Miklós Góth

ORCID: 0000-0003-2290-0109
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Research Areas
  • Pituitary Gland Disorders and Treatments
  • Growth Hormone and Insulin-like Growth Factors
  • Adrenal and Paraganglionic Tumors
  • Thyroid Disorders and Treatments
  • Adrenal Hormones and Disorders
  • Thyroid Cancer Diagnosis and Treatment
  • Neuroendocrine Tumor Research Advances
  • Diet and metabolism studies
  • Neuroblastoma Research and Treatments
  • Cancer, Hypoxia, and Metabolism
  • TGF-β signaling in diseases
  • Hypothalamic control of reproductive hormones
  • Childhood Cancer Survivors' Quality of Life
  • Endometriosis Research and Treatment
  • Glioma Diagnosis and Treatment
  • Pharmacological Effects and Toxicity Studies
  • Diabetes and associated disorders
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Diet, Metabolism, and Disease
  • Lipid metabolism and disorders
  • Regulation of Appetite and Obesity
  • Hormonal and reproductive studies
  • Adipose Tissue and Metabolism
  • Hormonal Regulation and Hypertension
  • Dermatological and COVID-19 studies

Cliniques Universitaires Saint-Luc
2019-2023

Lohmann (Germany)
2023

Institut für Frauengesundheit
2018-2020

Universitätsklinikum Tübingen
2018-2020

Wroclaw Medical University
2018

Buda Health Center
2016

BM Központi Kórház
2011-2012

Molina Center for Energy and the Environment
2012

Állami Szívkórház
2010

Health Center
2009

GH secretion has been thought traditionally to be regulated by the two hypothalamic hormones, GH-releasing hormone (GHRH) and somatostatin (SRIF). Recent evidence suggested that other factors may involved. These include natural ligand for synthetic hexapeptide peptide (GHRP) putative hypophysiotropic factor pituitary adenylate cyclase-activating polypeptide (PA-CAP). Accordingly, we examined effects of GHRP PACAP on at single cell level using reverse hemolytic plaque assay which allows...

10.1210/endo.130.2.1346381 article EN Endocrinology 1992-02-01

A novel oral octreotide formulation was tested for efficacy and safety in a phase III, multicenter, open-label, dose-titration, baseline-controlled study patients with acromegaly.We enrolled 155 complete or partially controlled (IGF-1 <1.3 × upper limit of normal [ULN], 2-h integrated GH <2.5 ng/mL) receiving injectable somatostatin receptor ligand (SRL) ≥ 3 months. Subjects were switched to 40 mg/d capsules (OOCs), the dose escalated 60 then up 80 control IGF-1. Subsequent fixed doses...

10.1210/jc.2014-4113 article EN The Journal of Clinical Endocrinology & Metabolism 2015-02-09
Laura C. Hernández‐Ramírez Plamena Gabrovska Judit Dénes Karen Stals Giampaolo Trivellin and 95 more Daniel Tilley Francesco Ferraù Jane Evanson Sian Ellard Ashley Grossman Federico Roncaroli Mônica R. Gadelha Márta Korbonits Amar Agha Scott Akker Elena Daniela Aflorei Sándor Alföldi Wiebke Arlt Brew Atkinson Anna Aulinas-Masó Simon Aylwin Philippe Backeljauw Corin Badiu Stephanie Baldeweg Gul Bano Ariel Barkan Julian Barwell Carmen Bernal-González G. M. Besser John S. Bevan Joanne Blair Pierre Bouloux Lisa Bradley Michael Buchfelder Mehtap Çakır Natalie Canham Paul Carroll Harvinder Chahal Tim Cheetham F. Chentli Richard N. Clayton Mark L. Cohen Trevor Cole Hamish Courtney Elizabeth Crowne Daniel J. Cuthbertson Jacob Dal Nadezhda Dalantaeva Christina Daousi Ken Darzy Mehul Dattani Justin H. Davies J.R. Davis Margaret de Castro Laura De Marinis William Drake Pinaki Dutta Larisa Dzeranova Britt Edén Engström Rosalind A. Eeles Maria Elfving Marianne S. Elston Louise Emmerson Naomi Fersht Simona Fica Stefan Fischli Daniel Flanagan Maria Fleseriu Pamela U. Freda Theodore C. Friedman Lawrence A. Frohman Patricia Gallego Evelien Gevers Edit Gláz James A. Goldman Anthony P. Goldstone Miklós Góth Lynn Greenhalgh Joan Grieve Mirtha Guitelman Alper Gürlek Mark Gurnell Katalin Horváth Trevor A. Howlett Charlotte Höybye Steven Hunter Donato Iacovazzo Péter Igaz Warrick J. Inder Takeo Iwata Louise Izatt Sujatha Jagadeesh Gregory Kaltsas Felicity Kaplan Niki Karavitaki Darko Kaštelan Michelle L. Katz Tara Kearney Bernard Khoo Cathy Kiraly‐Borri

