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Rare diseases caused by abnormal calcium sensing and signalling

Endocrine, 2021-03, Vol.71 (3), p.611-617

2021

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Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma

Scientific reports, 2023-09, Vol.13 (1), p.14658-14658, Article 14658

2023

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Multiple bronchial carcinoids associated with Cowden syndrome

Endocrine, 2024, Vol.84 (3), p.880-884

2024

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

European journal of endocrinology, 2009-04, Vol.160 (4), p.647

2009

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

Cancers, 2022-02, Vol.14 (4), p.895

2022

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

Frontiers in endocrinology (Lausanne), 2022-09, Vol.13, p.952418-952418

2022

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

Frontiers in oncology, 2021-05, Vol.11

2021

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

Frontiers in endocrinology (Lausanne), 2021-04, Vol.12, p.677187-677187

2021

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Parathyroid cancer with MTOR gene mutation: Case report and review of the literature

Annales d'endocrinologie, 2023-12, Vol.84 (6), p.761-763

2023

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Gradual Development of Brachydactyly in Pseudohypoparathyroidism

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.1945-1946

2014

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

Endokrynologia Polska, 2021-01, Vol.72 (3), p.286-287

2021

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

Endocrine, 2019-08, Vol.65 (2), p.451-459

2019

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Spontaneous and Treatment-Related Changes of Serum Calcitonin in Medullary Thyroid Cancer: Long-Term Experience in a Patient With Multiple Endocrine Neoplasia Type 2B

JCO precision oncology, 2024-05, Vol.8, p.e2300675

2024

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CYP24A1 gene defect manifesting with gestational hypercalcemia

Orvosi hetilap, 2022-07, Vol.163 (31), p.1237

2022

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

Diabetes/metabolism research and reviews, 2008-07, Vol.24 (5), p.343-352

2008

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

Steroids, 2011, Vol.76 (1), p.38-42

2011

Volltextzugriff (PDF)

The European Registry for Rare Bone and Mineral Conditions (EuRR-Bone): First year experience of the use of an e-reporting tool

Bone Reports, 2021-04, Vol.14, p.100849, Article 100849

2021

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

Orvosi hetilap, 2014-11, Vol.155 (45), p.1775

2014

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Publisher Correction: Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma

Scientific reports, 2023-09, Vol.13 (1), p.16339-16339, Article 16339

2023

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Letter to the Editor From Tőke and Tóth: "Shift in Calcium From Peripheral Bone to Axial Bone After Tumor Resection in Patients With Tumor-Induced Osteomalacia"

The journal of clinical endocrinology and metabolism, 2024-02, Vol.109 (7), p.e1554-e1554

2024

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

Endocrine, 2006-12, Vol.30 (3), p.255-260

2006

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Parathyroid hormone-dependent hypercalcemia

Wiener Klinische Wochenschrift, 2009, Vol.121 (7-8), p.236-245, Article 236

2009

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

Clinical endocrinology (Oxford), 2009-11, Vol.71 (5), p.636-643

2009

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Salt Wasting 21-Hydroxylase Deficiency

Practical Clinical Endocrinology, p.337-344

Volltextzugriff (PDF)

Simple Virilizing 21-Hydroxylase Deficiency

Practical Clinical Endocrinology, p.345-351

Volltextzugriff (PDF)

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Rare diseases caused by abnormal calcium sensing and signalling

Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma

Multiple bronchial carcinoids associated with Cowden syndrome

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

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

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

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

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

Parathyroid cancer with MTOR gene mutation: Case report and review of the literature

Gradual Development of Brachydactyly in Pseudohypoparathyroidism

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

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

Spontaneous and Treatment-Related Changes of Serum Calcitonin in Medullary Thyroid Cancer: Long-Term Experience in a Patient With Multiple Endocrine Neoplasia Type 2B

CYP24A1 gene defect manifesting with gestational hypercalcemia

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

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

The European Registry for Rare Bone and Mineral Conditions (EuRR-Bone): First year experience of the use of an e-reporting tool

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

Publisher Correction: Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma

Letter to the Editor From Tőke and Tóth: "Shift in Calcium From Peripheral Bone to Axial Bone After Tumor Resection in Patients With Tumor-Induced Osteomalacia"

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

Parathyroid hormone-dependent hypercalcemia

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

Salt Wasting 21-Hydroxylase Deficiency

Simple Virilizing 21-Hydroxylase Deficiency

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