Eğitim Bilgileri
2009 - 2012
2009 - 2012Lisans Yandal
Sağlık Bilimleri Üniversitesi, Ankara Dr. Sami Ulus Kadın Doğum Çocuk Sağlığı Ve Hastalıkları Sağlık Uygulama Ve Araştırma Merkezi, Türkiye
2003 - 2008
2003 - 2008Lisans
Gazi Üniversitesi, Tıp Fakültesi, Türkiye
Yabancı Diller
C1 İleri
C1 İleriİngilizce
Araştırma Alanları
Pediatrik Endokrinoloji ve Metabolizma
Akademik Unvanlar / Görevler
2019 - Devam Ediyor
2019 - Devam EdiyorDoç.Dr.
Kütahya Sağlık Bilimleri Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
2018
2018Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome.
Baştuğ F., Nalçacıoğlu H., Baş V. N. , Tekatlı-Çelik B., Çetinkaya H., Yel S.
The Turkish journal of pediatrics, cilt.60, ss.210-215, 2018 (SCI İndekslerine Giren Dergi)
2017
2017Effects of L-thyroxine treatment on heart functions in infants with congenital hypothyroidism.
Arslan A., Baş V. N. , Uytun S., Poyrazoğlu H.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.30, ss.557-560, 2017 (SCI İndekslerine Giren Dergi)
2017
2017Clinical Toxicity of Acute Overdoses With L-Thyroxin in Children.
Ergul A., Altuner T., Serbetci M., Ozcan A., Bas V. N.
Pediatric emergency care, 2017 (SCI İndekslerine Giren Dergi)
2017
2017Bone mineral density and bone metabolic markers' status in children with neurofibromatosis type 1.
Poyrazoğlu H., Baş V. N. , Arslan A., Bastug F., Canpolat M., Per H., et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.30, ss.175-180, 2017 (SCI Expanded İndekslerine Giren Dergi)
2016
2016Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations.
Demir K., van G., Büyükinan M., Çatlı G., Ayhan Y., Baş V. N. , et al.
The Journal of clinical endocrinology and metabolism, cilt.101, ss.2945-54, 2016 (SCI Expanded İndekslerine Giren Dergi)
2016
2016Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome.
Sari E., Bereket A., Yeşilkaya E., Baş F., Bundak R., Aydın B., et al.
American journal of medical genetics. Part A, ss.942-8, 2016 (SCI Expanded İndekslerine Giren Dergi)
2016
2016Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing.
Ağladıoğlu S., Aycan Z., Çetinkaya S., Baş V. N. , Önder A., Peltek K., et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.29, ss.487-96, 2016 (SCI Expanded İndekslerine Giren Dergi)
2015
2015Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes.
Ece S., Onay H., Atik T., Aykut A., Cerrah G., Ozalp Y., et al.
European journal of medical genetics, cilt.58, ss.689-94, 2015 (SCI Expanded İndekslerine Giren Dergi)
2015
2015Effects of GnRH analogue treatment on anterior pituitary hormones in children with central precocious puberty.
Kendirci H., Ağladıoğlu S., Önder A., Baş V. N. , Çetinkaya S., Aycan Z.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.28, ss.1145-51, 2015 (SCI İndekslerine Giren Dergi)
2015
2015Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group.
Darendeliler F., Yeşilkaya E., Bereket A., Baş F., Bundak R., Sarı E., et al.
Journal of clinical research in pediatric endocrinology, cilt.7, ss.183-91, 2015 (SCI Expanded İndekslerine Giren Dergi)
2015
2015Investigation of autoimmune diseases accompanying Hashimoto's thyroiditis in children and adolescents and evaluation of cardiac signs.
Baş V. N. , Yılmaz A., Özgür S., Karademir S., Aycan Z.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.28, ss.767-71, 2015 (SCI Expanded İndekslerine Giren Dergi)
2015
2015Diabetic euglycemic ketoacidosis in newly diagnosed type 1 diabetes mellitus during Ramadan fasting.
