Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Mariusz I, Furmanek"'
Autor:
Małgorzata Szperl, Ilona Michałowska, Jarosław B. Ćwikła, Mariola Pęczkowska, Andrzej Januszewicz, Aleksander Prejbisz, Urszula Swoboda-Rydz, Mariusz I. Furmanek, Anna Lewczuk
Publikováno v:
Polish Journal of Radiology
BACKGROUND: Hereditary head and neck paragangliomas (HNP) are very often associated with pheochromocytoma-paraganglioma syndromes, which are caused by mutations in genes encoding subunits of succinate dehydrogenase (SDHx) complex. The aim of this stu
Autor:
Mariusz I. Furmanek, Mateusz Spiewak, Maksymilian P. Opolski, Kajetan Grodecki, Ilona Michałowska
Publikováno v:
Arquivos Brasileiros de Cardiologia
Arquivos Brasileiros de Cardiologia, Vol 110, Iss 6, Pp 600-601
Arquivos Brasileiros de Cardiologia, Vol 110, Iss 6, Pp 600-601
A 45-year-old male without past medical history presented with retrosternal chest pain and ST-segment elevation in inferolateral leads at ECG. Invasive coronary angiography, along with optical coherence tomography performed as part of the clinical st
Autor:
Andrzej Januszewicz, Angelica Malinoc, Jolanta Antoniewicz, Piotr Pęczkowski, Anna Lewczuk, Wojciech Michalski, Hartmut P. H. Neumann, Grażyna Bednarek-Tupikowska, Marek Kabat, Małgorzata Szperl, Jarosław B. Ćwikła, Katarzyna Przybylowska, Jadwiga Janas, Andrzej Kawecki, Dariusz Moczulski, Andrzej Cichocki, Ilona Michałowska, Mariola Pęczkowska, Z. Szutkowski, Hanna Janaszek-Sitkowska, Mariusz I. Furmanek, John R. Buscombe, Maciej Otto, Aleksander Prejbisz
Publikováno v:
Neuroendocrinology. 101:321-330
Aims: The aim of this study was to assess the usefulness of somatostatin receptor scintigraphy (SRS) using 99mTc-[HYNIC, Tyr3]-octreotide (TOC) and 123I-metaiodobenzylguanidine (mIBG) in patients with SDHx-related syndromes in which paragangliomas we
Autor:
Ashley B. Grossman, Ilona Michałowska, Anouk N A van der Horst-Schrivers, Satz Mengensatzproduktion, Hironobu Sasano, Andrzej Cichocki, Francesca Spada, Jadwiga Janas, Nicola Fazio, Thamara E. Osinga, Simona Grozinsky-Glasberg, David J. Gross, Jonathan R. Strosberg, Silvia Giatti, Andrzej Januszewicz, Wojciech Michalski, Saulo J.A. Felizola, Anna Koumarianou, Piotr Pęczkowski, Larissa C. Faustino, Caterina Fumagalli, Gregory Kaltsas, Druckerei Stückle, Maciej Otto, Kjell Öberg, Thera P. Links, Barbara Viviani, Marek Kabat, Roberta Rigolio, Anna Lewczuk, Angelica Malinoc, Małgorzata Szperl, Aleksander Prejbisz, Alfredo Berruti, Ronald R. de Krijger, Mika Watanabe, Ido P. Kema, Andrzej Kawecki, Yasuhiro Nakamura, Michiaki Unno, Simone Romano, Hiroko Ogata, Guido Cavaletti, Bernard F. A. M. van der Laan, Hartmut P. H. Neumann, Massimo Barberis, Dariusz Moczulski, Grażyna Bednarek-Tupikowska, Esther Korpershoek, Mariola Pęczkowska, Yoshiaki Onodera, J. R. Buscombe, Tania M. Ortiga-Carvalho, Samaneh Yazdani, Nico Mitro, Katarzyna Przybyłowska, Jolanta Antoniewicz, Luis M. Garcia-Segura, Matthew H. Kulke, Salvatore Galdy, Jarosław B. Ćwikła, Robin P. F. Dullaart, Donald W. Pfaff, Michiel N. Kerstens, Donatella Caruso, Zbigniew Szutkowski, Mariusz I. Furmanek, Khatuna Gagnidze, Atsuko Kasajima, Hanna Janaszek-Sitkowska, Roberto Cosimo Melcangi, Fuyuhiko Motoi
