Attila Patocs, Ph.D. - Publications

Affiliations: 
2004 Semmelweis Egyetem, Hungary 
Area:
Oncology

99 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Sarkadi B, Meszaros K, Krencz I, Canu L, Krokker L, Zakarias S, Barna G, Sebestyen A, Papay J, Hujber Z, Butz H, Darvasi O, Igaz P, Doczi J, Luconi M, ... ... Patocs A, et al. Glutaminases as a Novel Target for SDHB-Associated Pheochromocytomas/Paragangliomas. Cancers. 12. PMID 32150977 DOI: 10.3390/cancers12030599  1
2020 Sumanszki C, Kovacs K, Karvaly GB, Kiss E, Simon E, Patocs A, Toth M, Komka Z, Reismann P. Metabolic and catecholamine response to sympathetic stimulation in early-treated adult male patients with phenylketonuria. Hormones (Athens, Greece). PMID 31993977 DOI: 10.1007/s42000-020-00176-z  0.32
2019 Németh K, Darvasi O, Likó I, Szücs N, Czirják S, Reiniger L, Szabó B, Krokker L, Pállinger É, Igaz P, Patócs A, Butz H. Comprehensive analysis of circulating microRNAs in plasma of patients with pituitary adenomas. The Journal of Clinical Endocrinology and Metabolism. PMID 31112271 DOI: 10.1210/jc.2018-02479  1
2019 Krokker L, Nyírő G, Reiniger L, Darvasi O, Szücs N, Czirják S, Tóth M, Igaz P, Patócs A, Butz H. Differentially Expressed miRNAs Influence Metabolic Processes in Pituitary Oncocytoma. Neurochemical Research. PMID 30945144 DOI: 10.1007/s11064-019-02789-2  1
2019 Decmann A, Bancos I, Khanna A, Thomas MA, Turai P, Perge P, Pintér JZ, Tóth M, Patócs A, Igaz P. Comparison of plasma and urinary microRNA-483-5p for the diagnosis of adrenocortical malignancy. Journal of Biotechnology. PMID 30940435 DOI: 10.1016/j.jbiotec.2019.03.017  0.48
2019 Csajbók ÉA, Kocsis ÁK, Faragó N, Furdan S, Kovács B, Lovas S, Molnár G, Likó I, Zvara Á, Puskás LG, Patócs A, Tamás G. Expression of GLP-1 receptors in insulin-containing interneurons of rat cerebral cortex. Diabetologia. PMID 30637442 DOI: 10.1007/s00125-018-4803-z  0.48
2018 Ali SR, Bryce J, Cools M, Korbonits M, Beun JG, Taruscio D, Danne T, Dattani MT, Dekkers O, Linglart A, Netchine I, Nordenstrom A, Patocs A, Persani L, Reisch N, et al. The current landscape of European registries for rare endocrine conditions. European Journal of Endocrinology. PMID 30407922 DOI: 10.1530/EJE-18-0861  0.48
2018 Németh K, Szücs N, Czirják S, Reiniger L, Szabó B, Barna G, Karászi K, Igaz P, Zivkovic V, Korbonits M, Patócs A, Butz H. Survivin as a potential therapeutic target of acetylsalicylic acid in pituitary adenomas. Oncotarget. 9: 29180-29192. PMID 30018744 DOI: 10.18632/oncotarget.25650  1
2018 Grolmusz VK, Kövesdi A, Borka K, Igaz P, Patocs A. Prognostic relevance of proliferation-related miRNAs in pancreatic neuroendocrine neoplasms. European Journal of Endocrinology. PMID 30006373 DOI: 10.1530/EJE-18-0305  0.48
2018 Decmann A, Perge P, Nyíro G, Darvasi O, Likó I, Borka K, Micsik T, Tóth Z, Bancos I, Pezzani R, Iacobone M, Patócs A, Igaz P. MicroRNA expression profiling in adrenal myelolipoma. The Journal of Clinical Endocrinology and Metabolism. PMID 29982598 DOI: 10.1210/jc.2018-00817  0.48
2018 Marczell I, Balogh P, Nyiro G, Kiss AL, Kovacs B, Bekesi G, Racz K, Patocs A. Membrane-bound estrogen receptor alpha initiated signaling is dynamin dependent in breast cancer cells. European Journal of Medical Research. 23: 31. PMID 29880033 DOI: 10.1186/s40001-018-0328-7  0.72
2018 Molnár Á, Patócs A, Likó I, Nyírő G, Rácz K, Tóth M, Sármán B. An unexpected, mild phenotype of glucocorticoid resistance associated with glucocorticoid receptor gene mutation case report and review of the literature. Bmc Medical Genetics. 19: 37. PMID 29510671 DOI: 10.1186/s12881-018-0552-6  0.6
