Gravenhorst, Verena D.

[["dc.bibliographiccitation.firstpage","292"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Catheterization and Cardiovascular Interventions"],["dc.bibliographiccitation.lastpage","295"],["dc.bibliographiccitation.volume","91"],["dc.contributor.author","Schneider, Heike E."],["dc.contributor.author","Gravenhorst, Verena"],["dc.contributor.author","Paul, Thomas"],["dc.contributor.author","Jacobshagen, Claudius"],["dc.date.accessioned","2021-06-01T10:49:45Z"],["dc.date.available","2021-06-01T10:49:45Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1002/ccd.27445"],["dc.identifier.issn","1522-1946"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86404"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.issn","1522-1946"],["dc.title","Insufficiency of a Damus-Kaye-Stansel anastomosis in a Fontan patient: Transfemoral implantation of an Edwards Sapien 3 valve"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","234"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","American Journal of Medical Genetics Part A"],["dc.bibliographiccitation.lastpage","237"],["dc.bibliographiccitation.volume","127A"],["dc.contributor.author","Wessel, Alok D."],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Buchhorn, Reiner"],["dc.contributor.author","Gosch, A."],["dc.contributor.author","Partsch, C. J."],["dc.contributor.author","Pankau, R."],["dc.date.accessioned","2018-11-07T10:48:04Z"],["dc.date.available","2018-11-07T10:48:04Z"],["dc.date.issued","2004"],["dc.description.abstract","Williams-Beuren syndrome (WBS) is a genetic disorder characterized by a distinctive facial gestalt, mental retardation, mild growth deficiency, and cardiovascular disease. The occurrence of sudden death in the WBS is known from several case reports, but information about the risk of sudden death as derived from the data of a large cohort of patients is lacking. We analyzed the data of 293 WBS patients who had been treated for 43 years at the same two institutions. We thus collected 5,190 patient years without loss to follow-up. During this period ten patients died. Five of them died from: reticulosarcoma (1), after accident (1), heart failure (1), following heart surgery (2). Of the remaining five patients, four died suddenly and one died of unknown cause suggestive of sudden cardiac death. Thus, the incidence of sudden death in our WBS cohort amounts to 1/1,000 patient years. This risk of sudden death is comparable to that following surgery for congenital heart disease, and is 25-100-fold higher compared to the age-matched normal population. (C) 2004 Wiley-Liss, Inc."],["dc.identifier.doi","10.1002/ajmg.a.30012"],["dc.identifier.isi","000221707000004"],["dc.identifier.pmid","15150772"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/48111"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-liss"],["dc.relation.issn","0148-7299"],["dc.title","Risk of sudden death in the Williams-Beuren syndrome"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1063"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE"],["dc.bibliographiccitation.lastpage","1068"],["dc.bibliographiccitation.volume","159"],["dc.contributor.author","Norozi, K."],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Hobbiebrunken, Elke"],["dc.contributor.author","Wessel, Alok D."],["dc.date.accessioned","2018-11-07T10:54:28Z"],["dc.date.available","2018-11-07T10:54:28Z"],["dc.date.issued","2005"],["dc.description.abstract","Background: One of the main goals of corrective surgery of congenital heart defects in children is the improvement of quality of life, which in young children is predominantly determined by exercise capacity. It is not known whether this goal can be achieved in school-aged children who have undergone cardiac surgery in infancy. Objectives: To determine if primary school-aged children who under-went surgery to correct congenital heart defects in infancy are physically as fit as their peers. Methods: We examined 84 children with congenital heart defects, aged 4 to 11 years, after surgical repair. Fifty-two children had simple defects (ie, atrial or ventricular septal defect, coarctation of the aorta). Thirty-two children had complex defects (ie, tetralogy of Fallot, pulmonary atresia with ventricular septal defect). All patients underwent exercise testing performed on a specially modified bicycle ergometer. Ninety-eight sex- and age-matched healthy children served as the control group. Results: There was no gender difference, either in healthy children or in the group with congenital heart defects, regarding exercise testing and that the healthy children reached a mean +/- SD normalized maximal performance of 2.8 +/- 0.3 W/kg. The same range was found for the children who had undergone surgery to correct simple heart defects. The children operated on to correct complex heart defects showed significantly impaired mean normalized maximal performance, although this tended to be lower in the