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Showing 1 to 12 of 36 entries
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What Should the Cardiologist know about Lamin Disease?.

Arrhythmia & electrophysiology review

Charron P, Arbustini E, Bonne G.
PMID: 26835025
Arrhythm Electrophysiol Rev. 2012 Sep;1(1):22-28. doi: 10.15420/aer.2012.1.22.

Lamins are intermediate filament proteins able to polymerise and form an organised meshwork underlying the inner nuclear membrane in most differentiated somatic cells. Mutations in the LMNA gene, which encodes the two major lamin A and C isoforms, cause...

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Charron P, Arbustini E, Bonne G. What Should the Cardiologist know about Lamin Disease?. Arrhythm Electrophysiol Rev. 2012;1(1):22-28doi: 10.15420/aer.2012.1.22.
Charron, P., Arbustini, E., & Bonne, G. (2012). What Should the Cardiologist know about Lamin Disease?. Arrhythmia & electrophysiology review, 1(1), 22-28. https://doi.org/10.15420/aer.2012.1.22
Charron, Philippe, et al. "What Should the Cardiologist know about Lamin Disease?." Arrhythmia & electrophysiology review vol. 1,1 (2012): 22-28. doi: https://doi.org/10.15420/aer.2012.1.22
Charron P, Arbustini E, Bonne G. What Should the Cardiologist know about Lamin Disease?. Arrhythm Electrophysiol Rev. 2012 Sep;1(1):22-28. doi: 10.15420/aer.2012.1.22. PMID: 26835025; PMCID: PMC4711561.
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Immediate causes of death in short-term surviving heart transplant recipients.

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology

Gallo P, Agozzino L, Arbustini E, Bartoloni G, Baroldi G, Bonacina E, Bosman C, Catani G, di Gioia C, Motta T, Pucci A, Rocco M, Thiene G.
PMID: 25990994
Cardiovasc Pathol. 1994 Jul-Sep;3(3):173-81. doi: 10.1016/1054-8807(94)90027-2.

From 1985 to 1992, 1068 cardiac transplants have been performed in the Italian units. The immediate causes of death of 142 of the 148 orthotopic cardiac transplantation recipients who died within the first 6 postoperative months were surveyed. Deaths...

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Gallo P, Agozzino L, Arbustini E, et al. Immediate causes of death in short-term surviving heart transplant recipients. Cardiovasc Pathol. 1994;3(3):173-81doi: 10.1016/1054-8807(94)90027-2.
Gallo, P., Agozzino, L., Arbustini, E., Bartoloni, G., Baroldi, G., Bonacina, E., Bosman, C., Catani, G., di Gioia, C., Motta, T., Pucci, A., Rocco, M., & Thiene, G. (1994). Immediate causes of death in short-term surviving heart transplant recipients. Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology, 3(3), 173-81. https://doi.org/10.1016/1054-8807(94)90027-2
Gallo, P, et al. "Immediate causes of death in short-term surviving heart transplant recipients." Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology vol. 3,3 (1994): 173-81. doi: https://doi.org/10.1016/1054-8807(94)90027-2
Gallo P, Agozzino L, Arbustini E, Bartoloni G, Baroldi G, Bonacina E, Bosman C, Catani G, di Gioia C, Motta T, Pucci A, Rocco M, Thiene G. Immediate causes of death in short-term surviving heart transplant recipients. Cardiovasc Pathol. 1994 Jul-Sep;3(3):173-81. doi: 10.1016/1054-8807(94)90027-2. PMID: 25990994.
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Implantable Cardioverter-Defibrillator in Dilated Cardiomyopathy after the DANISH-Trial Lesson. A Poly-Parametric Risk Evaluation Is Needed to Improve the Selection of Patients.

Frontiers in physiology

Disertori M, Masè M, Rigoni M, Nollo G, Arbustini E, Ravelli F.
PMID: 29163215
Front Physiol. 2017 Oct 31;8:873. doi: 10.3389/fphys.2017.00873. eCollection 2017.

No abstract available.

