Prof.

VEYSEL NİJAT BAŞ


Tıp Fakültesi

Dahili Tıp Bilimleri

Çocuk Sağlığı ve Hastalıkları

Education Information

2009 - 2012

2009 - 2012

Undergraduate Minor

Sağlık Bilimleri Üniversitesi, Ankara Dr. Sami Ulus Kadın Doğum Çocuk Sağlığı Ve Hastalıkları Sağlık Uygulama Ve Araştırma Merkezi, Turkey

2003 - 2008

2003 - 2008

Undergraduate

Gazi Üniversitesi, Tıp Fakültesi, Turkey

Foreign Languages

C1 Advanced

C1 Advanced

English

Research Areas

Pediatric Endocrinology and Metabolism

Academic Titles / Tasks

2019 - Continues

2019 - Continues

Associate Professor

Kütahya Sağlık Bilimleri Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

2017

2017

Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism

Aycan Z., Cangul H., Muzza M., Bas V. N. , Fugazzola L., Chatterjee V. K. , et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.102, no.9, pp.3085-3090, 2017 (Journal Indexed in SCI) identifier identifier identifier

2017

2017

Effects 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, vol.30, pp.557-560, 2017 (Journal Indexed in SCI) identifier identifier identifier

2017

2017

Bone 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, vol.30, pp.175-180, 2017 (Journal Indexed in SCI Expanded) identifier identifier identifier

2016

2016

Diverse 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, vol.101, pp.2945-54, 2016 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier identifier

2016

2016

Maturity 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, vol.29, pp.487-96, 2016 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2016

2016

Effects of vitamin D levels on asthma control and severity in pre-school children

TÜRKELİ A. , AYAZ O., UNCU A., ÖZHAN B., BAŞ V. N. , Tufan A. K. , et al.

EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES, vol.20, no.1, pp.26-36, 2016 (Journal Indexed in SCI) identifier identifier identifier

2015

2015

Effects 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, vol.28, pp.1145-51, 2015 (Journal Indexed in SCI) identifier identifier identifier

2015

2015

Growth 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, vol.7, pp.183-91, 2015 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier identifier

2015

2015

Investigation 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, vol.28, pp.767-71, 2015 (Journal Indexed in SCI Expanded) identifier identifier identifier

2015

2015

Turner 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, vol.7, pp.27-36, 2015 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier identifier

2015

2015

Diabetic 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, vol.28, pp.333-5, 2015 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2015

2015

Evaluating 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, vol.2015, pp.247386, 2015 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

A 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, vol.27, pp.1101-5, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

Iatrogenic Cushing's syndrome due to overuse of topical steroid in the diaper area.

Ozdemir A., Bas V. N.

Journal of tropical pediatrics, vol.60, pp.404-6, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

Corneal biomechanical characteristics in children with diabetes mellitus.

Nalcacioglu-Yuksekkaya P., Sen E., Cetinkaya S., Bas V. N. , Aycan Z., Ozturk F.

International ophthalmology, vol.34, pp.881-6, 2014 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2014

2014

What has national screening program changed in cases with congenital hypothyroidism?

Özgelen Ş., Nijat B. , Çetinkaya S., Aycan Z.

Iranian journal of pediatrics, vol.24, pp.255-60, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

Diseases accompanying congenital hypothyroidism.

Baş V. N. , Ozgelen S., Cetinkaya S., Aycan Z.

Journal of pediatric endocrinology & metabolism : JPEM, vol.27, pp.485-9, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

A 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, vol.27, pp.383-7, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

A 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, vol.27, pp.323-7, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

Evaluation 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, vol.6, pp.22-7, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

Adherence 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, vol.20, pp.46-51, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

An 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, vol.82, pp.278-82, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2014

2014

Prader-Willi syndrome and growth hormone deficiency.

Aycan Z., Baş V. N.

Journal of clinical research in pediatric endocrinology, vol.6, pp.62-7, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

2013

2013

Report of the first case of precocious puberty in Rett syndrome

Bas V. N. , Cetinkaya S., Agladioglu S. Y. , Aksoy A., Gulpinar B., Aycan Z.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.26, pp.937-939, 2013 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2013

2013

Hyperinsulinemic 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, vol.5, pp.150-5, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

2013

2013

Long-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, vol.5, pp.202-5, 2013 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

2013

2013

Thyroid 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, vol.79, pp.275-81, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

2013

2013

Short- 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, vol.55, pp.365-70, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

2013

2013

Prevalence of hyperthyrotropinemia in obese children before and after weight loss.

Baş V. N. , Aycan Z., Ağladıoğlu S., Kendirci H.

Eating and weight disorders : EWD, vol.18, pp.87-90, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

2013

2013

Diabetes 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, vol.26, pp.955-8, 2013 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2012

2012

A 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, vol.4, pp.213-5, 2012 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier identifier

2012

2012

Assessment 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, vol.4, pp.199-203, 2012 (Journal Indexed in SCI Expanded) Creative Commons License Sustainable Development identifier identifier identifier

2012

2012

Iatrogenic Cushing syndrome due to nasal steroid drops.

