Wissenschaftliche Arbeiten

Doç. Dr. Saygın Abalı

93 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.

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  1. The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography

    International Ophthalmology, 2016

    DOI 10.1007/s10792-016-0371-8 PMID 27718081 21 Zitationen (Europe PMC) Quelle: OpenAlex

  2. Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females

    Pediatric Diabetes, 2016

    DOI 10.1111/pedi.12470 PMID 27873431 24 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  3. GCK gene mutations are a common cause of childhood‐onset MODY (maturity‐onset diabetes of the young) in Turkey

    Clinical Endocrinology, 2016

    DOI 10.1111/cen.13121 PMID 27256595 18 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  4. The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

    Journal of Clinical Research in Pediatric Endocrinology, 2016

    DOI 10.4274/jcrpe.3013 PMID 27125300 20 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  5. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

    American Journal of Medical Genetics Part A, 2016

    DOI 10.1002/ajmg.a.37498 PMID 26788866 8 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  6. Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes

    Dspace Repository (Marmara Üniversitesi), 2016

    DOI 10.5072/zenodo.15248 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  7. Etiologic Distribution and Characteristics of Patients with Short Stature in a Pediatric Endocrinology Clinic

    Dspace Repository (Marmara Üniversitesi), 2016

    Frei zugänglicher VolltextQuelle: OpenAlex

  8. Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta

    55th ESPE Meeting, 2016

    DOI 10.5072/zenodo.15050 Quelle: OpenAlex

  9. [beta]-hCG from an Occult Source Causing Peripheral Precocious Puberty: Identification of the Tumour 6 Years After Presentation

    Dspace Repository (Marmara Üniversitesi), 2016

    Frei zugänglicher VolltextQuelle: OpenAlex

  10. Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.1771 PMID 25800473 44 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  11. Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children

    Hormone Research in Paediatrics, 2015

    DOI 10.1159/000369395 PMID 25676144 24 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  12. Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours

    Pediatric Obesity, 2015

    DOI 10.1111/ijpo.12076 PMID 26463004 14 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  13. Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

    Journal of Clinical Research in Pediatric Endocrinology, 2015

    DOI 10.4274/jcrpe.2023 PMID 26831551 7 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  14. Dysosteosclerosis from a unique mutation in SLC29A3

    Bone Abstracts, 2015

    DOI 10.1530/boneabs.4.p97 7 Zitationen (OpenAlex) Quelle: OpenAlex

  15. Growth without growth hormone syndrome in a patient with craniopharyngioma

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2015

    1 Zitation (OpenAlex) Quelle: OpenAlex

  16. Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome

    54th ESPE Meeting (ESPE 2015), 2015

    Quelle: OpenAlex

  17. Follow-up of two cases of medulloblastoma with/without growth hormone therapy

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2015

    Quelle: OpenAlex

  18. Hereditary Vitamin D-Resistant Rickets: Report of Four Cases with Successful Use of Intermittent Intravenous Calcium Via Peripheral Route

    54th ESPE Meeting (ESPE 2015), 2015

    Quelle: OpenAlex

  19. Friedreich's Ataxia Presenting with Diabetes Mellitus in an Adolescent

    2015

    Quelle: OpenAlex

  20. The Growth Characteristics of Patients with Noonan Syndrome, and First 2 Years Results of GH Treatment: A Nationwide Multicentre Study

    54th ESPE Meeting (ESPE 2015), 2015

    Quelle: OpenAlex

  21. Turner Sendromlu Türk Kızlarının Büyüme Eğrileri: FAVOR Turner Sendromu Çalışma Grubu

    Çanakkale Onsekiz Mart University AVESIS, 2015

    Quelle: OpenAlex

  22. Turner Sendromlu Türk Kızlarının Büyüme Eğrileri:

    Çanakkale Onsekiz Mart University AVESIS, 2015

    Quelle: OpenAlex

  23. Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS

    Bone, 2014

    DOI 10.1016/j.bone.2014.10.006 PMID 25464124 25 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  24. Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet