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Disertori M, Masè M, Rigoni M, et al. Implantable Cardioverter-Defibrillator in Dilated Cardiomyopathy after the DANISH-Trial Lesson. A Poly-Parametric Risk Evaluation Is Needed to Improve the Selection of Patients. Front Physiol. 2017;8:873doi: 10.3389/fphys.2017.00873.
Disertori, M., Masè, M., Rigoni, M., Nollo, G., Arbustini, E., & Ravelli, F. (2017). Implantable Cardioverter-Defibrillator in Dilated Cardiomyopathy after the DANISH-Trial Lesson. A Poly-Parametric Risk Evaluation Is Needed to Improve the Selection of Patients. Frontiers in physiology, 8873. https://doi.org/10.3389/fphys.2017.00873
Disertori, Marcello, et al. "Implantable Cardioverter-Defibrillator in Dilated Cardiomyopathy after the DANISH-Trial Lesson. A Poly-Parametric Risk Evaluation Is Needed to Improve the Selection of Patients." Frontiers in physiology vol. 8 (2017): 873. doi: https://doi.org/10.3389/fphys.2017.00873
Disertori M, Masè M, Rigoni M, Nollo G, Arbustini E, Ravelli F. Implantable Cardioverter-Defibrillator in Dilated Cardiomyopathy after the DANISH-Trial Lesson. A Poly-Parametric Risk Evaluation Is Needed to Improve the Selection of Patients. Front Physiol. 2017 Oct 31;8:873. doi: 10.3389/fphys.2017.00873. eCollection 2017. PMID: 29163215; PMCID: PMC5671592.
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Aortic Smooth Muscle Detraining in Continuous Flow LVAD: Out of Practice.

Journal of the American College of Cardiology

Arbustini E, Narula N.
PMID: 34711338
J Am Coll Cardiol. 2021 Nov 02;78(18):1796-1799. doi: 10.1016/j.jacc.2021.08.045.

No abstract available.

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Arbustini E, Narula N. Aortic Smooth Muscle Detraining in Continuous Flow LVAD: Out of Practice. J Am Coll Cardiol. 2021;78(18):1796-1799doi: 10.1016/j.jacc.2021.08.045.
Arbustini, E., & Narula, N. (2021). Aortic Smooth Muscle Detraining in Continuous Flow LVAD: Out of Practice. Journal of the American College of Cardiology, 78(18), 1796-1799. https://doi.org/10.1016/j.jacc.2021.08.045
Arbustini, Eloisa, and Narula, Navneet. "Aortic Smooth Muscle Detraining in Continuous Flow LVAD: Out of Practice." Journal of the American College of Cardiology vol. 78,18 (2021): 1796-1799. doi: https://doi.org/10.1016/j.jacc.2021.08.045
Arbustini E, Narula N. Aortic Smooth Muscle Detraining in Continuous Flow LVAD: Out of Practice. J Am Coll Cardiol. 2021 Nov 02;78(18):1796-1799. doi: 10.1016/j.jacc.2021.08.045. PMID: 34711338.
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Myths to debunk: the non-compacted myocardium.

European heart journal supplements : journal of the European Society of Cardiology

Di Toro A, Giuliani L, Smirnova A, Favalli V, Serio A, Urtis M, Grasso M, Arbustini E.
PMID: 33654460
Eur Heart J Suppl. 2020 Nov 18;22:L6-L10. doi: 10.1093/eurheartj/suaa124. eCollection 2020 Nov.

Left ventricular non-compaction (LVNC) is defined by the triad: prominent trabecular anatomy, thin compacted layer, and deep inter-trabecular recesses. No person, sick or healthy, demonstrates identical anatomy of the trabeculae; their configuration represents a sort of individual dynamic 'cardiac...

