Zobrazeno 1 - 10
of 87
pro vyhledávání: '"Michal Krsek"'
Publikováno v:
Biomedical Papers, Vol 168, Iss 1, Pp 85-91 (2024)
Background. We report four pediatric subjects with Cushing's disease (CD) diagnosed in the Czech Republic. We focus on initial symptoms of Cushing's syndrome (CS) which can lead to early diagnosis, on typical symptoms of CS in children, their age and
Externí odkaz:
https://doaj.org/article/e009776022c14678ba1c82a76d4116f4
Publikováno v:
Bone Reports, Vol 16, Iss , Pp 101180- (2022)
Tumor-induced osteomalacia (TIO) is an uncommon type of osteomalacia associated with phosphaturic mesenchymal tumors (PMTs). Due to nonspecific symptoms, the diagnosis and appropriate management of the disease is often delayed for many years. Involve
Externí odkaz:
https://doaj.org/article/2dabc43d44b84167a4ecff2bb3ebdfa3
Autor:
Filip Ctvrtlik, Zbynek Tudos, Paulina Szasz, Zuzana Sedlackova, Igor Hartmann, Jan Schovanek, Zdenek Frysak, Iva Macova, Tomas Zelinka, Milan Hora, Eva Kocova, Jaroslav Pacovsky, Michal Krsek, Viera Lehotska, Emilia Mojtova, Josef Molnar, Vladimir Vanek, Karel Pacak, Jan Baxa
Publikováno v:
Biomedical Papers, Vol 163, Iss 3, Pp 212-219 (2019)
Objectives: The aim of the study was to evaluate the CT features of adrenal tumors in an effort to identify features specific to pheochromocytomas and second, to define a feasible probability calculation model. Methods: This multicentric retrospectiv
Externí odkaz:
https://doaj.org/article/2cb24a5944d1483e811b894ee59e56ba
Publikováno v:
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Thymic neuroendocrine tumor as a cause of Cushing syndrome is extremely rare in children. Case presentation We report a case of a 10-year-old girl who presented with typical symptoms and signs of hypercortisolemia, including bone
Externí odkaz:
https://doaj.org/article/3fdbe77b3fd1486084cca3584631b063
Autor:
Zdeňka Lacinová, Jana Klouckova, Antonín Pařízek, Martin Haluzik, Helena Kratochvilova, Patrik Šimják, Kateřina Anderlová, Milos Mraz, Michal Krsek, Anna Cinkajzlová, Hana Krejčí
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:e3892-e3902
Context Gestational diabetes mellitus (GDM) is accompanied by subclinical inflammation; however, little is known about local inflammation in adipose tissue and placenta. Objective To analyze systemic and local subclinical inflammation and adipose tis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7069edc595fd86c64d173a1403d398f0
https://doi.org/10.1210/clinem/dgaa528
https://doi.org/10.1210/clinem/dgaa528
Autor:
Dana Benešová, Martin Haluzik, Michal Krsek, Antonín Pařízek, Kateřina Anderlová, Hana Krejčí, Vratislav Krejčí, Patrik Šimják
Publikováno v:
Ceska gynekologie. 86(5)
Introduction: Despite the ever-improving medical care, pregnancies of women with type 1 diabetes mellitus (T1DM) are at increased risk of complications for both mother and child. Optimal compensation of diabetes before and during pregnancy is an esse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0363b796b21279294c6823f66e8dea7
https://pubmed.ncbi.nlm.nih.gov/34736329
https://pubmed.ncbi.nlm.nih.gov/34736329
Autor:
Patrik Simjak, Katerina Anderlova, Dagmar Smetanová, Michal Kršek, Miloš Mráz, Martin Haluzík
Publikováno v:
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Maternal diabetes adversely affects fetal cardiovascular system development. Previous studies have reported that the fetuses of mothers with diabetes exhibit both structural and functional changes; nevertheless, prior studies have
Externí odkaz:
https://doaj.org/article/992b7f516495468a9763d6e93a6f6165
Autor:
Eggermann T., Elbracht M., Kurth I., Juul A., Johannsen T. H., Netchine I., Mastorakos G., Johannsson G., Musholt T. J., Zenker M., Prawitt D., Pereira A. M., Hiort O., Stefan Riedl, Birgit Rami-Merhar, Greisa Vila, Sabina Baumgartner-Parzner, Walter Bonfig, Claudine Heinrichs, Dominique Maiter, Inge Gies, Martine Cools, Kristina Casteels, Albert Beckers, Sabina Zacharieva, Violeta Iotova, Tomislav Jukic, Dario Rahelic, Vassos Neocleous, Leonidas Phylactou, Michal Krsek, Jan Lebl, Claus Gravholt, Anders Juul, Vallo Tillmann, Vallo Volke, Tapani Ebeling, Thierry Brue, Patrice Rodien, Jérôme Bertherat, Christine Poitou Bernert, Philippe Touraine, Philippe Chanson, Michel