Zobrazeno 1 - 10
of 153
pro vyhledávání: '"U Arbenz"'
Publikováno v:
Zeitschrift für Kardiologie. 90:127-132
Double aortic arch is a rare vascular anomaly which usually causes tracheal and esophageal compression in the first few months of life. During the last 30 years, 7 children, 2 to 24 months old, and one 29-year-old woman with double aortic arches have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcefe3477366be87c04bb3c94622ffbc
https://doi.org/10.1007/s003920170199
https://doi.org/10.1007/s003920170199
Publikováno v:
Scopus-Elsevier
Coronary artery fistula is a very rare congenital malformation with an abnormal coronary-cameral communication that may involve any chamber and any or all coronary artery branches. We present our experience with 11 consecutive patients (mean age 16.6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d95cf314b8e0e6b0958873c3dde7b01
https://doi.org/10.1159/000177114
https://doi.org/10.1159/000177114
Autor:
M. Pasic, L. von Segesser, T. Carrel, U. Arbenz, M. Tönz, U. Niederhäuser, P. Vogt, M. Turina
Publikováno v:
Cardiovascular Surgery. 1:608-612
Between 1977 and 1992, four infants with an anomalous left pulmonary artery and subsequent compression of the tracheobronchial tree were operated on at the University Hospital Zurich. The operation consisted of mobilization of the abnormal left pulmo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ab9e7fdd62e595db06d252c44d7f101
https://doi.org/10.1177/096721099300100529
https://doi.org/10.1177/096721099300100529
Autor:
G. Karrer, J. Behr, Joseph T. Chambers, Dan Lewinthal, H. Bauer, D.J. Hansell, Per Aim, U. Arbenz, Adrian Ionescu, Lopez Bernal, Juhani Toivonen, Lennart Bondeson, S. Heinzl, Ehud Kukia, Ron Tepper, H. Baumann, Pål Øian, A. Huch, H. Riedmiller, Shlomo Mashiach, Jennifer C. Wilson, M. Winkler, F. Casper, Evan Sundström, J. Dudenhausen, Tapani Luukkainen, Johannes Skjerris, Khail Nahoul, Pekka Lähteenmäki, P.J. Keller, Peter E. Schwartz, K. Vetter, Jens-Jörgen Platz-Christensen, Veronique Amice, Josef Blankstein, Mohamed-Hassan Hatahet, G.C. Liggins, T.Y. Khong, J.W. Keeling, N. Deslex, Olof Löfgren, Per-Göran Larsson, Bjarne Østerud, Ch. Rudin, Ivar H. Omsjø, Josef Shalev, A.C. Turnbull, N. Pavić, P.M. Lamont, Jean-Pierre Bercovici, Mordechai Goldenberg, J.C. Schellenberg, Jan Martin Maltau, R. Seufert, Maria J. Merino, H. Ellis, Ernest I. Kohorn, Kari Ratsula, Jean Amice
Publikováno v:
Gynäkologisch-geburtshilfliche Rundschau. 30:57-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c41886729d434eb9f21f35df963651e
https://doi.org/10.1159/000271188
https://doi.org/10.1159/000271188
A boy aged 2 years 10 months was admitted to the hospital because of high fever for three days, a rash over the trunk, oedema, redness of the palms without peeling skin, conjunctivitis affecting both eyes, redness of the lips, reddened throat with st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::526572c5b88e238b1a2ff3f55fc27f83
https://europepmc.org/articles/PMC1768567/
https://europepmc.org/articles/PMC1768567/
Publikováno v:
Zeitschrift fur Kardiologie. 90(2)
Double aortic arch is a rare vascular anomaly which usually causes tracheal and esophageal compression in the first few months of life. During the last 30 years, 7 children, 2 to 24 months old, and one 29-year-old woman with double aortic arches have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::441a0a7b52fddde07f7641caf588a7ad
https://pubmed.ncbi.nlm.nih.gov/11263002
https://pubmed.ncbi.nlm.nih.gov/11263002
Can dopamine prevent the renal side effects of indomethacin? A prospective randomized clinical study
Publikováno v:
Klinische Padiatrie. 211(6)
Indomethacin therapy for closure of a patent ductus arteriosus in preterm neonates is responsible for transient renal insufficiency. Dopamine theoretically reduces the renal side effects of indomethacin therapy.33 neonates with a mean gestational age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6812b522ada8297a1f45122d71c95f33
https://pubmed.ncbi.nlm.nih.gov/10592922
https://pubmed.ncbi.nlm.nih.gov/10592922
Publikováno v:
Schweizerische medizinische Wochenschrift. 129(21)
In a retrospective study we evaluated the predictive value of the traditional risk factors (Fontan criteria) for mortality and morbidity after total cavopulmonary anastomosis (Fontan operation).We studied 51 consecutive patients who underwent Fontan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5406d8babb8feb14ce316d36874d79c7
https://pubmed.ncbi.nlm.nih.gov/10413814
https://pubmed.ncbi.nlm.nih.gov/10413814
Autor:
J. Uehlinger, Burkhard Simma, Reinhard Seger, U. Arbenz, Margrit Fasnacht, Sergio Fanconi, R. Biedermann, G. Ferrazzini, P. Dangel
Publikováno v:
Intensive care medicine. 22(5)
We report a case of neonatal lupus erythematosus (NLE) with congenital heart block and severe myocardial failure, which was followed from the 25th week of gestation because of fetal bradycardia. The child was delivered at the 37th week of gestation b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcfa76efb7efc192fd294b8c8267eab3
https://pubmed.ncbi.nlm.nih.gov/8796403
https://pubmed.ncbi.nlm.nih.gov/8796403
Publikováno v:
The Journal of cardiovascular surgery. 37(1)
Coronary artery fistula is a very rare congenital malformation with abnormal coronary-cameral communication that may involve any chamber and any or all coronary artery branches. We present our experience with 11 consecutive patients [mean age 16.6 ye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5bce713e045ce13f5695cd56c3372724
https://pubmed.ncbi.nlm.nih.gov/8606205
https://pubmed.ncbi.nlm.nih.gov/8606205