Faculty Opinions recommendation of Causes of death in patients with Berardinelli-Seip congenital generalized lipodystrophy.

Author(s):  
Eric J Belin de Chantemele
PLoS ONE ◽  
2018 ◽  
Vol 13 (6) ◽  
pp. e0199052 ◽  
Author(s):  
Josivan Gomes Lima ◽  
Lucia Helena C. Nobrega ◽  
Natalia Nobrega Lima ◽  
Marcel Catão Ferreira dos Santos ◽  
Pedro Henrique Dantas Silva ◽  
...  

2006 ◽  
Vol 5 (1) ◽  
pp. 188-189
Author(s):  
M ANASTASIU ◽  
C MIHAI ◽  
C CALTEA ◽  
C SINESCU

Crisis ◽  
2009 ◽  
Vol 30 (1) ◽  
pp. 6-12 ◽  
Author(s):  
D.P. Doessel ◽  
Ruth F.G. Williams ◽  
Harvey Whiteford

Background. Concern with suicide measurement is a positive, albeit relatively recent, development. A concern with “the social loss from suicide” requires careful attention to appropriately measuring the phenomenon. This paper applies two different methods of measuring suicide data: the conventional age-standardized suicide (count) rate; and the alternative rate, the potential years of life lost (PYLL) rate. Aims. The purpose of applying these two measures is to place suicide in Queensland in a historical and comparative (relative to other causes of death) perspective. Methods. Both measures are applied to suicide data for Queensland since 1920. These measures are applied also to two “largish” causes of death and two “smaller” causes of death, i.e., circulatory diseases, cancers, motor vehicle accidents, suicide. Results. The two measures generate quite different pictures of suicide in Queensland: Using the PYLL measure, suicide is a quantitatively larger issue than is indicated by the count measure. Conclusions. The PYLL measure is the more appropriate measure for evaluation exercise of public health prevention strategies. This is because the PYLL measure is weighted by years of life lost and, thus, it incorporates more information than the count measure which implicitly weights each death with a somewhat partial value, viz. unity.


Author(s):  
Nadine R. Sahyoun ◽  
Harold Lentzner ◽  
Donna Hoyert ◽  
Kristen N. Robinson
Keyword(s):  

2009 ◽  
Vol 29 (S 01) ◽  
pp. S7-S12
Author(s):  
M. Spannagl ◽  
W. Schramm ◽  
H. Krebs ◽  

SummarySince 1978 an annual multicentric survey regarding the epidemiology of patients suffering of haemophilia is performed with support of haemophilia treating centres of any size. Again the actual compilation is resting upon a broad database returning to over 30 years of inquiry well representing both the actual and retrospective status of mortality. Prompted was exclusively information about patients with haemophilia A, B and von Willebrand disease. In particular anonymous data concerning the last 12 months about number of treated patients, type and severity of illness, HIV-status and detailed information about causes of death was inquired. This data was merged with existing data and analyzed statistically. In the 2007/2008 survey, a total


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