2018 Sarkadi B, Grolmusz VK, Butz H, Kövesdi A, Likó I, Nyirő G, Igaz P, Patócs A. [Evolution of molecular genetic methods in the clinical diagnosis of hereditary endocrine tumour syndromes]. Orvosi Hetilap. 159: 285-292. PMID 29429353 DOI: 10.1556/650.2018.31036  1
2018 Szappanos Á, Mészáros K, Nagy Z, Kövesdi A, Likó I, Kiss E, Tóth M, Patócs A. [Extraadrenal glucocorticoid synthesis]. Orvosi Hetilap. 159: 260-268. PMID 29429352 DOI: 10.1556/650.2018.31019  0.48
2018 Doleschall M, Török D, Mészáros K, Luczay A, Halász Z, Németh K, Szücs N, Kiss R, Tőke J, Sólyom J, Fekete G, Patócs A, Igaz P, Tóth M. [Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia]. Orvosi Hetilap. 159: 269-277. PMID 29429350 DOI: 10.1556/650.2018.30986  0.48
2018 Perge P, Decmann Á, Pezzani R, Bancos I, Fassina A, Luconi M, Canu L, Tóth M, Boscaro M, Patócs A, Igaz P. Analysis of circulating extracellular vesicle-associated microRNAs in cortisol-producing adrenocortical tumors. Endocrine. PMID 29299796 DOI: 10.1007/s12020-017-1506-z  0.48
2017 Darvasi O, Szabo PM, Nemeth K, Szabo K, Spisak S, Liko I, Czirjak S, Racz K, Igaz P, Patocs A, Butz H. Limitations of high throughput methods for miRNA expression profiles in non-functioning pituitary adenomas. Pathology Oncology Research : Por. PMID 29043608 DOI: 10.1007/s12253-017-0330-3  1
2017 Dávid A, Butz H, Halász Z, Török D, Nyirő G, Muzsnai Á, Csákváry V, Luczay A, Sallai Á, Hosszú É, Felszeghy E, Tar A, Szántó Z, Fekete GL, Kun I, et al. [The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study]. Orvosi Hetilap. 158: 1351-1356. PMID 28823207 DOI: 10.1556/650.2017.30829  1
2017 Perge P, Butz H, Pezzani R, Bancos I, Nagy Z, Pálóczi K, Nyírő G, Decmann Á, Pap E, Luconi M, Mannelli M, Buzás EI, Tóth M, Boscaro M, Patócs A, et al. Evaluation and diagnostic potential of circulating extracellular vesicle-associated microRNAs in adrenocortical tumors. Scientific Reports. 7: 5474. PMID 28710381 DOI: 10.1038/s41598-017-05777-0  1
2017 Doleschall M, Luczay A, Koncz K, Hadzsiev K, Erhardt É, Szilágyi Á, Doleschall Z, Németh K, Török D, Prohászka Z, Gereben B, Fekete G, Gláz E, Igaz P, Korbonits M, et al. A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics. European Journal of Human Genetics : Ejhg. PMID 28401898 DOI: 10.1038/ejhg.2017.38  0.6
2017 Bausch B, Schiavi F, Ni Y, Welander J, Patocs A, Ngeow J, Wellner U, Malinoc A, Taschin E, Barbon G, Lanza V, Söderkvist P, Stenman A, Larsson C, Svahn F, et al. Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention. Jama Oncology. PMID 28384794 DOI: 10.1001/jamaoncol.2017.0223  0.72
2017 Zotter Z, Nagy Z, Patócs A, Csuka D, Veszeli N, Kőhalmi KV, Farkas H. Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency. Orphanet Journal of Rare Diseases. 12: 5. PMID 28069032 DOI: 10.1186/s13023-016-0552-6  0.48
2016 Butz H, Németh K, Czenke D, Likó I, Czirják S, Zivkovic V, Baghy K, Korbonits M, Kovalszky I, Igaz P, Rácz K, Patócs A. Systematic Investigation of Expression of G2/M Transition Genes Reveals CDC25 Alteration in Nonfunctioning Pituitary Adenomas. Pathology Oncology Research : Por. PMID 28004354 DOI: 10.1007/s12253-016-0163-5  1
2016 Nagy Z, Marta A, Butz H, Liko I, Racz K, Patocs A. Modulation of the circadian clock by glucocorticoid receptor isoforms in the H295R cell line. Steroids. PMID 27725099 DOI: 10.1016/j.steroids.2016.10.002  1