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Di Toro A, Giuliani L, Smirnova A, et al. Myths to debunk: the non-compacted myocardium. Eur Heart J Suppl. 2020;22:L6-L10doi: 10.1093/eurheartj/suaa124.
Di Toro, A., Giuliani, L., Smirnova, A., Favalli, V., Serio, A., Urtis, M., Grasso, M., & Arbustini, E. (2020). Myths to debunk: the non-compacted myocardium. European heart journal supplements : journal of the European Society of Cardiology, 22L6-L10. https://doi.org/10.1093/eurheartj/suaa124
Di Toro, Alessandro, et al. "Myths to debunk: the non-compacted myocardium." European heart journal supplements : journal of the European Society of Cardiology vol. 22 (2020): L6-L10. doi: https://doi.org/10.1093/eurheartj/suaa124
Di Toro A, Giuliani L, Smirnova A, Favalli V, Serio A, Urtis M, Grasso M, Arbustini E. Myths to debunk: the non-compacted myocardium. Eur Heart J Suppl. 2020 Nov 18;22:L6-L10. doi: 10.1093/eurheartj/suaa124. eCollection 2020 Nov. PMID: 33654460; PMCID: PMC7904063.
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A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy.

RNA biology

Martens L, Rühle F, Witten A, Meder B, Katus HA, Arbustini E, Hasenfuß G, Sinner MF, Kääb S, Pankuweit S, Angermann C, Bornberg-Bauer E, Stoll M.
PMID: 34313541
RNA Biol. 2021 Oct 15;18:409-415. doi: 10.1080/15476286.2021.1952756. Epub 2021 Jul 27.

lncRNAs are at the core of many regulatory processes and have also been recognized to be involved in various complex diseases. They affect gene regulation through direct interactions with RNA, DNA or proteins. Accordingly, lncRNA structure is likely to...

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Martens L, Rühle F, Witten A, et al. A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. RNA Biol. 2021;18:409-415doi: 10.1080/15476286.2021.1952756.
Martens, L., Rühle, F., Witten, A., Meder, B., Katus, H. A., Arbustini, E., Hasenfuß, G., Sinner, M. F., Kääb, S., Pankuweit, S., Angermann, C., Bornberg-Bauer, E., & Stoll, M. (2021). A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. RNA biology, 18409-415. https://doi.org/10.1080/15476286.2021.1952756
Martens, Leonie, et al. "A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy." RNA biology vol. 18 (2021): 409-415. doi: https://doi.org/10.1080/15476286.2021.1952756
Martens L, Rühle F, Witten A, Meder B, Katus HA, Arbustini E, Hasenfuß G, Sinner MF, Kääb S, Pankuweit S, Angermann C, Bornberg-Bauer E, Stoll M. A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. RNA Biol. 2021 Oct 15;18:409-415. doi: 10.1080/15476286.2021.1952756. Epub 2021 Jul 27. PMID: 34313541.
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Macrophages and Monocytes: "Trojan Horses" in COVID-19.

Viruses

Percivalle E, Sammartino JC, Cassaniti I, Arbustini E, Urtis M, Smirnova A, Concardi M, Belgiovine C, Ferrari A, Lilleri D, Piralla A, Baldanti F.
PMID: 34834984
Viruses. 2021 Oct 28;13(11). doi: 10.3390/v13112178.

We aimed to explore whether variants of SARS-CoV-2 (Chinese-derived strain (D614, lineage A), Italian strain PV10734 (D614G, lineage B.1.1) and Alpha strain (lineage B.1.1.7)) were able to infect monocytes (MN) and monocyte-derived macrophages (MDM) and whether these infected cells...

