Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Daiva-Elzbieta Optazaite"'
Autor:
Patricia Leutz-Schmidt, Daiva-Elzbieta Optazaite, Olaf Sommerburg, Monika Eichinger, Sabine Wege, Eva Steinke, Simon Y. Graeber, Michael U. Puderbach, Jens-Peter Schenk, Abdulsattar Alrajab, Simon M.F. Triphan, Hans-Ulrich Kauczor, Mirjam Stahl, Marcus A. Mall, Mark O. Wielpütz
Publikováno v:
ERJ Open Research, Vol 9, Iss 2 (2023)
Background Bronchial artery dilatation (BAD) is associated with haemoptysis in advanced cystic fibrosis (CF) lung disease. Our aim was to evaluate BAD onset and its association with disease severity by magnetic resonance imaging (MRI). Methods 188 CF
Externí odkaz:
https://doaj.org/article/88967b4379074ce3884f0c3d5830b010
Autor:
Ieva Dimiene, Kristina Bieksiene, Jurgita Zaveckiene, Mindaugas Andrulis, Daiva-Elzbieta Optazaite, Neringa Vaguliene, Marius Zemaitis, Skaidrius Miliauskas
Publikováno v:
Medicina, Vol 57, Iss 12, p 1308 (2021)
Diffuse pulmonary lymphangiomatosis (DPL), an exceptionally rare disease, mainly occurs in children and young adults of both sexes. Even though DPL is considered to be a benign disease, its prognosis is relatively poor. Because of its rarity, little
Externí odkaz:
https://doaj.org/article/48d82428fe984f57a29389187609ff63
Autor:
Daiva-Elzbieta Optazaite, Mindaugas Andrulis, Skaidrius Miliauskas, Neringa Vaguliene, Kristina Bieksiene, Jurgita Zaveckiene, Ieva Dimiene, Marius Zemaitis
Publikováno v:
Medicina, Vol 57, Iss 1308, p 1308 (2021)
Medicina
Medicina
Diffuse pulmonary lymphangiomatosis (DPL), an exceptionally rare disease, mainly occurs in children and young adults of both sexes. Even though DPL is considered to be a benign disease, its prognosis is relatively poor. Because of its rarity, little
Autor:
Daiva Elzbieta Optazaite, Annette Kopp-Schneider, C. Hintze, Mark O. Wielpütz, Jürgen Biederer, Michael Puderbach, Anne Niemann, Marcus A. Mall, Monika Eichinger, Hans-Ulrich Kauczor
Publikováno v:
European journal of radiology. 81(6)
Magnetic resonance imaging (MRI) gains increasing importance in the assessment of cystic fibrosis (CF) lung disease. The aim of this study was to develop a morpho-functional MR-scoring-system and to evaluate its intra- and inter-observer reproducibil
Autor:
Hans-Ulrich Kauczor, Monika Eichinger, Michael Puderbach, Marcus A. Mall, Daiva-Elzbieta Optazaite, Anne Niemann
Publikováno v:
A53. CYSTIC FIBROSIS: CLINICAL PEDIATRIC STUDIES.
Autor:
C. Hintze, Marcus A. Mall, Juergen Biederer, Hans-Ulrich Kauczor, Monika Eichinger, Anne Niemann, Annette Kopp-Schneider, Daiva-Elzbieta Optazaite, Michael Puderbach
Publikováno v:
A53. CYSTIC FIBROSIS: CLINICAL PEDIATRIC STUDIES.