An altered repertoire of T cell receptor V gene expression by rheumatoid synovial fluid T lymphocytes.

Por Lunardi, C, Marguerie, C, So, A K
Publicado em 1992

EcoRI polymorphism in the human third complement component (C3) gene

Por Botto, M., Fong, K.Y., So, A.K.
Publicado em 1990

Hypogammaglobulinaemia associated with gold therapy.

Por So, A K, Peskett, S A, Webster, A D
Publicado em 1984

CD4 T cells in the rheumatoid joint are oligoclonally activated and change during the course of disease.

Por Khazaei, H A, Lunardi, C, So, A K
Publicado em 1995

Back pain in the older patient.

Por Baumgartner, E, Heitmann, L, Duvoisin, B, So, A K
Publicado em 1996

Common variable immunodeficiency is associated with polymorphic markers in the human major histocompatibility complex.

Por Howe, H S, So, A K, Farrant, J, Webster, A D
Publicado em 1991

Lack of association of T cell receptor V beta 8 polymorphism with rheumatoid arthritis in United Kingdom and Italian white patients.

Por Lunardi, C, Ibberson, M, Zeminian, S, De Sandre, G, So, A K
Publicado em 1994

Arthritis caused by Mycoplasma salivarium in hypogammaglobulinaemia.

Por So, A K, Furr, P M, Taylor-Robinson, D, Webster, A D
Publicado em 1983

Reduction in T gamma delta cell numbers and alteration in subset distribution in systemic lupus erythematosus.

Por Lunardi, C, Marguerie, C, Bowness, P, Walport, M J, So, A K
Publicado em 1991

Molecular basis of hereditary C3 deficiency.

Por Botto, M, Fong, K Y, So, A K, Rudge, A, Walport, M J
Publicado em 1990

Homozygous hereditary C3 deficiency due to a partial gene deletion.

Por Botto, M, Fong, K Y, So, A K, Barlow, R, Routier, R, Morley, B J, Walport, M J
Publicado em 1992