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Mutations in the X-linked spondyloepiphyseal dysplasia tarda (SEDL) coding sequence are not a common cause of early primary osteoarthritis in men.
- Published in:
- Clinical Genetics, 2002, v. 62, n. 1, p. 94, doi. 10.1034/j.1399-0004.2002.620114.x
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- Article
Perinatal hypophosphatasia: diagnosis and detection of heterozygote carriers within the family.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 4, p. 313, doi. 10.1034/j.1399-0004.1999.560409.x
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- Article
Serum concentrations of procollagen I C-terminal propeptide, osteocalcin and insulin-like growth factor-I in patients with non-lethal osteogenesis irnperfecta.
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- Acta Paediatrica, 1993, v. 82, n. 10, p. 764, doi. 10.1111/j.1651-2227.1993.tb12554.x
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- Article
Surface coating strategies to prevent biofilm formation on implant surfaces.
- Published in:
- 2010
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- Publication type:
- journal article
Differential effects of p38MAP kinase inhibitors on the expression of inflammation-associated genes in primary, interleukin-1beta-stimulated human chondrocytes.
- Published in:
- 2010
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- Publication type:
- journal article
Schmid-type metaphyseal chondrodysplasia as the result of a collagen type X defect due to a novel COL10A1 nonsense mutation : A case report of a novel COL10A1 mutation.
- Published in:
- 2011
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- Publication type:
- Journal Article
Optimizing Manufacturing and Osseointegration of Ti6Al4V Implants through Precision Casting and Calcium and Phosphorus Ion Implantation? In Vivo Results of a Large-Scale Animal Trial.
- Published in:
- Materials (1996-1944), 2020, v. 13, n. 7, p. 1670, doi. 10.3390/ma13071670
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- Publication type:
- Article