T. M. Doyle

发表

Pediatric granulomatous arthritis: an international registry.

C. Wouters, J. Rosenbaum, C. Rosé, 2006, Arthritis and rheumatism.

Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15).

Justine R. Smith, J. Rosenbaum, T. Martin, 2003, American journal of ophthalmology.

Interstitial pneumonitis in Blau syndrome with documented mutation in CARD15.

C. Rosé, T. Martin, M. Becker, 2007, Arthritis and rheumatism.

Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis.

J. Rosenbaum, C. Rosé, T. Martin, 2005, The Journal of rheumatology.

Infantile onset panniculitis with uveitis and systemic granulomatosis: a new clinicopathologic entity.

C. Wouters, D. Stichweh, M. Punaro, 2007, The Journal of pediatrics.

Incomplete penetrance of the NOD2 E383K substitution among members of a pediatric granulomatous arthritis pedigree.

C. Wouters, C. Rosé, F. Saulsbury, 2009, Arthritis and rheumatism.

Association of Interleukin 23 Receptor Gene with Sarcoidosis

Justine R. Smith, Dongseok Choi, J. Rosenbaum, 2011, Disease markers.

Analysis of the ARMD1 locus: evidence that a mutation in HEMICENTIN-1 is associated with age-related macular degeneration in a large family.

M. Klein, P. Francis, A. Humpert, 2003, Human molecular genetics.

Surface smoothness and marginal fit with phosphate-bonded investments.

A. Caputo, J. Cooney, T. M. Doyle, 1979, The Journal of prosthetic dentistry.

A locus on chromosome 9p predisposes to a specific disease manifestation, acute anterior uveitis, in ankylosing spondylitis, a genetically complex, multisystem, inflammatory disease.

Justine R. Smith, Jingchun Luo, J. Reveille, 2005, Arthritis and rheumatism.