Prof. Dr. Hasan ÖNAL

1. Diagnostic utility of FGF-21 and GDF-15 for differentiating primary mitochondrial diseases from lysosomal storage disorders associated with secondary mitochondrial dysfunction: a machine learning–based multimetabolite approach

Yildiz A., YILDIZ M. T., ÖNAL H.

Molecular Genetics and Metabolism , cilt.149, sa.1-2, 2026 (SCI-Expanded, Scopus)

2. Expanding the clinical and molecular spectrum of NGLY1 deficiency: A multicenter cohort

Yılmaz-Gümüş E., KILAVUZ S., Demir Ş., Aydoğan A., Genç E., Akar H. T., et al.

Molecular Genetics and Metabolism , cilt.148, sa.4, 2026 (SCI-Expanded, Scopus)

3. Metabolic and mitochondrial alterations in children with autism spectrum disorder: The role of FGF-21 and GDF-15

Yildiz A., Topuz H. S., ÖNAL H.

Clinica Chimica Acta , cilt.588, 2026 (SCI-Expanded, Scopus)

4. Impact of Growth-promoting Therapies on Puberty, Growth, and Final Height in Classical 21-hydroxylase Deficiency

YAVAŞ ABALI Z., Yildiz M., ABALI S., Moniri A., BAŞ F., ÖNAL H., et al.

Journal of Clinical Endocrinology and Metabolism , cilt.111, sa.5, ss.1348-1355, 2026 (SCI-Expanded, Scopus)

5. Evaluation of adrenomedullin levels in adolescents with Hashimoto’s thyroiditis: association with clinical and laboratory findings

Kurt N. C., Sütçü Z. K., Şener G., ÖNAL H.

Journal of Pediatric Endocrinology and Metabolism , cilt.39, sa.3, ss.265-272, 2026 (SCI-Expanded, Scopus)

6. Clinical, hormonal, and genetic spectrum of cryptorchidism: a comprehensive evaluation of patients referred for pediatric endocrinological assessment

Sütçü Z. K., Kaplan E. H. A., ÖNAL H.

Journal of Pediatric Endocrinology and Metabolism , 2026 (SCI-Expanded, Scopus)

7. Atypical pediatric presentation of hyperparathyroidism: CDC73 gene mutation and parathyroid carcinoma

Aytaç Kaplan E. H., ÇAKMAK M. E., Yilmaz Özgüven M. B., Tuna Şentürk Ş., ÖNAL H., Bozlak S., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.38, sa.12, ss.1356-1360, 2025 (SCI-Expanded, Scopus)

8. Clinical characteristics, surgical and endocrinological outcomes of sellar and parasellar masses in pediatric patients: a single-center experience

Kocabey Sütçü Z., Aytaç Kaplan E. H., Erkan B., ÖNAL H.

Pituitary , cilt.28, sa.5, 2025 (SCI-Expanded, Scopus)

9. A Rare Case of Monogenic Obesity Due to a Novel Variant in the ADCY3 Gene: Challenges in Follow-up and Treatment

Özcabı B., Durmaz A., Aykut A., ÖNAL H., Özen S.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.17, sa.3, ss.337-344, 2025 (SCI-Expanded, Scopus, TRDizin)

10. Control of Coagulation Abnormalities with Sodium Benzoate in Patients with Argininemia

Ergun N. Ü., Gezdirici A., ÖNAL H.

Journal of Pediatric Research , cilt.12, sa.2, ss.102-107, 2025 (ESCI, Scopus, TRDizin)

11. Developmental outcomes of children with biotinidase deficiency and the psychological state of their parents

Bozduman Çelebi S., Akdağ B., Cimbar H., Dağ C., Topal F., Noyan B., et al.

European Journal of Pediatrics , cilt.184, sa.3, 2025 (SCI-Expanded, Scopus)

12. Pediatric hypoparathyroidism: etiological and clinical evaluation in a tertiary center

Kocabey Sütçü Z., Aytaç Kaplan E. H., ÖNAL H.

Endocrine , cilt.87, sa.3, ss.1235-1245, 2025 (SCI-Expanded, Scopus)

13. Profiles of paediatric patients experiencing stroke-like episodes associated with mitochondrial disease

Molla G. K., Uzun Ö. Ü., Agakisili H. B., Genç E., Gülten Z. A., Yıldırım T., et al.