    Bone, 2014

    DOI 10.1016/j.bone.2014.04.010 PMID 24735972 30 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  25. Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus

    Pediatric Diabetes, 2014

    DOI 10.1111/pedi.12167 PMID 25039448 16 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  26. Final Height in Girls with Idiopathic Central Precocious Puberty Treated with GNRH Analog: Comparison with Untreated Controls

    53rd ESPE Meeting, 2014

    1 Zitation (OpenAlex) Quelle: OpenAlex

  27. Hypoglycemia: An unrecognized problem in cystic fibrosis (CF) patients unmasked by continues glucose monitorisation (CGM)

    European Respiratory Journal, 2014

    DOI 10.1183/13993003/erj.44.suppl_58.p1216 1 Zitation (OpenAlex) Quelle: OpenAlex

  28. ABSTRACT 286

    Pediatric Critical Care Medicine, 2014

    DOI 10.1097/01.pcc.0000449012.06013.49 Quelle: OpenAlex

  29. Department of Pediatric Endocrinology, Marmara University

    Dspace Repository (Marmara Üniversitesi), 2014

    Quelle: OpenAlex

  30. Younger Age and BMI [gt]3SD are Risk Factors for Mortality in Children with Hypothalamic Obesity

    ESPE 2014, 2014

    Quelle: OpenAlex

  31. Papillary Thyroid Cancer with Diffuse Pulmonary Metastasis: How to Manage?

    53rd ESPE Meeting, 2014

    Quelle: OpenAlex

  32. Eleven Years of Letrozole Treatment in a Child with 11-[beta] Hydroxylase Deficiency: Effect on Bone Age and Height Prognosis

    53rd ESPE Meeting, 2014

    Quelle: OpenAlex

  33. Sleep-related Breathing Disorders in Pycnodysostosis

    53rd ESPE Meeting, 2014

    Quelle: OpenAlex

  34. Is There a Change in the Presentation of Childhood Type-1 Diabetes Mellitus in the Last 15 Years? Data from a Tertiary Care Center in Turkey

    ESPE 2014, 2014

    Quelle: OpenAlex

  35. Hyperthyroidism Due to TSH Secreting Pituitary Adenoma in a 7-Year-Old Boy

    53rd ESPE Meeting, 2014

    Quelle: OpenAlex

  36. GAD Antibody Positivity is Associated with Higher Prevalence of Autoimmune Thyroiditis in Children with Type 1 Diabetes Mellitus

    53rd ESPE Meeting, 2014

    Quelle: OpenAlex

  37. Turner Sendromlu Çocukların Başvuru Özellikleri ve Eşlik Eden Patolojiler: 842 Vakanın Ulusal Veritabanında Değerlendirme Sonuçları

    AYBU AVESIS, 2014

    Quelle: OpenAlex

  38. Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and “Apparent” Thyroid Dysgenesis

    The Journal of Clinical Endocrinology & Metabolism, 2013

    DOI 10.1210/jc.2013-2619 PMID 24248179 37 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  39. Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

    European Journal of Pediatrics, 2012

    DOI 10.1007/s00431-012-1868-4 PMID 23093139 7 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  40. Türk çocuklarında kulaç uzunluğu ve oturma yüksekliği referansları

    Turkiye Klinikleri Pediatric Sciences - Special Topics, 2012

    Quelle: OpenAlex

  41. 651 Evaluation of Thyroid Functions in Preterm Newborns Less Than 34 Weeks of Gestation

    Archives of Disease in Childhood, 2012

    DOI 10.1136/archdischild-2012-302724.0651 Quelle: OpenAlex

  42. GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.

    Quelle: Profilseite auf acibadem.com.tr

  43. igher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus.

    Quelle: Profilseite auf acibadem.com.tr