Familial isolated pituitary adenoma (FIPA) due to aryl hydrocarbon receptor interacting protein (AIP) gene mutations is an autosomal dominant disease with incomplete penetrance. Clinical screening of apparently unaffected AIP mutation (AIPmut) carriers could identify previously unrecognized disease. To determine the mutational status FIPA and young patients, analyzing their clinical characteristics, perform AIPmut carrier family members. This was observational, longitudinal study conducted...

10.1210/jc.2015-1869 article EN cc-by The Journal of Clinical Endocrinology & Metabolism 2015-07-17

Raf/MEK/ERK and phosphatidylinositol 3-kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) cascades are key signalling pathways interacting with each other to regulate cell growth tumourigenesis. We have previously shown B-Raf Akt overexpression and/or overactivation in pituitary adenomas. The aim this study is assess the expression their downstream components (MEK1/2, ERK1/2, mTOR, TSC2, p70S6K) effectors (c-MYC CYCLIN D1). studied tissue from 16 non-functioning adenomas (NFPAs), six...

10.1677/erc-09-0101 article EN Endocrine Related Cancer 2009-07-21

Lanreotide Autogel is a new long-acting aqueous preparation of lanreotide for the treatment acromegaly and administered by deep sc injection from small volume, prefilled syringe. The aim this study was to evaluate efficacy safety formulation in large population acromegalic patients previously responsive 30 mg, im (sustained release microparticle formulation). every 28 d 107 (54 males 53 females; mean age, 54 ± 1.2 yr). All had been treated with (30 mg) at least 3 months before entry GH level...

10.1210/jcem.87.1.8153 article EN The Journal of Clinical Endocrinology & Metabolism 2002-01-01

To investigate the effect of varying amounts iodine intake on prevalence thyroid dysfunction, autoimmunity and goitre in old age.The first screening study where elderly subjects with supply but from same geographical ethnographical region (Carpathian basin) were compared, all hormone measurements ultrasonography performed by laboratory or person.Nursing home residents screened for disorders from: (A) an iodine-deficient area, Northern Hungary (n = 119; median age 81 years; excretion (MIE)...

10.1046/j.1365-2265.1997.2271040.x article EN Clinical Endocrinology 1997-07-01

The aim of the present study was to clarify relationship between GH deficiency (GHD) and some cardiovascular risk factors analyse effect replacement therapy in a large number patients over prolonged period time.Data for analysis were retrieved from KIMS (Pfizer International Metabolic Database). Serum concentrations total cholesterol, high-density lipoprotein (HDL)-cholesterol, low-density (LDL)-cholesterol triglycerides obtained 2589 at baseline 1206 after 1 2 years therapy. Body mass index...

10.1530/eje.1.02179 article EN European Journal of Endocrinology 2006-06-22

The study was designed to evaluate the long-term efficacy and safety of 28-day prolonged-release Autogel formulation somatostatin analogue lanreotide (Lan-Autogel) in unselected patients with acromegaly. comprised four phases: washout; a double-blind comparison placebo, at single randomized dose (60, 90 or 120 mg) Lan-Autogel; single-blind, fixed-dose phase for injections (placebo group re-allocated active treatment); eight doses tailored according biochemical response. Serum samples were...