Baş V. N. , Uytun S., Torun Y.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.28, ss.333-5, 2015 (SCI Expanded İndekslerine Giren Dergi)
2015
2015Turner syndrome and associated problems in Turkish children: a multicenter study.
Yeşilkaya E., Bereket A., Darendeliler F., Baş F., Poyrazoğlu Ş., Küçükemre A., et al.
Journal of clinical research in pediatric endocrinology, cilt.7, ss.27-36, 2015 (SCI Expanded İndekslerine Giren Dergi)
2015
2015Effect of obesity on left ventricular longitudinal myocardial strain by speckle tracking echocardiography in children and adolescents.
Kibar A., Pac F., Ece İ., Oflaz M., Ballı Ş., Bas V. N. , et al.
Balkan medical journal, cilt.32, ss.56-63, 2015 (SCI Expanded İndekslerine Giren Dergi)
2015
2015Evaluating the Efficacy of Treatment with a GnRH Analogue in Patients with Central Precocious Puberty.
Kendirci H., Ağladıoğlu S., Baş V. N. , Önder A., Çetinkaya S., Aycan Z.
International journal of endocrinology, cilt.2015, ss.247386, 2015 (SCI Expanded İndekslerine Giren Dergi)
2014
2014A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects.
Cangul H., Bas V. N. , Saglam Y., Kendall M., Barrett T., Maher E., et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.27, ss.1101-5, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014Iatrogenic Cushing's syndrome due to overuse of topical steroid in the diaper area.
Ozdemir A., Bas V. N.
Journal of tropical pediatrics, cilt.60, ss.404-6, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014Corneal biomechanical characteristics in children with diabetes mellitus.
Nalcacioglu-Yuksekkaya P., Sen E., Cetinkaya S., Bas V. N. , Aycan Z., Ozturk F.
International ophthalmology, cilt.34, ss.881-6, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014What has national screening program changed in cases with congenital hypothyroidism?
Özgelen Ş., Nijat B. , Çetinkaya S., Aycan Z.
Iranian journal of pediatrics, cilt.24, ss.255-60, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014Diseases accompanying congenital hypothyroidism.
Baş V. N. , Ozgelen S., Cetinkaya S., Aycan Z.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.27, ss.485-9, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism.
Cangul H., Aycan Z., Kendall M., Bas V. N. , Saglam Y., Barrett T., et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.27, ss.323-7, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect.
Baş V. N. , Aycan Z., Cangul H., Kendall M., Ağladıoğlu S., Çetinkaya S., et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.27, ss.383-7, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014Evaluation of asymmetric dimethylarginine (ADMA) levels in children with growth hormone deficiency.
Önder A., Aycan Z., Koca C., Ergin M., Çetinkaya S., Ağladıoğlu S., et al.
Journal of clinical research in pediatric endocrinology, cilt.6, ss.22-7, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014An uncommon cause of hypoglycemia: insulin autoimmune syndrome.
Savas-Erdeve S., Yılmaz A., Onder A., Peltek K., Bas V. N. , Sagsak E., et al.
Hormone research in paediatrics, cilt.82, ss.278-82, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014Adherence to growth hormone therapy: results of a multicenter study.
Aydın B., Aycan Z., Sıklar Z., Berberoğlu M., Ocal G., Cetinkaya S., et al.
Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists, cilt.20, ss.46-51, 2014 (SCI Expanded İndekslerine Giren Dergi)
2014
2014Prader-Willi syndrome and growth hormone deficiency.
Aycan Z., Baş V. N.
Journal of clinical research in pediatric endocrinology, cilt.6, ss.62-7, 2014 (SCI Expanded İndekslerine Giren Dergi)
2013
2013Long-term follow-up of Cushing's disease:a case report.
Baş V. N. , Ağladıoğlu S., Onder A., Ozışık P., Peltek K., Cetinkaya S., et al.