2016 Tóth G, Patócs A, Tóth M. [Hereditary phaeochromocytoma in twins]. Orvosi Hetilap. 157: 1326-1330. PMID 27523316 DOI: 10.1556/650.2016.30513  0.48
2016 Kacso G, Ravasz D, Doczi J, Nemeth B, Madgar O, Saada A, Ilin P, Miller C, Ostergaard E, Iordanov I, Adams D, Vargedo Z, Araki M, Araki K, Nakahara M, ... ... Patocs A, et al. Two transgenic mouse models for beta subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations. The Biochemical Journal. PMID 27496549 DOI: 10.1042/BCJ20160594  0.48
2016 Marczell I, Hrabak A, Nyiro G, Patocs A, Stark J, Dinya E, Kukor Z, Toth S, Tulassay ZS, Racz K, Bekesi G. 17-β-estradiol Decreases Neutrophil Superoxide Production through Rac1. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. PMID 27437916 DOI: 10.1055/s-0042-105556  0.72
2016 Molnár Á, Kövesdi A, Szücs N, Tóth M, Igaz P, Rácz K, Patócs A. Polymorphisms of the GR and HSD11B1genes influence body mass index and weight gain during hormone replacement treatment in patients with Addison's disease. Clinical Endocrinology. PMID 26800219 DOI: 10.1111/cen.13022  0.6
2015 Butz H, Patócs A. Technical Aspects Related to the Analysis of Circulating microRNAs. Exs. 106: 55-71. PMID 26608199 DOI: 10.1007/978-3-0348-0955-9_3  1
2015 Nagy Z, Acs B, Butz H, Feldman K, Marta A, Szabo PM, Baghy K, Pazmany T, Racz K, Liko I, Patocs A. Overexpression of GRß in colonic mucosal cell line partly reflects altered gene expression in colonic mucosa of patients with inflammatory bowel disease. The Journal of Steroid Biochemistry and Molecular Biology. 155: 76-84. PMID 26480216 DOI: 10.1016/j.jsbmb.2015.10.006  1
2015 Igaz I, Nyírő G, Nagy Z, Butz H, Nagy Z, Perge P, Sahin P, Tóth M, Rácz K, Igaz P, Patócs A. Analysis of Circulating MicroRNAs In Vivo following Administration of Dexamethasone and Adrenocorticotropin. International Journal of Endocrinology. 2015: 589230. PMID 26161091 DOI: 10.1155/2015/589230  0.6
2015 Butz H, Kinga N, Racz K, Patocs A. Circulating miRNAs as biomarkers for endocrine disorders. Journal of Endocrinological Investigation. PMID 26015318 DOI: 10.1007/s40618-015-0316-5  1
2015 Butz H, Szabó PM, Khella HW, Nofech-Mozes R, Patocs A, Yousef GM. miRNA-target network reveals miR-124as a key miRNA contributing to clear cell renal cell carcinoma aggressive behaviour by targeting CAV1 and FLOT1. Oncotarget. 6: 12543-57. PMID 26002553 DOI: 10.18632/oncotarget.3815  0.6
2015 Balogh P, Szabó A, Likó I, Patócs A, L Kiss A. Autophagy may contribute to the recovery of rat mesothelium following acute inflammation in vivo. Cell and Tissue Research. 362: 127-37. PMID 25943092 DOI: 10.1007/s00441-015-2188-6  0.48
2015 Balog B, T?ke J, Róna K, Szücs N, Igaz P, Pusztai P, Sármán B, Gláz E, Kiss R, Patócs A, Rácz K, Tóth M. [Analysis of laboratory data of 155 patients with pheochromocytoma-paraganglioma syndrome diagnosed during the past 20 years]. Orvosi Hetilap. 156: 626-35. PMID 25864138 DOI: 10.1556/OH.2015.30127  0.6
2015 Szelényi Z, Fazakas Á, Szénási G, Kiss M, Tegze N, Fekete BC, Nagy E, Bodó I, Nagy B, Molvarec A, Patócs A, Pepó L, Prohászka Z, Vereckei A. Inflammation and oxidative stress caused by nitric oxide synthase uncoupling might lead to left ventricular diastolic and systolic dysfunction in patients with hypertension. Journal of Geriatric Cardiology : Jgc. 12: 1-10. PMID 25678898 DOI: 10.11909/j.issn.1671-5411.2015.01.001  0.6
2015 Igaz P, Igaz I, Nagy Z, NyírÅ‘ G, Szabó PM, Falus A, Patócs A, Rácz K. MicroRNAs in adrenal tumors: relevance for pathogenesis, diagnosis, and therapy. Cellular and Molecular Life Sciences : Cmls. 72: 417-28. PMID 25297921 DOI: 10.1007/s00018-014-1752-7  0.6
