C. Buchanan

发表

A monoclonal antibody to human insulin-like growth factor-I: characterization, use in radioimmunoassay and effect on the biological activities of the growth factor.

M. Preece, H. Dadi, A. Taylor, 1989, Journal of molecular endocrinology.

Mortality, neoplasia, and Creutzfeldt-Jakob disease in patients treated with human pituitary growth hormone in the United Kingdom.

M. Preece, R. Milner, R. Milner, 1991, BMJ.

ANTIGENICITY AND EFFICACY OF AUTHENTIC SEQUENCE RECOMBINANT HUMAN GROWTH HORMONE (SOMATROPIN): FIRST‐YEAR EXPERIENCE IN THE UNITED KINGDOM

M. Preece, D. Morrell, F. Buzi, 1989, Clinical endocrinology.

Double blind placebo controlled trial of low dose oxandrolone in the treatment of boys with constitutional delay of growth and puberty.

M. Preece, R. Stanhope, G. C. Fenn, 1988, Archives of disease in childhood.

Changes in skeletal muscle and body composition after discontinuation of growth hormone treatment in growth hormone deficient young adults *

O. Rutherford, D. Jones, M. Preece, 1991, Clinical endocrinology.

Identification, localization, and regulation of insulin-like growth factor binding proteins and their messenger ribonucleic acids in the newborn rat olfactory bulb.

G. Werther, V. Russo, F. Mercuri, 1994, Endocrinology.

GONADOTROPHIN, GROWTH HORMONE AND PROLACTIN SECRETION IN CHILDREN WITH PRIMARY HYPOTHYROIDISM

M. Preece, R. Stanhope, D. Grant, 1988, Clinical endocrinology.

A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH‐binding activity by abolishing receptor homodimerization.

M. Preece, S. Amselem, M. Savage, 1994, The EMBO journal.

Identification of growth hormone receptors on human growth plate chondrocytes

G. Werther, S. Edmondson, K. Haynes, 1993, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Growth hormone in short, slowly growing children and those with Turner's syndrome.

C. Law, R. Milner, C. Buchanan, 1987, Archives of disease in childhood.

MOLECULAR ANALYSIS OF TWO FAMILIES WITH LARON SYNDROME AND POSITIVE GROWTH HORMONE BINDING PROTEIN

S. Amselem, M. Savage, M. Goossens, 1993, Pediatric Research.

Laron‐type dwarfism with apparently normal high affinity serum growth hormone‐binding protein

M. Preece, H. Maheshwari, D. Morrell, 1991, Clinical endocrinology.

The evolution of changes in immunoreactive serum insulin-like growth factors (IGFs), IGF-binding proteins, circulating growth hormone (GH) and GH-binding protein as a result of short-term dexamethasone treatment.

W. Blum, H. Maheshwari, J. Miell, 1994, The Journal of endocrinology.