Frontiers in Neurology , cilt.16, 2025 (SCI-Expanded, Scopus)

14. Evaluation of cardiac autonomic dysfunctions in children with type 1 diabetes mellitus

Gözüküçük D., İleri B. A., Başkan S. K., Öztarhan E., Güller D., ÖNAL H., et al.

BMC Pediatrics , cilt.24, sa.1, 2024 (SCI-Expanded, Scopus)

15. A novel graphene oxide-based fluorescence method for detection of urine glycosaminoglycans

Kösoğlu C. B., DEDE S., KARAKUŞ E., ERDOĞMUŞ A., KESKİN B., ÖNAL H.

Biotechnology and Applied Biochemistry , cilt.71, sa.3, ss.651-660, 2024 (SCI-Expanded, Scopus)

16. Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes

Altuntaş C., Uzunhan T. A., Ertürk B., Petmezci M. T., ÇAKAR N. E., Noyan B., et al.

Clinical Neurology and Neurosurgery , cilt.236, 2024 (SCI-Expanded, Scopus)

17. Ambulatory blood pressure monitorisation in children with recombinant growth hormone treatment

Aytaç Kaplan E. H., Kocabey Sütçü Z., Soyaltln E., ÖNAL H.

Journal of Pediatric Endocrinology and Metabolism , cilt.37, sa.1, ss.69-73, 2024 (SCI-Expanded, Scopus)

18. Investigation of (Epi)genetic causes in syndromic short children born small for gestational age

Tüysüz B., Kasap B., ULUDAĞ ALKAYA D., Alp Ünkar Z., Köseoğlu P., GEYİK F., et al.

European Journal of Medical Genetics , cilt.66, sa.11, 2023 (SCI-Expanded, Scopus)

19. A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy

Altuntaş C., Uzunhan T. A., Ertürk B., Petmezci M. T., ÇAKAR N. E., Noyan B., et al.

Clinical Neurology and Neurosurgery , cilt.229, 2023 (SCI-Expanded, Scopus)

20. Can we predict risk for cardiac involvement in paediatric inflammatory multi-system syndrome?

Yakut N., Tanidir I. C., Yakut K., Sahin S., Kilinc A., Kabasakal I., et al.

Cardiology in the Young , cilt.32, sa.12, ss.1944-1951, 2022 (SCI-Expanded, Scopus)

21. Angiotensin (1−7) peptide replacement therapy with plasma transfusion in COVID-19

ÖNAL H., Ergun N. U., Arslan B., Topuz S., Semerci S. Y., UĞUREL O. M., et al.

Transfusion and Apheresis Science , cilt.61, sa.4, 2022 (SCI-Expanded, Scopus)

22. Clinical, biochemical and genotypical characteristics in biotinidase deficiency

Akgun A., Sen A., ÖNAL H.

Journal of Pediatric Endocrinology and Metabolism , cilt.34, sa.11, ss.1425-1433, 2021 (SCI-Expanded, Scopus)

23. Clinical and Hormonal Profiles Correlate with Molecular Characteristics in Patients with 11β-Hydroxylase Deficiency

Yildiz M., Isik E., Abali Z. Y., Keskin M., Ozbek M. N., BAŞ F., et al.

Journal of Clinical Endocrinology and Metabolism , cilt.106, sa.9, 2021 (SCI-Expanded, Scopus)

24. The frequency of and factors affecting functional gastrointestinal disorders in infants that presented to tertiary care hospitals

BEŞER Ö. F., Cullu Cokugras F., Dogan G., Akgun O., ELEVLİ M., Yilmazbas P., et al.

European Journal of Pediatrics , cilt.180, sa.8, ss.2443-2452, 2021 (SCI-Expanded, Scopus)

25. GENDER DSYPHORIA AND PSYCHIATRIC DISORDERS IN CHILDREN AND ADOLESCENTS WITH CONGENITAL ADRENAL HYPERPLASIA

Doktur H., Tanidir C., Güneş H., Aytemiz T., DURCAN G., ÖNAL H., et al.

