721 results on '"Valery, Patricia C"'
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52. Partnering with support persons and clinicians to improve the health care experiences of patients with cirrhosis.
53. Differences in the pattern and cost of hospital care between Indigenous and non‐Indigenous Australians with cirrhosis: an exploratory study.
54. Breast cancer diagnosis, patterns of care and burden of disease in Queensland, Australia (1998–2004): does being Indigenous make a difference?
55. Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
56. Targeted antiviral treatment of hepatitis B virus in culturally and linguistically diverse populations to achieve elimination targets in Australia
57. Towards collaborative management of non‐alcoholic fatty liver disease: a ‘real‐world’ pathway for fibrosis risk assessment in primary care
58. Childhood cancer survival and avoided deaths in Australia, 1983–2016
59. Epidemiology of ascites fluid infections in patients with cirrhosis in Queensland, Australia from 2008 to 2017
60. Liver Disease and Poor Adherence Limit Hepatitis C Cure: A Real-World Australian Treatment Cohort
61. Patient‐oriented medication education intervention has long‐term benefits for people with decompensated cirrhosis
62. Aboriginal and Torres Strait Islander Australians and cancer
63. Changes in cancer incidence and survival among Aboriginal and Torres Strait Islander children in Australia, 1997–2016
64. Indigenous Australians with non–small cell lung cancer or cervical cancer receive suboptimal treatment
65. Childhood cancer mortality in Australia
66. Partnering with support persons and clinicians to improve the health care experiences of patients with cirrhosis
67. Development and Evaluation of the Supportive Needs Assessment Tool for Cirrhosis (SNAC)
68. Additional file 1 of Poor disease knowledge is associated with higher healthcare service use and costs among patients with cirrhosis: an exploratory study
69. Additional file 1 of Hepatitis C treatment outcomes for Australian First Nations Peoples: equivalent SVR rate but higher rates of loss to follow-up
70. An exploration of barriers and facilitators to implementing a nonalcoholic fatty liver disease pathway for people with type 2 diabetes in primary care.
71. Changes in cancer incidence and survival among Aboriginal and Torres Strait Islander children in Australia, 1997–2016
72. Bacteraemia, sepsis and antibiotic resistance in Australian patients with cirrhosis: a population-based study
73. Medication Discrepancies and Regimen Complexity in Decompensated Cirrhosis: Implications for Medication Safety
74. Aboriginal and Torres Strait Islander patients’ cancer care pathways in Queensland: Insights from health professionals
75. Fitting Health Care to People: Understanding and Adapting to the Epidemiology and Health Literacy of People Affected by Viral Hepatitis from Culturally and Linguistically Diverse Migrant Backgrounds
76. Predicting Liver‐Related Outcomes in People With Nonalcoholic Fatty Liver Disease: The Prognostic Value of Noninvasive Fibrosis Tests
77. Disparities in Unmet Needs in Indigenous and Non-Indigenous Australians with Cirrhosis: An Exploratory Study
78. Colorectal cancer among Indigenous and non-Indigenous people in Queensland, Australia: Toward survival equality
79. The first comprehensive report on Indigenous Australian womenʼs inequalities in cervical screening: A retrospective registry cohort study in Queensland, Australia (2000-2011)
80. Childhood cancer survival and avoided deaths in Australia, 1983–2016.
81. Psychological distress and quality of life in lung cancer: the role of health-related stigma, illness appraisals and social constraints
82. Psychometric properties of an Australian supportive care needs assessment tool for Indigenous patients with cancer
83. Cancer outcomes for Aboriginal and Torres Strait Islander Australians in rural and remote areas
84. Protecting persons at-risk of viral hepatitis and alcohol-related liver disease during the pandemic and beyond: mitigating the impact of coronavirus disease 2019 on liver health
85. Treatment and outcomes for indigenous and non‐indigenous lung cancer patients in the Top End of the Northern Territory
86. Remoteness of residence predicts tumor stage, receipt of treatment, and mortality in patients with hepatocellular carcinoma
87. Changing prevalence of aetiological factors and comorbidities among Australians hospitalised for cirrhosis
88. Changing prevalence of aetiological factors and comorbidities among Australians hospitalised for cirrhosis
89. Assessment of health-related quality of life and health utilities in Australian patients with cirrhosis
90. Disparities in Unmet Needs in Indigenous and Non-Indigenous Australians with Cirrhosis: An Exploratory Study
91. Respiratory Exacerbations in Indigenous Children From Two Countries With Non-Cystic Fibrosis Chronic Suppurative Lung Disease/Bronchiectasis
92. Exploring the cancer risk perception and interest in genetic services among Indigenous people in Queensland, Australia
93. Indigenous Children From Three Countries With Non-Cystic Fibrosis Chronic Suppurative Lung Disease/Bronchiectasis
94. Sustainable care for indigenous children with cancer
95. Fitting health care to people: understanding and adapting to the epidemiology and health literacy of people affected by viral hepatitis from culturally and linguistically diverse migrant backgrounds
96. The Patient’s Perspective in Cirrhosis: Unmet Supportive Care Needs Differ by Disease Severity, Etiology, and Age
97. Detecting non-alcoholic fatty liver disease and risk factors in health databases: accuracy and limitations of the ICD-10-AM
98. A decade on: Follow-up findings of indigenous children with bronchiectasis
99. Development and Evaluation of the Supportive Needs Assessment Tool for Cirrhosis (SNAC)
100. Communication, collaboration and care coordination : The three-point guide to cancer care provision for aboriginal and Torres Strait Islander Australians
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