I. Stoeva

发表

Serum IGF-1 levels measured by different ELISA assays and IRMA – a comparability study

Shina Pashova, G. Kirilov, A. Aroyo, 2015 .

Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism.

A. Grüters, H. Biebermann, P. Ambrugger, 2001, European journal of endocrinology.

CORTISOL IN SALIVA - A MARKER FOR INCREASED ANXIETY IN CHILDREN

M. Rashkova, L. Ribagin, K. Ohridski, 2011 .

Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

H. Ropers, H. Christen, A. Grüters, 2014, Journal of Medical Genetics.

Growth and endocrine disorders in thalassemia: The international network on endocrine complications in thalassemia (I-CET) position statement and guidelines

M. Angastiniotis, V. De Sanctis, A. Soliman, 2013, Indian journal of endocrinology and metabolism.

The Resurgence of Populism in Europe

I. Stoeva, 2018 .

[The regulation of prolactin secretion].

I. Stoeva, P. Matrozov, 1989, Akusherstvo i ginekologiia.

The ICET-A Recommendations for the Diagnosis and Management of Disturbances of Glucose Homeostasis in Thalassemia Major Patients

M. Angastiniotis, V. De Sanctis, A. Soliman, 2016, Mediterranean journal of hematology and infectious diseases.

International network on endocrine complications in thalassaemia (I-CET): an opportunity to grow.

M. Angastiniotis, A. Eleftheriou, V. De Sanctis, 2012, Georgian medical news.

Preliminary Data on COVID-19 in Patients with Hemoglobinopathies: A Multicentre ICET-A Study

Y. Oymak, T. Zarei, V. De Sanctis, 2020, Mediterranean journal of hematology and infectious diseases.

The ICET-A Survey on Current Criteria Used by Clinicians for the Assessment of Central Adrenal Insufficiency in Thalassemia: Analysis of Results and Recommendations

M. Di Maio, V. De Sanctis, A. Soliman, 2016, Mediterranean journal of hematology and infectious diseases.

Role of Prostaglandin E2 (PGE2) on the Corticotropin-Releasing Hormone (CRH)-Induced ACTH Release in Healthy Men

S. Zacharieva, A. Borissova, I. Stoeva, 1992, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

A case of a boy with SOD and 7q11.23 microduplication syndrome

D. Pencheva, A. Aroyo, I. Stoeva, 2017 .

The effect of angiotensin-converting enzyme inhibition on ACTH response to corticotropin-releasing hormone (CRH) in normal men.

S. Zacharieva, I. Stoeva, K. Andonova, 1991, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

THE ROLE OF THE NEWBORN SCREENING PROGRAMME (NSP) FOR THE DIAGNOSIS OF A 17-YEAR-OLD BOY WITH CONGENITAL ADRENAL HYPERPLASIA (CAH) DUE TO 21 OH DEFICIENCY

T. Todorov, A. Todorova, A. Aroyo, 2014 .

Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

H. Ropers, H. Christen, A. Grüters, 2014, Journal of Medical Genetics.