Acta Endocrinologica , cilt.17, sa.3, ss.365-371, 2021 (SCI-Expanded, Scopus)

26. Possible genotype-phenotype correlations in niemann-pick type c patients and miglustat treatment Lehetseges genotipus-fenotipus korrelaciok c tipusu niemann-pick-korban es a betegek miglustatkezelese

Eakar' N. E., ÖNAL H.

Ideggyogyaszati Szemle , cilt.74, sa.3-4, ss.139-144, 2021 (SCI-Expanded, Scopus)

27. Treatment of COVID-19 patients with quercetin: A prospective, single center, randomized, controlled trial

ÖNAL H., Arslan B., Üçüncü Ergun N., Topuz Ş., Yilmaz Semerci S., Kurnaz M. E., et al.

Turkish Journal of Biology , cilt.45, sa.Special Issue 1, ss.518-529, 2021 (SCI-Expanded, Scopus, TRDizin)

28. The Effect of The Height of a Second-Degree Relative on Children with Short Stature

Semerci S. Y., ÖNAL H., Topal N., Şiraneci R.

Trends in Pediatrics , cilt.2, sa.2, ss.60-66, 2021 (Scopus)

29. The factors relevant to partial remission in children with type 1 diabetes mellitus after measles vaccination: A retrospective study

Bektaş G., ÖNAL H., Adal E.

Journal of Medical Virology , cilt.92, sa.12, ss.2955-2960, 2020 (SCI-Expanded, Scopus)

30. Clinical characteristics and long-term follow-up of patients with diabetes due to ptf1a enhancer mutations

DEMİRBİLEK H., Cayir A., Flanagan S. E., Yildirim R., Kor Y., GÜRBÜZ F., et al.

Journal of Clinical Endocrinology and Metabolism , cilt.105, sa.12, 2020 (SCI-Expanded, Scopus)

31. Novel variants in Turkish patients with glycogen storage disease

ÇAKAR N. E., Gezdirici A., Topuz H. Ş., ÖNAL H.

Pediatrics International , cilt.62, sa.10, ss.1145-1150, 2020 (SCI-Expanded, Scopus)

32. Revisiting classical 3β-hydroxysteroid dehydrogenase 2 deficiency: Lessons from 31 pediatric cases

GÜRAN T., Kara C., Yildiz M., Bitkin E. C., HAKLAR G., Lin J., et al.

Journal of Clinical Endocrinology and Metabolism , cilt.105, sa.4, 2020 (SCI-Expanded, Scopus)

33. Children with hashimoto’s thyroiditis have increased intestinal permeability: Results of a pilot study

Aydın B. K., Yıldız M., Akgün A., Topal N., Adal E., ÖNAL H.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.12, sa.3, ss.303-307, 2020 (SCI-Expanded, Scopus, TRDizin)

34. Prenatal androgens and autistic, attention deficit hyperactivity disorder, and disruptive behavior disorders traits Prenatal androjenler ve otizm spektrum bozukluğu, dikkat eksikliği hiperaktivite bozukluğu, yıkıcı davranış bozuklukları belirtileri

Güneş H., Tanidir C., Doktur H., Önal Z., Kutlu E., ÖNAL H., et al.

Anadolu Psikiyatri Dergisi , cilt.21, sa.4, ss.435-442, 2020 (SCI-Expanded, Scopus, TRDizin)

35. Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study

Hatun S., Yesiltepe Mutlu G., Cinaz P., DEMİRCİOĞLU S., Ekberzade A., BEREKET A., et al.

Diabetic Medicine , cilt.36, sa.10, ss.1243-1250, 2019 (SCI-Expanded, Scopus)

36. Sense of smell and quality of life in children with diabetes mellitus

Yilmaz Y., Polat S., Yildiz M., Turgut S. B., Topal N., Aydin B., et al.

