Browse by UCL people
Group by: Type | Date
Jump to: Article
Number of items: 23.
Article
Akhtar, M;
Elliott, P;
(2018)
The genetics of hypertrophic cardiomyopathy.
Global Cardiology Science and Practice
, 2018
(3)
, Article 36. 10.21542/gcsp.2018.36.
|
 |
|
Akhtar, M;
Elliott, PM;
(2019)
Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy.
Current Cardiology Reports
, 21
, Article 155. 10.1007/s11886-019-1236-3.
|
|
|
Akhtar, MM;
Bhan, A;
Lim, ZY;
Akhtar, MA;
Sekhri, N;
Bharadwaj, P;
Mullen, M;
(2018)
Percutaneous extraction of an embolized progesterone contraceptive implant from the pulmonary artery.
Open Access Journal of Contraception
, 9
pp. 57-61.
10.2147/OAJC.S165827.
|
|
|
Akhtar, MM;
Elliott, P;
(2019)
Impact of left bundle branch block (LBBB) in dilated cardiomyopathy (DCM) with intermediate left ventricular systolic dysfunction (LVSD).
International Journal of Cardiology
, 278
pp. 199-201.
10.1016/j.ijcard.2018.12.036.
|
|
Akhtar, MM;
Elliott, PM;
(2018)
Anderson-Fabry disease in heart failure.
Biophysical Reviews
, 10
(4)
pp. 1107-1119.
10.1007/s12551-018-0432-5.
|
|
|
Akhtar, MM;
Elliott, PM;
(2017)
Rare Disease in Cardiovascular Medicine I.
[Editorial comment].
European Heart Journal
, 38
(21)
pp. 1625-1628.
10.1093/eurheartj/ehx241.
|
|
Akhtar, MM;
Lorenzini, M;
Cicerchia, M;
Ochoa, JP;
Hey, TM;
Sabater Molina, M;
Restrepo-Cordoba, MA;
... European Genetic Cardiomyopathies Initiative Investigators; + view all
(2020)
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene.
Circulation: Heart Failure
, 13
(10)
, Article e006832. 10.1161/CIRCHEARTFAILURE.119.006832.
|
|
Akhtar, MM;
Lorenzini, M;
Pavlou, M;
Ochoa, JP;
O'Mahony, C;
Restrepo-Cordoba, MA;
Segura-Rodriguez, D;
... Elliott, PM; + view all
(2021)
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure.
JAMA Cardiology
10.1001/jamacardio.2021.1106.
(In press).
|
|
Augusto, JB;
Eiros, R;
Nakou, E;
Moura-Ferreira, S;
Treibel, TA;
Captur, G;
Akhtar, MA;
... Lopes, LR; + view all
(2020)
Dilated cardiomyopathy and arrhythmogenic left ventricular cardiomyopathy: a comprehensive genotype-imaging phenotype study.
European Heart Journal: Cardiovascular Imaging
, 21
(3)
pp. 326-336.
10.1093/ehjci/jez188.
|
|
Bugiardini, Enrico;
Nunes, Andreia M;
Oliveira-Santos, Ariany;
Dagda, Marisela;
Fontelonga, Tatiana M;
Barraza-Flores, Pamela;
Pittman, Alan M;
... Burkin, Dean J; + view all
(2022)
Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice.
Journal of the American Heart Association Cardiovascular and Cerebrovascular Disease
, Article e026494. 10.1161/JAHA.122.026494.
(In press).
|
|
Cannie, DE;
Akhtar, MM;
Elliott, P;
(2019)
Hidden in Heart Failure.
European Cardiology Review
, 14
(2)
pp. 89-96.
10.15420/ecr.2019.19.2.
|
|
|
Chen, Y;
Rathod, KS;
Hamshere, S;
Choudry, F;
Akhtar, MM;
Curtis, M;
Amersey, R;
... Jones, DA; + view all
(2021)
COVID-19 and changes in activity and treatment of ST elevation MI from a UK cardiac centre.
IJC Heart and Vasculature
, 33
, Article 100736. 10.1016/j.ijcha.2021.100736.
|
|
Domínguez, F;
Cuenca, S;
Bilińska, Z;
Toro, R;
Villard, E;
Barriales-Villa, R;
Ochoa, JP;
... European Genetic Cardiomyopathies Initiative Investigators, .; + view all
(2018)
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.
