Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Morten Helvind"'
Publikováno v:
Case Reports in Genetics, Vol 2021 (2021)
In this clinical report, we describe a male infant and his mother, who had similar congenital heart defects. They were both diagnosed neonatally with total anomalous pulmonary venous connection (TAPVC) in combination with other heart defects. Neither
Externí odkaz:
https://doaj.org/article/2e172a49011f45d7963b3e6666ddf0a3
Autor:
Thomas, Holm-Weber, Jacob, Gjedsted, Michael Rahbek, Schmidt, Morten, Helvind, Vibeke E, Hjortdal
Publikováno v:
Ugeskrift for laeger. 184(33)
Protein-losing enteropathy (PLE) is a severe Fontan complication. This is a case report of the first hybrid treatment of PLE in Denmark of an 11-year-old Fontan patient with severe symptoms (diarrhoea, fatigue and swelling) and low albumin level. Dia
Autor:
Morten Helvind, Bohdan Maruszewski, Emile A. Bacha, Kisaburo Sakamoto, Christo I. Tchervenkov, Susan Vosloo, Cheul Lee, James S. Tweddell, Christian Kreutzer, Attilio A. Lotto, Hani K. Najm, Giovanni Stellin, Nguyen Ly Thinh Truong, Piya Samankatiwat, Jeffrey P. Jacobs, Joseph A. Dearani, Drissi Boumzebra, Miguel Arboleda, Krishna S Iyer, Pedro Becker, Tae-Gook Jun, James D St Louis, Valdano Manuel, Claudia Herbst, Bistra Zheleva, George E. Sarris, Richard A. Jonas, Frank Edwin, Kirsten Finucane, Sivakumar Sivalingam, Hafil B Abdulgani, Hao Zhang, David M. Overman, Marcelo B. Jatene, Vladimiro L. Vida, David J. Barron, Zohair Al-Halees, José Fragata, Adel Elgamal, Budi Rahmat, Elizabeth H. Stephens, Jorge Cervantes, Nestor Sandoval, Darshan Reddy, James K. Kirklin, Justin T. Tretter
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 12:394-405
The optimal training of the highly specialized congenital heart surgeon is a long and complex process, which is a significant challenge in most parts of the world. The World Society for Pediatric and Congenital Heart Surgery (WSPCHS) has established
Publikováno v:
Case Reports in Genetics, Vol 2021 (2021)
Case Reports in Genetics
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, 5539855 . https://doi.org/10.1155/2021/5539855
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, pp. 5539855 . https://doi.org/10.1155/2021/5539855
Case Reports in Genetics
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, 5539855 . https://doi.org/10.1155/2021/5539855
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, pp. 5539855 . https://doi.org/10.1155/2021/5539855
In this clinical report, we describe a male infant and his mother, who had similar congenital heart defects. They were both diagnosed neonatally with total anomalous pulmonary venous connection (TAPVC) in combination with other heart defects. Neither
Autor:
Robin P. F. Dullaart, Bjoern Dahlback, Henrik Ørbæk Andersen, Lars Bo Nielsen, Eva Martha Madsen Svarrer, Maartje C. J. Slagman, Morten Helvind, Gerjan Navis
Publikováno v:
Biomarkers in medicine, 10(1), 81-93. FUTURE MEDICINE LTD
Aim: To investigate whether apoM is excreted in urine of children undergoing heart surgery and the potential of apoM as early biomarker of acute kidney injury (AKI). Materials & methods: Urine was collected in children undergoing heart surgery. ApoM
Autor:
Henrik Ørbæk Andersen, Naima Borg Tahri, Mathis Gröning, Morten Helvind, Lars Søndergaard, Mads Ersbøll
Publikováno v:
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery. 56(1)
OBJECTIVES The aim was to investigate the incidence of infective endocarditis (IE) in right ventricle-to-pulmonary artery conduits implanted at a Danish tertiary centre. METHODS Cases of IE in patients with homografts, Contegra grafts and Melody tran
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 4:286-289
We report on a 10-year-old boy with medically refractory pulmonary arterial hypertension (PAH) and end-stage right heart failure after closure of a ventricular septal defect. The boy was a candidate for lung transplantation (LTX), but an alternative
Autor:
Harald Lindberg, Bart Meyns, Jeffrey P. Jacobs, Mark G. Hazekamp, Massimo A. Padalino, Jean Rubay, Rudolphus Berger, Ilkka Mattila, Marco Pozzi, Djoeke Wolff, Tjark Ebels, Guido Michielon, Duccio Di Carlo, Nosal M, Stojan Lazarov, José Fragata, Tomáš Tláskal, René Prêtre, Alexander Kadner, Morten Helvind, Hakan Berggren, George E. Sarris, Viktor Hraska, Joost P. van Melle, Emre Belli, Jürgen Hörer
Publikováno v:
Heart (British Cardiac Society), 102(14), 1127-1133. BMJ Publishing Group
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Heart, 102(14), 1127-1133
Heart, 102(14), 1127-1133. BMJ PUBLISHING GROUP
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Heart, 102(14), 1127-1133
Heart, 102(14), 1127-1133. BMJ PUBLISHING GROUP
OBJECTIVE: The objective of this European multicenter study was to report surgical outcomes of Fontan takedown, Fontan conversion and heart transplantation (HTX) for failing Fontan patients in terms of all-cause mortality and (re-)HTX.METHODS: A retr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d16ed999481446936bc0db9086cd978
http://hdl.handle.net/11577/3314820
http://hdl.handle.net/11577/3314820
Publikováno v:
Interactive CardioVascular and Thoracic Surgery. 7:84-89
The number of patients with grown-up congenital heart (GUCH) disease is steadily increasing. Although there is agreement that the medical service for GUCH patients should be expanded in coming years, it is still unknown whether this should also inclu
Publikováno v:
Danish medical journal. 62(9)
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is an uncommon congenital heart abnormality. The aim of this study was to describe a single-centre experience with surgical repair of this condition.We performed a retros