ON-LINE IDENTIFICATION OF CONGENITAL AMUSIA

2008 ◽  
Vol 25 (4) ◽  
pp. 331-343 ◽  
Author(s):  
ISABELLE PERETZ ◽  
NATHALIE GOSSELIN ◽  
BARBARA TILLMANN ◽  
LOLA L. CUDDY ◽  
BENOİİT GAGNON ◽  
...  

RECENTLY, WE POINTED OUT THAT A SMALL number of individuals fail to acquire basic musical abilities, and that these deficiencies might have neuronal and genetic underpinnings. Such a musical disorder is now termed "congenital amusia," an umbrella term for lifelong musical disabilities that cannot be attributed to mental retardation, deafness, or lack of exposure. Congenital amusia is a condition that is estimated to affect 4% of the general population. Despite this relatively high prevalence, cases of congenital amusia have been difficult to identify.We present here a novel on-line test that can be used to identify such cases in 15 minutes, provided that the cohort of the participant is taken into account. The results also confirm that congenital amusia is typically expressed by a deficit in perceiving musical pitch but not musical time.

2008 ◽  
Vol 17 (5) ◽  
pp. 329-333 ◽  
Author(s):  
Isabelle Peretz

Research over the last decade has provided compelling evidence that the ability to engage with music is a fundamental human trait, yet the biological basis of music remains largely unknown. Recent findings indicate that a small number of individuals have severe musical problems that have neurogenetic underpinnings. Such deficiencies are termed congenital amusia, an umbrella term for lifelong musical disabilities that cannot be attributed to mental retardation, deafness, lack of exposure to music, or brain damage after birth. Congenital amusia constitutes a natural experiment, giving us a rare chance to examine the biological basis of music by tracing causal links among genes, environment, brain, and behavior.


CCIT Journal ◽  
2010 ◽  
Vol 3 (3) ◽  
pp. 377-402
Author(s):  
Ermatita Ermatita ◽  
Huda Ubaya ◽  
Dwirosa Indah

Pengembangan perangkat lunak adalah tugas kompleks dan membutuhkan adaptasi untuk mengakomodasi kebutuhan pengguna. Untuk membuat konsep dan perubahan perangkat lunak, dalam pemeliharaan, sekarang telah dikembangkan lebih mudah dalam pengembangan perangkat lunak, pola model-view-controller, yang merupakan arsitektur yang dapat membantu memfasilitasi dalam pengembangan dan pemeliharaan perangkat luna. Hal ini, karena dalam arsitektur model tiga-lapis, yaitu: tampilan dan pengontrolan dalam pembangunan dilakukan secara independen, sehingga dapat memberikan dahan dalam pengembangan dan pemeliharaan. Selain itu, arsitektur ini juga dapat melihat hal-hal yang sederhana dan menarik bagi pengguna. Software sistem on-line test adalah perangkat lunak yang memerlukan interaksi dengan pengguna, dan pemeliharaan perangkat adaptif. Karena sistem ujian on-line memerlukan pengembangan perangkat lunak untuk mengakomodasi kebutuhan ini berkembang dengan cepat. Makalah ini untuk menganalisis Model-View-Controller dan mencoba pembangunan, untuk menerapkannya dalam pengembangan perangkat lunak sistem pengujian on-line. 


2021 ◽  
Vol 10 (6) ◽  
pp. 1314
Author(s):  
Rebeca Lorca ◽  
Isaac Pascual ◽  
Andrea Aparicio ◽  
Alejandro Junco-Vicente ◽  
Rut Alvarez-Velasco ◽  
...  

Background: Coronary artery disease (CAD) is the most frequent cause of ST-segment elevation myocardial infarction (STEMI). Etiopathogenic and prognostic characteristics in young patients may differ from older patients and young women may present worse outcomes than men. We aimed to evaluate the clinical characteristics and prognosis of men and women with premature STEMI. Methods: A total 1404 consecutive patients were referred to our institution for emergency cardiac catheterization due to STEMI suspicion (1 January 2014–31 December 2018). Patients with confirmed premature (<55 years old in men and <60 in women) STEMI (366 patients, 83% men and 17% women) were included (359 atherothrombotic and 7 spontaneous coronary artery dissection (SCAD)). Results: Premature STEMI patients had a high prevalence of classical cardiovascular risk factors. Mean follow-up was 4.1 years (±1.75 SD). Mortality rates, re-hospitalization, and hospital stay showed no significant differences between sexes. More than 10% of women with premature STEMI suffered SCAD. There were no significant differences between sexes, neither among cholesterol levels nor in hypolipemiant therapy. The global survival rates were similar to that expected in the general population of the same sex and age in our region with a significantly higher excess of mortality at 6 years among men compared with the general population. Conclusion: Our results showed a high incidence of cardiovascular risk factors, a high prevalence of SCAD among young women, and a generally good prognosis after standardized treatment. During follow-up, 23% suffered a major cardiovascular event (MACE), without significant differences between sexes and observed survival at 1, 3, and 6 years of follow-up was 96.57% (95% CI 94.04–98.04), 95.64% (95% CI 92.87–97.35), and 94.5% (95% CI 91.12–97.66). An extra effort to prevent/delay STEMI should be invested focusing on smoking avoidance and optimal hypolipemiant treatment both in primary and secondary prevention.


1979 ◽  
Vol 21 (7) ◽  
pp. 1239-1249 ◽  
Author(s):  
J. P. Bravard ◽  
M. Cordonnier ◽  
J. P. Kernevez ◽  
J. M. Lebeault

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