Maite Tome
Overview
Explore the profile of Maite Tome including associated specialties, affiliations and a list of published articles.
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Articles
40
Citations
743
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Recent Articles
1.
Basu J, Nikoletou D, Miles C, MacLachlan H, Parry-Williams G, Tilby-Jones F, et al.
Eur Heart J
. 2025 Mar;
PMID: 40037382
Background And Aims: The feasibility and impact of high intensity exercise programmes in patients with hypertrophic cardiomyopathy (HCM) are unknown. This study was conducted to determine the feasibility of a...
2.
Khoury S, Zornitzki L, Laufer-Perl M, Bhatia R, Marwaha S, Tome M, et al.
Int J Cardiol Heart Vasc
. 2024 Jun;
53:101427.
PMID: 38846157
Background: In many conditions characterised by septal hypertrophy, females have been shown to have worse outcomes compared to males. In clinical practice and research, similar cutoff points for septal hypertrophy...
3.
Lorca R, Salgado M, Alvarez-Velasco R, Reguro J, Alonso V, Gomez J, et al.
Int J Cardiol
. 2024 May;
408:132117.
PMID: 38710232
Background: Hypertrophic cardiomyopathy (HCM) is believed to have low overall mortality rate, that could be influenced by gender, particularly among probands. We aimed to evaluate the survival rates and possible...
4.
Joy G, Lopes L, Webber M, Ardissino A, Wilson J, Chan F, et al.
J Am Coll Cardiol
. 2024 Feb;
83(11):1042-1055.
PMID: 38385929
Background: Ventricular arrhythmia in hypertrophic cardiomyopathy (HCM) relates to adverse structural change and genetic status. Cardiovascular magnetic resonance (CMR)-guided electrocardiographic imaging (ECGI) noninvasively maps cardiac structural and electrophysiological (EP) properties....
5.
Coroyannakis C, Tome M, Watt-Coote I, Cauldwell M
Obstet Med
. 2023 Sep;
16(3):200-202.
PMID: 37719992
Marfan syndrome (MFS) is linked with adverse pregnancy events, one of the most significant being aortic dissection. We present a case of a woman with MFS with prior aortic root...
6.
Khoury S, Bhatia R, Marwaha S, Miles C, Kasiakogias A, Bunce N, et al.
Int J Cardiol
. 2023 Aug;
391:131265.
PMID: 37574022
Background: We investigated whether ethnicity and sex are associated with different clinical presentations and cardiovascular magnetic resonance (CMR) findings in individuals with apical hypertrophic cardiomyopathy (ApHCM). Methods: A retrospective observational...
7.
Joy G, Kelly C, Webber M, Pierce I, Teh I, McGrath L, et al.
Circulation
. 2023 Jul;
148(10):808-818.
PMID: 37463608
Background: In hypertrophic cardiomyopathy (HCM), myocyte disarray and microvascular disease (MVD) have been implicated in adverse events, and recent evidence suggests that these may occur early. As novel therapy provides...
8.
Chatrath N, Bhatia R, Fyyaz S, MacLachlan H, Tome M, Sharma S, et al.
JACC Case Rep
. 2023 May;
13:101495.
PMID: 37153479
The physiologic cardiac adaptations caused by intensive exercise and the pathophysiologic changes caused by significant regurgitant valvular lesions can be challenging to differentiate. We describe the clinical course of an...
9.
Hughes R, Augusto J, Knott K, Davies R, Shiwani H, Seraphim A, et al.
Circ Cardiovasc Imaging
. 2023 Mar;
16(3):e014907.
PMID: 36943913
Background: Apical hypertrophic cardiomyopathy (ApHCM) accounts for ≈10% of hypertrophic cardiomyopathy cases and is characterized by apical hypertrophy, apical cavity obliteration, and tall ECG R waves with ischemic-looking deep T-wave...
10.
Moccia E, Papatheodorou E, Miles C, Merghani A, Malhotra A, Dhutia H, et al.
Int J Cardiovasc Imaging
. 2022 Nov;
38(12):2723-2732.
PMID: 36445664
To describe the overlap between structural abnormalities typical of arrhythmogenic right ventricular cardiomyopathy (ARVC) and physiological right ventricular adaptation to exercise and differentiate between pathologic and physiologic findings using CMR....