2014 Doleschall M, Szabó JA, Pázmándi J, Szilágyi Á, Koncz K, Farkas H, Tóth M, Igaz P, Gláz E, Prohászka Z, Korbonits M, Rácz K, Füst G, Patócs A. Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels. Plos One. 9: e107244. PMID 25210767 DOI: 10.1371/journal.pone.0107244  0.6
2014 Butz H, Szabó PM, Nofech-Mozes R, Rotondo F, Kovacs K, Mirham L, Girgis H, Boles D, Patocs A, Yousef GM. Integrative bioinformatics analysis reveals new prognostic biomarkers of clear cell renal cell carcinoma. Clinical Chemistry. 60: 1314-26. PMID 25139457 DOI: 10.1373/clinchem.2014.225854  0.6
2014 Grolmusz VK, Acs OD, Feldman-Kovács K, Szappanos Á, Stenczer B, Fekete T, Szendei G, Reismann P, Rácz K, Patócs A. Genetic variants of the HSD11B1 gene promoter may be protective against polycystic ovary syndrome. Molecular Biology Reports. 41: 5961-9. PMID 24969481 DOI: 10.1007/s11033-014-3473-2  0.6
2014 TÅ‘ke J, Czirják G, Bezzegh A, Vásárhelyi B, Rácz K, Patócs A. [Effects and significance of estradiol in men]. Orvosi Hetilap. 155: 891-6. PMID 24880967 DOI: 10.1556/OH.2014.29914  0.6
2014 Castinetti F, Qi XP, Walz MK, Maia AL, Sansó G, Peczkowska M, Hasse-Lazar K, Links TP, Dvorakova S, Toledo RA, Mian C, Bugalho MJ, Wohllk N, Kollyukh O, Canu L, ... ... Patocs A, et al. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study. The Lancet. Oncology. 15: 648-55. PMID 24745698 DOI: 10.1016/S1470-2045(14)70154-8  0.6
2014 Szabó DR, Luconi M, Szabó PM, Tóth M, Szücs N, Horányi J, Nagy Z, Mannelli M, Patócs A, Rácz K, Igaz P. Analysis of circulating microRNAs in adrenocortical tumors. Laboratory Investigation; a Journal of Technical Methods and Pathology. 94: 331-9. PMID 24336071 DOI: 10.1038/labinvest.2013.148  0.6
2014 Lendvai N, Pawlosky R, Bullova P, Eisenhofer G, Patocs A, Veech RL, Pacak K. Succinate-to-fumarate ratio as a new metabolic marker to detect the presence of SDHB/D-related paraganglioma: initial experimental and ex vivo findings. Endocrinology. 155: 27-32. PMID 24189137 DOI: 10.1210/en.2013-1549  0.6
2014 Bausch B, Wellner U, Bausch D, Schiavi F, Barontini M, Sanso G, Walz MK, Peczkowska M, Weryha G, Dall'igna P, Cecchetto G, Bisogno G, Moeller LC, Bockenhauer D, Patocs A, et al. Long-term prognosis of patients with pediatric pheochromocytoma. Endocrine-Related Cancer. 21: 17-25. PMID 24169644 DOI: 10.1530/ERC-13-0415  0.6
2013 Szabó JA, Szilágyi Á, Doleschall Z, Patócs A, Farkas H, Prohászka Z, Rácz K, Füst G, Doleschall M. Both positive and negative selection pressures contribute to the polymorphism pattern of the duplicated human CYP21A2 gene. Plos One. 8: e81977. PMID 24312389 DOI: 10.1371/journal.pone.0081977  0.6
2013 Balogh P, Szabó A, Katz S, Likó I, Patócs A, Kiss AL. Estrogen receptor alpha is expressed in mesenteric mesothelial cells and is internalized in caveolae upon Freund's adjuvant treatment. Plos One. 8: e79508. PMID 24244516 DOI: 10.1371/journal.pone.0079508  0.48
2013 Zsippai A, Szabó PM, Szabó DR, Nagy Z, Patócs A, Rácz K, Igaz P. In silico analysis of pathways affected by differentially expressed microRNA in adrenocortical tumors. Journal of Endocrinological Investigation. 36: 1011-9. PMID 23812403 DOI: 10.3275/9024  0.6
2013 Grolmusz VK, Stenczer B, Fekete T, Szendei G, Patócs A, Rácz K, Reismann P. Lack of association between C385A functional polymorphism of the fatty acid amide hydrolase gene and polycystic ovary syndrome. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. 121: 338-42. PMID 23616186 DOI: 10.1055/s-0033-1337941  0.6
