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1.
Neth Heart J ; 24(12): 699-700, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27830447
2.
Neth Heart J ; 24(10): 561-2, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27561282
3.
Neth Heart J ; 24(9): 493-4, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27484323
4.
Neth Heart J ; 24(9): 495-7, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27461421
5.
Neth Heart J ; 24(7-8): 439-40, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27165314
6.
Neth Heart J ; 24(6): 369-371, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27189215
7.
Neth Heart J ; 24(5): 303-5, 2016 May.
Article in English | MEDLINE | ID: mdl-27052893
8.
Neth Heart J ; 24(5): 306-7, 2016 May.
Article in English | MEDLINE | ID: mdl-27040677

ABSTRACT

At the annual 2016 Spring Congress of the NVVC, the Durrer prizes were awarded to the authors of two of the best original articles published in the year 2015, one paper being more basically oriented and one paper being more clinically oriented. This annual tradition has existed since the year 2006.

9.
Neth Heart J ; 24(5): 355-62, 2016 May.
Article in English | MEDLINE | ID: mdl-27081006
11.
Neth Heart J ; 24(3): 159-60, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26857785
12.
Neth Heart J ; 24(2): 93-5, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26645713
13.
Neth Heart J ; 24(1): 1-3, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26643306
14.
Neth Heart J ; 23(12): 559-62, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26530462
15.
Neth Heart J ; 23(12): 557-8, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26490368
16.
Neth Heart J ; 23(10): 455-456, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26324192
17.
Neth Heart J ; 23(11): 505-7, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26408033
18.
Neth Heart J ; 23(7-8): 351-2, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26135225
19.
Neth Heart J ; 23(9): 405-6, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26199141
20.
Neth Heart J ; 23(6): 314-20, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25963529

ABSTRACT

OBJECTIVE: Atherosclerotic large vessel disease is potentially involved in the pathogenesis of cerebral small vessel disease related to occurrence of white matter lesions (WMLs) in the brain. We aimed to assess morphological and functional carotid vessel wall properties in relation to WML using magnetic resonance imaging (MRI) in myocardial infarction (MI) patients. MATERIALS AND METHODS: A total of 20 MI patients (90 % male, 61 ± 11 years) underwent carotid artery and brain MRI. Carotid vessel wall thickness (VWT) was assessed, by detecting lumen and outer wall contours. Carotid pulse wave velocity (PWV), a measure of elasticity, was determined using the transit-time method. Patients were divided according to the median VWT into two groups. Brain MRI allowed for the WML score. RESULTS: Mean VWT was 1.41 ± 0.29 mm and mean carotid PWV was 7.0 ± 2.2 m/s. A significant correlation (Pearson r = 0.45, p = 0.046) between VWT and PWV was observed. Furthermore, in the group of high VWT, the median WML score was higher as compared with the group with lower VWT (4.0 vs 3.0, p = 0.035). CONCLUSIONS: Carotid artery morphological and functional alterations are correlated in MI patients. Patients with high VWT showed a higher amount of periventricular WMLs. These findings support the hypothesis that atherosclerotic large vessel disease is potentially involved in the pathogenesis of cerebral small vessel disease.

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