J. Tőke

发表

[Extracellular calcium sensing under normal and pathological conditions].

Z. Tulassay, K. Rácz, M. Tóth, 2009, Orvosi hetilap.

Autoimmune polyglandular syndrome type 3 with multiple genetic alterations in a young male patient with type 1 diabetes mellitus.

A. Somogyi, Ábel Decmann, É. Csöregh, 2021, Endokrynologia Polska.

[Evaluation of the accuracy of inferior petrosal sinus sampling in the differential diagnosis of ACTH-dependent Cushing's syndrome].

R. Kiss, S. Czirják, K. Rácz, 2007, Orvosi hetilap.

[Effects and significance of estradiol in men].

K. Rácz, A. Bezzegh, B. Vásárhelyi, 2014, Orvosi hetilap.

Association between birth weight in preterm neonates and the BclI polymorphism of the glucocorticoid receptor gene

K. Rácz, I. Varga, B. Vásárhelyi, 2008, The Journal of Steroid Biochemistry and Molecular Biology.

Ghrelin: a new peptide regulating the neurohormonal system, energy homeostasis and glucose metabolism

Z. Tulassay, K. Rácz, A. Somogyi, 2008, Diabetes/metabolism research and reviews.

Plasma ghrelin response to an oral glucose load in growth hormone-deficient adults treated with growth hormone

Z. Tulassay, K. Rácz, A. Somogyi, 2007, Wiener klinische Wochenschrift.

Skeletal differences in bone mineral area and content before and after cure of endogenous Cushing’s syndrome

Z. Tulassay, K. Rácz, M. Tóth, 2008, Osteoporosis International.

[Analysis of laboratory data of 155 patients with pheochromocytoma-paraganglioma syndrome diagnosed during the past 20 years].

R. Kiss, P. Igaz, K. Rácz, 2015, Orvosi hetilap.

Rare diseases caused by abnormal calcium sensing and signalling

M. Tóth, G. Czirják, P. Enyedi, 2021, Endocrine.

True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndrome

P. Igaz, M. Tóth, A. Patócs, 2019, Endocrine.

Diagnostic performance of a newly developed salivary cortisol and cortisone measurement using an LC–MS/MS method with simple and rapid sample preparation

K. Rácz, M. Tóth, A. Patócs, 2018, Journal of Endocrinological Investigation.

Diagnostic performance of salivary cortisol and serum osteocalcin measurements in patients with overt and subclinical Cushing's syndrome

P. Igaz, S. Czirják, K. Rácz, 2011, Steroids.

Prognostic factors and mitotane treatment of adrenocortical cancer. Two decades of experience from an institutional case series

P. Igaz, M. Tóth, T. Micsik, 2022, Frontiers in Endocrinology.

Bone turnover in patients with endogenous Cushing’s syndrome before and after successful treatment

P. Igaz, K. Rácz, M. Tóth, 2010, Osteoporosis International.

Complete Remission of Advanced Adrenocortical Cancer Following Mitotane Monotherapy: A Case Report and Literature Review of Predictive Markers

M. Tóth, Z. Jakab, J. Stark, 2021, Frontiers in Oncology.

Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency

K. Rácz, M. Tóth, E. Gláz, 2008, Journal of endocrinological investigation.

Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium‐sensing receptor gene

M. Tóth, A. Patócs, G. Czirják, 2007, Clinical endocrinology.

Atherosclerotic risk factors and complications in patients with non-functioning adrenal adenomas treated with or without adrenalectomy: a long-term follow-up study.

K. Karlinger, K. Rácz, M. Tóth, 2009, European journal of endocrinology.

Parathyroid hormone-dependent hypercalcemia

K. Rácz, M. Tóth, A. Patócs, 2009, Wiener klinische Wochenschrift.

BclI polymorphism of the glucocorticoid receptor gene is associated with decreased bone mineral density in patients with endogenous hypercortisolism

K. Rácz, M. Tóth, I. Varga, 2009, Clinical endocrinology.

Case Report: Complete Necrosis of a Large Adrenocortical Cancer and Liver Metastases Achieved by Selective Arterial Embolization: A Case Study and Review of Literature

P. Igaz, M. Tóth, L. Kóbori, 2021, Frontiers in Endocrinology.

Secondary Aldosteronism

Csaba Sumánszki, J. Tőke, K. Pócsai, 2021, Practical Clinical Endocrinology.

[Methods for the analysis of large gene deletions and their application in some hereditary diseases].

P. Igaz, K. Rácz, M. Tóth, 2009, Orvosi hetilap.

Tissue miRNA Combinations for the Differential Diagnosis of Adrenocortical Carcinoma and Adenoma Established by Artificial Intelligence

P. Igaz, M. Tóth, A. Patócs, 2022, Cancers.

Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka

R. Kiss, P. Igaz, M. Tóth, 2018 .

Metyrapone treatment in endogenous Cushings syndrome. Long term efficacy and safety results of the extension of the phase III/IV study PROMPT

L. Nieman, R. Giordano, M. Tóth, 2021 .

Salt Wasting 21-Hydroxylase Deficiency

J. Tőke, D. Török, 2021, Practical Clinical Endocrinology.

Simple Virilizing 21-Hydroxylase Deficiency

J. Tőke, D. Török, 2020, Practical Clinical Endocrinology.

High prevalence of PROP1 gene mutations in hungarian patients with childhood-onset combined anterior pituitary hormone deficiency

K. Rácz, L. Kovács, Z. Tömböl, 2006, Endocrine.

[Significance of biochemical markers in the diagnosis of neuroendocrine tumours and for the follow-up of patients].

K. Rácz, M. Tóth, A. Patócs, 2014, Orvosi hetilap.

Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma

H. Butz, A. Bánvölgyi, A. Bozsik, 2023, Scientific reports.

Bone turnover in patients with endogenous Cushing's syndrome before and after successful treatment

P. Igaz, A. Patócs, D. Lippai, 2009 .

[Significance of biochemical markers in the diagnosis of neuroendocrine tumours and for the follow-up of patients].

K. Rácz, M. Tóth, A. Patócs, 2014, Orvosi hetilap.

[Methods for the analysis of large gene deletions and their application in some hereditary diseases].

P. Igaz, K. Rácz, M. Tóth, 2009, Orvosi hetilap.