Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ulrike Bartram"'
Publikováno v:
Pediatric and Developmental Pathology. 11:266-273
Congenital interruption of the inferior vena cava (IVC) due to absence of its hepatic segment is usually found in patients with polysplenia. The occurrence without other features of the heterotaxy syndrome is rare, and the frequency of associated add
Publikováno v:
Pediatric Cardiology. 28:325-332
This review compiles the current knowledge of normal and abnormal myocardial morphogenesis to facilitate an unambiguous diagnosis of primary myocardial noncompaction. During the early stages of development, the formation of trabeculae with the result
Autor:
Ulrike Bartram, Kassa Darge
Publikováno v:
Pediatric Radiology. 35:655-660
Background:Harmonic imaging (HI) is a relatively new US method. Its usefulness in children has yet to be determined. Objective: To evaluate the value of HI in urinary tract imaging of infants and children. Materials and methods: The bladder and kidne
Publikováno v:
Neonatology. 88:278-290
Heterotaxy results from failure of the developing embryo to establish normal left-right asymmetry. Typical manifestations include abnormal symmetry and malposition of the thoraco-abdominal organs and vessels, complex congenital heart disease and extr
Autor:
Ulrike Bartram, Christian P. Speer
Publikováno v:
Chest. 125:754-765
Transforming growth factor (TGF) beta plays an important role in normal pulmonary morphogenesis and function and in the pathogenesis of lung disease. The effect of TGFbeta is regulated via a selective pathway of TGFbeta synthesis and signaling that i
Autor:
Christian P. Speer, Azhar Mohamad, L. Philip Sanford, Adriana C. Gittenberger-de Groot, Ulrike Bartram, Thomas Doetschman, Lambertus J. Wisse, Daniel G. M. Molin, Robert E. Poelmann
Publikováno v:
Circulation. 103:2745-2752
Background —Transforming growth factor-β 2 (TGF-β 2 ) is a member of a family of growth factors with the potential to modify multiple processes. Mice deficient in the TGF-β 2 gene die around birth and show a variety of defects of different organ
Publikováno v:
Pediatric Cardiology. 22:93-101
This review outlines the morphologic and pathogenetic characteristics of congenital polyvalvular disease. Two cases are used for exemplification. The macroscopic and histologic features of the valves as well as associated cardiac lesions and clinical
Publikováno v:
Medizinische Klinik. 92:8-14
BACKGROUND: The question whether patients suffering from end-stage emphysema who are candidates for lung transplantation should be treated with a single lung or with a double lung transplantation is still unanswered. METHODS: We reviewed 24 consecuti
Autor:
Jürgen Bauer, Ulrike Bartram, Hakan Akintuerk, Ina Michel-Behnke, Mathias Müller, Dietmar Schranz
Publikováno v:
The American journal of cardiology. 96(4)
Ventricular septal defects (VSDs) complicate the arterial switch operation (ASO) in newborns with transposition of the great arteries because of prolonged cardiac arrest time and subsequent ventricular dysfunction. Three newborns with paramembranous
Autor:
Daniel G.M. Molin, Ulrike Bartram, Kim Van der Heiden, Liesbeth van Iperen, Beerend P. Hierck, Christian P. Speer, Robert E. Poelmann, Adriana C. Gittenberger-de-Groot
Publikováno v:
Developmental dynamics : an official publication of the American Association of Anatomists. 227(3)
Transforming growth factor-beta (Tgfbeta) is essential for normal embryogenesis. The cardiac phenotypes obtained after knockout of each of the three mammalian isoforms suggest different roles during morphogenesis. We studied cardiovascular expression