Journal of clinical research in pediatric endocrinology, cilt.5, ss.202-5, 2013 (SCI İndekslerine Giren Dergi)
2013
2013Hyperinsulinemic hypoglycemia: experience in a series of 17 cases.
Ağladıoğlu S., Savaş E., Cetinkaya S., Baş V. N. , Peltek K., Onder A., et al.
Journal of clinical research in pediatric endocrinology, cilt.5, ss.150-5, 2013 (SCI Expanded İndekslerine Giren Dergi)
2013
2013Early subclinical left-ventricular dysfunction in obese nonhypertensive children: a tissue Doppler imaging study.
Kibar A., Pac F., Ballı S., Oflaz M., Ece I., Bas V. N. , et al.
Pediatric cardiology, cilt.34, ss.1482-90, 2013 (SCI Expanded İndekslerine Giren Dergi)
2013
2013Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community.
Cangul H., Aycan Z., Olivera-Nappa A., Saglam H., Schoenmakers N., Boelaert K., et al.
Clinical endocrinology, cilt.79, ss.275-81, 2013 (SCI Expanded İndekslerine Giren Dergi)
2013
2013Short- and long-term effects of individualized enteral protein supplementation in preterm newborns.
Ergenekon E., Soysal Ş., Hirfanoğlu İ., Baş V. N. , Gücüyener K., Turan Ö., et al.
The Turkish journal of pediatrics, cilt.55, ss.365-70, 2013 (SCI Expanded İndekslerine Giren Dergi)
2013
2013Prevalence and long-term follow-up outcomes of testicular adrenal rest tumours in children and adolescent males with congenital adrenal hyperplasia.
Aycan Z., Bas V. N. , Cetinkaya S., Yilmaz A., Tiryaki T.
Clinical endocrinology, cilt.78, ss.667-72, 2013 (SCI Expanded İndekslerine Giren Dergi)
2013
2013Prevalence of hyperthyrotropinemia in obese children before and after weight loss.
Baş V. N. , Aycan Z., Ağladıoğlu S., Kendirci H.
Eating and weight disorders : EWD, cilt.18, ss.87-90, 2013 (SCI Expanded İndekslerine Giren Dergi)
2013
2013Diabetes mellitus with Laron syndrome: case report.
Agladıoglu S., Cetınkaya S., Savas E., Onder A., Kendırcı H., Bas V. N. , et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.26, ss.955-8, 2013 (SCI Expanded İndekslerine Giren Dergi)
2012
2012A rare combination: congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome.
Kendirci H., Aycan Z., Çetinkaya S., Baş V. N. , Ağladıoğlu S., Önder A.
Journal of clinical research in pediatric endocrinology, cilt.4, ss.213-5, 2012 (SCI Expanded İndekslerine Giren Dergi)
2012
2012Assessment of the knowledge of diabetes mellitus among school teachers within the scope of the managing diabetes at school program.
Aycan Z., Önder A., Çetinkaya S., Bilgili H., Yıldırım N., Baş V. N. , et al.
Journal of clinical research in pediatric endocrinology, cilt.4, ss.199-203, 2012 (SCI Expanded İndekslerine Giren Dergi)
2012
2012Iatrogenic Cushing syndrome due to nasal steroid drops.
Baş V. N. , Cetinkaya S., Aycan Z.
European journal of pediatrics, cilt.171, ss.735-6, 2012 (SCI Expanded İndekslerine Giren Dergi)
2012
2012Assessment of the 21-hydroxylase deficiency and the adrenal functions in young females with Turner syndrome.
Onder A., Aycan Z., Cetinkaya S., Kendirci H., Bas V. N. , Agladioglu S.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.25, ss.681-5, 2012 (SCI İndekslerine Giren Dergi)
2012
2012Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation.
Baş V. N. , Ozkan M., Zenciroğlu A., Cavuşoğlu Y., Cetinkaya S., Aycan Z.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.25, ss.553-5, 2012 (SCI Expanded İndekslerine Giren Dergi)
2012
2012Thyroid nodules in children and adolescents: a single institution's experience.
