Prof. VEYSEL NİJAT BAŞ

Metrics

Publication

Publication (WoS)

Publication (Scopus)

Citation (WoS)

560

H-Index (WoS)

Citation (Scopus)

1176

H-Index (Scopus)

Citation (TrDizin)

H-Index (TrDizin)

Citation (Sum Other)

Project

Open Access

UN Sustainable Development Goals

Education

2009 - 2012

Undergraduate Minor

University Of Health Sciences, Ankara Keçiören Educatıon And Research Hospıtal, Turkey

2003 - 2008

Undergraduate

Gazi University, Tıp Fakültesi, Turkey

Foreign Languages

C1 Advanced

English

Research Areas

Pediatric Endocrinology and Metabolism

Research Areas Based on Academic Activities

Avesis Research Areas

WoS Research Areas

Scopus Research Areas

Academic Positions

2019 - Present

Professor

Kütahya Health Sciences University, Tıp Fakültesi, Dahili Tıp Bilimleri

Articles

2026

1. Symptoms and quality of life in long COVID-19: effects on children and parents Síntomas y calidad de vida en el COVID-19 prolongado: efectos en los niños y los padres

Yılmaz Y., Geçkalan D., Baş V. N.

Andes Pediatrica , vol.97, no.2, 2026 (ESCI, Scopus)

2025

2. Lipoatrophy following weekly growth hormone therapy: a case report

Hazer İ., Bas V. N.

Journal of Pediatric Endocrinology and Metabolism , vol.38, no.10, pp.1098-1102, 2025 (SCI-Expanded, Scopus)

2024

3. Macro-TSH: A Diagnostic Dilemma

IŞIKLAR Ö. Ö., ELİFOĞLU İ., BAŞ V. N.

Osmangazi Tıp Dergisi , vol.46, no.6, pp.986-989, 2024 (TRDizin)

2022

4. Edinsel Adrenal Yetmezlik

ELİFOĞLU İ., BAŞ V. N.

Türkiye Klinikleri , 2022 (TRDizin)

2022

5. Evaluation of the Effects of Adolescent Obesity on Electrocardiography and Pulmonary Function Tests

KARAKUŞ Y., ERGEN DİBEKLİOĞLU S., ÖZDEMİR R., BAŞ V. N., ÇİÇEK M.

GUNCEL PEDIATRI , vol.20, 2022 (ESCI, Scopus)

2022

6. Identification of A Novel Hemizygous SLC16A2 Nonsense Mutation in Allen-Herndon-Dudley Syndrome

KOCAAĞA A., YİMENİCİOĞLU S., BAŞ V. N., ÇİLİNGİR O., BİLDİRİCİ Y.

Eskisehir Medical Journal , vol.3, no.22, pp.219-222, 2022 (Peer-Reviewed Journal)

2022

7. Tek Taraflı İnmemiş Testisi olan İnfantlarda Orşiopeksi Sonrası Serum AMH Seviyelerinin Değerlendirilmesi

TOPCUOĞLU M., BAŞ V. N.

Osmangazi Tıp Dergisi , vol.44, no.4, pp.569-575, 2022 (TRDizin)

2021

8. Proximal hypospadias and 46XY disorder of sex development; which patient with hypospadias needs to be investigated?

BAYRAMOĞLU E., BAŞ V. N., AYCAN Z.

Annals of Medical Research , vol.28, no.10, pp.1795-800, 2021 (TRDizin)

2020

9. Phenylketonuria and Puberty Precoccious Association A Case Report

KILIÇ YILDIRIM G., BAŞ V. N.

Osmangazi Tıp Dergisi , vol.42, no.6, pp.710-713, 2020 (TRDizin)

2018

10. Acute 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 , vol.60, pp.210-215, 2018 (SCI-Expanded, Scopus, TRDizin)

2017

11. 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 (SCI-Expanded, Scopus)

2017

12. 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 (SCI-Expanded, Scopus)

2017

13. 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-Expanded, Scopus)

2017

14. 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 (SCI-Expanded, Scopus)

2016

15. 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 (TRDizin)

2016

16. 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 (SCI-Expanded, Scopus)

2016

17. Anthropometric 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 , pp.942-8, 2016 (SCI-Expanded, Scopus)

2016

18. 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 (TRDizin)

2016

19. 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 (SCI-Expanded, Scopus)

2016

20. 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 (SCI-Expanded, Scopus)

