Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Janina, Bacher"'
Autor:
Hartmut P.H. Neumann, Angelica Malinoc, Janina Bacher, Zinaida Nabulsi, Vera Ivanovas, Nadine Ortiz Bruechle, Irina Mader, Michael M. Hoffmann, Peter Riegler, Annette Kraemer-Guth, Christian Burchardi, Elke Schaeffner, Rodolfo S. Martin, Pablo J. Azurmendi, Klaus Zerres, Cordula Jilg, Charis Eng, Sven Gläsker
Publikováno v:
Cerebrovascular Diseases Extra, Vol 2, Iss 1, Pp 71-79 (2012)
Background: Patients who harbor intracranial aneurysms (IAs) run a risk for aneurysm rupture and subsequent subarachnoid hemorrhage which frequently results in permanent deficits or death. Prophylactic treatment of unruptured aneurysms is possible an
Externí odkaz:
https://doaj.org/article/1924638bf3554e139167274304b7256f
Autor:
Hartmut P H, Neumann, Cordula, Jilg, Janina, Bacher, Zinaida, Nabulsi, Angelica, Malinoc, Barbara, Hummel, Michael M, Hoffmann, Nadina, Ortiz-Bruechle, Sven, Glasker, Przemyslaw, Pisarski, Hannes, Neeff, Annette, Krämer-Guth, Markus, Cybulla, Martin, Hornberger, Jochen, Wilpert, Ludwig, Funk, Jörg, Baumert, Dietrich, Paatz, Dieter, Baumann, Markus, Lahl, Helmut, Felten, Martin, Hausberg, Klaus, Zerres, Charis, Eng, Dieter, Lang
Publikováno v:
Nephrology Dialysis Transplantation. 28:1472-1487
BACKGROUND As we emerge into the genomic medicine era, the epidemiology of diseases is taken for granted. Accurate prevalence figures, especially of rare diseases (RDs, ≤50/100,000), will become even more important for purposes of health care and s
Autor:
Malte Schwardt, Angelica Malinoc, Pablo Javier Azurmendi, Mercedes Nunez, Wolfgang Schultze-Seemann, Alexander Weber, Vanessa Drendel, Hartmut P. H. Neumann, Zoran Erlic, Janina Bacher, Hannes P. Neeff, Martin Werner, Cordula A. Jilg, Sven Gläsker, Przemyslaw Pisarski, Oliver Drognitz
Background: The role of autosomal dominant polycystic kidney disease (ADPKD) as a risk factor for renal cell carcinoma (RCC) is still under discussion. Data on prevalence of RCC in ADPKD are limited, especially on a large population scale. The aim of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f7c7c3c0db87538ed301e66a003a5b0
https://doi.org/10.1159/000351049
https://doi.org/10.1159/000351049
Autor:
Klaus Zerres, Robert Corradini, Janina Bacher, Markus Cybulla, Jens Nürnberger, Hartmut P. H. Neumann, Jochen Wilpert, Elke Schaeffner, Cordula A. Jilg, Sven Gläsker, Annette Kraemer-Guth, Peter Dr. Riegler, Pablo Javier Azurmendi, Michael M. Hoffmann, Mercedes Nunez, Nadine Ortiz Brüchle, Zinaida Nabulsi
BACKGROUND: ADPKD is one of the most common inherited disorders, with high risk for end-stage renal disease. Numerous patients, however, have no relatives in whom this disorder is known and are unsure whether they may transmit the disease to their of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32b811348b58873dad5c4a6218142888
https://doi.org/10.1007/s11255-012-0125-0
https://doi.org/10.1007/s11255-012-0125-0
Autor:
Nadine Ortiz Bruechle, Peter Dr. Riegler, Elke Schaeffner, Christian Burchardi, Janina Bacher, Pablo Javier Azurmendi, Michael Hoffmann, Hartmut P. H. Neumann, Zinaida Nabulsi, Angelica Malinoc, Sven Gläsker, Annette Kraemer-Guth, Vera Ivanovas, Charis Eng, Rodolfo S. Martin, Klaus Zerres, Irina Mader, Cordula A. Jilg
Publikováno v:
Cerebrovascular diseases / Extra 2(1), 71-79 (2012). doi:10.1159/000342620
Cerebrovascular Diseases Extra, Vol 2, Iss 1, Pp 71-79 (2012)
Cerebrovascular Diseases Extra
Cerebrovascular Diseases Extra, Vol 2, Iss 1, Pp 71-79 (2012)
Cerebrovascular Diseases Extra
Cerebrovascular diseases / Extra 2(1), 71-79 (2012). doi:10.1159/000342620
Published by Karger, Basel
Published by Karger, Basel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93b1543900c9e902038d779bb10fde07
