Zobrazeno 1 - 10
of 123
pro vyhledávání: '"I. Hammerer"'
Autor:
I. Hammerer
Publikováno v:
Pädiatrie & Pädologie. 48:18-20
Seltene Krankheiten („orphan diseases“) und Krankheiten, deren Diagnostik und Behandlung eine spezialisierte Ausbildung und kostspielige Apparaturen und Einrichtungen erfordern, mussen zentralisiert betreut werden. Das entsprechend ausgebildete a
Publikováno v:
Pediatric cardiology. 20(3)
A 13-year-old boy with hypertrophic obstructive cardiomyopathy was treated with dual-chamber pacing after severe progression of left ventricular outflow tract obstruction and of clinical symptoms despite drug therapy. Rapid intrinsic atrioventricular
Publikováno v:
Klinische Pädiatrie. 202:183-185
We report a child with a rare cardiac involvement in GM1 gangliosidosis. At the age of 9 months a secondary dilatative cardiomyopathy due to the metabolic disorder was diagnosed. During 2 years the functional echocardiographic signs became normal, th
Publikováno v:
Klinische Padiatrie. 209(3)
PS is a rare congenital vascular anomaly in which the left pulmonary artery originates from the right pulmonary artery and courses between trachea and esophagus to the hilus of the left lung causing compression of the right mainstem bronchus and trac
Publikováno v:
British heart journal. 74(1)
OBJECTIVE--To establish criteria for the accurate diagnosis of different forms of left sided pericardial defects on magnetic resonance imaging. Early detection of a partial apical defect is essential as it is potentially fatal. DESIGN--Examination of
Autor:
A, Beitzke, J I, Stein, M, Haidvogl, A, Pilhatsch, C, Suppan, I, Hammerer, C, Fink, M, Fritz, M, Schlemmer, M, Wimmer
Publikováno v:
Zeitschrift fur Kardiologie. 83(12)
From July 1987 to December 1992, 52 patients underwent balloon-angioplasty of aortic coarctation at three units of pediatric cardiology in Austria (Graz = 35 patients, Innsbruck = 15 patients, and Vienna = 2 patients). 35 patients had postoperative a
Publikováno v:
European journal of pediatrics. 150(7)
We report a 3-year-old girl with the cardio-facio-cutaneous (CFC) syndrome. She presented the typical combination of mild developmental delay, postnatal onset short stature with relative macrocephaly, a wide and prominent forehead with posteriorly ro
Publikováno v:
Padiatrie und Padologie. 26(1)
The congenital heart disease incidence study was designed to collect valid data with respect to new diagnostic methods and to an improved system of preventive health care in order to compare the results with former studies. In the years 1979-1983 the
Publikováno v:
Klinische Padiatrie. 202(3)
We report a child with a rare cardiac involvement in GM1 gangliosidosis. At the age of 9 months a secondary dilatative cardiomyopathy due to the metabolic disorder was diagnosed. During 2 years the functional echocardiographic signs became normal, th
Autor:
H. Ringe, H. J. Feickert, H. C. Kallfelz, Dang Phuong Kiet, Nguyen Xuan Thu, William Meadow, Brian Rudinsky, Anthony Bell, A. Eicken, W. Sebening, G. Balling, K. Bühlmeyer, Majidah Shadid, Paul Steendijk, Ralph Moison, Enno T. van de Velde, Jan Baan, Howard M. Berger, Frank van Bel, G. Ya Gebel, A. G. Kruglov, L. M. Golostenova, A. N. Dasaev, V. N. Utkin, V. E. Bagdatjev, N. G. Ignatov, S. G. Suvorov, C. Fink, B. Simma, M. Fritz, R. Trawöger, R. Geiger, I. Hammerer
Publikováno v:
Intensive Care Medicine. 22:S245-S246