group that had pulmonary atresia with a ventricular septal defect than in the group with tetralogy of Fallot (mean normalized maximal performance, 1.9 W/kg vs 2.3 W/kg). Conclusions: The goal of normal exercise capacity in childhood after heart surgery is achieved in those with simple heart defects only. In children with complex heart defects impaired exercise performance persists, depending on the severity of the heart defect and probably on chronotropic incompetence."],["dc.identifier.doi","10.1001/archpedi.159.11.1063"],["dc.identifier.isi","000233051300013"],["dc.identifier.pmid","16275798"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/49570"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Medical Assoc"],["dc.relation.issn","1072-4710"],["dc.title","Normality of cardiopulmonary capacity in children operated on to correct congenital heart defects"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Clinical Research in Cardiology"],["dc.bibliographiccitation.volume","98"],["dc.contributor.author","Schneider, H."],["dc.contributor.author","Kriebel, TA"],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Paul, Thomas"],["dc.date.accessioned","2018-11-07T11:24:38Z"],["dc.date.available","2018-11-07T11:24:38Z"],["dc.date.issued","2009"],["dc.format.extent","614"],["dc.identifier.isi","000269926600104"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/56450"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Dr Dietrich Steinkopff Verlag"],["dc.publisher.place","Heidelberg"],["dc.relation.issn","1861-0684"],["dc.title","Systematic work-up of young patients suspected of electrical cardiomyopathy"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","521"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","The American Journal of Cardiology"],["dc.bibliographiccitation.lastpage","525"],["dc.bibliographiccitation.volume","101"],["dc.contributor.author","Kaemmerer, Harald"],["dc.contributor.author","Bauer, Ulrike"],["dc.contributor.author","Pensl, Ulrike"],["dc.contributor.author","Oechslin, Erwin"],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Franke, Andreas"],["dc.contributor.author","Hager, Alfred"],["dc.contributor.author","Balling, Gunter"],["dc.contributor.author","Hauser, Michael"],["dc.contributor.author","Eicken, Andreas"],["dc.contributor.author","Hess, John"],["dc.date.accessioned","2018-11-07T11:18:17Z"],["dc.date.available","2018-11-07T11:18:17Z"],["dc.date.issued","2008"],["dc.description.abstract","The aim of the study was to assess the quantity and nature of emergencies affecting adults with congenital cardiac disease (CCD) and evaluate infrastructural requirements for adequate management. There is an increasing number of adults with CCD requiring specialized complex care. This multicenter study evaluated all emergency admissions to I of 5 centers for adults with CCD within 1 year. Within 1 year, there were 1,033 admissions of adults with CCD, and 201 (160 patients; age 16 to 71 years) were emergencies. Underlying cardiac anomalies were univentricular heart (22%), complete transposition (14%), tetralogy of Fallot (21%), and others (43%). Seventy percent of patients had undergone previous cardiac surgery. The main reason for acute admission was cardiovascular (arrhythmia, heart failure, syncope, aortic dissection, and endocarditis). Diagnostic procedures most often assigned were echocardiography (n = 223), chest x-ray (n = 95), Holter electrocardiography (n = 85), cardiac catheterization/electrophysiologic study (n = 39), and others (n = 143). Forty-six patients underwent surgery (cardiovascular n = 41, general n = 5) or electrophysiologic treatment (n = 41). One hundred twenty-six of 201 emergencies (63%) required cooperation with another specialized department: surgery (n = 46), internal medicine (n = 42), neurology (n = 12), ophthalmology (n 6), otorhinolaryngology (n = 5), gynecology (n = 5), psychiatry (n = 4), radiology (n 3), dermatology (n = 2), and orthopedics (n = 2). In conclusion, physicians and consultants attending adult patients with CCD need a high degree of specialized experience concerning the cardiac anomaly to manage emergencies properly. Furthermore, a wide range of noncardiac diagnostic and therapeutic procedures must be available. Data support the demand for a multidisciplinary approach in specialized centers for adequate care of adults with CCD. (C) 2008 Elsevier Inc. All rights reserved."],["dc.identifier.doi","10.1016/j.amjcard.2007.09.110"],["dc.identifier.isi","000253173900021"],["dc.identifier.pmid","18312770"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/55000"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Excerpta Medica Inc-elsevier Science Inc"],["dc.relation.issn","0002-9149"],["dc.title","Management of emergencies in adults with congenital cardiac disease"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Clinical Research in Cardiology"],["dc.bibliographiccitation.volume","100"],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Ebenebe, Chinedu