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Items: 17

1.

Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy.

Roberts JD, Murphy NP, Hamilton RM, Lubbers ER, James CA, Kline CF, Gollob MH, Krahn AD, Sturm AC, Musa H, El-Refaey M, Koenig S, Aneq MÅ, Hoorntje ET, Graw SL, Davies RW, Rafiq MA, Koopmann TT, Aafaqi S, Fatah M, Chiasson DA, Taylor MR, Simmons SL, Han M, van Opbergen CJ, Wold LE, Sinagra G, Mittal K, Tichnell C, Murray B, Codima A, Nazer B, Nguyen DT, Marcus FI, Sobriera N, Lodder EM, van den Berg MP, Spears DA, Robinson JF, Ursell PC, Green AK, Skanes AC, Tang AS, Gardner MJ, Hegele RA, van Veen TA, Wilde AA, Healey JS, Janssen PM, Mestroni L, van Tintelen JP, Calkins H, Judge DP, Hund TJ, Scheinman MM, Mohler PJ.

J Clin Invest. 2019 Jul 2;129(8):3171-3184. doi: 10.1172/JCI125538. eCollection 2019 Jul 2.

2.

Brugada syndrome: Let's talk about sex.

Jons C, Gollob MH.

Heart Rhythm. 2018 Oct;15(10):1466-1467. doi: 10.1016/j.hrthm.2018.07.004. Epub 2018 Jul 4. No abstract available.

PMID:
29981479
3.

Reappraisal of Reported Genes for Sudden Arrhythmic Death.

Hosseini SM, Kim R, Udupa S, Costain G, Jobling R, Liston E, Jamal SM, Szybowska M, Morel CF, Bowdin S, Garcia J, Care M, Sturm AC, Novelli V, Ackerman MJ, Ware JS, Hershberger RE, Wilde AAM, Gollob MH; National Institutes of Health Clinical Genome Resource Consortium.

Circulation. 2018 Sep 18;138(12):1195-1205. doi: 10.1161/CIRCULATIONAHA.118.035070.

4.

Complex interactions in a novel SCN5A compound mutation associated with long QT and Brugada syndrome: Implications for Na+ channel blocking pharmacotherapy for de novo conduction disease.

Liu J, Bayer JD, Aschar-Sobbi R, Wauchop M, Spears D, Gollob M, Vigmond EJ, Tsushima R, Backx PH, Chauhan VS.

PLoS One. 2018 May 23;13(5):e0197273. doi: 10.1371/journal.pone.0197273. eCollection 2018.

5.

T-Wave Morphology Analysis in Congenital Long QT Syndrome Discriminates Patients From Healthy Individuals.

Porta-Sánchez A, Spillane DR, Harris L, Xue J, Dorsey P, Care M, Chauhan V, Gollob MH, Spears DA.

JACC Clin Electrophysiol. 2017 Apr;3(4):374-381. doi: 10.1016/j.jacep.2016.10.013. Epub 2016 Dec 21.

6.

Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability.

Bianchi B, Ozhathil LC, Medeiros-Domingo A, Gollob MH, Abriel H.

Front Physiol. 2018 Mar 8;9:177. doi: 10.3389/fphys.2018.00177. eCollection 2018.

7.

Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy: Revisiting the Gene-Dose Effect.

Fourey D, Care M, Siminovitch KA, Weissler-Snir A, Hindieh W, Chan RH, Gollob MH, Rakowski H, Adler A.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001685. doi: 10.1161/CIRCGENETICS.116.001685. Erratum in: Circ Cardiovasc Genet. 2017 Aug;10(4):e000038.

PMID:
28420666
8.

Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia.

Roberts JD, Gollob MH, Young C, Connors SP, Gray C, Wilton SB, Green MS, Zhu DW, Hodgkinson KA, Poon A, Li Q, Orr N, Tang AS, Klein GJ, Wojciak J, Campagna J, Olgin JE, Badhwar N, Vedantham V, Marcus GM, Kwok PY, Deo RC, Scheinman MM.