International Journal of Pediatric Otorhinolaryngology , cilt.123, ss.43-46, 2019 (SCI-Expanded, Scopus)

37. Assessment of retinal thickness as a marker of brain masculinization in children with congenital adrenal hyperplasia: A pilot study

ÖNAL H., Kutlu E., Aydln B., Ersen A., Topal N., Adal E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.32, sa.7, ss.683-687, 2019 (SCI-Expanded, Scopus)

38. Management of thyrotoxicosis in children and adolescents: A Turkish multi-center experience

Esen İ., BAYRAMOĞLU E., Yildiz M., Aydın M., Özturhan E. K., Aycan Z., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.11, sa.2, ss.164-172, 2019 (SCI-Expanded, Scopus, TRDizin)

39. Evaluation of unfavorable cardiovascular and metabolic risk factors in children and young adults with haemophilia

YILDIZ M., Özdemir N., ÖNAL H., Koç B., Tipici B. E., ZÜLFİKAR O. B.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.11, sa.2, ss.173-180, 2019 (SCI-Expanded, Scopus, TRDizin)

40. A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome

Odaman-Al I., Gezdirici A., Yıldız M., Ersoy G., Aydoğan G., Şalcıoğlu Z., et al.

Turkish Journal of Pediatrics , cilt.61, sa.2, ss.257-260, 2019 (SCI-Expanded, Scopus, TRDizin)

41. Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report

ÖNAL H., Ersen A., Gemici H., Adal E., GÜLER S., Sander S., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.10, sa.4, ss.391-394, 2018 (SCI-Expanded, Scopus, TRDizin)

42. Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

POYRAZOĞLU Ş., Bundak R., Abalı Z. Y., ÖNAL H., Sarıkaya S., Akgün A., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.10, sa.4, ss.336-342, 2018 (SCI-Expanded, Scopus, TRDizin)

43. Autoimmunity and intestinal colonization by candida albicans in patients with type 1 diabetes at the time of the diagnosis

GÜRSOY S., Koçkar T., UGAN ATİK S., Önal Z., ÖNAL H., Adal E.

Korean Journal of Pediatrics , cilt.61, sa.7, ss.217-220, 2018 (Scopus)

44. Emergence of insulin resistance following empirical glibenclamide therapy: A case report of neonatal diabetes with a recessive INS gene mutation

Yildiz M., Akcay T., Aydin B., Akgun A., Dogan B. B., De Franco E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.31, sa.3, ss.345-348, 2018 (SCI-Expanded, Scopus)

45. Endocrinological evaluations of a neurofibromatosis type 1 cohort: Is it necessary to evaluate autoimmune thyroiditis in neurofibromatosis type 1?

GÜLER S., Yeşil G., ÖNAL H.

Balkan Medical Journal , cilt.34, sa.6, ss.522-526, 2017 (SCI-Expanded, Scopus, TRDizin)

46. Possible effects of neonatal vitamin B12 status on TSH-screening program: A cross-sectional study from Turkey

Onal Z., Balkaya S., Ersen A., Mutlu N., ÖNAL H., Adal E.

Journal of Pediatric Endocrinology and Metabolism , cilt.30, sa.5, ss.551-555, 2017 (SCI-Expanded, Scopus)

47. Treatment of ichthyosis and hypernatremia in a patient with Netherton syndrome with a SPINK5 c.153delT mutation using kallikrein inhibiting ointment

Tiryakioğlu N. O., Önal Z., SAYGILI S. K., ÖNAL H., Ersoy Tunali N.

International Journal of Dermatology , cilt.56, sa.1, ss.106-108, 2017 (SCI-Expanded, Scopus)

48. Clinical, molecular, and genetic evaluation of galactosemia in Turkish children Galaktozemi tanılı olgularımızın klinik ve genetic değerlendirilmesi

UGAN ATİK S., GÜRSOY S., Koçkar T., ÖNAL H., Adal S. E.

Turk Pediatri Arsivi , cilt.51, sa.4, ss.204-209, 2016 (Scopus, TRDizin)

49. Seroprotection status of hepatitis B and measles vaccines in children with type 1 diabetes mellitus

Onal Z., Ersen A., BAYRAMOĞLU E., Yaroglu Kazancl S., ÖNAL H., Adal E.

Journal of Pediatric Endocrinology and Metabolism , cilt.29, sa.9, ss.1013-1017, 2016 (SCI-Expanded, Scopus)

50. Sleep disturbances and serum vitamin D levels in children with autism spectrum disorder

GÜLER S., Yesil G., Ozdil M., Ekici B., ÖNAL H.

