Evaluation of demographic, clinical, and aetiological data of patients admitted to cardiology clinics and diagnosed with left ventricular hypertrophy in Turkish population (LVH-TR)-Reference-Cited by-同舟云学术

Evaluation of demographic, clinical, and aetiological data of patients admitted to cardiology clinics and diagnosed with left ventricular hypertrophy in Turkish population (LVH-TR)

Published:2022-10-12 Issue:9 Volume:77 Page:836-845
ISSN:0001-5385
Container-title:Acta Cardiologica
language:en
Short-container-title:Acta Cardiologica

Author:

Kis Mehmet¹^ORCID,Dogan Yasemin²^ORCID,Yildirim Abdullah³^ORCID,Güzel Tuncay⁴^ORCID,Bekar Lutfu⁵^ORCID,Akhan Onur⁶,Dogdus Mustafa⁷^ORCID,Harbalıoğlu Hazar⁸^ORCID,Karabulut Dilay⁹^ORCID,Soydan Elton¹⁰^ORCID,Zoghi Mehdi¹⁰^ORCID,Ergene Oktay¹^ORCID,

Affiliation:

1. Department of Cardiology, Dokuz Eylul University, Izmir, Turkey

2. Department of Cardiology, Kayseri City Hospital, Kayseri, Turkey

3. Department of Cardiology, Adana City Training and Research Hospital, Adana, Turkey

4. Department of Cardiology, Akhisar State Hospital, Manisa, Turkey

5. Department of Cardiology, Hitit University Faculty of Medicine, Corum, Turkey

6. Department of Cardiology, Bilecik State Hospital, Bilecik, Turkey

7. Department of Cardiology, Usak University Training and Research Hospital, Usak, Turkey

8. Department of Cardiology, Düzce Atatürk State Hospital, Duzce, Turkey

9. Department of Cardiology, Bakırkoy Dr. Sadi Konuk Training and Research Hospital, Istanbul, Turkey

10. Department of Cardiology, EGE University, Izmir, Turkey

Publisher

Informa UK Limited

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/00015385.2022.2119670

Reference45 articles.

1. Left Ventricular Hypertrophy

2. Bornstein AB, Rao SS, Marwaha K. Left ventricular hypertrophy. StatPearls; 2022. Available from: https://www.ncbi.nlm.nih.gov/books/NBK557534/.

3. THAOS – The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis

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