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Percivalle E, Sammartino JC, Cassaniti I, et al. Macrophages and Monocytes: "Trojan Horses" in COVID-19. Viruses. 2021;13(11)doi: 10.3390/v13112178.
Percivalle, E., Sammartino, J. C., Cassaniti, I., Arbustini, E., Urtis, M., Smirnova, A., Concardi, M., Belgiovine, C., Ferrari, A., Lilleri, D., Piralla, A., & Baldanti, F. (2021). Macrophages and Monocytes: "Trojan Horses" in COVID-19. Viruses, 13(11), . https://doi.org/10.3390/v13112178
Percivalle, Elena, et al. "Macrophages and Monocytes: "Trojan Horses" in COVID-19." Viruses vol. 13,11 (2021). doi: https://doi.org/10.3390/v13112178
Percivalle E, Sammartino JC, Cassaniti I, Arbustini E, Urtis M, Smirnova A, Concardi M, Belgiovine C, Ferrari A, Lilleri D, Piralla A, Baldanti F. Macrophages and Monocytes: "Trojan Horses" in COVID-19. Viruses. 2021 Oct 28;13(11). doi: 10.3390/v13112178. PMID: 34834984; PMCID: PMC8624282.
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Is Occult Genetic Substrate the Missing Link Between Arrhythmic Mitral Annular Disjunction Syndrome and Sudden Cardiac Death?.

The Canadian journal of cardiology

Appignani M, Khanji MY, Arbustini E, Stuppia L, Ceriello L, Girolamo ED, Mantini C, Gallina S, Chahal CAA, Ricci F.
PMID: 33933609
Can J Cardiol. 2021 Oct;37(10):1651-1653. doi: 10.1016/j.cjca.2021.04.014. Epub 2021 Apr 29.

We present the case of a 28-year-old man with a history of unexplained syncope, frequent ventricular arrhythmias, familial LMNA-related dilated cardiomyopathy (DCM), and mitral annular disjunction (MAD). We provide the first association of a novel truncating LMNA variant serving...

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Appignani M, Khanji MY, Arbustini E, et al. Is Occult Genetic Substrate the Missing Link Between Arrhythmic Mitral Annular Disjunction Syndrome and Sudden Cardiac Death?. Can J Cardiol. 2021;37(10):1651-1653doi: 10.1016/j.cjca.2021.04.014.
Appignani, M., Khanji, M. Y., Arbustini, E., Stuppia, L., Ceriello, L., Girolamo, E. D., Mantini, C., Gallina, S., Chahal, C. A. A., & Ricci, F. (2021). Is Occult Genetic Substrate the Missing Link Between Arrhythmic Mitral Annular Disjunction Syndrome and Sudden Cardiac Death?. The Canadian journal of cardiology, 37(10), 1651-1653. https://doi.org/10.1016/j.cjca.2021.04.014
Appignani, Marianna, et al. "Is Occult Genetic Substrate the Missing Link Between Arrhythmic Mitral Annular Disjunction Syndrome and Sudden Cardiac Death?." The Canadian journal of cardiology vol. 37,10 (2021): 1651-1653. doi: https://doi.org/10.1016/j.cjca.2021.04.014
Appignani M, Khanji MY, Arbustini E, Stuppia L, Ceriello L, Girolamo ED, Mantini C, Gallina S, Chahal CAA, Ricci F. Is Occult Genetic Substrate the Missing Link Between Arrhythmic Mitral Annular Disjunction Syndrome and Sudden Cardiac Death?. Can J Cardiol. 2021 Oct;37(10):1651-1653. doi: 10.1016/j.cjca.2021.04.014. Epub 2021 Apr 29. PMID: 33933609.
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Multivessel endovascular therapy for undiagnosed vascular type Ehlers-Danlos syndrome. Successful percutaneous transcatheter coil embolization of hepatic artery pseudoaneurysm with stenting of right renal and iliac arteries in emergency setting.

BJR case reports

Moramarco LP, Capodaglio CA, Quaretti P, Cionfoli N, Fiorina I, Disabella E, D'agostino AM, Urtis M, Arbustini E.
PMID: 33299587
BJR Case Rep. 2020 Jul 06;6(4):20200025. doi: 10.1259/bjrcr.20200025. eCollection 2020 Dec 01.

Among Ehlers-Danlos syndromes, the vascular type is the most severe because of its vascular complications. Transcatheter embolization of medium-sized arteries has become the first-line therapy for life-threatening hemorrhage. Ongoing multiple lesions causing hemorrhagic or ischemic complications in the acute...

