Authors:
WARD BK
STUCKEY BGA
GUTTERIDGE DH
LAING NG
PULLAN PT
RATAJCZAK T
Citation: Bk. Ward et al., A NOVEL MUTATION (L174R) IN THE CA2-SENSING RECEPTOR GENE ASSOCIATED WITH FAMILIAL HYPOCALCIURIC HYPERCALCEMIA(), Human mutation, 10(3), 1997, pp. 233-235
Citation: Jp. Walsh et Pt. Pullan, HYPERPROLACTINEMIA IN MALES - A HETEROGENEOUS DISORDER, Australian and New Zealand Journal of Medicine, 27(4), 1997, pp. 385-390
Authors:
GLENDENNING P
PULLAN PT
GULLAND D
EDIS AJ
Citation: P. Glendenning et al., SURGICALLY PROVEN PRIMARY HYPERPARATHYROIDISM WITH A SUPPRESSED INTACT PARATHYROID-HORMONE, Medical journal of Australia, 165(4), 1996, pp. 197-198
Citation: Jp. Walsh et Pt. Pullan, RELAPSE OF CUSHINGS-SYNDROME FOLLOWING THE TREATMENT OF PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DISEASE BY UNILATERAL ADRENALECTOMY, Australian and New Zealand Journal of Medicine, 26(3), 1996, pp. 426-427
Authors:
GRIMMOND SM
TEH BT
HII SI
CARDINAL J
WALTERS M
EPSTEIN M
EDWARDS M
HOCKEY A
PULLAN PT
PERRYKEENE D
BOYAGES S
CAMERON D
HAYWARD NK
Citation: Sm. Grimmond et al., PREDICTIVE DIAGNOSIS OF MULTIPLE ENDOCRINE NEOPLASIA (MEN-1) IN 4 AUSTRALIAN KINDREDS, Australian and New Zealand Journal of Medicine, 26(1), 1996, pp. 27-32
Citation: Jp. Walsh et al., PRIMARY-TREATMENT OF A COMBINED SOMATOTROPIN-SECRETING AND THYROTROPIN-SECRETING PITUITARY-TUMOR WITH OCTREOTIDE, Australian and New Zealand Journal of Medicine, 26(1), 1996, pp. 124-125