2015

21. Targeted 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 , vol.58, pp.689-94, 2015 (SCI-Expanded, Scopus)

2015

22. 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 (SCI-Expanded, Scopus)

2015

23. 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 (SCI-Expanded, Scopus, TRDizin)

2015

24. 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 (SCI-Expanded, Scopus)

2015

25. 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 (Peer-Reviewed Journal)

2015

26. 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 (SCI-Expanded, Scopus)

2015

27. 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 (SCI-Expanded, Scopus, TRDizin)

2015

28. Effect 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 , vol.32, pp.56-63, 2015 (SCI-Expanded, Scopus, TRDizin)

2015

29. 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 (SCI-Expanded, Scopus)

2014

30. 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 (SCI-Expanded, Scopus)

2014

31. 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 (SCI-Expanded, Scopus)

2014

32. 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 (SCI-Expanded, Scopus)

2014

33. 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 (SCI-Expanded, Scopus)

2014

34. 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 (SCI-Expanded, Scopus)

2014

35. 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 (SCI-Expanded, Scopus)

2014

36. 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 (SCI-Expanded, Scopus)

2014

37. 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 (SCI-Expanded, Scopus)

2014

38. 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 (SCI-Expanded, Scopus)

2014

39. 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 (SCI-Expanded, Scopus)

2014

40. 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 (SCI-Expanded, Scopus)

2013

41. 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 (SCI-Expanded, Scopus)

2013

42. 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 (SCI-Expanded, Scopus)

2013

43. 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 (SCI-Expanded, Scopus)

2013

44. 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 , vol.34, pp.1482-90, 2013 (SCI-Expanded, Scopus)

2013

45. 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 (SCI-Expanded, Scopus)

2013

46. 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 (SCI-Expanded, Scopus)

2013

47. Prevalence 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 , vol.78, pp.667-72, 2013 (SCI-Expanded, Scopus)

2013

48. 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 (SCI-Expanded, Scopus)

2013

49. 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 (SCI-Expanded, Scopus)

2012

50. 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 (SCI-Expanded, Scopus)

2012

51. 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 (SCI-Expanded, Scopus)

2012

52. 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 (SCI-Expanded, Scopus)

2012

53. 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 (SCI-Expanded, Scopus)

2012

54. 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 (SCI-Expanded, Scopus)

2012

55. 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 (SCI-Expanded, Scopus)

2012

56. 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 (SCI-Expanded, Scopus)

2012

57. 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 (SCI-Expanded, Scopus)

2012

58. 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 (SCI-Expanded, Scopus)

2011

59. 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 (SCI-Expanded, Scopus)

2011

60. 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 (SCI-Expanded, Scopus)

2011

61. Combination antifungal therapy with voriconazole for persistent candidemia in very low birth weight neonates

Turan O., ERGENEKON N. E., HIRFANOĞLU İ. M., ÖNAL E. E., Bas V. N., TÜRKYILMAZ C., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.53, no.1, pp.19-26, 2011 (SCI-Expanded, Scopus)

2011

62. 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 (SCI-Expanded, Scopus)

2010

63. 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 (SCI-Expanded, Scopus)

2010

64. 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 (SCI-Expanded, Scopus)

2010

65. 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 (SCI-Expanded, Scopus)

2010

66. 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 (SCI-Expanded, Scopus)

Papers Presented at Peer-Reviewed Scientific Conferences

2025

1. Diyabetik Ketoasidozlu Çocuk Hastalarda Nötrofil/Lenfosit Oranı ve Diğer hematolojik Bulguların Değerlendirilmesi

HAZER İ., kasap demir z. s., ÖZSOYLU S., BAŞ V. N.

21. Ulusal Uludağ Pediatri Kış Kongresi, 10 April 2025, pp.49, (Summary Text)

2023

2. Tip 1 diyabetes mellitus tanılı çocuklarda kardiyak repolarizasyon inhomejenitesinin değerlendirilmesi

ELİFOĞLU İ., BAŞ V. N., GEÇKALAN D., ÖZDEMİR R.

27. ulusal pediatrik endokrinoloji ve diyabet kongresi, Turkey, 02 May 2023, (Summary Text)

2023

3. Tanı karmaşasına yol açan Makro-TSH Olgusu 27. ulusal pediatrik endokrinoloji ve diyabet kongresi

ELİFOĞLU İ., BAŞ V. N., IŞIKLAR Ö. Ö.

