Browsing by Author Walsh, John P

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Issue DateTitleAuthor(s)Citation
2006Are Australian children iodine deficient? Results of the Australian National Iodine Nutrition Study.Byth Wilson, Karen; Eastman, Creswell; Li, Mu; Doyle, Zelda; Harding, Philip E.; Ma, Gary; Mackenzie, Emily J.; Mortimer, Robin H.; Topliss, Duncan J.; Waite, Kay; Walsh, John P; Ward, Lynley C.; Zacharin, Margaret R.; NH&MRC Clinical Trials Centre; Western Clinical School: Medicine (Westmead); School of Public Health: Public HealthAre Australian children iodine deficient? Results of the Australian National Iodine Nutrition Study., Medical Journal of Australia, vol.184, 4, 2006,pp 165-169
2006Are Australian children iodine deficient? Results of the Australian National Iodine Nutrition Study.Byth Wilson, Karen; Eastman, Creswell; Li, Mu; Doyle, Zelda; Harding, Philip E.; Ma, Gary; Mackenzie, Emily J.; Mortimer, Robin H.; Topliss, Duncan J.; Waite, Kay; Walsh, John P; Ward, Lynley C.; Zacharin, Margaret R.; NH&MRC Clinical Trials Centre; Western Clinical School: Medicine (Westmead); School of Public Health: Public HealthAre Australian children iodine deficient? Results of the Australian National Iodine Nutrition Study., Medical Journal of Australia, vol.184, 4, 2006,pp 165-169
2014Association of the CASQ1 gene SNP rs3838216 with ophthalmopathy in patients with thyroid autoimmunityChampion, Bernard; Cregan, Patrick; Cultrone, Daniele; Delbridge, Leigh; Edirimanne, Senarath; El Kochairi, Ilhem; Lahooti, Hooshang; Wall, Jack; Walsh, John P; Nepean Clinical School: Medicine; Nepean Clinical School: Surgery; Nepean Clinical School: Medicine; Northern Clinical School: Surgery; Nepean Clinical School: Surgery; Central Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: MedicineAssociation of the CASQ1 gene SNP rs3838216 with ophthalmopathy in patients with thyroid autoimmunity, Ophthalmology Research: An International Journal, vol.2, 6, 2014,pp 281-293
2010Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of boneHooper, Michael; Albagha, Omar M E; Alonso, Nerea; Cundy, Tim; Dargie, Rosemary; del Pino Montes, Javier; di Stefano, Marco; Dunlop, Malcolm G; Fraser, William D; Gonzalez-Sarmiento, Rogelio; Isaia, Gianluca; Langston, Anne L; Nicholson, Geoff C; Ralston, Stuart H; Tenesa, Albert; Visconti, Micaela R; Walsh, John P; Concord Clinical School: MedicineGenome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone, Nature Genetics, vol.42, 6,pp 520-524
2013Improving diagnosis of tumor-induced osteomalacia with gallium-68 DOTATATE PET/CTClifton-Bligh, Roderick; Gill, Anthony; Clarkson, Adele; Darnell, David; Duncan, Emma; Ebeling, Peter R; Hicks, Rodney J; Hofman, Michael S; Sim, li-Wen; Walsh, John P; Wong, Tricia; Northern Clinical School: Medicine; Northern Clinical School: PathologyImproving diagnosis of tumor-induced osteomalacia with gallium-68 DOTATATE PET/CT, Journal of Clinical Endocrinology and Metabolism, vol.98, 2, 2013,pp 687-694
2015Novel single-nucleotide polymorphisms in the calsequestrin-1 gene are associated with Graves' ophthalmopathy and Hashimoto's thyroiditisChampion, Bernard; Cregan, Patrick; Cultrone, Daniele; Delbridge, Leigh; Edirimanne, Senarath; Lahooti, Hooshang; Wall, Jack; Walsh, John P; Nepean Clinical School: Medicine; Nepean Clinical School: Surgery; Nepean Clinical School: Medicine; Northern Clinical School: Surgery; Nepean Clinical School: Surgery; Nepean Clinical School: Medicine; Nepean Clinical School: MedicineNovel single-nucleotide polymorphisms in the calsequestrin-1 gene are associated with Graves' ophthalmopathy and Hashimoto's thyroiditis, Clinical Ophthalmology, vol.9, N/A, 2015,pp 1731-1740
2017Single nucleotide polymorphism 1623 A/G (Rs180195) in the promoter of the thyroglobulin gene is associated with autoimmune thyroid disease but not with thyroid ophthalmopathyDelbridge, Leigh; Edirimanne, Senarath; Lahooti, Hooshang; Wall, Jack; Walsh, John P; Northern Clinical School: Surgery; Nepean Clinical School: Surgery; Nepean Clinical School: Medicine; Nepean Clinical School: MedicineSingle nucleotide polymorphism 1623 A/G (Rs180195) in the promoter of the thyroglobulin gene is associated with autoimmune thyroid disease but not with thyroid ophthalmopathy, Clinical Ophthalmology, vol.11, N/A, 2017,pp 1337-1345
2008Treatment of Paget's disease of bone: a survey of clinical practice in AustraliaHooper, Michael; Attewell, R; Eisman, John A.; Ferrari, G; Fletcher, S; Stuckey, B G A; Walsh, John P; Wark, John D.; Concord Clinical School: MedicineTreatment of Paget's disease of bone: a survey of clinical practice in Australia, Bone, vol.42,(6),2008,pp 1219-1225
2005Ubiquitin-Associated Domain Mutations of SQSTM1 in Paget’s Disease of Bone: Evidence for a Founder Effect in Patients of British DescentHooper, Michael; Meier, Christian; Cundy, Tim; Daroszewska, Anna; Fraser, William D; Hocking, Lynne J; Lucas, Gavin JA; Nicholson, Geoff C; Ralston, Stuart H; Walsh, John P; Concord Clinical School: Medicine; MedicineUbiquitin-Associated Domain Mutations of SQSTM1 in Paget’s Disease of Bone: Evidence for a Founder Effect in Patients of British Descent, JOURNAL OF BONE AND MINERAL RESEARCH 2005, vol.20,(2),2005,pp 227-231