International Journal of Clinical and Experimental Medicine , cilt.9, sa.7, ss.14691-14697, 2016 (SCI-Expanded, Scopus)

51. 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., Aydin B. K., et al.

American Journal of Medical Genetics, Part A , cilt.170, sa.4, ss.942-948, 2016 (SCI-Expanded, Scopus)

52. A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family

Caridi G., Gulec E. Y., Campagnoli M., Lugani F., ÖNAL H., Kilic D., et al.

Biochemia Medica , cilt.26, sa.2, ss.264-271, 2016 (SCI-Expanded, Scopus)

53. 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.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.7, sa.3, ss.183-191, 2015 (SCI-Expanded, Scopus, TRDizin)

54. Recognizing the psychosocial aspects of type 1 diabetes in adolescents

Adal E., Önal Z., Ersen A., Yalçın K., ÖNAL H., AYDIN A.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.7, sa.1, ss.57-62, 2015 (SCI-Expanded, Scopus, TRDizin)

55. Turner syndrome and associated problems in turkish children: A multicenter study

Yeşilkaya E., BEREKET A., Darendeliler F., BAŞ F., POYRAZOĞLU Ş., Aydın B. K., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.7, sa.1, ss.27-36, 2015 (SCI-Expanded, Scopus, TRDizin)

56. Differences in the gut microbiota of healthy children and those with type 1 diabetes

Soyucen E., GÜLCAN A., AKTUĞLU ZEYBEK A. Ç., ÖNAL H., KIYKIM E., AYDIN A.

Pediatrics International , cilt.56, sa.3, ss.336-343, 2014 (SCI-Expanded, Scopus)

57. Evaluation of subfoveal choroidal thickness in children with type 1 diabetes mellitus: An EDI-OCT study

SAYIN N., Kara N., PİRHAN D., VURAL A., Ersan H. B. A., ÖNAL H., et al.

Seminars in Ophthalmology , cilt.29, sa.1, ss.27-31, 2014 (SCI-Expanded, Scopus)

58. A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: Functional analysis of the mutant protein

Ersoy Tunali N., Marobbio C. M., Tiryakioǧlu N. O., Punzi G., SAYGILI S. K., ÖNAL H., et al.

Molecular Genetics and Metabolism , cilt.112, sa.1, ss.25-29, 2014 (SCI-Expanded, Scopus)

59. Response to growth hormone therapy in turner syndrome Turner sendromlu hastalarda büyüme hormonu tedavisine yanıt

Özgen I. T., Adal E., Ünüvar T., ÖNAL H., Sarikaya A. S., Akın L.

Turk Pediatri Arsivi , cilt.48, sa.4, ss.294-298, 2013 (Scopus, TRDizin)

60. Miliaria rubra and thrombocytosis in pseudohypoaldosteronism: Case report

ÖNAL H., Adal E., Ersen A., Onal Z., KESKİNDEMİRCİ G.

Platelets , cilt.23, sa.8, ss.645-647, 2012 (SCI-Expanded, Scopus)

61. Effects of selenium supplementation in the early stage of autoimmune thyroiditis in childhood: An open-label pilot study

ÖNAL H., KESKİNDEMİRCİ G., Adal E., Ersen A., Korkmaz O.

Journal of Pediatric Endocrinology and Metabolism , cilt.25, sa.7-8, ss.639-644, 2012 (SCI-Expanded, Scopus)

62. Subclinical hypothyroidism in in vitro fertilization babies

ÖNAL H., Ercan O., Adal E., Ersen A., Onal Z.

Acta Paediatrica, International Journal of Paediatrics , cilt.101, sa.6, 2012 (SCI-Expanded, Scopus)

63. Ovarian and uterine ultrasonography and relation to puberty in healthy girls between 6 and 16 years in the Turkish population: A cross-sectional study

Ersen A., ÖNAL H., Yildirim D., Adal E.

Journal of Pediatric Endocrinology and Metabolism , cilt.25, sa.5-6, ss.447-451, 2012 (SCI-Expanded, Scopus)

64. Turner syndrome with a ring X chromosome and atypical skin manifestation: Port wine stain

ÖNAL H., Adal E., Ersen A., Onal Z.

