Horizontal equity in the design of Australian family payments for newborns

2021 ◽  
Author(s):  
Matthew Taylor
Keyword(s):  
Horizontal Equity ◽  
Australian Family

α Thalassemia british type (αα/--BRIT) in an australian family

Pathology ◽  
1986 ◽  
Vol 18 (2) ◽  
pp. 193-195 ◽  
Author(s):  
Thomas Wilkinson ◽  
J. Yakas ◽  
H. Kronenberg ◽  
R.J. Trent
Keyword(s):  
Australian Family

A second australian family with hemoglobin north shore (β134 VAL→GLU)

Pathology ◽  
1987 ◽  
Vol 19 (1) ◽  
pp. 62-63 ◽  
Author(s):  
Howard Gurney ◽  
Ibrahim Baig ◽  
Susan Gordon ◽  
Kiran Phadke ◽  
Heather Kearsley ◽  
...  
Keyword(s):  
North Shore ◽  
Australian Family

Horizontal Equity in Health Care Utilization in Canada

2006 ◽  
Author(s):  
Michel Grignon ◽  
Jeremiah Hurley ◽  
Alina Gildiner ◽  
Martin Hering
Keyword(s):  
Health Care ◽  
Health Care Utilization ◽  
Horizontal Equity ◽  
Care Utilization ◽  
Equity In Health ◽  
Equity In Health Care

HAEMOGLOBIN J BALTIMORE INTERACTING WITH BETA‐THALASSAEMIA IN AN AUSTRALIAN FAMILY

1967 ◽  
Vol 1 (18) ◽  
pp. 907-910 ◽  
Author(s):  
T. Wilkinson ◽  
H. Kronenberg ◽  
W. A. Isaacs ◽  
H. Lehmann
Keyword(s):  
Beta Thalassaemia ◽  
Australian Family

HOUSING TENURE AND HORIZONTAL EQUITY

1978 ◽  
Vol 31 (4) ◽  
pp. 329-338
Author(s):  
J. FRED GIERTZ ◽  
DENNIS H. SULLIVAN
Keyword(s):  
Housing Tenure ◽  
Horizontal Equity

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

Blood ◽  
2002 ◽  
Vol 100 (2) ◽  
pp. 692-694 ◽  
Author(s):  
Daniel F. Wallace ◽  
Palle Pedersen ◽  
Jeannette L. Dixon ◽  
Peter Stephenson ◽  
Jeffrey W. Searle ◽  
...  
Keyword(s):  
Iron Transport ◽  
Autosomal Recessive ◽  
Iron Homeostasis ◽  
Autosomal Dominant ◽  
Novel Mutation ◽  
Hfe Gene ◽  
Excess Iron ◽  
Chromosome 1Q ◽  
Australian Family ◽  
Autosomal Recessive Pattern

Abstract Hemochromatosis is a common disorder characterized by excess iron absorption and accumulation of iron in tissues. Usually hemochromatosis is inherited in an autosomal recessive pattern and is caused by mutations in the HFE gene. Less common non-HFE–related forms of hemochromatosis have been reported and are caused by mutations in the transferrin receptor 2 gene and in a gene localized to chromosome 1q. Autosomal dominant forms of hemochromatosis have also been described. Recently, 2 mutations in theferroportin1 gene, which encodes the iron transport protein ferroportin1, have been implicated in families with autosomal dominant hemochromatosis from the Netherlands and Italy. We report the finding of a novel mutation (V162del) in ferroportin1 in an Australian family with autosomal dominant hemochromatosis. We propose that this mutation disrupts the function of the ferroportin1 protein, leading to impaired iron homeostasis and iron overload.

scholarly journals Achieving Horizontal Equity: Must We Have a Single-Payer Health System?

2009 ◽  
Vol 34 (4) ◽  
pp. 617-633 ◽  
Author(s):  
Michael K. Gusmano ◽  
Daniel Weisz ◽  
Victor G. Rodwin
Keyword(s):  
Health System ◽  
Horizontal Equity ◽  
Single Payer
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