Füsun SALGÜR, MD - Doctors - Kent Health Group | +90 850 222 53 68
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Medical Doctor
Füsun SALGÜR

Academic Title

Medical Doctor

 

Specialty

Internal Diseases, Endocrinology and metabolism diseases

Languages
Native Turkish
English

 

Education and Experiences

2004-2010: Eskişehir Osmangazi University Faculty of Medicine International Medicine

Mayıs –Ağustos 2010: Uşak Eşme State Hospital International Medicine

2010-2013: İzmir Katip Çelebi University Faculty of Medicine and Atatürk Training and Research Hospital Endocrinology Lateral Education

2014-2015: Adıyaman University Training and Research Hospital  Endocrinology

 

Professioanal Areas of Interests

Thesis studies

Frequency, characteristics and evaluation findings with transcranial doppler headache in patients with Behcet's disease 2010
Retrospective Evaluation of Changes in Growth Hormone Levels and Pituitary Adenoma Size in Patients with Acromegaly Diagnosed and Using Long-acting Somatostatin Analogue in a Training and Research Hospital 2013

 

Memberships of Assosiations

Turkey Association of Endocrinology and Metabolic Diseases

Turkish Diabetes Foundation

Turkish Medical  Assosiation

 

Researches and ve Publications
Combined thrombophilic factors increase the risk of recurrent thrombotic events in Behcet's disease.

Yaşar NŞ, Salgür F, Cansu DÜ, Kaşifoğlu T, Korkmaz C. Clin Rheumatol. 2010     Dec;29(12):1367-72.. Epub 2010 Apr 11.

Coexistence of gastrointestinal stromal tumors (GISTs) and pheochromocytoma in three cases of neurofibromatosis type 1 (NF1) with a review of the literature.

Gorgel A, Cetinkaya DD, Salgur F, Demirpence M, Yilmaz H, Karaman EH, Tutuncuoglu P, Oruk G, Bahceci M, Sari AA, Altinboga AA, Paker I.Intern Med. 2014;53(16):1783-9. Epub 2014 Aug 15.

Evaluation of the Effetcs of Octreoide and Lanreotide on Growth Hormone and Adenoma Size in Acromegalic Patients
Fusun Salgur, Pelin Tutuncuoglu, Mithat Bahceci, Ahmet Gorgel, Hüsnü Yılmaz and Gonca Oruk Endocrine Society's 96th Annual Meeting and Expo, June 21–24,

A Rare Association of Monosomy 18p Syndrome and Polyglandular Autoimmune Syndrome Type IIIA.

Dolek-Cetinkaya D, Demirpence M, Gorgel A, Salgur F, Bahceci M. Balkan J Med Genet. 2013 Jun;16(1):81-4. doi: 10.2478/bjmg-2013-0023.

A rare cause of hypocalemia: familial hypoparathyroidism

Mitat Bahceci, Fusun Salgur, Aliye Pelin Tutuncuoglu, Husnu Yilmaz & Gonca Oruk

Endocrine Abstracts (2014) 35 P284

A Very Rare Assocıatıon; Coexıstence of Breast Cancer, Pheochromocytoma and   

Neurofıbromatosıs Type 1 in a Female Patıent

Demirpence M M,  Bahceci M, Devrim Dolek, Salgur F, Gorgel  A. International Journal of

Case Reports in Medicine April 2013

 

International Congress oral pronounce

Endobridge 2013

A Rare Cause of Primary Amenorrhea and Hypokalemia; 17-A-Hydroxylase Deficiency (17OHD)  

 

Pronounce

Evaluation of the Effetcs of Octreoide and Lanreotide on Growth Hormone and Adenoma Size in Acromegalic Patients

Fusun Salgur, Pelin Tutuncuoglu, MD, Mithat Bahceci, Ahmet Gorgel, Hüsnü Yilmaz and Gonca Oruk, MD
İzmir Katip Celebi University Atatürk Training and Research Hospital, İzmir, Turkey, İzmir Katip Celebi University Ataturk Training and Research

ICE/ENDO 2014