Harald Kaemmerer
Overview
Explore the profile of Harald Kaemmerer including associated specialties, affiliations and a list of published articles.
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Articles
143
Citations
2772
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Recent Articles
11.
Niwa K, von Kodolitsch Y, Oto O, Kaemmerer H
Cardiovasc Diagn Ther
. 2023 Aug;
13(2):323-325.
PMID: 37583689
No abstract available.
12.
Freiberger A, Richter C, Huber M, Beckmann J, Freilinger S, Kaemmerer H, et al.
Am J Cardiol
. 2023 Jul;
203:9-16.
PMID: 37478638
The stressful and potentially traumatic perception of repeated hospitalization, outpatient check-ups, and medical interventions places a high stress burden on patients with congenital heart disease (CHD). These experiences can lead...
13.
Neidenbach R, Freilinger S, Stocker F, Ewert P, Nagdyman N, Oberhoffer-Fritz R, et al.
Cardiovasc Diagn Ther
. 2023 Mar;
13(1):11-24.
PMID: 36864956
Background: Since 1968, thousands of patients with a morphologically or functionally univentricular heart have been treated with a total cavopulmonary connection/Fontan operation. Because of the resulting passive pulmonary perfusion, blood...
14.
Busse A, Freilinger S, Eicken A, Ewert P, Freiberger A, Huntgeburth M, et al.
Cardiovasc Diagn Ther
. 2023 Jan;
12(6):840-852.
PMID: 36605078
Background: In the long-term course of treated and untreated congenital heart defects (CHD), pulmonary hypertension (PH) is one of the most relevant complications. Since PH carries a high risk for...
15.
Suleiman M, Freilinger S, Meierhofer C, May M, Bischoff G, Ewert P, et al.
Cardiovasc Diagn Ther
. 2023 Jan;
12(6):787-802.
PMID: 36605074
Background: Aortic aneurysm and aortic dissection can have a major impact on the life expectancy of Marfan syndrome (MFS) or Loeys-Dietz syndrome (LDS) patients. Although obesity can influence the development...
16.
Freiberger A, Busse A, Ewert P, Huntgeburth M, Kaemmerer H, Kohls N, et al.
Cardiovasc Diagn Ther
. 2023 Jan;
12(6):758-766.
PMID: 36605070
Background: Pulmonary vascular disease and pulmonary hypertension (PH) belong to the most relevant complications of congenital heart disease (CHD) in the long-term course. Although PH might lead to a severely...
17.
Strack K, Freilinger S, Busse A, Ewert P, Hauser M, Huntgeburth M, et al.
Cardiovasc Diagn Ther
. 2022 Nov;
12(5):655-670.
PMID: 36329967
Background: Pulmonary arterial hypertension (PAH), a common complication in adults with congenital heart disease (CHD), leads to significant morbidity and mortality. Targeted PAH medication is available, but PAH-CHD patient data...
18.
Sinning C, Huntgeburth M, Fukushima N, Tompkins R, Huh J, Tataneo S, et al.
Cardiovasc Diagn Ther
. 2022 Nov;
12(5):727-743.
PMID: 36329959
Background And Objective: The number of adults with congenital heart disease (ACHD) is increasing worldwide. Almost all congenital cardiac lesions can be successfully treated due to the progress in neonatal...
19.
Andonian C, Beckmann J, Mayer O, Ewert P, Freiberger A, Huber M, et al.
Cardiovasc Diagn Ther
. 2022 Aug;
12(4):426-435.
PMID: 36033224
Background: Fabry disease (FD) is a multi-organ disorder associated with severe physical and psychological impairments, particularly in adulthood. To date, comprehensive data on the psychological burden of FD are lacking....
20.
Freiberger A, Beckmann J, Freilinger S, Kaemmerer H, Huber M, Nagdyman N, et al.
Cardiovasc Diagn Ther
. 2022 Aug;
12(4):389-399.
PMID: 36033219
Background: Improved treatment options for congenital heart disease (CHD) lead to a growing number of women with CHD at reproductive age. Due to physical and psychological burden, pregnancies in women...