Journal of the American College of Cardiology
, 72
(20)
pp. 2471-2481.
10.1016/j.jacc.2018.08.2181.
|
|
Hall, CL;
Akhtar, MM;
Sabater-Molina, M;
Futema, M;
Asimaki, A;
Protonotarios, A;
Dalageorgou, C;
... McKenna, WJ; + view all
(2020)
Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype.
International Journal of Cardiology
, 307
pp. 101-108.
10.1016/j.ijcard.2019.09.048.
|
|
|
Linhart, A;
Germain, DP;
Olivotto, I;
Akhtar, MM;
Anastasakis, A;
Hughes, D;
Namdar, M;
... Elliott, P; + view all
(2020)
An Expert Consensus Document on the Management of Cardiovascular Manifestations of Fabry Disease.
European Journal of Heart Failure
, 22
(7)
pp. 1076-1096.
10.1002/ejhf.1960.
|
|
|
Lopes, LR;
Murphy, D;
Bugiardini, E;
Salem, R;
Jager, J;
Futema, M;
Akhtar, MM;
... Elliott, PM; + view all
(2021)
Iterative Reanalysis of Hypertrophic Cardiomyopathy Exome Data Reveals Causative Pathogenic Mitochondrial DNA Variants.
Circulation: Genomic and Precision Medicine
, 14
(3)
, Article e003388. 10.1161/CIRCGEN.121.003388.
|
|
Lopes, LR;
Futema, M;
Akhtar, MM;
Lorenzini, M;
Pittman, A;
Syrris, P;
Elliott, PM;
(2019)
Prevalence of TTR variants detected by whole-exome sequencing in hypertrophic cardiomyopathy.
The Journal of Protein Folding Disorders
, 26
(4)
pp. 243-247.
10.1080/13506129.2019.1665996.
|
|
Lopes, LR;
Garcia-Hernández, S;
Lorenzini, M;
Futema, M;
Chumakova, O;
Zateyshchikov, D;
Isidoro-Garcia, M;
... Elliott, PM; + view all
(2021)
Alpha-protein kinase 3 (ALPK3)-truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy.
European Heart Journal
10.1093/eurheartj/ehab424.
(In press).
|
|
|
Lorenzini, M;
Norrish, G;
Field, E;
Ochoa, JP;
Cicerchia, M;
Akhtar, MM;
Syrris, P;
... Elliott, PM; + view all
(2020)
Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers.
Journal of the American College of Cardiology
, 76
(5)
pp. 550-559.
10.1016/j.jacc.2020.06.011.
|
|
|
O'Mahony, C;
Akhtar, MM;
Anastasiou, Z;
Guttmann, OP;
Vriesendorp, PA;
Michels, M;
Magrì, D;
... Elliott, PM; + view all
(2019)
Effectiveness of the 2014 European Society of Cardiology guideline on sudden cardiac death in hypertrophic cardiomyopathy: a systematic review and meta-analysis.
Heart
, 105
(8)
pp. 623-631.
10.1136/heartjnl-2018-313700.
|
|
|
Ochoa, JP;
Sabater-Molina, M;
García-Pinilla, JM;
Mogensen, J;
Restrepo-Córdoba, A;
Palomino-Doza, J;
Villacorta, E;
... Monserrat, L; + view all
(2018)
Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.
Journal of the American College of Cardiology
, 72
(20)
pp. 2457-2467.
10.1016/j.jacc.2018.10.001.
|
|
|
Protonotarios, A;
Brodehl, A;
Asimaki, A;
Jager, J;
Quinn, E;
Stanasiuk, C;
Ratnavadivel, S;
... Lopes, LR; + view all
(2021)
The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy.
Canadian Journal of Cardiology
, 37
(6)
pp. 857-866.
10.1016/j.cjca.2020.11.017.
|
|
Salazar-Mendiguchía, J;
Ochoa, JP;
Palomino-Doza, J;
Domínguez, F;
Díez-López, C;
Akhtar, M;
Ramiro-León, S;
... GENESCOPIC Research Group, .; + view all
(2020)
Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy.
Heart
10.1136/heartjnl-2020-316913.
(In press).
|
|