27. ulusal pediatrik endokrinoloji ve diyabet kongresi(, Turkey, 02 May 2023, (Full Text)

2021

4. Transvers testiküler ektopi ile persistan müllerian kanal sendromu; AMH yeni mutasyon saptanan olgu sunumu

YILMAZ Z., GEÇKALAN SOYSAL D., URFALI M., BAŞ V. N.

56.Türk Pediatri Kongresi, Turkey, 17 October - 22 November 2021, (Summary Text)

2021

5. Tip 1 Diyabetes Melitus tanılı çocuk hastalarda otoimmun hastalıkların değerlendirilmesi

SİVAS O., GEÇKALAN SOYSAL D., BAŞ V. N.

56.Türk Pediatri Kongresi, Turkey, 17 - 22 November 2021, (Summary Text)

2016

6. Hipo hiperkalsemi ile giden subkutan yag dokusu nekrozu ve brakiyal pleksopati

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

18. Ulusal Çocuk Nöroloji Kongresi, Antalya, Turkey, 20 - 24 April 2016

2016

7. 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

8. 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

2015

9. 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

Books

2025

1. KIZLARDA NUTRİSYONEL BOY KISALIĞI

UĞURLU M., BAŞ V. N.

in: yaşamda kadın, ARITÜRK ATILGAN ZUHAL, HASPOLAT YUSUF KENAN, KARA MUSTAFA, Editor, Orient Yayınları, pp.156-167, 2025

2025

2. klinifelter syndrome

HAZER İ., BAŞ V. N.

in: Gonadal diseases in boys and male adolescents, PELTEK KENDİRCİ HAVVA NUR, HASPOLAT YUSUF KENAN, Editor, orient publications, pp.100-108, 2025

2025

3. ÇOCUKLARDA FAST FOOD BESLENME

DEĞİRMEN ŞİŞMAN E., BAŞ V. N.

in: ÇOCUKLARDA BESLENME VE BESİN KAYNAKLARI, HASPOLAT YUSUF KENAN, DÖNERAY HAKAN, ATICI SERKAN, ÇAYIR ATİLLA, Editor, ORİENT YAYINLARI, pp.215-224, 2025

2025

4. KIZ ERGENLERDE JİNEKOLOJİK SORUNLAR

DEĞİRMEN ŞİŞMAN E., BAŞ V. N.

in: KADIN VE JİNEKOLOJİK SORUNLAR, PEKER NURULLAH, HASPOLAT YUSUF KENAN, DUMAN MESUDE, Editor, ORİENT YAYINLARI, pp.21-31, 2025

2025

5. kız ergenlerde gelişim sorunları

ELİFOĞLU İ., BAŞ V. N.

in: kadın sağlığı, PEKER NURULLAH, HASPOLAT YUSUF KENAN, BAYSAL YILDIRIM ZEYNEP, Editor, Orient Yayınları, pp.1-9, 2025

2025

6. ERİŞKİNLERDE FAST FOOD BESLENME

ELİFOĞLU İ., BAŞ V. N.

in: obezite, HASPOLAT YUSUF KENAN, PELTEK KENDİRCİ HAVVA NUR, BAŞ VEYSEL NİJAT, Editor, Orient Yayınları, pp.56-63, 2025

2024

7. Çocukluk Döneminde Arı Ürünleri ile Beslenme

BAŞ V. N., DEĞİRMEN ŞİŞMAN E.

in: Çocuk Sağlığı ve Gelişimi Cilt 2, , Editor, Orient Yayınları, pp.99-114, 2024

2023

8. ACQUIRED ADRENAL INSUFFIENCY

elifoğlu İ., BAŞ V. N.

in: ADRENAL DISEASES IN CHILDREN AND ADOLESCENTS, , Editor, orient publications, pp.76-83, 2023

2023

9. MENSTRUATION DISORDERS IN CHILDREN

GEÇKALAN D., BAŞ V. N.

in: GONADAL DISEASES IN GIRLS AND FEMALE ADOLESCENTS, KABAY ŞAHİN, ÖZLÜLERDEN YUSUF, ÇELEN SİNAN, GÜNSEREN KADİR ÖMÜR, BAŞER AYKUT, Editor, orient publications, pp.78-85, 2023

2020

10. 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

Congress and Symposium Activities

17 April 2019 - 21 April 2019

XXIII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi

Session Moderator

Antalya-Turkey

18 April 2018 - 22 April 2018

XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi

Invited Speaker

Antalya-Turkey

26 April 2017 - 30 April 2017