Baş V. N. , Cetinkaya S., Aycan Z.

European journal of pediatrics, vol.171, pp.735-6, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

2012

2012

Seizure 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, vol.25, pp.553-5, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

2012

2012

Mild 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, vol.25, pp.1153-6, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

2012

2012

Thyroid 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, vol.25, pp.633-8, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

2012

2012

Assessment 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, vol.25, pp.681-5, 2012 (Journal Indexed in SCI) identifier identifier identifier

2012

2012

TSHR 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, vol.25, pp.419-26, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

2012

2012

A pediatric Conn syndrome case.

Onder A., Kendirci H., Bas V. N. , Agladioglu S., Cetinkaya S., Aycan Z.

Journal of pediatric endocrinology & metabolism : JPEM, vol.25, pp.203-6, 2012 (Journal Indexed in SCI Expanded) identifier identifier identifier

2011

2011

Thiamine-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, vol.33, pp.144-7, 2011 (Journal Indexed in SCI Expanded) identifier identifier identifier

2011

2011

A 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, vol.24, pp.1059-61, 2011 (Journal Indexed in SCI Expanded) identifier identifier identifier

2011

2011

Does 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, vol.3, pp.219-21, 2011 (Journal Indexed in SCI) identifier identifier identifier

2010

2010

Novel 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, vol.73, pp.671-7, 2010 (Journal Indexed in SCI Expanded) identifier identifier identifier

2010

2010

Sporadic 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, vol.2, pp.168-72, 2010 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier

2010

2010

Insulin 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, vol.2, pp.46-8, 2010 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier

2010

2010

Hypothyroidism 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, vol.2, pp.126-30, 2010 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier

Articles Published in Other Journals

2016

2016

Effects of Vitamin D Levels on Asthma Control and Severity in Children

TÜRKELİ A. , AYAZ O., UNCU A., ÖZHAN B., BAŞ V. N. , KAVAZ TUFAN A., et al.

ASTIM ALLERJI IMMUNOLOJI, vol.14, pp.148-156, 2016 (Refereed Journals of Other Institutions) Creative Commons License identifier

2016

2016

Hipo hiperkalsemi ile giden Subkutan Yağ Dokusu Nekrozu ve Brakiyal Pleksopati

YİMENİCİOĞLU S., YİMENİCİOĞLU M. F. , TÜRKELİ A. , EKİCİ A., AÇIKALIN D., BAŞ V. N.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI, vol.6, pp.81-84, 2016 (Other Refereed National Journals)

2015

2015

Hypopituitarism and Legg-Calve-Perthes disease related to difficult delivery.

Baş V. N. , Uytun S., Vurdem Ü., Torun Y.

Korean journal of pediatrics, vol.58, pp.270-3, 2015 (Refereed Journals of Other Institutions) identifier identifier

Refereed Congress / Symposium Publications in Proceedings

2016

2016

Çocuklarda D Vitamini Eksikliğinin Astım Kontrolü ve Şiddeti Üzerine Etkisi

TÜRKELİ A. , AYAZ O., UNCU A., KAVAZ TUFAN A., ÖZHAN B., BAŞ V. N. , et al.

Türk Toraks Derneği 19. Yıllık Kongresi, Turkey, 6 - 10 April 2016

2015

2015

Okul Öncesi Astımlı Çocuklarda Vitamin D Düzeyi Düzeyi ve Astım Kontrolü

TÜRKELİ A. , AYAZ O., UNCU A., KAVAZ TUFAN A., ÖZHAN B., BAŞ V. N. , et al.

22. Ulusal Allerji ve İmmünoloji Kongresi, Antalya, Turkey, 28 November - 02 December 2015

2015

2015

Okul Öncesi Astımlı Çocuklarda Serum Vitamin D düzeyi

TÜRKELİ A. , AYAZ O., UNCU A., KAVAZ TUFAN A., ÖZHAN B., BAŞ V. N. , et al.

22. Ulusal Allerji ve İmmünoloji Kongresi, Antalya, Turkey, 28 November - 02 December 2015

Books & Book Chapters

2020

2020

Diyabet Nedir ?

EVLİYAOĞLU S. O. , PİRGON M. Ö. , akyürek n., BAŞ V. N. , yılmaz s.

in: Çocukluk Çağı Diyabeti Eğitici Rehberi, zehra aycan, Editor, Sağlık Bakanlığı, pp.2-7, 2020 Sustainable Development


Edit Congress and Symposium Activities

2019

2019

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet KongresiSustainable Development

Session Moderator

Antalya-Turkey

2018

2018

XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet KongresiSustainable Development

Invited Speaker

Antalya-Turkey

2017

2017

XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet KongresiSustainable Development

Invited Speaker

Antalya-Turkey

Citations

Total Citations (WOS): 564

h-index (WOS): 14