Suchergebnisse - "Efstathiadou, Zoe A"

PubPharm (29)

1

Current and Emerging Pharmacological Therapies for Cushing's Disease

enthalten in: Current pharmaceutical design | 2024

von Divaris, E. | Kostopoulos, G. | Efstathiadou, Z.

2

Complete and sustained remission of hypercortisolism with pasireotide treatment of an adrenocorticotropic hormone (ACTH)-secreting thoracic neuroendocrine tumor : an n-of-1 trial

enthalten in: Endocrine journal | 2023

von Efstathiadou, Z. | Divaris, E. | Michou, A. | +2

3

Postmenopausal osteoporosis coexisting with other metabolic diseases : Treatment considerations

enthalten in: Maturitas | 2021

von Polyzos, S. | Anastasilakis, A. | Efstathiadou, Z. | +2

4

Benefits and Limitations of TKIs in Patients with Medullary Thyroid Cancer : A Systematic Review and Meta-Analysis

enthalten in: European thyroid journal | 2021

von Efstathiadou, Z. | Tsentidis, C. | Bargiota, A. | +8

5

A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family : diversity in phenotype and response to treatment

enthalten in: Endocrine | 2021

von Efstathiadou, Z. | Kostoulas, C. | Polyzos, S. | +3

ErratumIn: Endocrine. 2020 Oct 6;:. - PMID 33025564

6

Correction to : A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family: diversity in phenotype and response to treatment

enthalten in: Endocrine | 2020

von Efstathiadou, Z. | Kostoulas, C. | Polyzos, S. | +3

ErratumFor: Endocrine. 2020 Aug 9;:. - PMID 32772338

7

Comparative effectiveness of glucagon-like peptide-1 receptor agonists versus dipeptidyl peptidase-4 inhibitors on noninvasive indices of hepatic steatosis and fibrosis in patients with type 2 diabetes mellitus

enthalten in: Diabetes & metabolic syndrome | 2020

von Makri, E. | Kita, M. | Goulas, A. | +4

8

Correction to: A mutation in NOTCH2 gene first associated with Hajdu–Cheney syndrome in a Greek family: diversity in phenotype and response to treatment

enthalten in: Endocrine | 2020

von Efstathiadou, Z. | Kostoulas, C. | Polyzos, S. | +3

9

Correction to: A mutation in NOTCH2 gene first associated with Hajdu–Cheney syndrome in a Greek family: diversity in phenotype and response to treatment

enthalten in: Endocrine | 2020

von Efstathiadou, Z. | Kostoulas, C. | Polyzos, S. | +3

10

Correction to: A mutation in NOTCH2 gene first associated with Hajdu–Cheney syndrome in a Greek family: diversity in phenotype and response to treatment

enthalten in: Endocrine | 2020

von Efstathiadou, Z. | Kostoulas, C. | Polyzos, S. | +3