Moskowitz RW - Search Results

1

Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct founders.

Bleasel JF, Holderbaum D, Brancolini V, Moskowitz RW, Considine EL, Prockop DJ, Devoto M, Williams CJ. Bleasel JF, et al. Among authors: moskowitz rw. Hum Mutat. 1998;12(3):172-6. doi: 10.1002/(SICI)1098-1004(1998)12:3<172::AID-HUMU4>3.0.CO;2-J. Hum Mutat. 1998. PMID: 9711874

2

Arg519-Cys mutation in COL2A1: evidence for multiple founders.

Bleasel JF, Holderbaum D, Brancolini V, Moskowitz RW, Haqqi TM, Considine E, Prockop DJ, Devoto M, Williams CJ. Bleasel JF, et al. Among authors: moskowitz rw. Ann N Y Acad Sci. 1996 Jun 8;785:215-8. doi: 10.1111/j.1749-6632.1996.tb56265.x. Ann N Y Acad Sci. 1996. PMID: 8702133 No abstract available.

3

Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.

Ala-Kokko L, Baldwin CT, Moskowitz RW, Prockop DJ. Ala-Kokko L, et al. Among authors: moskowitz rw. Proc Natl Acad Sci U S A. 1990 Sep;87(17):6565-8. doi: 10.1073/pnas.87.17.6565. Proc Natl Acad Sci U S A. 1990. PMID: 1975693 Free PMC article.

4

Hereditary osteoarthritis with mild spondyloepiphyseal dysplasia--are there "hot spots" on COL2A1?

Bleasel JF, Holderbaum D, Mallock V, Haqqi TM, Williams HJ, Moskowitz RW. Bleasel JF, et al. Among authors: moskowitz rw. J Rheumatol. 1996 Sep;23(9):1594-8. J Rheumatol. 1996. PMID: 8877930

5

Clinical correlations of osteoarthritis associated with a single-base mutation (arginine519 to cysteine) in type II procollagen gene. A newly defined pathogenesis.

Pun YL, Moskowitz RW, Lie S, Sundstrom WR, Block SR, McEwen C, Williams HJ, Bleasel JF, Holderbaum D, Haqqi TM. Pun YL, et al. Among authors: moskowitz rw. Arthritis Rheum. 1994 Feb;37(2):264-9. doi: 10.1002/art.1780370216. Arthritis Rheum. 1994. PMID: 8129781

6

Type II procollagen gene (COL2A1) mutation in exon 11 associated with spondyloepiphyseal dysplasia, tall stature and precocious osteoarthritis.

Bleasel JF, Bisagni-Faure A, Holderbaum D, Vacher-Lavenu MC, Haqqi TM, Moskowitz RW, Menkes CJ. Bleasel JF, et al. Among authors: moskowitz rw. J Rheumatol. 1995 Feb;22(2):255-61. J Rheumatol. 1995. PMID: 7738948

7

Clinical correlations of osteoarthritis associated with single base mutations in the type II procollagen gene.

Bleasel JF, Holderbaum D, Haqqi TM, Moskowitz RW. Bleasel JF, et al. Among authors: moskowitz rw. J Rheumatol Suppl. 1995 Feb;43:34-6. J Rheumatol Suppl. 1995. PMID: 7752131

8

Changes in serum cartilage marker levels indicate altered cartilage metabolism in families with the osteoarthritis-related type II collagen gene COL2A1 mutation.

Bleasel JF, Poole AR, Heinegård D, Saxne T, Holderbaum D, Ionescu M, Jones P, Moskowitz RW. Bleasel JF, et al. Among authors: moskowitz rw. Arthritis Rheum. 1999 Jan;42(1):39-45. doi: 10.1002/1529-0131(199901)42:1<39::AID-ANR5>3.0.CO;2-Y. Arthritis Rheum. 1999. PMID: 9920012 Free article.

9

[Mutation of collagen genes and familial osteoarthritis].

Moskowitz RW, Bleasel JF, Holderbaum D, Haqqi TM. Moskowitz RW, et al. Rev Rhum Ed Fr. 1993 Jul-Sep;60(7-8):477-80. Rev Rhum Ed Fr. 1993. PMID: 8148845 French. No abstract available.

10

Osteoarthritis in children associated with a mutation in the type II procollagen gene (COL2A1).

Mier RJ, Holderbaum D, Ferguson R, Moskowitz R. Mier RJ, et al. Mol Genet Metab. 2001 Nov;74(3):338-41. doi: 10.1006/mgme.2001.3250. Mol Genet Metab. 2001. PMID: 11708863

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