Baş V. N. , Aycan Z., Cetinkaya S., Uner C., Cavuşoğlu Y., Arda N.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.25, ss.633-8, 2012 (SCI Expanded İndekslerine Giren Dergi)
2012
2012Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.
Baş V. N. , Cangul H., Agladioglu S., Kendall M., Cetinkaya S., Maher E., et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.25, ss.1153-6, 2012 (SCI Expanded İndekslerine Giren Dergi)
2012
2012TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis.
Cangul H., Aycan Z., Saglam H., Forman J., Cetinkaya S., Tarim O., et al.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.25, ss.419-26, 2012 (SCI Expanded İndekslerine Giren Dergi)
2012
2012A pediatric Conn syndrome case.
Onder A., Kendirci H., Bas V. N. , Agladioglu S., Cetinkaya S., Aycan Z.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.25, ss.203-6, 2012 (SCI Expanded İndekslerine Giren Dergi)
2011
2011Thiamine-responsive megaloblastic anemia syndrome with atrial standstill: a case report.
Aycan Z., Baş V. N. , Cetinkaya S., Ağladioğlu S., Kendirci H., Senocak F.
Journal of pediatric hematology/oncology, cilt.33, ss.144-7, 2011 (SCI Expanded İndekslerine Giren Dergi)
2011
2011Does pseudohypoaldosteronism mask the diagnosis of congenital adrenal hyperplasia?
Ağladıoğlu S., Aycan Z., Kendirci H., Erkek N., Baş V. N.
Journal of clinical research in pediatric endocrinology, cilt.3, ss.219-21, 2011 (SCI İndekslerine Giren Dergi)
2011
2011A case of Langerhans cell histiocytosis with thyroid involvement.
Baş V. N. , Cetinkaya S., Apaydin S., Bozkurt C., Cavuşoğlu Y., Aycan Z.
Journal of pediatric endocrinology & metabolism : JPEM, cilt.24, ss.1059-61, 2011 (SCI Expanded İndekslerine Giren Dergi)
2010
2010Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.
Cangul H., Morgan N., Forman J., Saglam H., Aycan Z., Yakut T., et al.
Clinical endocrinology, cilt.73, ss.671-7, 2010 (SCI Expanded İndekslerine Giren Dergi)
2010
2010Insulin oedema in newly diagnosed type 1 diabetes mellitus.
Baş V. N. , Çetinkaya S., Ağladıoğlu S., Kendirici H., Bilgili H., Yıldırım N., et al.
Journal of clinical research in pediatric endocrinology, cilt.2, ss.46-8, 2010 (SCI Expanded İndekslerine Giren Dergi)
2010
2010Hypothyroidism due to hepatic hemangioendothelioma: a case report.
Çetinkaya S., Kendirci H., Ağladioğlu S., Baş V. N. , Özdemir S., Bozkurt C., et al.
Journal of clinical research in pediatric endocrinology, cilt.2, ss.126-30, 2010 (SCI Expanded İndekslerine Giren Dergi)
2010
2010Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor gene.
Aycan Z., Ağladıoğlu S., Ceylaner S., Cetinkaya S., Baş V. N. , Kendirici H.
Journal of clinical research in pediatric endocrinology, cilt.2, ss.168-72, 2010 (SCI Expanded İndekslerine Giren Dergi)
Diğer Dergilerde Yayınlanan Makaleler
2015
2015Hypopituitarism and Legg-Calve-Perthes disease related to difficult delivery.
Baş V. N. , Uytun S., Vurdem Ü., Torun Y.
Korean journal of pediatrics, cilt.58, ss.270-3, 2015 (Diğer Kurumların Hakemli Dergileri)
Davetli Kongre ve Sempozyum Faaliyetleri
2019
2019XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi
Oturum Başkanı
Antalya-Türkiye
2018
2018XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi
Davetli Konuşmacı
Antalya-Türkiye
2017
2017