Publikováno v:
Neuroendocrinology. 101:I-IV
Autor:
Mariusz I. Furmanek
Publikováno v:
Życie i starzenie się z wirusem HIV. Podejście interdyscyplinarne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7109a25f1af7860dddcf0223cd1c861f
https://doi.org/10.31338/uw.9788323528111.pp.57-66
https://doi.org/10.31338/uw.9788323528111.pp.57-66
Autor:
Mirosław Kowalski, Piotr Hoffman, Ilona Michałowska, Tomasz Hryniewiecki, Mariusz Kruk, Mariusz I. Furmanek, Joanna Waniewska, Paweł Kwiatek, Tomasz Oleksiuk
Publikováno v:
Journal of Thoracic Imaging. 29:113-117
The aim of the study was to assess thoracic aorta pathologies coexisting with bicuspid aortic valve (BAV) using dual-source computed tomography.A total of 102 patients with BAV diagnosed by electrocardiogram-gated computed tomography angiography of t
Autor:
Aleksander Prejbisz, Hartmut P. H. Neumann, Charis Eng, Agata Kubaszek, Mariusz I. Furmanek, Alberto Cascón, B Jarosław Cwikła, Mariola Pęczkowska, Andrzej Januszewicz, Zoran Erlic
Publikováno v:
Nature Clinical Practice Endocrinology & Metabolism. 4:111-115
There is a high frequency of germline mutations in patients with pheochromocytomas and paragangliomas. This article describes a patient with a pheochromocytoma and a novelSDHCmutation. The authors highlight the importance of genetic testing in patien
Autor:
Ilona, Michałowska, Jarosław B, Ćwikła, Mariola, Pęczkowska, Mariusz I, Furmanek, John R, Buscombe, Wojciech, Michalski, Aleksander, Prejbisz, Małgorzata, Szperl, Angelica, Malinoc, Dariusz, Moczulski, Zbigniew, Szutkowski, Andrzej, Kawecki, Jolanta, Antoniewicz, Piotr, Pęczkowski, Anna, Lewczuk, Maciej, Otto, Andrzej, Cichocki, Grażyna, Bednarek-Tupikowska, Marek, Kabat, Hanna, Janaszek-Sitkowska, Katarzyna, Przybyłowska, Jadwiga, Janas, Hartmut P H, Neumann, Andrzej, Januszewicz
Publikováno v:
Neuroendocrinology. 101(4)
The aim of this study was to assess the usefulness of somatostatin receptor scintigraphy (SRS) using (99m)Tc-[HYNIC, Tyr3]-octreotide (TOC) and 123I-metaiodobenzylguanidine (mIBG) in patients with SDHx-related syndromes in which paragangliomas were d
Publikováno v:
Otolaryngologia polska = The Polish otolaryngology. 66(5)
The aberrant internal carotid artery (ICA) is a rare congenital vascular anomaly. Misdiagnosed may result in life threatening complications during middle ear surgery. Authors present a case of a 6-year old boy in whom ventilation tube insertion was c
Autor:
Anna Lewczuk, Z. Szutkowski, Andrzej Januszewicz, Maren Sullivan, Witold Szyfter, Krzysztof Chojnowski, Mieczysław Litwin, Charis Eng, Aleksander Prejbisz, Agata Kubaszek, Michael Hoffmann, Hartmut P. H. Neumann, Jarosław B. Ćwikła, Mariusz I. Furmanek, Martin A. Walter, Andrzej Kawecki, Zoran Erlic, Mariola Pęczkowska
Publikováno v:
The Journal of clinical endocrinology and metabolism. 93(12)
Context and Objective: Germline mutations of the genes SDHB, SDHC, and SDHD predispose to paraganglioma syndromes. Mutation-specific counseling, risk assessment, and management recommendations ideally should be performed. Here, we provide data for a