Wordsworth P - Search Results

1

Molecular analysis of eight mutations in FBN1.

Halliday D, Hutchinson S, Kettle S, Firth H, Wordsworth P, Handford PA. Halliday D, et al. Among authors: wordsworth p. Hum Genet. 1999 Dec;105(6):587-97. doi: 10.1007/s004399900190. Hum Genet. 1999. PMID: 10647894

2

Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice.

Halliday DJ, Hutchinson S, Lonie L, Hurst JA, Firth H, Handford PA, Wordsworth P. Halliday DJ, et al. Among authors: wordsworth p. J Med Genet. 2002 Aug;39(8):589-93. doi: 10.1136/jmg.39.8.589. J Med Genet. 2002. PMID: 12161601 Free PMC article. No abstract available.

3

The real connective tissue diseases.

Wordsworth P, Halliday D. Wordsworth P, et al. Clin Med (Lond). 2001 Jan-Feb;1(1):21-4. doi: 10.7861/clinmedicine.1-1-21. Clin Med (Lond). 2001. PMID: 11358071 Free PMC article. Review. No abstract available.

4

Linkage of the gene that encodes the alpha 1 chain of type V collagen (COL5A1) to type II Ehlers-Danlos syndrome (EDS II).

Loughlin J, Irven C, Hardwick LJ, Butcher S, Walsh S, Wordsworth P, Sykes B. Loughlin J, et al. Among authors: wordsworth p. Hum Mol Genet. 1995 Sep;4(9):1649-51. doi: 10.1093/hmg/4.9.1649. Hum Mol Genet. 1995. PMID: 8541855

5

The revised Ghent nosology for the Marfan syndrome.

Loeys BL, Dietz HC, Braverman AC, Callewaert BL, De Backer J, Devereux RB, Hilhorst-Hofstee Y, Jondeau G, Faivre L, Milewicz DM, Pyeritz RE, Sponseller PD, Wordsworth P, De Paepe AM. Loeys BL, et al. Among authors: wordsworth p. J Med Genet. 2010 Jul;47(7):476-85. doi: 10.1136/jmg.2009.072785. J Med Genet. 2010. PMID: 20591885

6

Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.

Sykes B, Ogilvie D, Wordsworth P, Wallis G, Mathew C, Beighton P, Nicholls A, Pope FM, Thompson E, Tsipouras P, et al. Sykes B, et al. Among authors: wordsworth p. Am J Hum Genet. 1990 Feb;46(2):293-307. Am J Hum Genet. 1990. PMID: 1967900 Free PMC article.

7

HLA heterozygosity contributes to susceptibility to rheumatoid arthritis.

Wordsworth P, Pile KD, Buckely JD, Lanchbury JS, Ollier B, Lathrop M, Bell JI. Wordsworth P, et al. Am J Hum Genet. 1992 Sep;51(3):585-91. Am J Hum Genet. 1992. PMID: 1496989 Free PMC article.

8

Bone mineral density in adults with Marfan syndrome.

Carter N, Duncan E, Wordsworth P. Carter N, et al. Among authors: wordsworth p. Rheumatology (Oxford). 2000 Mar;39(3):307-9. doi: 10.1093/rheumatology/39.3.307. Rheumatology (Oxford). 2000. PMID: 10788540

9

The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and Management.

Pollock L, Ridout A, Teh J, Nnadi C, Stavroulias D, Pitcher A, Blair E, Wordsworth P, Vincent TL. Pollock L, et al. Among authors: wordsworth p. Curr Rheumatol Rep. 2021 Nov 26;23(11):81. doi: 10.1007/s11926-021-01045-3. Curr Rheumatol Rep. 2021. PMID: 34825999 Free PMC article. Review.

10

Structural and segregation analysis of the type II collagen gene (COL2A1) in some heritable chondrodysplasias.

Wordsworth P, Ogilvie D, Priestley L, Smith R, Wynne-Davies R, Sykes B. Wordsworth P, et al. J Med Genet. 1988 Aug;25(8):521-7. doi: 10.1136/jmg.25.8.521. J Med Genet. 1988. PMID: 2902229 Free PMC article.

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