2013 Bencze A, Szücs N, Igaz P, Leiszter K, Nagy Z, Patócs A, Rácz K. [Carcinoid heart disease]. Orvosi Hetilap. 154: 546-50. PMID 23545233 DOI: 10.1556/OH.2013.29583  0.6
2013 Feldman K, Likó I, Nagy Z, Szappanos A, Grolmusz VK, Tóth M, Rácz K, Patócs A. [Importance of the 11β-hydroxysteroid dehydrogenase enzyme in clinical disorders]. Orvosi Hetilap. 154: 283-93. PMID 23419529 DOI: 10.1556/OH.2013.29558  0.6
2013 Szabó PM, Butz H, Igaz P, Rácz K, Hunyady L, Patócs A. Minireview: miRomics in endocrinology: a novel approach for modeling endocrine diseases. Molecular Endocrinology (Baltimore, Md.). 27: 573-85. PMID 23349525 DOI: 10.1210/me.2012-1220  0.6
2013 Bekő G, Butz H, Berta K, Tislér A, Olajos F, Vásárhelyi B, Patócs A. Switching between parathormone (PTH) assays: the impact on the diagnosis of renal osteodystrophy. Clinical Chemistry and Laboratory Medicine. 51: 1251-6. PMID 23241601 DOI: 10.1515/cclm-2012-0485  1
2012 Szabó PM, Pintér M, Szabó DR, Zsippai A, Patócs A, Falus A, Rácz K, Igaz P. Integrative analysis of neuroblastoma and pheochromocytoma genomics data. Bmc Medical Genomics. 5: 48. PMID 23106811 DOI: 10.1186/1755-8794-5-48  0.6
2012 Zsippai A, Szabó DR, Tömböl Z, Szabó PM, Eder K, Pállinger E, Gaillard RC, Patócs A, Tóth S, Falus A, Rácz K, Igaz P. Effects of mitotane on gene expression in the adrenocortical cell line NCI-H295R: a microarray study. Pharmacogenomics. 13: 1351-61. PMID 22966885 DOI: 10.2217/pgs.12.116  0.6
2012 Trivellin G, Butz H, Delhove J, Igreja S, Chahal HS, Zivkovic V, McKay T, Patócs A, Grossman AB, Korbonits M. MicroRNA miR-107 is overexpressed in pituitary adenomas and inhibits the expression of aryl hydrocarbon receptor-interacting protein in vitro. American Journal of Physiology. Endocrinology and Metabolism. 303: E708-19. PMID 22811466 DOI: 10.1152/ajpendo.00546.2011  0.6
2012 Butz H, Rácz K, Hunyady L, Patócs A. Crosstalk between TGF-β signaling and the microRNA machinery. Trends in Pharmacological Sciences. 33: 382-93. PMID 22613783 DOI: 10.1016/j.tips.2012.04.003  0.6
2012 Lendvai N, Tóth M, Valkusz Z, BekÅ‘ G, Szücs N, Csajbók E, Igaz P, Kriszt B, Kovács B, Rácz K, Patócs A. Over-representation of the G12S polymorphism of the SDHD gene in patients with MEN2A syndrome. Clinics (SãO Paulo, Brazil). 67: 85-9. PMID 22584711 DOI: 10.6061/clinics/2012(Sup01)15  0.6
2012 Offergeld C, Brase C, Yaremchuk S, Mader I, Rischke HC, Gläsker S, Schmid KW, Wiech T, Preuss SF, Suárez C, Kopeć T, Patocs A, Wohllk N, Malekpour M, Boedeker CC, et al. Head and neck paragangliomas: clinical and molecular genetic classification. Clinics (SãO Paulo, Brazil). 67: 19-28. PMID 22584701 DOI: 10.6061/clinics/2012(Sup01)05  0.6
2012 Halászlaki C, Takács I, Butz H, Patócs A, Lakatos P. Novel genetic mutation in the background of Carney complex. Pathology Oncology Research : Por. 18: 149-52. PMID 22297707 DOI: 10.1007/s12253-012-9502-3  1
2011 Halászlaki C, Takács I, Patócs A, Lakatos P. [Novel mutation in a patient with Carney complex]. Orvosi Hetilap. 152: 802-4. PMID 21540154 DOI: 10.1556/OH.2011.29117  0.32
2011 Pregun I, Herszényi L, Juhász M, Miheller P, Hritz I, Patócs A, Rácz K, Tulassay Z. Effect of proton-pump inhibitor therapy on serum chromogranin a level. Digestion. 84: 22-8. PMID 21304238 DOI: 10.1159/000321535  0.6
