harper JI, Lacour M, Magee G, Lane EB, McGrath JA, McLean WH. Corden LD, et al. Among authors: mcgrath ja. Hum Mutat. 1998;11(4):279-85. doi: 10.1002/(SICI)1098-1004(1998)11:4<279::AID-HUMU5>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9554744

4

The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21.

Whittock NV, Coleman CM, McLean WH, Ashton GH, Acland KM, Eady RA, McGrath JA. Whittock NV, et al. Among authors: mcgrath ja. J Invest Dermatol. 2000 Oct;115(4):694-8. doi: 10.1046/j.1523-1747.2000.00097.x. J Invest Dermatol. 2000. PMID: 10998145 Free article.

5

Genomic localization, organization and amplification of the human zinc transporter protein gene, ZNT4, and exclusion as a candidate gene in different clinical variants of acrodermatitis enteropathica.

Bleck O, Ashton GH, Mallipeddi R, South AP, Whittock NV, McLean WH, Atherton DJ, McGrath JA. Bleck O, et al. Among authors: mcgrath ja. Arch Dermatol Res. 2001 Aug;293(8):392-6. doi: 10.1007/s004030100246. Arch Dermatol Res. 2001. PMID: 11686514

6

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis.

South AP, Ashton GH, Willoughby C, Ellis IH, Bleck O, Hamada T, Mannion G, Wessagowit V, Hashimoto T, Eady RA, McGrath JA. South AP, et al. Among authors: mcgrath ja. Br J Dermatol. 2002 Feb;146(2):216-20. doi: 10.1046/j.1365-2133.2002.04638.x. Br J Dermatol. 2002. PMID: 11903230

7

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. Among authors: mcgrath ja. Exp Dermatol. 2002 Apr;11(2):107-14. doi: 10.1034/j.1600-0625.2002.110202.x. Exp Dermatol. 2002. PMID: 11994137

8

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: mcgrath ja. Clin Exp Dermatol. 2003 Sep;28(5):545-8. doi: 10.1046/j.1365-2230.2003.01341.x. Clin Exp Dermatol. 2003. PMID: 12950350

9

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: mcgrath ja. Clin Exp Dermatol. 2004 Jan;29(1):77-80. doi: 10.1111/j.1365-2230.2004.01439.x. Clin Exp Dermatol. 2004. PMID: 14723729

10

Ectodermal dysplasia showing clinical overlap between AEC, Rapp-Hodgkin and CHAND syndromes.

Sahin MT, Türel-Ermertcan A, Chan I, McGrath JA, Oztürkcan S. Sahin MT, et al. Among authors: mcgrath ja. Clin Exp Dermatol. 2004 Sep;29(5):486-8. doi: 10.1111/j.1365-2230.2004.01584.x. Clin Exp Dermatol. 2004. PMID: 15347331

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