Cardiac phenotype in familial partial lipodystrophy-Reference-Cited by-同舟云学术

Cardiac phenotype in familial partial lipodystrophy

Published:2021-02-22 Issue:6 Volume:94 Page:1043-1053
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Eldin Abdelwahab Jalal¹^ORCID,Akinci Baris¹²^ORCID,Rocha Andre Monteiro³^ORCID,Meral Rasimcan¹^ORCID,Simsir Ilgin Yildirim⁴,Adiyaman Suleyman Cem²,Ozpelit Ebru⁵,Bhave Nicole⁶,Gen Ramazan⁷,Yurekli Banu⁴^ORCID,Ozdemir Kutbay Nilufer⁸^ORCID,Siklar Zeynep⁹^ORCID,Neidert Adam H.¹,Hench Rita¹,Tayeh Marwan K.¹⁰,Innis Jeffrey W.¹⁰¹¹,Jalife Jose⁶¹²,Oral Hakan⁶,Oral Elif A.¹^ORCID

Affiliation:

1. Division of Metabolism, Endocrinology and Diabetes (MEND) Department of Internal Medicine Michigan Medicine University of Michigan Ann Arbor MI USA

2. Division of Endocrinology Department of Internal Medicine Dokuz Eylul University Izmir Turkey

3. Center for Arrhythmia Research Department of Internal Medicine University of Michigan Ann Arbor MI USA

4. Division of Endocrinology Department of Internal Medicine Ege University Izmir Turkey

5. Division of Cardiology Department of Internal Medicine Dokuz Eylul University Izmir Turkey

6. Division of Cardiovascular Medicine Department of Internal Medicine University of Michigan Ann Arbor MI USA

7. Division of Endocrinology Department of Internal Medicine Mersin University Mersin Turkey

8. Division of Endocrinology Department of Internal Medicine Celal Bayar University Manisa Turkey

9. Division of Endocrinology Department of Pediatrics Ankara University Ankara Turkey

10. Departments of Pediatrics University of Michigan Ann Arbor MI USA

11. Human Genetics University of Michigan Ann Arbor MI USA

12. Cardiac Arrhythmia Section Centro Nacional de Investigaciones Cardiovasculares (CNIC) Carlos III Madrid Spain

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14426

Reference34 articles.

1. Phenotypic and Genetic Characteristics of Lipodystrophy: Pathophysiology, Metabolic Abnormalities, and Comorbidities

2. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy

3. Laminopathies

4. LMNA mutation position predicts organ system involvement in laminopathies

5. Lamin A/C and cardiac diseases

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lipodystrophic Laminopathies: From Dunnigan Disease to Progeroid Syndromes;International Journal of Molecular Sciences;2024-08-28

2. Early B-cell transcription factor-2 defect as a novel cause of lipodystrophy: disruption of the adipose tissue character and integrity;2024-06-24

3. A rapid action plan to improve diagnosis and management of lipodystrophy syndromes;Frontiers in Endocrinology;2024-06-04

4. Comprehensive analysis of morbidity and mortality patterns in familial partial lipodystrophy patients: insights from a population study;Frontiers in Endocrinology;2024-06-03

5. Understanding Cardiac Alterations in Familial Partial Lipodystrophy: Insights from Echocardiography;Arquivos Brasileiros de Cardiologia;2024