Zobrazeno 1 - 10
of 383
pro vyhledávání: '"Marcus Quinkler"'
Autor:
Anke Tönjes, Marleen Würfel, Marcus Quinkler, Ulrich J. Knappe, Jürgen Honegger, Nina Krause-Joppig, Konrad Bacher, Timo Deutschbein, Sylvère Störmann, Jochen Schopohl, Sebastian M. Meyhöfer, the participants of the German Acromegaly Registry
Publikováno v:
Reproductive Biology and Endocrinology, Vol 22, Iss 1, Pp 1-8 (2024)
Abstract Context Acromegaly is a rare disease caused by excessive growth hormone (GH) secretion, mostly induced by pituitary adenomas. The care of pregnant women with acromegaly is challenging, in part due to existing clinical data being limited and
Externí odkaz:
https://doaj.org/article/91dde4d6e61c417a9b4449784289f2ea
Autor:
Leah T. Braun, Andrea Osswald, Stephanie Zopp, German Rubinstein, Frederick Vogel, Anna Riester, Jürgen Honegger, Graeme Eisenhofer, Georgiana Constantinescu, Timo Deutschbein, Marcus Quinkler, Ulf Elbelt, Heike Künzel, Hanna F. Nowotny, Nicole Reisch, Michaela F. Hartmann, Felix Beuschlein, Jörn Pons-Kühnemann, Martin Reincke, Stefan A. Wudy
Publikováno v:
EBioMedicine, Vol 99, Iss , Pp 104907- (2024)
Summary: Background: Diagnosing Cushing’s syndrome (CS) is highly complex. As the diagnostic potential of urinary steroid metabolome analysis by gas chromatography-mass spectrometry (GC-MS) in combination with systems biology has not yet been fully
Externí odkaz:
https://doaj.org/article/150c72c68c42466f90f11b1e75850b6a
Autor:
Otilia Kimpel, Barbara Altieri, Marta Laganà, Thomas J. Vogl, Hamzah Adwan, Tina Dusek, Vittoria Basile, James Pittaway, Ulrich Dischinger, Marcus Quinkler, Matthias Kroiss, Soraya Puglisi, Deborah Cosentini, Ralph Kickuth, Darko Kastelan, Martin Fassnacht
Publikováno v:
Cancers, Vol 16, Iss 4, p 706 (2024)
International guidelines recommend local therapies (LTs) such as local thermal ablation (LTA; radiofrequency, microwave, cryoablation), transarterial (chemo)embolisation (TA(C)E), and transarterial radioembolisation (TARE) as therapeutic options for
Externí odkaz:
https://doaj.org/article/7547c518e8154205a3deac23027de497
Autor:
Bruna Calsina, Elena Piñeiro-Yáñez, Ángel M. Martínez-Montes, Eduardo Caleiras, Ángel Fernández-Sanromán, María Monteagudo, Rafael Torres-Pérez, Coral Fustero-Torre, Marta Pulgarín-Alfaro, Eduardo Gil, Rocío Letón, Scherezade Jiménez, Santiago García-Martín, Maria Carmen Martin, Juan María Roldán-Romero, Javier Lanillos, Sara Mellid, María Santos, Alberto Díaz-Talavera, Ángeles Rubio, Patricia González, Barbara Hernando, Nicole Bechmann, Margo Dona, María Calatayud, Sonsoles Guadalix, Cristina Álvarez-Escolá, Rita M. Regojo, Javier Aller, Maria Isabel Del Olmo-Garcia, Adrià López-Fernández, Stephanie M. J. Fliedner, Elena Rapizzi, Martin Fassnacht, Felix Beuschlein, Marcus Quinkler, Rodrigo A. Toledo, Massimo Mannelli, Henri J. Timmers, Graeme Eisenhofer, Sandra Rodríguez-Perales, Orlando Domínguez, Geoffrey Macintyre, Maria Currás-Freixes, Cristina Rodríguez-Antona, Alberto Cascón, Luis J. Leandro-García, Cristina Montero-Conde, Giovanna Roncador, Juan Fernando García-García, Karel Pacak, Fátima Al-Shahrour, Mercedes Robledo
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
The molecular mechanisms underlying metastasis in pheochromocytoma/paraganglioma (mPPGL) remain to be explored. Here, the authors perform genomic and immunogenomic profiling of mPPGL tumors and suggest potential biomarkers for risk of metastasis and
Externí odkaz:
https://doaj.org/article/69b48437dc7349d2ae46afb0ace70885