10.1007/s11102-009-0191-1 article EN cc-by-nc Pituitary 2009-07-28
Elena Valassi Antoine Tabarin Thierry Brue Richard A. Feelders Martín Reincke and 94 more Romana T. Netea‐Maier Miklós Tóth Sabina Zacharieva Susan M. Webb Stylianos Tsagarakis Philippe Chanson Marija Pfeiffer Michael Droste Irina Komerdus Darko Kaštelan Dominique Maiter Olivier Chabre Holger Franz Alicia Santos Christian J. Strasburger Peter Trainer John Newell‐Price Óskar Ragnarsson NULL AUTHOR_ID NULL AUTHOR_ID Alberto Giacinto Ambrogio Gloria Aranda Maura Arosio Maria Balomenaki P. Beck-Peccoz C Berr-Kirmair M. Bolanowski Jens Bollerslev Brue Thierry Davide Carvalho Francesco Cavagnini Emanuel Christ F Demtröder Zentrum fur Endokrinologi Judit Dénes Christina Dimopoulou Alexander Dreval Tina Dušek E Erdinc Johan Arild Evang Julia Fazel Simona Fica Ezio Ghigo Miklós Góth Yona Greenman V Greisa Ilana Halperin Felicia A. Hanzu A. R. M. M. Hermus Gudmundur Johannsson Peter Kamenický A Kasperlik-Załuska Jasmin Kirchner Kastelan Darko Ivana Kraljević Aleksandra Kruszyńska Ioana Maria Lambrescu Sean M. Lang A Luger N Marpole Sorina Martin Monique Martinie O Moros John Newell‐Price Maria Orbetzova Isabel Paiva Francesca Pecori Giraldi Alberto M. Pereira James Pickel Valdis Pīrāgs Óskar Ragnarsson AD Reghina Pedro Riesgo Myron Roberts S. H. P. P. Roerink Olga Roig Chris Rowan П. А. Руденко MA Sahnoun Javier Salvador HA Sigurjonsdottir Tanja Škorić Polovina Rachel L. Smith Barbara Stachowska Günter K. Stalla Judit Tőke Esther Ubiña S Vinay Margreet A. E. M. Wagenmakers Sigbritt Werner Jacques Young Piotr Zdunowski Kathrin Zopf Stephanie Zopp Ioana Zosin

Patients with Cushing's syndrome (CS) have increased mortality. The aim of this study was to evaluate the causes and time death in a large cohort patients CS establish factors associated mortality.In study, we analyzed 1564 included European Registry on (ERCUSYN); 1045 (67%) had pituitary-dependent CS, 385 (25%) adrenal-dependent 89 (5%) an ectopic source 45 (3%) other causes. median (IQR) overall follow-up ERCUSYN 2.7 (1.2-5.5) years.Forty-nine died at analysis; 23 (47%) 6 (12%) 18 (37%)...

10.1530/eje-19-0464 article EN European Journal of Endocrinology 2019-09-03
Vincent Amodru Amandine Ferrière Antoine Tabarin Fréderic Castinetti Stylianos Tsagarakis and 95 more Miklós Tóth Richard A. Feelders Susan M. Webb Martín Reincke Romana T. Netea‐Maier Darko Kaštelan Атанаска Еленкова Dominique Maiter Óskar Ragnarsson Alicia Santos Elena Valassi C Amaral Alberto Giacinto Ambrogio Gloria Aranda Maura Arosio Maria Balomenaki C Berr-Kirmair Jérôme Bertherat Marek Bolanowski Jens Bollerslev Helena Cardoso Davide Carvalho Francesco Cavagnini P Ceccato Olivier Chabre Philippe Chanson Emanuel Christ F Demtröder Zentrum fur Endokrinologie Judit Dénes Timo Deutschbein Christina Dimopoulou Alexander Dreval Michael Droste J Duarte Tina Dušek Emre Ertürk Johan Arild Evang Christian Fajardo Julia Fazel Richard A. Feelders Simona Fica Rogelio García-Centeno Ezio Ghigo Miklós Góth Magdalena Godlewska Yona Greenman Ilana Halperin Felicia A. Hanzu A. R. M. M. Hermus Gudmundur Johannsson Erika Hubina A Gilis Januszewska Peter Kamenický A Kasperlik-Załuska Jasmin Kirchner Darko Kaštelan Irina Komerdus Ivana Kraljević Michal Kršek Aleksandra Kruszyńska Cristina Lamas Ioana Maria Lambrescu Sean M. Lang A Luger Dominique Maiter N Marpole Sorina Martin Monique Martinie M J Martins Oliveira O Moros Romana T. Netea‐Maier John Newell‐Price Maria Orbetzova Isabel Paiva Francesca Pecori Giraldi Juan Carlos Percovich Alberto M. Pereira Marija Pfeifer James Pickel Valdis Pīrāgs Óskar Ragnarsson Aura Reghină Martín Reincke Pedro Riesgo Myron Roberts S. H. P. P. Roerink Olga Roig Chris Rowan П. А. Руденко Javier Salvador Alicia Santos C Scaroni Helga Ágústa Sigurjónsdóttir Tanja Škorić Polovina Rachel L. Smith

