Marfan Syndrome Latest Advances

Aortic surgery during pregnancy: A retrospective case series in a single tertiary cardiovascular center.

Journal: Asian cardiovascular & thoracic annals

Published: September 04, 2026

Clinical manifestation and analysis of FBN1 gene variants in eight patients with Marfan syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 28, 2026

Too tall, too young, too hypertensive: Abraham Lincoln disease in a 19‑year‑old patient. When should we suspect Marfan syndrome?

Journal: Polish archives of internal medicine

Published: August 25, 2026

Aortic Dissection or Aneurysm and In-Hospital Mortality in Patients With Turner Syndrome　- A Retrospective Cohort Study in Japan.

Journal: Circulation journal : official journal of the Japanese Circulation Society

Published: August 23, 2026

Single-Cell Proteomics Uncovers Cell-Specific Proteins in Vascular Health and Marfan Syndrome Disease.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: August 13, 2026

Sequential Transcatheter Valve-in-Valve-in-Valve Implantation Within a Degenerated Bio-Bentall Conduit in a Patient with Marfan Syndrome.

Journal: Anatolian journal of cardiology

Published: August 12, 2026

Coexistence of Neurofibromatosis Type 1 and Marfan Syndrome in a 13-Year-Old Boy: A Case Report.

Journal: The American journal of case reports

Published: August 04, 2026

Lymphatic therapies open the valve in Marfan syndrome.

Journal: The Journal of clinical investigation

Published: August 03, 2026

Clinical characteristics of pregnant women with different high-risk factors for Stanford type A aortic dissection

Journal: Zhonghua fu chan ke za zhi

Published: July 21, 2026

The Effect of Exercise on Quality of Life in Patients With Thoracic Aortic Disease Pre- and Post-Surgery: A SCOPING REVIEW.

Journal: Journal of cardiopulmonary rehabilitation and prevention

Published: July 17, 2026

Cardiovascular involvement and outcomes in Marfan syndrome: new observations on evolving aortic risk associations in a single-center cohort from Poland.

Journal: Polish archives of internal medicine

Published: July 09, 2026

Dysregulated Proteins in Plasma Distinguishing Loeys-Dietz Syndrome from Other Heritable Thoracic Aortic Disease - An Explorative Study.

Journal: Scandinavian cardiovascular journal : SCJ

Published: July 07, 2026

Marfan Syndrome Latest Advances

Find the Latest Research About Marfan Syndrome

Aortic surgery during pregnancy: A retrospective case series in a single tertiary cardiovascular center.

Aortic surgery during pregnancy: A retrospective case series in a single tertiary cardiovascular center.

Clinical manifestation and analysis of FBN1 gene variants in eight patients with Marfan syndrome

Clinical manifestation and analysis of FBN1 gene variants in eight patients with Marfan syndrome

Too tall, too young, too hypertensive: Abraham Lincoln disease in a 19‑year‑old patient. When should we suspect Marfan syndrome?

Too tall, too young, too hypertensive: Abraham Lincoln disease in a 19‑year‑old patient. When should we suspect Marfan syndrome?

Aortic Dissection or Aneurysm and In-Hospital Mortality in Patients With Turner Syndrome - A Retrospective Cohort Study in Japan.

Aortic Dissection or Aneurysm and In-Hospital Mortality in Patients With Turner Syndrome - A Retrospective Cohort Study in Japan.

Single-Cell Proteomics Uncovers Cell-Specific Proteins in Vascular Health and Marfan Syndrome Disease.

Single-Cell Proteomics Uncovers Cell-Specific Proteins in Vascular Health and Marfan Syndrome Disease.

Sequential Transcatheter Valve-in-Valve-in-Valve Implantation Within a Degenerated Bio-Bentall Conduit in a Patient with Marfan Syndrome.

Sequential Transcatheter Valve-in-Valve-in-Valve Implantation Within a Degenerated Bio-Bentall Conduit in a Patient with Marfan Syndrome.

Coexistence of Neurofibromatosis Type 1 and Marfan Syndrome in a 13-Year-Old Boy: A Case Report.

Coexistence of Neurofibromatosis Type 1 and Marfan Syndrome in a 13-Year-Old Boy: A Case Report.

Lymphatic therapies open the valve in Marfan syndrome.

Lymphatic therapies open the valve in Marfan syndrome.

Clinical characteristics of pregnant women with different high-risk factors for Stanford type A aortic dissection

Clinical characteristics of pregnant women with different high-risk factors for Stanford type A aortic dissection

The Effect of Exercise on Quality of Life in Patients With Thoracic Aortic Disease Pre- and Post-Surgery: A SCOPING REVIEW.

The Effect of Exercise on Quality of Life in Patients With Thoracic Aortic Disease Pre- and Post-Surgery: A SCOPING REVIEW.

Cardiovascular involvement and outcomes in Marfan syndrome: new observations on evolving aortic risk associations in a single-center cohort from Poland.

Cardiovascular involvement and outcomes in Marfan syndrome: new observations on evolving aortic risk associations in a single-center cohort from Poland.

Dysregulated Proteins in Plasma Distinguishing Loeys-Dietz Syndrome from Other Heritable Thoracic Aortic Disease - An Explorative Study.

Dysregulated Proteins in Plasma Distinguishing Loeys-Dietz Syndrome from Other Heritable Thoracic Aortic Disease - An Explorative Study.

Aortic Dissection or Aneurysm and In-Hospital Mortality in Patients With Turner Syndrome　- A Retrospective Cohort Study in Japan.

Aortic Dissection or Aneurysm and In-Hospital Mortality in Patients With Turner Syndrome　- A Retrospective Cohort Study in Japan.