Marfan syndrome and related connective tissue disorders in the current era in Switzerland in 103 patients: medical and surgical management and impact of genetic testing-Reference-Cited by-同舟云学术

Marfan syndrome and related connective tissue disorders in the current era in Switzerland in 103 patients: medical and surgical management and impact of genetic testing

Published:2020-04-03 Issue: Volume: Page:
ISSN:1424-3997
Container-title:Swiss Medical Weekly
language:en
Short-container-title:Swiss Med Wkly

Author:

Bombardieri Elisa¹,Rohrbach Marianne²,Greutmann Matthias¹,Matyas Gabor³,Weber Roland⁴,Radulovic Jovana⁵,Fasnacht Boillat Margrit⁶,Linka Andr⁷,De Pasquale Gabriela⁸,Bonassin Francesca¹,Attenhofer Jost Christine H.⁵

Affiliation:

1. Cardiology, University Hospital, Zurich, Switzerland

2. Division of Metabolism, University Children’s Hospital, Zurich, Switzerland

3. Centre for Cardiovascular Genetics and Gene Diagnostics, Schlieren, Switzerland

4. Cardiology, Division of Cardiology, University Children’s Hospital, Zurich; and Children’s Research Centre, University Children’s Hospital, Zurich, Switzerland

5. Cardiovascular Centre, Klinik Im Park, Zurich, Switzerland

6. Department of Paediatric Cardiology, Paediatrics, Kantonsspital Winterthur, Switzerland

7. Department of Cardiology, Kantonsspital Winterthur, Switzerland

8. Department of Cardiology, Stadtspital Triemli, Zurich, Switzerland

Publisher

EMH Swiss Medical Publishers, Ltd.

Subject

General Medicine

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1. Unique Features of Cardiovascular Involvement and Progression in Children with Marfan Syndrome Justify Dedicated Multidisciplinary Care;Journal of Cardiovascular Development and Disease;2024-04-03

2. Predicting Marfan Syndrome in Children With Congenital Ectopia Lentis: Development and Validation of a Nomogram;Translational Vision Science & Technology;2024-03-19

3. Midterm Clinical Outcomes of Reimplantation Versus Remodeling Valve-Sparing Aortic Root Replacement in Patients With Connective Tissue Disorders: A Meta-Analysis;The American Journal of Cardiology;2024-02

4. Targeted Panel Sequencing Identifies an Intronic c.5225-3C>G Variant of the FBN1 Gene Causing Sporadic Marfan Syndrome with Annuloaortic Ectasia;Genes;2022-11-13

5. Tricuspid valve prolapse as an early predictor for severe phenotype in children with Marfan syndrome;Acta Paediatrica;2022-02-27