Found: 27
Select item for more details and to access through your institution.
Complete Remission of Advanced Adrenocortical Cancer Following Mitotane Monotherapy: A Case Report and Literature Review of Predictive Markers.
- Published in:
- Frontiers in Oncology, 2021, v. 11, p. N.PAG, doi. 10.3389/fonc.2021.680853
- By:
- Publication type:
- Article
Type 3 autoimmune polyglandular syndrome with multiple genetic alterations in a young male patient with type 1 diabetes mellitus.
- Published in:
- Polish Journal of Endocrinology / Endokrynologia Polska, 2021, v. 72, n. 3, p. 286, doi. 10.5603/EP.a2021.0035
- By:
- Publication type:
- Article
Parathyroid hormone-dependent hypercalcemia.
- Published in:
- Wiener Klinische Wochenschrift, 2009, v. 121, n. 7/8, p. 1, doi. 10.1007/s00508-009-1149-z
- By:
- Publication type:
- Article
Plasma ghrelin response to an oral glucose load in growth hormone-deficient adults treated with growth hormone.
- Published in:
- Wiener Klinische Wochenschrift, 2007, v. 119, n. 3/4, p. 99, doi. 10.1007/s00508-006-0743-6
- By:
- Publication type:
- Article
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".
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 7, p. e1554, doi. 10.1210/clinem/dgae077
- By:
- Publication type:
- Article
Secondary hypertension due to middle aortic syndrome in a young adult.
- Published in:
- Polish Archives of Internal Medicine, 2021, v. 131, p. 9
- By:
- Publication type:
- Article
Parathyroid adenoma in Li-Fraumeni syndrome: a novel manifestation of the disease.
- Published in:
- Polish Archives of Internal Medicine, 2021, v. 131, p. 7
- By:
- Publication type:
- Article
Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka: Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2018, v. 159, n. 7, p. 269, doi. 10.1556/650.2018.30986
- By:
- Publication type:
- Article
Genetikai tényezők a hypopituitarismus kialakulásában. A transzkripciós faktorok szerepe az agyalapimirigy-elégtelenség hátterében: Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2018, v. 159, n. 7, p. 278, doi. 10.1556/650.2018.31029
- By:
- Publication type:
- Article
Rare diseases caused by abnormal calcium sensing and signalling.
- Published in:
- Endocrine (1355008X), 2021, v. 71, n. 3, p. 611, doi. 10.1007/s12020-021-02620-5
- By:
- Publication type:
- Article
True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndrome.
- Published in:
- Endocrine (1355008X), 2019, v. 65, n. 2, p. 451, doi. 10.1007/s12020-019-01932-x
- By:
- Publication type:
- Article
Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene.
- Published in:
- Clinical Endocrinology, 2007, v. 67, n. 3, p. 385, doi. 10.1111/j.1365-2265.2007.02896.x
- By:
- Publication type:
- Article
Prognostic factors and mitotane treatment of adrenocortical cancer. Two decades of experience from an institutional case series.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.952418
- By:
- Publication type:
- Article
Gradual development of brachydactyly in pseudohypoparathyroidism.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Ghrelin: a new peptide regulating the neurohormonal system, energy homeostasis and glucose metabolism.
- Published in:
- Diabetes/Metabolism Research & Reviews, 2008, v. 24, n. 5, p. 343, doi. 10.1002/dmrr.830
- By:
- Publication type:
- Article
A mellékvesekéreg-carcinoma diagnosztikája.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2024, v. 165, n. 4, p. 123, doi. 10.1556/650.2024.32958
- By:
- Publication type:
- Article
Cushing-szindrómát okozó macronodularis mellékvese-hyperplasia ARMC5-génmutáció következtében.: Az első hazai eset.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2023, v. 164, n. 32, p. 1271, doi. 10.1556/650.2023.32817
- By:
- Publication type:
- Article
A CYP24A1-gén terhességi hypercalcaemiát okozó defektusa.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2022, v. 163, n. 31, p. 1237, doi. 10.1556/650.2022.32520
- By:
- Publication type:
- Article
Egy különleges pancreaselváltozás: kevert differenciációjú nodularitás és diffúz szigetsejtes hyperplasia.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2021, v. 162, n. 6, p. 227, doi. 10.1556/650.2021.31989
- By:
- Publication type:
- Article
Az endogén fémionok koncentrációinak változása különböző kórokú, idült májbetegségekben.
- Published in:
- Hungarian Medical Journal / Orvosi Hetilap, 2020, v. 161, n. 22, p. 917, doi. 10.1556/650.2020.31747
- By:
- Publication type:
- Article
Tissue miRNA Combinations for the Differential Diagnosis of Adrenocortical Carcinoma and Adenoma Established by Artificial Intelligence.
- Published in:
- Cancers, 2022, v. 14, n. 4, p. 895, doi. 10.3390/cancers14040895
- By:
- Publication type:
- Article
Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41878-9
- By:
- Publication type:
- Article
Publisher Correction: Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma.
- Published in:
- 2023
- By:
- Publication type:
- Correction Notice
Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41878-9
- By:
- Publication type:
- Article
Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41878-9
- By:
- Publication type:
- Article
BclI polymorphism of the glucocorticoid receptor gene is associated with decreased bone mineral density in patients with endogenous hypercortisolism.
- Published in:
- Clinical Endocrinology, 2009, v. 71, n. 5, p. 636, doi. 10.1111/j.1365-2265.2009.03528.x
- By:
- Publication type:
- Article
Case Report: Complete Necrosis of a Large Adrenocortical Cancer and Liver Metastases Achieved by Selective Arterial Embolization: A Case Study and Review of Literature.
- Published in:
- Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2021.677187
- By:
- Publication type:
- Article