Abstract Objective To evaluate whether age-related differences exist in clinical characteristics, diagnostic approach, and management strategies patients with Cushing's syndrome (CS) included the European Registry on Syndrome (ERCUSYN). Design Cohort study. Methods We analyzed 1791 CS, of whom 1234 (69%) had pituitary-dependent CS (PIT-CS), 450 (25%) adrenal-dependent (ADR-CS), 107 (6%) an ectopic source (ECT-CS). According to WHO criteria, 1616 (90.2%) were classified as younger (&amp;lt;65...

10.1093/ejendo/lvad008 article EN European Journal of Endocrinology 2023-02-07

The prevalence of thyroid microcarcinomas found at autopsies is 100–1000 times higher than in clinical cancer. epidemiological and histological characteristics consecutive series performed two areas different iodine intake were investigated. Iodine deficient (ID) area: n = 222 (M 109, F 113), median age: 74–76 years, excretion (MIE) nursing home residents from this 70 µg/g creatinine. sufficient (IS) 221 132, 89), 68 MIE: 500 When compared to the IS area, results obtained ID area showed a...

10.1089/thy.2005.15.152 article EN Thyroid 2005-02-01

Somatostatin (SST) analogues play an important role in the medical management of somatotroph pituitary adenomas and new agonists have potential to be effective a wider group other tumours. The anti-proliferative effect SST occurs through multiple mechanisms, one which is cell-cycle arrest, where p27, cyclin-dependent kinase inhibitor, regulator. We hypothesised that may upregulate p27 protein levels downregulate MAP pathway these tumours.Human adenoma cells rat cell line (GH3) were cultured...

10.1530/eje.1.02213 article EN European Journal of Endocrinology 2006-07-25

OBJECTIVE Growth hormone (GH) deficiency is associated with insulin resistance and diabetes. The aim of the current study was to determine incidence diabetes during GH replacement therapy (GHRT) effect GHRT on fasting plasma glucose concentrations HbA1c in adult patients deficiency. RESEARCH DESIGN AND METHODS A total 5,143 GH-deficient (male 49.9%; mean age ± SD, 49 13 years; BMI 29.1 5.9 kg/m2) were analyzed. Mean observation period 3.9 years (range 0.01–13). Total number patient-years...

10.2337/dc11-0449 article EN cc-by-nc-nd Diabetes Care 2011-11-11

Objective An increased risk of cardiovascular morbidity and mortality in adult GH deficiency (GHD) may be related to hypopituitarism but also the presence metabolic syndrome (MetS). Our objective was investigate characteristics prevalence MetS as well its comorbidities GHD. Design In KIMS (Pfizer International Metabolic Database) 2479 patients with severe adult-onset GHD, naïve replacement, complete information on all components were found. defined according National Cholesterol Education...

