Search Results - "Curnow, L"

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    New guidelines from the Thrombosis and Haemostasis Society of Australia and New Zealand for the diagnosis and management of venous thromboembolism by Tran, Huyen A, Gibbs, Harry, Merriman, Eileen, Curnow, Jennifer L, Young, Laura, Bennett, Ashwini, Tan, Chee Wee, Chunilal, Sanjeev D, Ward, Chris M, Baker, Ross, Nandurkar, Harshal

    Published in Medical journal of Australia (01-03-2019)
    “…Introduction Venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE), is the third most common cardiovascular disease…”
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    Detection of hypofibrinolysis in stable coronary artery disease using the overall haemostatic potential assay by Reddel, Caroline J, Curnow, Jennifer L, Voitl, Jasmin, Rosenov, Alexander, Pennings, Gabrielle J, Morel-Kopp, Marie-Christine, Brieger, David B

    Published in Thrombosis research (01-05-2013)
    “…Abstract Introduction Patients with stable coronary artery disease (CAD) are at risk of arterial thrombosis causing myocardial infarction. Detection of global…”
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    Receiving Enzyme Replacement Therapy for a Lysosomal Storage Disorder: A Preliminary Exploration of the Experiences of Young Patients and Their Families by Freedman, R., Sahhar, M., Curnow, L., Lee, J., Peters, H.

    Published in Journal of genetic counseling (01-08-2013)
    “…Medical intervention for lysosomal storage disorders becomes part of life, shaping the reality of the condition for affected individuals and families. Enzyme…”
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    Updated Australian consensus statement on management of inherited bleeding disorders in pregnancy by Dunkley, Scott, Curtin, Julie A, Marren, Anthony J, Heavener, Robert P, McRae, Simon, Curnow, Jennifer L

    Published in Medical journal of Australia (01-04-2019)
    “…Introduction There have been significant advances in the understanding of the management of inherited bleeding disorders in pregnancy since the last Australian…”
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    Genetic counselling after carrier detection by newborn screening when one parent carries ΔF508 and the other R117H by Curnow, L, Savarirayan, R, Massie, J

    Published in Archives of disease in childhood (01-10-2003)
    “…Newborn screening (NBS) for cystic fibrosis (CF) has been carried out in Victoria, Australia since 1989. The primary screen is immunoreactive trypsinogen (IRT)…”
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    Markedly elevated neonatal immunoreactive trypsinogen levels in the absence of cystic fibrosis gene mutations is not an indication for further testing by Massie, J, Curnow, L, Tzanakos, N, Francis, I, Robertson, C F

    Published in Archives of disease in childhood (01-03-2006)
    “…Aims: To investigate the immunoreactive trypsinogen (IRT) values above the usual 99th centile laboratory cut-off and determine the value of offering further…”
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    Defining the V5/MT neuronal pool for perceptual decisions in a visual stereo-motion task by Krug, Kristine, Curnow, Tamara L., Parker, Andrew J.

    “…In the primate visual cortex, neurons signal differences in the appearance of objects with high precision. However, not all activated neurons contribute…”
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    Analysis of factors that could affect symptomatic outcome in patients having laparoscopic excision of deep rectovaginal endometriosis in BSGE endometriosis centres by Byrne, D.L., Curnow, T.L., Vashisht, A., Clark, T.J.

    “…Investigate factors that influence quality of life after laparoscopic excision of deep rectovaginal endometriosis. A multicentre prospective cohort study…”
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    Increased thrombin generation in a mouse model of cancer cachexia is partially interleukin‐6 dependent by Reddel, C. J., Allen, J. D., Ehteda, A., Taylor, R., Chen, V. M. Y., Curnow, J. L., Kritharides, L., Robertson, G.

    Published in Journal of thrombosis and haemostasis (01-03-2017)
    “…Essentials Cancer cachexia and cancer‐associated thrombosis have not previously been mechanistically linked. We assessed thrombin generation and coagulation…”
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    Factors Influencing Uptake of Genetic Testing For Colorectal Cancer Risk in an Australian Jewish Population by Warner, B. J., Curnow, L. J., Polglase, A. L., Debinski, H. S.

    Published in Journal of genetic counseling (01-10-2005)
    “…There is a significant excess of colorectal cancer in the Australian Ashkenazi Jewish community. This excess can partially be attributed to inherited factors…”
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    Characterization of the hypercoagulable state following severe orthopedic trauma by White, Amanda E, Edelman, J James B, Lott, Natalie, Bannon, Paul G, McElduff, Patrick, Curnow, Jennifer L, Balogh, Zsolt J

    “…Acute traumatic coagulopathy develops in seriously injured patients, which is followed by a paradoxical hypercoagulable state. The hypercoagulable state…”
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    Lessons learnt from the diagnosis and antimicrobial management of necrotising (malignant) otitis externa: our experience in a tertiary referral centre by Williams, S P, Curnow, T L, Almeyda, R

    Published in B-ENT (Leuven) (2014)
    “…Necrotising otitis externa is an uncommon and aggressive infection of the external auditory canal with a tendency to present in the elderly and…”
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    Reduced fibrinolysis and increased fibrin generation can be detected in hypercoagulable patients using the overall hemostatic potential assay by CURNOW, J. L., MOREL‐KOPP, M.‐C., RODDIE, C., ABOUD, M., WARD, C. M.

    Published in Journal of thrombosis and haemostasis (01-03-2007)
    “…Background: Routinely available coagulation assays are not capable of detecting clinically defined hypercoagulable states. A number of global coagulation…”
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    Declining prevalence of cystic fibrosis since the introduction of newborn screening by Massie, John, Curnow, Lisette, Gaffney, Lydia, Carlin, John, Francis, Ivan

    Published in Archives of disease in childhood (01-07-2010)
    “…Objectives Newborn screening for cystic fibrosis (CF) facilitates early diagnosis and genetic counselling for parents of affected infants. Many parents elect…”
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    An audit of clinical service examining the uptake of genetic testing by at-risk family members by Forrest, Laura, Delatycki, Martin, Curnow, Lisette, Gen Couns, M., Skene, Loane, Aitken, MaryAnne

    Published in Genetics in medicine (2012)
    “…Purpose: The aim of this study was to investigate the uptake of genetic testing by at-risk family members for four genetic conditions: chromosomal…”
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