2011 Szappanos A, Patócs A, Gergics P, Bertalan R, Kerti A, Acs B, Feldmann K, Rácz K, Tóth M. The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndrome. The Journal of Steroid Biochemistry and Molecular Biology. 123: 79-84. PMID 21111044 DOI: 10.1016/j.jsbmb.2010.11.009  0.6
2011 Butz H, Likó I, Czirják S, Igaz P, Korbonits M, Rácz K, Patócs A. MicroRNA profile indicates downregulation of the TGFβ pathway in sporadic non-functioning pituitary adenomas. Pituitary. 14: 112-24. PMID 21063788 DOI: 10.1007/s11102-010-0268-x  0.6
2011 Sereg M, Toke J, Patócs A, Varga I, Igaz P, Szücs N, Horányi J, Pusztai P, Czirják S, Gláz E, Rácz K, Tóth M. Diagnostic performance of salivary cortisol and serum osteocalcin measurements in patients with overt and subclinical Cushing's syndrome. Steroids. 76: 38-42. PMID 20813120 DOI: 10.1016/j.steroids.2010.08.007  0.6
2010 Tömböl Z, Eder K, Kovács A, Szabó PM, Kulka J, Likó I, Zalatnai A, Rácz G, Tóth M, Patócs A, Falus A, Rácz K, Igaz P. MicroRNA expression profiling in benign (sporadic and hereditary) and recurring adrenal pheochromocytomas. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. 23: 1583-95. PMID 20818339 DOI: 10.1038/modpathol.2010.164  0.6
2010 Halászlaki C, Horváth H, Kiss L, Takács I, Speer G, Nagy Z, Winternitz T, Dabasi G, Zalatnai A, Patócs A, Lakatos P. [Verner-Morrison syndrome: a case study]. Orvosi Hetilap. 151: 1111-4. PMID 20558361 DOI: 10.1556/OH.2010.28884  0.48
2010 Boyle B, Butz H, Liko I, Zalatnai A, Toth M, Feldman K, Horanyi J, Igaz P, Racz K, Patocs A. Expression of glucocorticoid receptor isoforms in human adrenocortical adenomas. Steroids. 75: 695-700. PMID 20438742 DOI: 10.1016/j.steroids.2010.04.008  0.6
2010 Balogh K, Patócs A, Hunyady L, Rácz K. Menin dynamics and functional insight: take your partners. Molecular and Cellular Endocrinology. 326: 80-4. PMID 20399832 DOI: 10.1016/j.mce.2010.04.011  0.6
2010 Szabó PM, Tamási V, Molnár V, Andrásfalvy M, Tömböl Z, Farkas R, Kövesdi K, Patócs A, Tóth M, Szalai C, Falus A, Rácz K, Igaz P. Meta-analysis of adrenocortical tumour genomics data: novel pathogenic pathways revealed. Oncogene. 29: 3163-72. PMID 20305693 DOI: 10.1038/onc.2010.80  0.6
2010 Beko G, Varga I, Glaz E, Sereg M, Feldman K, Toth M, Racz K, Patocs A. Cutoff values of midnight salivary cortisol for the diagnosis of overt hypercortisolism are highly influenced by methods. Clinica Chimica Acta; International Journal of Clinical Chemistry. 411: 364-7. PMID 19968981 DOI: 10.1016/j.cca.2009.11.033  0.72
2009 Patocs A, Balogh K, Racz K. Adrenal tumors in MEN1 syndrome and the role of menin in adrenal tumorigenesis. Advances in Experimental Medicine and Biology. 668: 97-103. PMID 20175457  0.6
2009 Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I, Fazakas F, Szabo I, Kovacs B, Glaz E, Racz K. Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas. European Journal of Endocrinology / European Federation of Endocrine Societies. 161: 495-502. PMID 19574279 DOI: 10.1530/EJE-09-0399  0.6
2009 Szabó PM, Wiener Z, Tömböl Z, Kovács A, Pócza P, Horányi J, Kulka J, Riesz P, Tóth M, Patócs A, Gaillard RC, Falus A, Rácz K, Igaz P. Differences in the expression of histamine-related genes and proteins in normal human adrenal cortex and adrenocortical tumors. Virchows Archiv : An International Journal of Pathology. 455: 133-42. PMID 19568768 DOI: 10.1007/s00428-009-0807-x  0.6
2009 Toke J, Patócs A, Balogh K, Gergics P, Stenczer B, Rácz K, Tóth M. Parathyroid hormone-dependent hypercalcemia. Wiener Klinische Wochenschrift. 121: 236-45. PMID 19562279 DOI: 10.1007/s00508-009-1149-z  0.6