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Moramarco LP, Capodaglio CA, Quaretti P, et al. Multivessel endovascular therapy for undiagnosed vascular type Ehlers-Danlos syndrome. Successful percutaneous transcatheter coil embolization of hepatic artery pseudoaneurysm with stenting of right renal and iliac arteries in emergency setting. BJR Case Rep. 2020;6(4):20200025doi: 10.1259/bjrcr.20200025.
Moramarco, L. P., Capodaglio, C. A., Quaretti, P., Cionfoli, N., Fiorina, I., Disabella, E., D'agostino, A. M., Urtis, M., & Arbustini, E. (2020). Multivessel endovascular therapy for undiagnosed vascular type Ehlers-Danlos syndrome. Successful percutaneous transcatheter coil embolization of hepatic artery pseudoaneurysm with stenting of right renal and iliac arteries in emergency setting. BJR case reports, 6(4), 20200025. https://doi.org/10.1259/bjrcr.20200025
Moramarco, Lorenzo Paolo, et al. "Multivessel endovascular therapy for undiagnosed vascular type Ehlers-Danlos syndrome. Successful percutaneous transcatheter coil embolization of hepatic artery pseudoaneurysm with stenting of right renal and iliac arteries in emergency setting." BJR case reports vol. 6,4 (2020): 20200025. doi: https://doi.org/10.1259/bjrcr.20200025
Moramarco LP, Capodaglio CA, Quaretti P, Cionfoli N, Fiorina I, Disabella E, D'agostino AM, Urtis M, Arbustini E. Multivessel endovascular therapy for undiagnosed vascular type Ehlers-Danlos syndrome. Successful percutaneous transcatheter coil embolization of hepatic artery pseudoaneurysm with stenting of right renal and iliac arteries in emergency setting. BJR Case Rep. 2020 Jul 06;6(4):20200025. doi: 10.1259/bjrcr.20200025. eCollection 2020 Dec 01. PMID: 33299587; PMCID: PMC7709055.
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A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy.

RNA biology

Martens L, Rühle F, Witten A, Meder B, Katus HA, Arbustini E, Hasenfuß G, Sinner MF, Kääb S, Pankuweit S, Angermann C, Bornberg-Bauer E, Stoll M.
PMID: 34313541
RNA Biol. 2021 Oct 15;18:409-415. doi: 10.1080/15476286.2021.1952756. Epub 2021 Jul 27.

lncRNAs are at the core of many regulatory processes and have also been recognized to be involved in various complex diseases. They affect gene regulation through direct interactions with RNA, DNA or proteins. Accordingly, lncRNA structure is likely to...

Cite
Martens L, Rühle F, Witten A, et al. A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. RNA Biol. 2021;18:409-415doi: 10.1080/15476286.2021.1952756.
Martens, L., Rühle, F., Witten, A., Meder, B., Katus, H. A., Arbustini, E., Hasenfuß, G., Sinner, M. F., Kääb, S., Pankuweit, S., Angermann, C., Bornberg-Bauer, E., & Stoll, M. (2021). A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. RNA biology, 18409-415. https://doi.org/10.1080/15476286.2021.1952756
Martens, Leonie, et al. "A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy." RNA biology vol. 18 (2021): 409-415. doi: https://doi.org/10.1080/15476286.2021.1952756
Martens L, Rühle F, Witten A, Meder B, Katus HA, Arbustini E, Hasenfuß G, Sinner MF, Kääb S, Pankuweit S, Angermann C, Bornberg-Bauer E, Stoll M. A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy. RNA Biol. 2021 Oct 15;18:409-415. doi: 10.1080/15476286.2021.1952756. Epub 2021 Jul 27. PMID: 34313541.
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Thoracoscopic Treatment of Pneumothorax in Marfan Syndrome: Hemostatic Patch to Support Lung Resection Recovery.

Case reports in surgery

Pelizzo G, Arbustini E, Pasqua N, Morbini P, Calcaterra V.
PMID: 30254783
Case Rep Surg. 2018 Sep 04;2018:7597215. doi: 10.1155/2018/7597215. eCollection 2018.

