Prof.Dr.

VEYSEL NİJAT BAŞ


Tıp Fakültesi

Dahili Tıp Bilimleri

Çocuk Sağlığı ve Hastalıkları

Eğitim Bilgileri

2009 - 2012

2009 - 2012

Lisans Yandal

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

2003 - 2008

2003 - 2008

Lisans

Gazi Üniversitesi, Tıp Fakültesi, Türkiye

Yabancı Diller

C1 İleri

C1 İleri

İngilizce

Araştırma Alanları

Pediatrik Endokrinoloji ve Metabolizma

Akademik Unvanlar / Görevler

2019 - Devam Ediyor

2019 - Devam Ediyor

Doç.Dr.

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

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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, cilt.30, ss.557-560, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

2017

2017

Clinical 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) 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, cilt.30, ss.175-180, 2017 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.101, ss.2945-54, 2016 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.29, ss.487-96, 2016 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.28, ss.1145-51, 2015 (SCI İndekslerine Giren Dergi) 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, cilt.7, ss.183-91, 2015 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.28, ss.767-71, 2015 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.28, ss.333-5, 2015 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.7, ss.27-36, 2015 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License 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, cilt.2015, ss.247386, 2015 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.27, ss.1101-5, 2014 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.60, ss.404-6, 2014 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.34, ss.881-6, 2014 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.24, ss.255-60, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

2014

2014

Diseases 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) 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, cilt.27, ss.323-7, 2014 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.27, ss.383-7, 2014 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.6, ss.22-7, 2014 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.82, ss.278-82, 2014 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.20, ss.46-51, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

2014

2014

Prader-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) 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, cilt.5, ss.202-5, 2013 (SCI İndekslerine Giren Dergi) Creative Commons License 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, cilt.5, ss.150-5, 2013 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

2013

2013

Early 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) 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, cilt.79, ss.275-81, 2013 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.55, ss.365-70, 2013 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.18, ss.87-90, 2013 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.26, ss.955-8, 2013 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.4, ss.213-5, 2012 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.4, ss.199-203, 2012 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

2012

2012

Iatrogenic 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) 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, cilt.25, ss.681-5, 2012 (SCI İndekslerine Giren Dergi) 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, cilt.25, ss.553-5, 2012 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.25, ss.633-8, 2012 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.25, ss.1153-6, 2012 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.25, ss.419-26, 2012 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.25, ss.203-6, 2012 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.33, ss.144-7, 2011 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.3, ss.219-21, 2011 (SCI İndekslerine Giren Dergi) 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, cilt.24, ss.1059-61, 2011 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.73, ss.671-7, 2010 (SCI Expanded İndekslerine Giren Dergi) identifier 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, cilt.2, ss.46-8, 2010 (SCI Expanded İndekslerine Giren Dergi) 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, cilt.2, ss.126-30, 2010 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License 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, cilt.2, ss.168-72, 2010 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

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, cilt.58, ss.270-3, 2015 (Diğer Kurumların Hakemli Dergileri) identifier identifier


Davetli Kongre ve Sempozyum Faaliyetleri

2019

2019

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi

Oturum Başkanı

Antalya-Türkiye

2018

2018

XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi

Davetli Konuşmacı

Antalya-Türkiye

2017

2017

XXI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi

Davetli Konuşmacı

Antalya-Türkiye

Atıflar

Toplam Atıf Sayısı (WOS): 438

h-indeksi (WOS): 12