Polak, Maithe Tauber, Thomas Eggermann, Joachim Spranger, Dagmar Fuhrer, Thomas Danne, Olaf Hiort, Klaus Mohnike, Dirk Prawitt, Markus Luster, Nicole Reisch, Martin Reincke, Julia Rohayem, Martin Fassnacht, Miklós Tóth, Alessandra Cassio, Sonia Toni, Csilla Krausz, Barbara Piccini, Diego Ferone, Gianni Russo, Luca Persani, Annamaria Colao, Mariacarolina Salerno, Marco Boscaro, Carla Scaroni, Ferruccio Santini, Giovanni Ceccarini, Ezio Ghigo, Iveta Dzivite-Krisane, Vita Rovite, Lauma Janozola, Rasa Verkauskiene, Michael Witsch, James Clark, Johannes Romijn, Thera Links, Nienke Biermasz, Sabine Hannema, Bas Havekes, Hedi Claahsen-van der Grinten, Henri Timmers, Robin Peeters, Gerlof Valk, A A Verrijn Stuart, Harm Haak, Eystein Husebye, Jens Bollerslev, Barbara Jarzab, Agnieszka 'Szypowska, João-Filipe Raposo, Dana Craiu, Doina Piciu, Ludmila Kostalova, Jarmila Vojtková, Tadej Battelino, Roque Cardona-Hernandez, Diego Yeste, Sonia Gaztambide, Anna Nordenström, Neil Gittoes, Trevor Cole, Elizabeth Crowne, Faisal Ahmed, Mohammed Didi, Marta Korbonits, Mehul Dattani, Peter Clayton, Justin Davies
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases: OJRD 15(1), 144 (2020). doi:10.1186/s13023-020-01420-w
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-16 (2020)
Eggermann, T, Elbracht, M, Kurth, I, Juul, A, Johannsen, T H, Netchine, I, Mastorakos, G, Johannsson, G, Musholt, T J, Zenker, M, Prawitt, D, Pereira, A M, Hiort, O & European Reference Network on Rare Endocrine Conditions (ENDO-ERN 2020, ' Genetic testing in inherited endocrine disorders : joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) ', Orphanet Journal of Rare Diseases, vol. 15, 144 . https://doi.org/10.1186/s13023-020-01420-w
Orphanet journal of rare diseases: OJRD 15(1), 144 (2020). doi:10.1186/s13023-020-01420-w
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-16 (2020)
Eggermann, T, Elbracht, M, Kurth, I, Juul, A, Johannsen, T H, Netchine, I, Mastorakos, G, Johannsson, G, Musholt, T J, Zenker, M, Prawitt, D, Pereira, A M, Hiort, O & European Reference Network on Rare Endocrine Conditions (ENDO-ERN 2020, ' Genetic testing in inherited endocrine disorders : joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) ', Orphanet Journal of Rare Diseases, vol. 15, 144 . https://doi.org/10.1186/s13023-020-01420-w
Orphanet journal of rare diseases: OJRD 15(1), 144 (2020). doi:10.1186/s13023-020-01420-w
Published by BioMed Central, London
Published by BioMed Central, London
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21bcdab9c1079b70ef2ccebfd8d9b677
Autor:
Hana Krejčí, P Kaválková, Milos Mraz, Jana Klouckova, Antonín Pařízek, Zdeňka Lacinová, Anna Cinkajzlová, Helena Kratochvilova, Michal Krsek, Patrik Šimják, Martin Haluzik, Kateřina Anderlová
Publikováno v:
Physiological Research. :807-816
The insulin-like growth factor (IGF) is involved in the regulation of growth and metabolism. The aim of this study was to determine selected parameters of IGF system at systemic and local levels [subcutaneous (SAT) and visceral adipose tissue (VAT)]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfe80af28b2bbe54dc3db4ea6432819d
https://doi.org/10.33549/physiolres.934093
https://doi.org/10.33549/physiolres.934093
Autor:
Inga S. Grills, Huai-Che Yang, Hideyuki Kano, Yan-Hua Su, Mikulas Kosak, Penny K. Sneed, Mary Lee Vance, Kevin Blas, Veronica Chiang, Nathaniel D Sisterson, Roman Liscak, Amr M N El-Shehaby, Wael A. Reda, Jason P. Sheehan, Nuria Martinez-Moreno, Michal Krsek, L. Dade Lunsford, Khaled Abdel Karim, Diogo Cordeiro, Roberto Martinez-Alvarez, Christopher P. Cifarelli, Dale Ding, Gene H. Barnett, Ahmed M. Nabeel, K.C. Lee, Cheng-Chia Lee, Gennadiy A. Katsevman, Gautam U. Mehta, Zhiyuan Xu, John Y K Lee, David Mathieu, Douglas Kondziolka
Publikováno v:
Journal of neurosurgery, vol 131, iss 4
J Neurosurg
J Neurosurg
OBJECTIVERecurrent or residual adenomas are frequently treated with Gamma Knife radiosurgery (GKRS). The most common complication after GKRS for pituitary adenomas is hypopituitarism. In the current study, the authors detail the timing and types of h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1148a8063bda303df882447ae90e1382
https://doi.org/10.3171/2018.5.jns18509
https://doi.org/10.3171/2018.5.jns18509