Concepedia

Roland Stengl

RS

Statistics

Publications

4

Citations

118

H-Index

4

Active since

2018

Affiliations

Semmelweis University(Current)

Foundation for People with Rare Diseases

Roland Stengl is an author at Semmelweis University specializing in medicine, genetic disorders, and molecular genetics.

Publications per year

2018–2022

4

Publications

4

Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement

Roland Stengl, András Bors, Bence Ágg et al. · Orphanet Journal of Rare Diseases · 2020 · 42 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Preventive Impella® Support in High-Risk Patients Undergoing Cardiac Surgery

Kálmán Benke, Edina Korça, Anniek Boltjes et al. · Journal of Clinical Medicine · 2022 · 35 citations · Full text

Medicine, Perioperative Medicine, Surgery +15

Increased visceral arterial tortuosity in Marfan syndrome

Bence Ágg, Bálint Szilveszter, Noémi Daradics et al. · Orphanet Journal of Rare Diseases · 2020 · 25 citations · Full text

Medicine, Anatomy, Surgery +11

Hungarian Marfan family with large FBN1 deletion calls attention to copy number variation detection in the current NGS era

Kálmán Benke, Bence Ágg, Janine Meienberg et al. · Journal of Thoracic Disease · 2018 · 16 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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