2009 Tömböl Z, Szabó PM, Molnár V, Wiener Z, Tölgyesi G, Horányi J, Riesz P, Reismann P, Patócs A, Likó I, Gaillard RC, Falus A, Rácz K, Igaz P. Integrative molecular bioinformatics study of human adrenocortical tumors: microRNA, tissue-specific target prediction, and pathway analysis. Endocrine-Related Cancer. 16: 895-906. PMID 19546168 DOI: 10.1677/ERC-09-0096  0.6
2009 Mondok A, Varga I, Glaz E, Szucs N, Tóth M, Patocs A, Beko G, Racz K. 11beta-hydroxysteroid dehydrogenase activity in acromegalic patients with normal or impaired carbohydrate metabolism. Steroids. 74: 725-9. PMID 19540999 DOI: 10.1016/j.steroids.2009.03.003  0.72
2009 Toke J, Patócs A, Gergics P, Bertalan R, Tóth M, Rácz K, Tulassay Z. [Extracellular calcium sensing under normal and pathological conditions]. Orvosi Hetilap. 150: 781-90. PMID 19362934 DOI: 10.1556/OH.2009.28602  0.36
2009 Bertalan R, Patocs A, Nagy B, Derzsy Z, Gullai N, Szappanos A, Rigo J, Racz K. Overrepresentation of BclI polymorphism of the glucocorticoid receptor gene in pregnant women with HELLP syndrome. Clinica Chimica Acta; International Journal of Clinical Chemistry. 405: 148-52. PMID 19336230 DOI: 10.1016/j.cca.2009.03.046  0.72
2009 Lendvai N, Szabó I, Butz H, Beko G, Horányi J, Tarjányi M, Alföldi S, Szabó I, Rácz K, Patócs A. [Extra-adrenal pheochromocytoma associated to SDHD gene mutation]. Orvosi Hetilap. 150: 645-9. PMID 19318336 DOI: 10.1556/OH.2009.28587  0.6
2009 Locsei Z, Racz K, Patocs A, Kovacs GL, Toldy E. Influence of sampling and storage conditions on plasma renin activity and plasma renin concentration. Clinica Chimica Acta; International Journal of Clinical Chemistry. 402: 203-5. PMID 19263530 DOI: 10.1016/j.cca.2009.01.013  0.6
2009 Bertalan R, Patócs A, Boyle B, Rigó J, Rácz K. The protective effect of the ER22/23EK polymorphism against an excessive weight gain during pregnancy. Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology. 25: 379-82. PMID 19241242 DOI: 10.1080/09513590902730762  0.6
2008 Bertalan R, Patocs A, Vasarhelyi B, Treszl A, Varga I, Szabo E, Tamas J, Toke J, Boyle B, Nobilis A, Rigo J, Racz K. Association between birth weight in preterm neonates and the BclI polymorphism of the glucocorticoid receptor gene. The Journal of Steroid Biochemistry and Molecular Biology. 111: 91-4. PMID 18595687 DOI: 10.1016/j.jsbmb.2008.05.002  0.72
2008 Patocs A, Gergics P, Balogh K, Toth M, Fazakas F, Liko I, Racz K. Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family. Bmc Medical Genetics. 9: 29. PMID 18416845 DOI: 10.1186/1471-2350-9-29  0.6
2008 Boyle B, Korányi K, Patocs A, Liko I, Szappanos A, Bertalan R, Racz K, Balazs C. Polymorphisms of the glucocorticoid receptor gene in Graves ophthalmopathy. The British Journal of Ophthalmology. 92: 131-4. PMID 18156379 DOI: 10.1136/bjo.2007.126789  0.72
2007 Balogh K, Hunyady L, Patocs A, Gergics P, Valkusz Z, Toth M, Racz K. MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1. Clinical Endocrinology. 67: 727-34. PMID 17953629 DOI: 10.1111/j.1365-2265.2007.02953.x  0.6
2007 Tõke J, Czirják G, Patócs A, Enyedi B, Gergics P, Csákváry V, Enyedi P, Tóth M. Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene. Clinical Endocrinology. 67: 385-92. PMID 17555508 DOI: 10.1111/j.1365-2265.2007.02896.x  0.48
2006 Balogh K, Rácz K, Patócs A, Hunyady L. Menin and its interacting proteins: elucidation of menin function. Trends in Endocrinology and Metabolism: Tem. 17: 357-64. PMID 16997566 DOI: 10.1016/j.tem.2006.09.004  0.6