10.1530/eje-11-0599 article EN European Journal of Endocrinology 2011-10-04
Kristina Isand Richard A. Feelders Thierry Brue Miklós Tóth Timo Deutschbein and 95 more Martín Reincke Michal Kršek Alicia Santos Frank Demtröder Olivier Chabre Christian J. Strasburger Anna Aulinas Masó Vallo Volke Alberto M. Pereira R Lohmann Ignasi Gich Saladich Cláudia Amaral Alberto Giacinto Ambrogio Gloria Aranda Maura Arosio Maria Balomenaki P. Beck-Peccoz C Berr-Kirmair Jérôme Bertherat Marek Bolanowski Jens Bollerslev Brue Thierry Helena Cardoso Davide Carvalho Francesco Cavagnini P Ceccato Olivier Chabre P. Chanson Emanuel Christ F Demtröder Zentrum fur Endokrinologie Judit Dénes Timo Deutschbein Christina Dimopoulou Alexander Dreval Michael Droste J Duarte Tina Dušek Emre Ertürk Johan Arild Evang Christian Fajardo Julia Fazel Richard A. Feelders Simona Fica Rogelio García-Centeno Ezio Ghigo Miklós Góth Yona Greenman Ilana Halperin Felicia A. Hanzu A. R. M. M. Hermus Gudmundur Johannsson Erika Hubina Peter Kamenický A Kasperlik-Załuska Jasmin Kirchner Darko Kaštelan Irina Komerdus Ivana Kraljević Michal Kršek Aleksandra Kruszyńska Cristina Lamas Ioana Maria Lambrescu Sean M. Lang A Luger Dominique Maiter N Marpole Sorina Martin Monique Martinie M J Martins Oliveira O Moros Romana T. Netea‐Maier John Newell‐Price Maria Orbetzova Isabel Paiva Francesca Pecori Giraldi Juan Carlos Percovich Alberto M. Pereira Melissa R. Pfeiffer James Pickel Valdis Pīrāgs Óskar Ragnarsson Aura Reghină Martín Reincke Pedro Riesgo Myron Roberts S. H. P. P. Roerink Chris Rowan П. А. Руденко Mariam Sahnoun Javier Salvador Alicia Santos C Scaroni Helga Ágústa Sigurjónsdóttir Tanja Škorić Polovina Rachel L. Smith

Abstract Objective The aim of this study was to evaluate the prevalence venous thromboembolism (VTE) in patients included European Registry on Cushing's syndrome (ERCUSYN), compare their clinical characteristics with those who did not develop VTE and identify risk factors for VTE. Design A retrospective observational cohort study. Methods Data extraction from registry taken February, 7, 2022. At time there were 2174 diagnosed (CS) 95 VTEs reported database. Results Of events 70 (74%)...

10.1093/ejendo/lvad176 article EN cc-by European Journal of Endocrinology 2023-12-22

GH deficiency (GHD) in adults is characterized by a tendency toward obesity and an adverse body composition with visceral fat deposit may thus predispose to the development of type 2 diabetes mellitus. The aim this study was assess observed prevalence proportion (PP) PP over expected ratio (standardized ratio, SPR) according International Diabetes Federation criteria large cohort GH-untreated adult-onset GHD patients.Associations between baseline variables 6050 patients from KIMS (Pfizer...

10.1530/eje-12-0807 article EN European Journal of Endocrinology 2012-12-05

Eur J Clin Invest 2012 Abstract Purpose While pituitary adenomas are common, carcinomas rare. It is unclear whether arise de novo or evolve from adenomas. Methods We studied the clinical characteristics and tissue samples eight surgeries autopsy a patient with carcinoma. A 16‐year‐old female was diagnosed an aggressive Crooke cell macroadenoma. Following transsphenoidal surgery, signs of Cushing disease quickly reappeared. During 14‐year course illness, surgeries, three courses extracranial...

10.1111/eci.12010 article EN European Journal of Clinical Investigation 2012-09-20

Objective Growth hormone (GH) replacement therapy currently requires daily injections, which may cause distress and low compliance. C-terminal peptide (CTP)-modified growth (MOD-4023) is being developed as a once-weekly dosing regimen in patients with GH deficiency (GHD). This study’s objective to evaluate the safety, pharmacokinetics (PK), pharmacodynamics (PD) efficacy of MOD-4023 administered GHD adults. Design 54 adults treated were normalized randomized into 4 weekly cohorts at 18.5%,...