International Journal of Dermatology , cilt.51, sa.2, ss.207-210, 2012 (SCI-Expanded, Scopus)

65. Arachnoid cysts in childhood with endocrinological outcomes

ÖNAL H., Adal E., Ersen A., Işik O., Önal Z., Arslan G.

Turkish Journal of Pediatrics , cilt.53, sa.3, ss.295-300, 2011 (SCI-Expanded, Scopus)

66. Decreased serum biotinidase activity in adult patients with decompensated liver cirrhosis

ÖZDEMİR S., Zeybek C. A., Baran A., Yalvaç S., Kahveci A., ÖNAL H., et al.

Medical Journal of Bakirkoy , cilt.7, sa.2, ss.68-70, 2011 (Scopus, TRDizin)

67. Is daily 400 IU of vitamin D supplementation appropriate for every country: A cross-sectional study

ÖNAL H., Adal E., Alpaslan S., Ersen A., Aydin A.

European Journal of Nutrition , cilt.49, sa.7, ss.395-400, 2010 (SCI-Expanded, Scopus)

68. A case of late-onset central hypoventilation syndrome with hypothalamic dysfunction: Through a new phenotype

ÖNAL H., Ersen A.

Turkish Journal of Pediatrics , cilt.52, sa.2, ss.198-202, 2010 (SCI-Expanded, Scopus)

69. Late effects of childhood ALL treatment on body mass index and serum leptin levels

KARAMAN S., Ercan O., YILDIZ İ., BOLAYIRLI İ. M., Celkan T., Apak H., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.23, sa.7, ss.669-674, 2010 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

70. An important problem in developing countries: Maternal and neonatal vitamin B12 deficiency Gelişmekte olan ülkelerde önemli bir sorun: Annede ve yenidoǧanda B12 vitamini eksikliǧi

ÖNAL H., Adal E., ÖNER T., Önal Z., Aydin A.

Turk Pediatri Arsivi , cilt.45, sa.3, ss.242-245, 2010 (Scopus, TRDizin)

71. The effect of low-carbohydrate diet on left ventricular diastolic function in obese children

Zeybek C., ÇELEBİ A., AKTUĞLU ZEYBEK A. Ç., ÖNAL H., Yalcin Y., Erdem A., et al.

Pediatrics International , cilt.52, sa.2, ss.218-223, 2010 (SCI-Expanded, Scopus)

72. Thiamine-responsive megaloblastic anemia: Early diagnosis may be effective in preventing deafness

ÖNAL H., BARIŞ S., Özdil M., Yeşil G., Altun G., Özyilmaz I., et al.

Turkish Journal of Pediatrics , cilt.51, sa.3, ss.301-304, 2009 (SCI-Expanded, Scopus)

73. Right ventricular subclinical diastolic dysfunction in obese children: The effect of weight reduction with a low-carbohydrate diet

Zeybek C., AKTUĞLU ZEYBEK A. Ç., ÖNAL H., Altay S., Erdem A., ÇELEBİ A.

Pediatric Cardiology , cilt.30, sa.7, ss.946-953, 2009 (SCI-Expanded, Scopus)

74. The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children

GÜRAN T., DEMİRCİOĞLU S., BEREKET A., Akcay T., Unluguzel G., BAŞ F., et al.

European Journal of Pediatrics , cilt.168, sa.9, ss.1043-1048, 2009 (SCI-Expanded, Scopus)

75. Dispersion of the P wave as a test for cardiac autonomic function in diabetic children

Imamoglu E. Y., Oztunc F., EROĞLU A. G., ÖNAL H., GÜZELTAŞ A.

Cardiology in the Young , cilt.18, sa.6, ss.581-585, 2008 (SCI-Expanded, Scopus)

76. Treatment of iron deficiency anemia in developing countries: Should zinc be added?

ÖNAL H., Adal E., Albayrak Z., Önal Z., Aydoǧan G.

International Pediatrics , cilt.23, sa.1, ss.11-16, 2008 (Scopus)

77. A new parameter in the differential diagnosis of bacterial and viral meningitis

ÖNAL H., ÖNAL Z., Ozdil M., BARIŞ S.