INTRODUCTION: In selected patients, the absorbable fibrin patch TachoSil® is superior to standard surgical treatment in reducing air leakage after pulmonary lobectomy. Pulmonary involvement is not considered a main feature of Marfan syndrome (MFS); however, spontaneous pneumothorax (SP) with...

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Pelizzo G, Arbustini E, Pasqua N, et al. Thoracoscopic Treatment of Pneumothorax in Marfan Syndrome: Hemostatic Patch to Support Lung Resection Recovery. Case Rep Surg. 2018;2018:7597215doi: 10.1155/2018/7597215.
Pelizzo, G., Arbustini, E., Pasqua, N., Morbini, P., & Calcaterra, V. (2018). Thoracoscopic Treatment of Pneumothorax in Marfan Syndrome: Hemostatic Patch to Support Lung Resection Recovery. Case reports in surgery, 20187597215. https://doi.org/10.1155/2018/7597215
Pelizzo, Gloria, et al. "Thoracoscopic Treatment of Pneumothorax in Marfan Syndrome: Hemostatic Patch to Support Lung Resection Recovery." Case reports in surgery vol. 2018 (2018): 7597215. doi: https://doi.org/10.1155/2018/7597215
Pelizzo G, Arbustini E, Pasqua N, Morbini P, Calcaterra V. Thoracoscopic Treatment of Pneumothorax in Marfan Syndrome: Hemostatic Patch to Support Lung Resection Recovery. Case Rep Surg. 2018 Sep 04;2018:7597215. doi: 10.1155/2018/7597215. eCollection 2018. PMID: 30254783; PMCID: PMC6142756.
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[Takotsubo cardiomyopathy: a consensus document].

Giornale italiano di cardiologia (2006)

Novo S, Akashi Y, Arbustini E, Assennato P, Azzarelli S, Barbaro G, Fazio G, Fedele F, Giordan M, Mazzarotto P, Modena MG, Novo G, Parodi G, Previtali M, Rapezzi C, Sconci F, Sganzerla P, Tona F, Salerno-Uriarte JA.
PMID: 19058673
G Ital Cardiol (Rome). 2008 Nov;9(11):785-97.

Takotsubo cardiomyopathy is a syndrome characterized by acute regional systolic dysfunction of the left ventricle, frequently related to psycho-physical acute stress, and usually reversible. This rare syndrome involves more often the female sex with the highest frequency of occurrence...

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Novo S, Akashi Y, Arbustini E, et al. La cardiomiopatia takotsubo: documento di consenso. [Takotsubo cardiomyopathy: a consensus document]. G Ital Cardiol (Rome). 2008;9(11):785-97
Novo, S., Akashi, Y., Arbustini, E., Assennato, P., Azzarelli, S., Barbaro, G., Fazio, G., Fedele, F., Giordan, M., Mazzarotto, P., Modena, M. G., Novo, G., Parodi, G., Previtali, M., Rapezzi, C., Sconci, F., Sganzerla, P., Tona, F., & Salerno-Uriarte, J. A. (2008). La cardiomiopatia takotsubo: documento di consenso. [Takotsubo cardiomyopathy: a consensus document]. Giornale italiano di cardiologia (2006), 9(11), 785-97.
Novo, Salvatore, et al. "La cardiomiopatia takotsubo: documento di consenso." [Takotsubo cardiomyopathy: a consensus document]. Giornale italiano di cardiologia (2006) vol. 9,11 (2008): 785-97.
Novo S, Akashi Y, Arbustini E, Assennato P, Azzarelli S, Barbaro G, Fazio G, Fedele F, Giordan M, Mazzarotto P, Modena MG, Novo G, Parodi G, Previtali M, Rapezzi C, Sconci F, Sganzerla P, Tona F, Salerno-Uriarte JA. La cardiomiopatia takotsubo: documento di consenso. [Takotsubo cardiomyopathy: a consensus document]. G Ital Cardiol (Rome). 2008 Nov;9(11):785-97. Italian. PMID: 19058673.
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