Autor:
Gesine Meyer, Madeleine Gruendl, Irina Chifu, Stefanie Hahner, Johanna Werner, Johannes Weiß, Tina Kienitz, Marcus Quinkler, Klaus Badenhoop, Eva Herrmann, Mireen Friedrich-Rust, Joerg Bojunga
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 19, p 6392 (2023)
Glucocorticoid excess is a known risk factor for non-alcoholic fatty liver disease (NAFLD). Our objective was to analyse the impact of glucocorticoid replacement therapy on the development of NAFLD and NAFLD-related fibrosis and, therefore, on cardio
Externí odkaz:
https://doaj.org/article/dcd75245d2f745589aa29411a7ec0833
Autor:
Anna-Karin Åkerman, Åse Bjorvatn Sævik, Per Medbøe Thorsby, Paal Methlie, Marcus Quinkler, Anders Palmstrøm Jørgensen, Charlotte Höybye, Aleksandra J. Debowska, Bjørn Gunnar Nedrebø, Anne Lise Dahle, Siri Carlsen, Aneta Tomkowicz, Stina Therese Sollid, Ingrid Nermoen, Kaja Grønning, Per Dahlqvist, Guri Grimnes, Jakob Skov, Trine Finnes, Jeanette Wahlberg, Synnøve Emblem Holte, Katerina Simunkova, Olle Kämpe, Eystein Sverre Husebye, Marianne Øksnes, Sophie Bensing
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 10, p 3602 (2023)
Purpose: Residual adrenocortical function, RAF, has recently been demonstrated in one-third of patients with autoimmune Addison’s disease (AAD). Here, we set out to explore any influence of RAF on the levels of plasma metanephrines and any changes
Externí odkaz:
https://doaj.org/article/4b18eea017514b7abe05fa854edd460a
Autor:
Mario Detomas, Katrin Ritzel, Isabella Nasi-Kordhishti, Stefan Wolfsberger, Marcus Quinkler, Marco Losa, Viola Tröger, Matthias Kroiss, Martin Fassnacht, Greisa Vila, Jürgen Bernd Honegger, Martin Reincke, Timo Deutschbein
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ObjectiveTo evaluate diagnostic accuracy of the corticotropin-releasing hormone (CRH) stimulation test and the overnight 8 mg dexamethasone suppression test (DST) for the differentiation of Cushing’s disease (CD) and ectopic Cushing’s syndrome (E
Externí odkaz:
https://doaj.org/article/f4471333053a43fe8bd82c377faafd46
Autor:
Tina Kienitz, Jörg Schwander, Ulrich Bogner, Michael Schwabe, Thomas Steinmüller, Marcus Quinkler
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2021)
Apart from adrenal myelolipomas, adrenal lipomatous tumors are rare and only seldom described in the literature. We present the case of a 50-year-old man, with a classical form of congenital adrenal hyperplasia (CAH), which was well treated with pred
Externí odkaz:
https://doaj.org/article/0ccf4f140dc2443d8af85ac27ad5ff8a
Autor:
Lea Tschaidse, Marcus Quinkler, Hedi Claahsen-van der Grinten, Anna Nordenström, Aude De Brac de la Perriere, Matthias K. Auer, Nicole Reisch
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 15, p 4506 (2022)
Objective: Women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH) may have poor quality of life (QoL) and low satisfaction with body appearance. We investigated the influence of the patients’ satisfaction with their suppor
Externí odkaz:
https://doaj.org/article/0785ed3f4c77497b9b6a0bf28c8cff3f
Publikováno v:
Endocrine Connections, Vol 7, Iss 6, Pp 811-818 (2018)
Context: Patients with primary adrenal insufficiency (PAI) or congenital adrenal hyperplasia (CAH) receive life-long glucocorticoid (GC) therapy. Daily GC doses are often above the physiological cortisol production rate and can cause long-term morbid
Externí odkaz:
https://doaj.org/article/46e3d5a6d48c48ac99e30424f453d297