Autor:
Zoran Erlic, Ursula Ploeckinger, Alberto Cascon, Michael M Hoffmann, Laura von Duecker, Aurelia Winter, Gerit Kammel, Janina Bacher, Maren Sullivan, Berend Isermann, Lars Fischer, Andreas Raffel, Wolfram Trudo Knoefel, Matthias Schott, Tobias Baumann, Oliver Schaefer, Tobias Keck, Richard P Baum, Ioana Milos, Mihaela Muresan, Mariola Peczkowska, Andrzej Januszewicz, Kenko Cupisti, Anke Tönjes, Mathias Fasshauer, Jan Langrehr, Peter von Wussow, Abbas Agaimy, Günter Schlimok, Regina Lamberts, Thorsten Wiech, Kurt Werner Schmid, Alexander Weber, Mercedes Nunez, Mercedes Robledo, Charis Eng, Hartmut P H Neumann
Pancreatic islet cell tumors (ICTs) occur as sporadic neoplasias or as a manifestation of multiple endocrine neoplasia type 1 (MEN1) and von Hippel–Lindau disease (VHL). Molecular classification of ICTs is mandatory for timely diagnosis and surveil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af591c43026d954e3b55d23424d9a1f0
https://doi.org/10.5167/uzh-45080
https://doi.org/10.5167/uzh-45080
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 49(1)
Tuberous sclerosis complex (TSC) was instrumented for identification of the gene causing autosomal dominant polycystic kidney disease type 1 (PKD1) because a patient showing both diseases gave rise to the suggestion that the TSC2 gene is located in c
Autor:
Pablo Pergola, Obinna D. Onodugo, Hiromichi Gotoh, Tobias Breidthardt, Pablo Javier Azurmendi, Amit Sharma, Mercedes Nunez, Satz Mengensatzproduktion, Alexander Weber, Ling-I Chen, Iain C. Macdougall, Yi-Chun Tsai, Martha S. Persky, Kevin Roe, Sven Gläsker, Christin Spatz, Julius U. Okoye, Stig Molsted, Jiun-Chi Huang, Orfeas Liangos, Angelica Malinoc, Shay Tzur, Christopher T. Chan, Cristian Pattaro, Bhupinder Singh, Zoran Erlic, Inge Eidemak, Jesper L. Andersen, Allan C. Skanes, Christopher J. Kirwan, Shih-Han S. Huang, Kiichiro Fujita, Przemyslaw Pisarski, Erik Lehman, Masahiro Inagaki, Daljit K. Hothi, Yuya Nakamura, Gerard Smits, Druck Reinhardt Druck Basel, Koichi Hayashi, Shingo Hori, Stephen Holt, Adrian P. Harrison, Hung-Chun Chen, F.L. Game, Mohamed Tarek Eldehni, Yutaka Shiina, Gunnar Sigurdsson, Szu-Chia Chen, Janina Bacher, Bogdan Momciu, Andrew D. Krahn, Bertrand L. Jaber, Hiroshi Itoh, Katsuji Oguchi, Saharon Rosset, Sean Platton, Uchenna N. Ijoma, Robert M. Lindsay, Michiyasu Inoue, Maurizio Bossola, Shu Wakino, Hannes Neeff, S. Hussain, Neil Ashman, Aghogho Odudu, James O. Burton, Revital Shemer, Cosetta Minelli, Shang-Jyh Hwang, Macaulay A C Onuigbo, Chinwuba K. Ijoma, Benjamin K.A. Thomson, Maria C. Comelli, Ngozi A. Ifebunandu, Seitaro Fujishima, Irena Glowinska, Nick Medford, Jan Marek, Lesley Rees, Koichiro Homma, Sverrir I. Gunnarsson, Navin Verma, Walter G. Wasser, Ewa Koc-Zorawska, Geoffrey A. Block, Wolfgang Schultze-Seemann, N.M. Selby, Tatsuo Shimizu, Karl Skorecki, Joseph V. Bonventre, Cajetan C. Onyedum, Gerald Stifter, Yasuhiko Homma, Ifeoma Ulasi, Peter P. Pramstaller, Etty Kruzel, Michal Mysliwiec, Marissa F. Baltazar, Ho-Ming Su, Jolanta Malyszko, Peter K. MacCullum, Mirko Modenese, Oliver Drognitz, Jacek S. Malyszko, Chinwe J. Chukwuka, Christopher W. McIntyre, J. Kazi, Peter Riegler, Brad L. Urquhart, George J. Klein, Jer-Ming Chang, Ejikeme B. Arodiwe, Paweena Susantitaphong, Masaru Suzuki, Flemming Dela, David Hildick-Smith, Runolfur Palsson, Olafur S. Indridason, Hartmut P. H. Neumann, Mary C. Perianayagam, Hocine Tighiouart, Malte Schwardt, Helen J. Jefferies, Beth M. Shamblin, Cordula A. Jilg, Elena Feigin, C.W. McIntyre, Martin Werner, Luigi Tazza, Adnan I Qureshi, Sudhakar George, Yoshikazu Goto, Zahid F. Baig, Emmanuel Nna, Vanessa Drendel
Publikováno v:
Nephron Physiology. 121:X-X