D. A. Brooks

Immunochemistry of Lysosomal Storage Disorders

P. Meikle, D. Brooks, J. Hopwood, 2005 .

Enzyme Replacement Therapy in Mucopolysaccharidosis I: Altered Distribution and Targeting of α-l-Iduronidase in Immunized Rats

D. Brooks, J. Hopwood, C. Turner, 2000 .

Immune response to enzyme replacement therapy in lysosomal storage disorder patients and animal models.

D. Brooks, D. A. Brooks, 1999, Molecular genetics and metabolism.

Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome.

D. Brooks, N. Fazzalari, J. Hopwood, 1996, The Journal of clinical investigation.

Diagnosis of lysosomal storage disorders: evaluation of lysosome-associated membrane protein LAMP-1 as a diagnostic marker.

P. Meikle, D. Brooks, L. Karageorgos, 1997, Clinical chemistry.

Human N-acetylgalactosamine-4-sulphate sulphatase. Purification, monoclonal antibody production and native and subunit Mr values.

D. Brooks, J. Hopwood, G. Gibson, 1987, The Biochemical journal.

Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes.

C. P. Morris, H. Scott, D. Brooks, 1993, American journal of human genetics.