Neurosciences , cilt.13, sa.1, ss.91-92, 2008 (SCI-Expanded, Scopus)

78. Combined methylmalonic aciduria and homocystinuria

ÖNAL H., BARIŞ S., Ozdil M., Ozyilmaz I., Altun G., AYDIN A.

Journal of Pediatric Neurology , cilt.6, sa.1, ss.73-76, 2008 (Scopus)

79. Encephalopathy in type I hyperlipidemia

ÖNAL H., AKTUĞLU ZEYBEK A. Ç., BARIŞ S., Altun G.

Indian Pediatrics , cilt.44, sa.4, ss.306-308, 2007 (SCI-Expanded, Scopus)

80. Capillary leak syndrome in a 5-month-old infant associated with intractable diarrhoea

ÖNAL H., AKTUĞLU ZEYBEK A. Ç., Altun G., Özyilmaz I., BARIŞ S., Aydin A.

Annals of Tropical Paediatrics , cilt.27, sa.1, ss.81-86, 2007 (SCI-Expanded, Scopus)

81. Fahr disease Fahr hastaliǧi

Akçay T., Arslan M., Toros E., ÖNAL H., Sarikaya S., GÜZELTAŞ A., et al.

Goztepe Tip Dergisi , cilt.21, sa.1, ss.61-63, 2006 (Scopus, TRDizin)

82. Hypophysis hyperplasia and growth hormon deficiency that immitate hypophysis macro adenoma secondary to hypothyroidism Hipotiroidiye ikincil hipofiz makroadenomunu taklit eden hipofiz hiperplazisi ve büyüme hormonu eksikliǧi

Akçay T., Adal E., ÖNAL H., Doǧangün E., Arslan M., Sarikaya S., et al.

Goztepe Tip Dergisi , cilt.21, sa.1, ss.40-43, 2006 (Scopus, TRDizin)

83. Bartter syndrome - Review Bartter sendromu - Derleme

ÖNAL H., Adal E., Ercan O.

Turk Pediatri Arsivi , cilt.41, sa.2, 2006 (Scopus, TRDizin)

84. Management of acute sinusitis in childhood Çocukluk çaǧinda akut sinüzit ve tedavisi

Birgül K., Özdemir P. G., ÖNAL H., Şiraneci R.

SENDROM , cilt.16, sa.12, ss.65-72, 2004 (Scopus)

85. Facial paralysis Fasiyal paralizi

ÖNAL H., Önal Z., Sezer S., Hacihasanoǧlu O., Akyol B., Adal E.

SENDROM , cilt.16, sa.8, ss.58-62, 2004 (Scopus)

86. Transfusion transmitted virus and its clinical implications Transfusion transmitted virus (TTV) ve klinik önemi

GÜZELTAŞ A., Akyol B., Yildiz H., ÖNAL H.

SENDROM , cilt.16, sa.5, ss.79-84, 2004 (Scopus)

87. Acute ischemic/hemorrhagic stroke in pediatric patiens Çocuklarda akut i̇skemik/hemorajik i̇nme

Önal Z., ÖNAL H., Yildiz E., Akyol M. B., Akin M. A., Adal E.

SENDROM , cilt.15, sa.4, ss.64-68, 2003 (Scopus)

88. Procalcitonin Prokalsitonin

Önal Z., ÖNAL H., Yildiz E., Yildiz C. K., Şiraneci R.

SENDROM , cilt.14, sa.12, ss.81-90, 2002 (Scopus)

89. Glutaric aciduria type-1 Glutarik asidüri tip 1

Önal Z., GÜZELTAŞ A., ÖNAL H., Yildiz E., Hacihasanoǧlu O.

SENDROM , cilt.13, sa.7, ss.67-68, 2001 (Scopus)

90. Zinc deficiency Çinko eksikligi

ÖNAL H., Akçay T., GÜZELTAŞ A., Yildiz H., Türel O.

SENDROM , cilt.13, sa.6, ss.61-64, 2001 (Scopus)

Yayınlar & Eserler

Yayın

Yayın (WoS)

Yayın (Scopus)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Atıf (TrDizin)

H-İndeks (TrDizin)

Atıf (Diğer Toplam)

Tez Danışmanlığı

Açık Erişim