| Preview | Issue Date | Title | Author(s) |
| 2014 | A case of Aromatase deficiency due to a novel CYP19A1 mutation | Gagliardi, L.; Scott, H.; Feng, J.; Torpy, D. |
| 2014 | ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia | Gagliardi, L.; Schreiber, A.; Hahn, C.; Feng, J.; Cranston, T.; Boon, H.; Hotu, C.; Oftedal, B.; Cutfield, R.; Adelson, D.; Braund, W.; Gordon, R.; Rees, D.; Grossman, A.; Torpy, D.; Scott, H. |
| 2016 | Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications | Gagliardi, L.; Burt, M.; Feng, J.; Poplawski, N.; Scott, H. |
| 2014 | Continuous subcutaneous hydrocortisone infusion therapy in Addison's disease: a randomized, placebo-controlled clinical trial | Gagliardi, L.; Nenke, M.; Thynne, T.; von der Borch, J.; Rankin, W.; Henley, D.; Sorbello, J.; Inder, W.; Torpy, D. |
| 2010 | Corticosteroid-binding globulin: The clinical significance of altered levels and heritable mutations | Gagliardi, L.; Ho, J.; Torpy, D. |
| 2009 | Familial vasopressin-sensitive ACTH-independent macronodular adrenal hyperplasia (VPs-AIMAH): clinical studies of three kindreads | Gagliardi, L.; Hotu, C.; Casey, G.; Braund, W.; Ling, K.; Dodd, T.; Manavis, J.; Devitt, P.; Cutfield, R.; Rudzki, Z.; Scott, H.; Torpy, D. |
| 2012 | Genome-wide gene expression profiling identifies overlap with malignant adrenocortical tumours and novel mechanisms of inefficient steroidogenesis in familial ACTH-independent macronodular adrenal hyperplasia | Gagliardi, L.; Ling, K.; Kok, C.; Carolan, J.; Brautigan, P.; Kenyon, R.; D'Andrea, R.; Van der Hoek, M.; Hahn, C.; Torpy, D.; Scott, H. |
| 2018 | Gestational weight gain charts for different body mass index groups for women in Europe, North America, and Oceania | Santos, S.; Eekhout, I.; Voerman, E.; Gaillard, R.; Barros, H.; Charles, M.A.; Chatzi, L.; Chevrier, C.; Chrousos, G.P.; Corpeleijn, E.; Costet, N.; Crozier, S.; Doyon, M.; Eggesbø, M.; Fantini, M.P.; Farchi, S.; Forastiere, F.; Gagliardi, L.; Georgiu, V.; Godfrey, K.M.; et al. |
| 2011 | Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia | Hahn, C.; Chong, C.; Carmichael, C.; Wilkins, E.; Brautigan, P.; Li, X.; Babic, M.; Lin, M.; Carmagnac, A.; Lee, Y.; Kok, C.; Gagliardi, L.; Friend, K.; Ekert, P.; Butcher, C.; Brown, A.; Lewis, I.; To, L.; Timms, A.; Storek, J.; et al. |
| 2015 | Low-dose hydrocortisone replacement improves wellbeing and pain tolerance in chronic pain patients with opioid-induced hypocortisolemic responses. A pilot randomized, placebo-controlled trial | Nenke, M.; Haylock, C.; Rankin, W.; Inder, W.; Gagliardi, L.; Eldridge, C.; Rolan, P.; Torpy, D. |
| 2007 | Management of obesity in patients with type 2 diabetes mellitus | Gagliardi, L.; Wittert, G. |
| 2013 | Neuro-endocrine function in older men with chronic pain - effects of chronic opioid usage | Haylock, C.; Maddison, J.; Foran, A.; Gagliardi, L.; Torpy, D.; Rolan, P.; The Australian and New Zealand Society for Geriatric Medicine Annual Scientific Meeting (17 Jun 2013 - 19 Jun 2013 : Adelaide, SA) |
| 2010 | Screening for subclinical Cushing's Syndrome in Type 2 Diabetes Mellitus: Low false-positive rates with nocturnal salivary cortisol | Gagliardi, L.; Chapman, I.; O'Loughlin, P.; Torpy, D. |
| 2010 | Subclinical Cushing's syndrome in adrenal incidentaloma: a common problem or an artefact of current diagnostic testing? | Gagliardi, L.; Torpy, D. |
| 2020 | Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss | Venugopal, P.; Gagliardi, L.; Forsyth, C.; Feng, J.; Phillips, K.; Babic, M.; Poplawski, N.K.; Rienhoff, H.Y.; Schreiber, A.W.; Hahn, C.N.; Brown, A.L.; Scott, H.S. |