2006 Patocs A, Klein I, Szilvasi A, Gergics P, Toth M, Valkusz Z, Forizs E, Igaz P, Al-Farhat Y, Tordai A, Varadi A, Racz K, Esik O. Genotype-phenotype correlations in Hungarian patients with hereditary medullary thyroid cancer. Wiener Klinische Wochenschrift. 118: 417-21. PMID 16865647 DOI: 10.1007/s00508-006-0635-9  0.72
2006 Gergics P, Patocs A, Majnik J, Balogh K, Szappanos A, Toth M, Racz K. Detection of the Bcl I polymorphism of the glucocorticoid receptor gene by single-tube allele-specific polymerase chain reaction. The Journal of Steroid Biochemistry and Molecular Biology. 100: 161-6. PMID 16806906 DOI: 10.1016/j.jsbmb.2006.04.004  0.6
2006 Majnik J, Patocs A, Balogh K, Toth M, Gergics P, Szappanos A, Mondok A, Borgulya G, Panczel P, Prohaszka Z, Racz K. Overrepresentation of the N363S variant of the glucocorticoid receptor gene in patients with bilateral adrenal incidentalomas. The Journal of Clinical Endocrinology and Metabolism. 91: 2796-9. PMID 16636127 DOI: 10.1210/jc.2006-0066  0.6
2005 Sweet K, Willis J, Zhou XP, Gallione C, Sawada T, Alhopuro P, Khoo SK, Patocs A, Martin C, Bridgeman S, Heinz J, Pilarski R, Lehtonen R, Prior TW, Frebourg T, et al. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis. Jama. 294: 2465-73. PMID 16287957 DOI: 10.1001/jama.294.19.2465  0.6
2005 Patocs A, Liko I, Varga I, Gergics P, Boros A, Futo L, Kun I, Bertalan R, Toth S, Pazmany T, Toth M, Szücs N, Horanyi J, Glaz E, Racz K. Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling. The Journal of Steroid Biochemistry and Molecular Biology. 97: 257-65. PMID 16176874 DOI: 10.1016/j.jsbmb.2005.06.035  0.72
2004 Majnik J, Patócs A, Balogh K, Tóth M, Rácz K. A rapid and simple method for detection of Asn363Ser polymorphism of the human glucocorticoid receptor gene. The Journal of Steroid Biochemistry and Molecular Biology. 92: 465-8. PMID 15698551 DOI: 10.1016/j.jsbmb.2004.08.005  0.6
2004 Majnik J, Szücs N, Patócs A, Tóth M, Balogh K, Varga I, Gláz E, Rácz K. Effect of single doses of dexamethasone and adrenocorticotrop hormone on serum bone markers in healthy subjects and in patients with adrenal incidentalomas and Cushing's syndrome. Journal of Endocrinological Investigation. 27: 747-53. PMID 15636428 DOI: 10.1007/BF03347517  0.6
2004 Balogh K, Patócs A, Majnik J, Rácz K, Hunyady L. Genetic screening methods for the detection of mutations responsible for multiple endocrine neoplasia type 1. Molecular Genetics and Metabolism. 83: 74-81. PMID 15464422 DOI: 10.1016/j.ymgme.2004.08.013  0.6
2004 Patócs A, Karádi E, Tóth M, Varga I, Szücs N, Balogh K, Majnik J, Gláz E, Rácz K. Clinical and biochemical features of sporadic and hereditary phaeochromocytomas: an analysis of 41 cases investigated in a single endocrine centre. European Journal of Cancer Prevention : the Official Journal of the European Cancer Prevention Organisation (Ecp). 13: 403-9. PMID 15452453 DOI: 10.1097/00008469-200410000-00008  0.6
2004 Balogh K, Patócs A, Majnik J, Varga F, Illyés G, Hunyady L, Rácz K. Unusual presentation of multiple endocrine neoplasia type 1 in a young woman with a novel mutation of the MEN1 gene. Journal of Human Genetics. 49: 380-6. PMID 15205994 DOI: 10.1007/s10038-004-0163-2  0.6
2003 Patócs A, Valkusz Z, Igaz P, Balogh K, Tóth M, Varga I, Rácz K. Segregation of the V804L mutation and S836S polymorphism of exon 14 of the RET gene in an extended kindred with familial medullary thyroid cancer. Clinical Genetics. 63: 219-23. PMID 12694233 DOI: 10.1034/j.1399-0004.2003.00044.x  0.6
Show low-probability matches.