10.1530/eje-16-0748 article EN cc-by European Journal of Endocrinology 2016-12-09
Elena Valassi Holger Franz Thierry Brue Richard A. Feelders Romana T. Netea‐Maier and 93 more Stylianos Tsagarakis Susan M. Webb Maria Yaneva Martín Reincke Michael Droste Irina Komerdus Dominique Maiter Darko Kaštelan Philippe Chanson Marija Pfeifer Christian J. Strasburger Miklós Tóth Olivier Chabre Michal Kršek Carmen Fajardo Marek Bolanowski Alicia Santos Peter Trainer John Wass Antoine Tabarin NULL AUTHOR_ID NULL AUTHOR_ID Alberto Giacinto Ambrogio Gloria Aranda Maura Arosio Maria Balomenaki P. Beck-Peccoz C Berr-Kirmair Jens Bollerslev Davide Carvalho Francesco Cavagnini Emanuel Christ Frank Demtröder Judit Dénes Christina Dimopoulou Alexander Dreval Tina Dušek E Erdinc Johan Arild Evang Julia Fazel Simona Fica Ezio Ghigo Miklós Góth Yona Greenman V Greisa Ilana Halperin Felicia A. Hanzu A. R. M. M. Hermus Gudmundur Johannsson Peter Kamenický A Kasperlik-Załuska Jasmin Kirchner Ivana Kraljević Aleksandra Kruszyńska Ioana Maria Lambrescu Sean M. Lang A Luger N Marpole Sorina Martin Monique Martinie O Moros John Newell‐Price Maria Orbetzova Isabel Paiva Francesca Pecori Giraldi Alberto M. Pereira James Pickel Valdis Pīrāgs Óskar Ragnarsson Aura Reghină Pedro Riesgo Myron Roberts S. H. P. P. Roerink Olga Roig Chris Rowan П. А. Руденко Mariam Sahnoun Javier Salvador HA Sigurjonsdottir Tanja Škorić Polovina Rachel L. Smith Barbara Stachowska Günter K. Stalla Judit Tőke Esther Ubiña S Vinay Margreet A. E. M. Wagenmakers Sandy Werner Jacques Young Piotr Zdunowski Kathrin Zopf Stephanie Zopp Ioana Zosin

Surgery is the definitive treatment of Cushing's syndrome (CS) but medications may also be used as a first-line therapy. Whether preoperative medical (PMT) affects postoperative outcome remains controversial.(1) Evaluate how frequently PMT given to CS patients across Europe; (2) examine differences in characteristics who receive and those undergo primary surgery (3) determine if influences pituitary-dependent (PIT-CS).1143 entered into ERCUSYN database from 57 centers 26 countries....

10.1530/eje-17-0997 article EN European Journal of Endocrinology 2018-02-13

Objective : Sheehan’s syndrome occurs as a result of ischaemic pituitary necrosis due to severe postpartum haemorrhage. It is one the most important causes hypopituitarism, and hence growth hormone deficiency (GHD), in developing countries. However, little known about effects (GH) replacement therapy patients with syndrome. Design The demographic background characteristics 91 GH-deficient (mean age ± s.d. , 46.3 9.4 years) were compared those group 156 women 51.5 13.1 non-functional adenoma...

10.1530/eje.1.01881 article EN European Journal of Endocrinology 2005-04-01

A voice assessment was performed before and after conservative treatment in 3 male-to-female transsexuals 2 nontreated serving as control persons. The characteristics studied were quality, habitual speaking pitch, vocal pitch range, intensity maximum phonation time ‘communicative impairment’, a subjective self-estimation by the patient. Based on these parameters Friedrich dysphonia index (DI) calculated. of who had received became female, contrast to that transsexuals, which remained...

10.1159/000083572 article EN Folia Phoniatrica et Logopaedica 2005-01-01

To assess its differential diagnostic value, dehydroepiandrosterone sulfate (DHEA-S) was measured in a nonselected cohort of 84 patients with incidentally detected adrenal tumors (incidentaloma). Of the 38 histologically confirmed cases, 6 12 primary or metastatic malignant tumor adrenals and 7 14 benign cortical adenoma had low DHEA-S levels. Thus, sensitivity, specificity, predictive value level to indicate were 0.35, 0.50, 0.60, values 0.67, 0.47, respectively. cases adenoma, 10 signs...

10.1210/jcem.81.5.8626824 article EN The Journal of Clinical Endocrinology & Metabolism 1996-05-01
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