Zobrazeno 1 - 10
of 310
pro vyhledávání: '"M. Puderbach"'
Autor:
J. M. Wild, H. Marshall, M. Bock, L. R. Schad, P. M. Jakob, M. Puderbach, F. Molinari, E. J. R. Van Beek, J. Biederer
Publikováno v:
Insights into Imaging, Vol 3, Iss 4, Pp 345-353 (2012)
Abstract Proton magnetic resonance imaging (MRI) has recently emerged as a clinical tool to image the lungs. This paper outlines the current technical aspects of MRI pulse sequences, radiofrequency (RF) coils and MRI system requirements needed for im
Externí odkaz:
https://doaj.org/article/abd1e9983954484bb6a39621cf42e378
Publikováno v:
Insights into Imaging, Vol 3, Iss 4, Pp 355-371 (2012)
Abstract Background Among the modalities for lung imaging, proton magnetic resonance imaging (MRI) has been the latest to be introduced into clinical practice. Its value to replace X-ray and computed tomography (CT) when radiation exposure or iodinat
Externí odkaz:
https://doaj.org/article/a6698d8f4fa94ba394ab642873210d4d
Autor:
Jürgen Biederer, S. Mirsadraee, M. Beer, F. Molinari, C. Hintze, G. Bauman, M. Both, E. J. R. Van Beek, J. Wild, M. Puderbach
Publikováno v:
Insights into Imaging, Vol 3, Iss 4, Pp 373-386 (2012)
Abstract Background MRI of the lung is recommended in a number of clinical indications. Having a non-radiation alternative is particularly attractive in children and young subjects, or pregnant women. Methods Provided there is sufficient expertise, m
Externí odkaz:
https://doaj.org/article/34be971c5458441ca907fb4f5e6fa578
Autor:
P. Leutz-Schmidt, Monika Eichinger, M. Puderbach, Mark O. Wielpütz, Marcus A. Mall, Olaf Sommerburg, Mirjam Stahl, Simon M. F. Triphan, H. U. Kauczor, S. Gehlen
Publikováno v:
Der Radiologe. 60:813-822
Die Schwere des Verlaufs und die Sterblichkeit der Mukoviszidose (zystische Fibrose, CF) ist wesentlich durch die pulmonale Manifestation gepragt. Eine fruhe Diagnose und rasch einsetzende Therapie sind entscheidend fur einen langfristigen Erhalt der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c05d47d2bb11d8eb1fef8dd4cd86981
https://doi.org/10.1007/s00117-020-00723-0
https://doi.org/10.1007/s00117-020-00723-0
Autor:
C, Schwarz, B, Schulte-Hubbert, J, Bend, M, Abele-Horn, I, Baumann, W, Bremer, F, Brunsmann, D, Dieninghoff, O, Eickmeier, H, Ellemunter, R, Fischer, J, Grosse-Onnebrink, J, Hammermann, H, Hebestreit, M, Hogardt, C, Hügel, M, Hug, S, Illing, A, Jung, B, Kahl, A, Koitschev, R, Mahlberg, J G, Mainz, F, Mattner, A, Mehl, A, Möller, C, Muche-Borowski, T, Nüßlein, M, Puderbach, S, Renner, E, Rietschel, F C, Ringshausen, S, Schmidt, L, Sedlacek, H, Sitter, C, Smaczny, B, Tümmler, R, Vonberg, M O, Wielpütz, H, Wilkens, B, Wollschläger, J, Zerlik, U, Düesberg, S, van Koningsbruggen-Rietschel
Publikováno v:
Pneumologie (Stuttgart, Germany). 72(5)
Cystic Fibrosis (CF) is the most common autosomal-recessive genetic disease affecting approximately 8000 people in Germany. The disease is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene leading to dysfuncti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f44773f4a4e349d1c30d91dcdb6f1e0
https://pubmed.ncbi.nlm.nih.gov/29758578
https://pubmed.ncbi.nlm.nih.gov/29758578
Autor:
Ingo Baumann, F.-M. Müller, J. Bend, A. Möller, Doris Staab, Carsten Schwarz, W. Bremer, Ernst Rietschel, R.-P. Vonberg, Burkhard Tümmler, R. Mahlberg, R. Bruns, Christina Smaczny, J. Riedler, B. Schulte-Hubbert, M. Abele-Horn, H. Hebestreit, R. Fischer, M. Kohlhäufl, F. Brunsmann, L. Sedlacek, S. Illing, J. Zerlik, Helmut Sitter, M. Puderbach, J. Bargon, Jochen G. Mainz, T. O. Hirche, Assen Koitschev, Michael Hogardt, Isidor Huttegger, Manfred Ballmann, S. Pfeiffer-Auler, C. Geidel, Tof Wagner
Publikováno v:
Monatsschrift Kinderheilkunde. 163:590-599
Mukoviszidose (zystische Fibrose, CF) ist eine der haufigsten autosomal-rezessiv vererbten Erkrankungen der kaukasischen Bevolkerung. Der genetische Defekt im CFTR-Gen fuhrt zu einer Verringerung des Chloridionentransports an der Zellmembran. Die res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cea5caf19930e1be2c21b34ebd157c6
https://doi.org/10.1007/s00112-015-3354-3
https://doi.org/10.1007/s00112-015-3354-3
Publikováno v:
MRI of the Lung ISBN: 9783319426167
Proton MRI is able to depict the major changes in CF lung disease in a similar way to CT, albeit there will be shortcomings in the detection of more subtle or smaller abnormalities. Further studies are warranted to determine whether the additional st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::421f571c29335bff68c9655b9cc163fe
https://doi.org/10.1007/174_2017_49
https://doi.org/10.1007/174_2017_49
Autor:
CP Heußel, Fjf Herth, Philipp A. Schnabel, Michael Kreuter, M. Puderbach, Benjamin Egenlauf, Arne Warth
Publikováno v:
Der Pneumologe. 11:255-258
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::915d85086dd0fbeaa1d14ad99efa931d
https://doi.org/10.1007/s10405-013-0773-5
https://doi.org/10.1007/s10405-013-0773-5
Autor:
M. Puderbach, K Palmowski, H Zabeck, Michael Kreuter, CP Heußel, M Schaaf, Arne Warth, U Oltmanns, Philipp A. Schnabel, Fjf Herth
Publikováno v:
Der Pneumologe. 11:61-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e07da0d91db80bef490328c1d1f32a0
https://doi.org/10.1007/s10405-013-0746-8
https://doi.org/10.1007/s10405-013-0746-8
Autor:
Hans U. Kauczor, C. Hintze, Monika Eichinger, Julien Dinkel, Omid Khalilzadeh, M Fabel, Jürgen Biederer, Michael Thomas, Heinz Peter Schlemmer, M. Thorn, M. Puderbach, Claus Peter Heussel
Publikováno v:
Lung Cancer. 82:76-82
Therapy monitoring in oncologic patient requires precise measurement methods. In order to improve the precision of measurements, we used a semi-automated generic segmentation algorithm to measure the size of large lung cancer tumors. The reproducibil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17daffef539b116774fd2a35c023df59
https://doi.org/10.1016/j.lungcan.2013.07.006
https://doi.org/10.1016/j.lungcan.2013.07.006