U."],["dc.contributor.author","Quentin, Thomas"],["dc.contributor.author","Jung, K."],["dc.contributor.author","Schneider, Heike E."],["dc.contributor.author","Paul, Thomas"],["dc.date.accessioned","2018-11-07T08:52:34Z"],["dc.date.available","2018-11-07T08:52:34Z"],["dc.date.issued","2011"],["dc.format.extent","828"],["dc.identifier.isi","000294690900044"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/22199"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.publisher.place","Heidelberg"],["dc.relation.issn","1861-0684"],["dc.title","Intraventricular dyssynchrony detected by 3-dimensional echocardiography in young patients with Duchenne muscular dystrophy and normal left ventricular ejection fraction"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","607"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","The International Journal of Cardiovascular Imaging"],["dc.bibliographiccitation.lastpage","613"],["dc.bibliographiccitation.volume","34"],["dc.contributor.author","Dellas, Claudia"],["dc.contributor.author","Kammerer, Laura"],["dc.contributor.author","Gravenhorst, Verena"],["dc.contributor.author","Lotz, Joachim"],["dc.contributor.author","Paul, Thomas"],["dc.contributor.author","Steinmetz, Michael"],["dc.date.accessioned","2020-12-10T14:11:26Z"],["dc.date.available","2020-12-10T14:11:26Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1007/s10554-017-1267-z"],["dc.identifier.eissn","1573-0743"],["dc.identifier.issn","1569-5794"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/71073"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Quantification of pulmonary regurgitation and prediction of pulmonary valve replacement by echocardiography in patients with congenital heart defects in comparison to cardiac magnetic resonance imaging"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","672"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Der Ophthalmologe"],["dc.bibliographiccitation.lastpage","675"],["dc.bibliographiccitation.volume","108"],["dc.contributor.author","Neunhoeffer, H."],["dc.contributor.author","Goldammer, Lena"],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Feltgen, Nicolas"],["dc.contributor.author","Hoerauf, Hans"],["dc.date.accessioned","2018-11-07T08:54:36Z"],["dc.date.available","2018-11-07T08:54:36Z"],["dc.date.issued","2011"],["dc.description.abstract","Anterior segment colobomas can be found isolated or in combination with changes in the posterior segment. A coloboma of the ciliary zonule leads to alteration of the lens profile with myopia and astigmatism. Amblyopia and cataract development may also occur. We present two cases with a coloboma of the zonule with different degrees of expression and the most important differential diagnoses are discussed."],["dc.identifier.doi","10.1007/s00347-011-2351-8"],["dc.identifier.isi","000293243100014"],["dc.identifier.pmid","21503820"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/22707"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0941-293X"],["dc.title","Bilateral ciliary zonule defect"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.subtype","letter_note"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Clinical Research in Cardiology"],["dc.bibliographiccitation.volume","96"],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Jux, Christian"],["dc.contributor.author","Kietz, Silke"],["dc.contributor.author","Paul, Thomas"],["dc.date.accessioned","2018-11-07T10:58:49Z"],["dc.date.available","2018-11-07T10:58:49Z"],["dc.date.issued","2007"],["dc.format.extent","698"],["dc.identifier.isi","000249258500147"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/50554"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Dr Dietrich Steinkopff Verlag"],["dc.publisher.place","Darmstadt"],["dc.relation.issn","1861-0684"],["dc.title","Reversible dilatative cardiomyopathy in extreme chronic anaemia (Hb 1,1 g/dl)"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","152"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Herzschrittmachertherapie + Elektrophysiologie"],["dc.bibliographiccitation.lastpage","157"],["dc.bibliographiccitation.volume","32"],["dc.contributor.author","Gravenhorst, Verena D."],["dc.contributor.author","Schneider, Heike E."],["dc.contributor.author","Müller, Matthias J."],["dc.contributor.author","Krause, Ulrich"],["dc.contributor.author","Felke, Barbara"],["dc.contributor.author","Paul, Thomas"],["dc.date.accessioned","2021-06-01T10:49:11Z"],["dc.date.available","2021-06-01T10:49:11Z"],["dc.date.issued","2021"],["dc.identifier.doi","10.1007/s00399-021-00758-3"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86198"],["dc.language.iso","de"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.eissn","1435-1544"],["dc.relation.issn","0938-7412"],["dc.title","Fetales EKG und Arrhythmien"],["dc.title.translated","Fetal ECG and arrhythmias"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]