JACC Clin Electrophysiol. 2017 Mar;3(3):276-288. doi: 10.1016/j.jacep.2016.09.019. Epub 2016 Dec 21.

9.

Evaluation of Prolonged QT Interval: Structural Heart Disease Mimicking Long QT Syndrome.

Weissler-Snir A, Gollob MH, Chauhan V, Care M, Spears DA.

Pacing Clin Electrophysiol. 2017 Apr;40(4):417-424. doi: 10.1111/pace.13040. Epub 2017 Mar 16.

PMID:
28155223
10.

Editorial commentary: Genetic testing in the absence of phenotype: When genetic testing may cause harm.

Gollob MH.

Trends Cardiovasc Med. 2017 Apr;27(3):214-215. doi: 10.1016/j.tcm.2016.10.001. Epub 2016 Oct 11. No abstract available.

PMID:
27780684
11.

Usefulness of 14-Day Holter for Detection of Nonsustained Ventricular Tachycardia in Patients With Hypertrophic Cardiomyopathy.

Weissler-Snir A, Chan RH, Adler A, Care M, Chauhan V, Gollob MH, Ziv-Baran T, Fourey D, Hindieh W, Rakowski H, Spears DA.

Am J Cardiol. 2016 Oct 15;118(8):1258-1263. doi: 10.1016/j.amjcard.2016.07.043. Epub 2016 Jul 29.

PMID:
27567133
12.

A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation.

Orr N, Arnaout R, Gula LJ, Spears DA, Leong-Sit P, Li Q, Tarhuni W, Reischauer S, Chauhan VS, Borkovich M, Uppal S, Adler A, Coughlin SR, Stainier DYR, Gollob MH.

Nat Commun. 2016 Apr 12;7:11303. doi: 10.1038/ncomms11303.

13.

Rapid Device-Detected Nonsustained Ventricular Tachycardia in the Risk Stratification of Hypertrophic Cardiomyopathy.

Viswanathan K, Suszko AM, DAS M, Jackson N, Gollob M, Cameron D, Spears D, Woo A, Rakowski H, Khurana M, Chauhan VS.

Pacing Clin Electrophysiol. 2016 Jul;39(7):642-51. doi: 10.1111/pace.12861. Epub 2016 May 4.

PMID:
27027856
14.

Primary prevention of idiopathic ventricular fibrillation: Not for the faint of heart.

Adler A, Gollob MH.

Heart Rhythm. 2016 Apr;13(4):913-4. doi: 10.1016/j.hrthm.2015.12.043. Epub 2015 Dec 29. No abstract available.

PMID:
26744096
15.

Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trials.

Suanprasert N, Berk JL, Benson MD, Dyck PJ, Klein CJ, Gollob JA, Bettencourt BR, Karsten V, Dyck PJ.

J Neurol Sci. 2014 Sep 15;344(1-2):121-8. doi: 10.1016/j.jns.2014.06.041. Epub 2014 Jun 27.

PMID:
25012480
16.

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H, Camm AJ, Ellinor PT, Gollob M, Hamilton R, Hershberger RE, Judge DP, Le Marec H, McKenna WJ, Schulze-Bahr E, Semsarian C, Towbin JA, Watkins H, Wilde A, Wolpert C, Zipes DP; Heart Rhythm Society (HRS); European Heart Rhythm Association (EHRA).

Europace. 2011 Aug;13(8):1077-109. doi: 10.1093/europace/eur245. No abstract available. Erratum in: Europace. 2012 Feb;14(2):277. Probst, Vincent [added]; Schwartz, Peter J [added]; Kääb, Stefan [added]; Kirchhof, Paulus [added].

PMID:
21810866
17.

The effect of age and gender on cytokine production by human peripheral blood mononuclear cells and markers of bone metabolism.

Pietschmann P, Gollob E, Brosch S, Hahn P, Kudlacek S, Willheim M, Woloszczuk W, Peterlik M, Tragl KH.

Exp Gerontol. 2003 Oct;38(10):1119-27.

PMID:
14580865

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