IR Reid

A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype (2002)

Cundy, T, Hegde, M, Naot, D, Chong, B, King, A, Wallace, R, ...

Idiopathic hyperphosphatasia is an autosomal recessive bone disease characterized by deformities of long bones, kyphosis and acetabular protrusion, increasing in severity as affected children pass...

Intravenous zoledronic acid in postmenopausal women with low bone mineral density. (2002)

REID, IR, BROWN, JP, BURCKHARDT, P, HOROWITZ, Z, RICHARDSON, P, TRECHSEL, U, ...

A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype (2002)

Cundy, T, Hegde, M, Naot, D, Chong, B, King, A, Wallace, R, ...

Idiopathic hyperphosphatasia is an autosomal recessive bone disease characterized by deformities of long bones, kyphosis and acetabular protrusion, increasing in severity as affected children pass...

Residential status and risk of hip fracture (1999)

Norton, R, Campbell, AJ, Reid, IR, Butler, M, Currie, R, Robinson, E, ...

Pathogenesis and treatment of glucocorticoid-induced osteoporosis (1988)

Reid, IR(Ian Reginald)