Milewicz DM - Search Results

1

Fibrillin 1 abnormalities in dermal fibroblast cultures from first-degree relatives of patients with systemic sclerosis (scleroderma).

Wallis DD, Tan FK, Kessler R, Kimball MD, Cretoiu JS, Arnett FC, Milewicz DM. Wallis DD, et al. Among authors: milewicz dm. Arthritis Rheum. 2004 Jan;50(1):329-32. doi: 10.1002/art.11437. Arthritis Rheum. 2004. PMID: 14730633 Free article. No abstract available.

2

Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.

Putnam EA, Zhang H, Ramirez F, Milewicz DM. Putnam EA, et al. Among authors: milewicz dm. Nat Genet. 1995 Dec;11(4):456-8. doi: 10.1038/ng1295-456. Nat Genet. 1995. PMID: 7493032

3

Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders.

Milewicz DM. Milewicz DM. Tex Heart Inst J. 1994;21(1):22-9. Tex Heart Inst J. 1994. PMID: 8180508 Free PMC article. Review.

4

Fibrillin-1 (FBN1) mutations in patients with thoracic aortic aneurysms.

Milewicz DM, Michael K, Fisher N, Coselli JS, Markello T, Biddinger A. Milewicz DM, et al. Circulation. 1996 Dec 1;94(11):2708-11. doi: 10.1161/01.cir.94.11.2708. Circulation. 1996. PMID: 8941093

5

Association of microsatellite markers near the fibrillin 1 gene on human chromosome 15q with scleroderma in a Native American population.

Tan FK, Stivers DN, Foster MW, Chakraborty R, Howard RF, Milewicz DM, Arnett FC. Tan FK, et al. Among authors: milewicz dm. Arthritis Rheum. 1998 Oct;41(10):1729-37. doi: 10.1002/1529-0131(199810)41:10<1729::AID-ART5>3.0.CO;2-8. Arthritis Rheum. 1998. PMID: 9778214

6

Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations.

Tan FK, Wang N, Kuwana M, Chakraborty R, Bona CA, Milewicz DM, Arnett FC. Tan FK, et al. Among authors: milewicz dm. Arthritis Rheum. 2001 Apr;44(4):893-901. doi: 10.1002/1529-0131(200104)44:4<893::AID-ANR146>3.0.CO;2-3. Arthritis Rheum. 2001. PMID: 11315929 Free article.

7

FBN1 exon 2 splicing error in a patient with Marfan syndrome.

Guo D, Tan FK, Cantu A, Plon SE, Milewicz DM. Guo D, et al. Among authors: milewicz dm. Am J Med Genet. 2001 Jun 15;101(2):130-4. doi: 10.1002/1096-8628(20010615)101:2<130::aid-ajmg1333>3.0.co;2-v. Am J Med Genet. 2001. PMID: 11391655

8

Abnormalities in fibrillin 1-containing microfibrils in dermal fibroblast cultures from patients with systemic sclerosis (scleroderma).

Wallis DD, Tan FK, Kielty CM, Kimball MD, Arnett FC, Milewicz DM. Wallis DD, et al. Among authors: milewicz dm. Arthritis Rheum. 2001 Aug;44(8):1855-64. doi: 10.1002/1529-0131(200108)44:8<1855::AID-ART324>3.0.CO;2-Q. Arthritis Rheum. 2001. PMID: 11508439 Free article.

9

Systemic sclerosis (scleroderma): specific autoantigen genes are selectively overexpressed in scleroderma fibroblasts.

Zhou X, Tan FK, Xiong M, Milewicz DM, Feghali CA, Fritzler MJ, Reveille JD, Arnett FC. Zhou X, et al. Among authors: milewicz dm. J Immunol. 2001 Dec 15;167(12):7126-33. doi: 10.4049/jimmunol.167.12.7126. J Immunol. 2001. PMID: 11739535

10

Association of novel polymorphisms with the expression of SPARC in normal fibroblasts and with susceptibility to scleroderma.

Zhou X, Tan FK, Reveille JD, Wallis D, Milewicz DM, Ahn C, Wang A, Arnett FC. Zhou X, et al. Among authors: milewicz dm. Arthritis Rheum. 2002 Nov;46(11):2990-9. doi: 10.1002/art.10601. Arthritis Rheum. 2002. PMID: 12428242 Free article.

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