Scientific work

Prof. Dr. Tülay Güran

389 publications. The source of the information is stated next to each publication.

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  1. Predictors of surgical complications in boys with hypospadias: Data from an internationa registry

    World Journal of Pediatric Surgery, 2023

    DOI 10.1136/wjps-2023-000599 PMID 37860275 3 citations (Europe PMC) Open-access full textSource: ORCID

  2. Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls

    Sexual Development, 2023

    DOI 10.1159/000526997 PMID 36917969 2 citations (Europe PMC) Open-access full textSource: ORCID

  3. Venous Thrombosis in a Pseudohypoparathyroidism Patient with a Novel GNAS Frameshift Mutation and Complete Resolution of Vascular Calcifications with Acetazolamide Treatment

    Hormone Research in Paediatrics, 2023

    DOI 10.1159/000534456 PMID 37906994 1 citation (Europe PMC) Open-access full textSource: ORCID

  4. An Overlooked Manifestation of Hypercortisolism: Cerebral Cortical Atrophy and Challenges in Identifying the Etiology of Hypercortisolism – A Report of 2 Pediatric Cases

    Hormone Research in Paediatrics, 2023

    DOI 10.1159/000530391 PMID 36972563 2 citations (OpenAlex) Open-access full textSource: OpenAlex

  5. Abstracts of the ESPE 61 Annual Society Meeting

    Hormone Research in Paediatrics, 2023

    DOI 10.1159/000533803 PMID 37725926 36 citations (OpenAlex) Open-access full textSource: OpenAlex

  6. The association between hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia

    Endocrine Abstracts, 2023

    DOI 10.1530/endoabs.90.oc5.2 1 citation (OpenAlex) Source: OpenAlex

  7. Differences of Sexual Development (DSD) and Gender Incongruence (GI)

    Yearbook of pediatric endocrinology, 2023

    DOI 10.1530/ey.20.4 Source: OpenAlex

  8. Association of newborn screening of congenital adrenal hyperplasia with outcomes in the first 90 days of life: a multi-centre I-CAH registry analysis of contemporary practice

    Endocrine Abstracts, 2023

    DOI 10.1530/endoabs.95.oc8.4 Source: OpenAlex

  9. An international study of the association between local health care resources and acute adrenal insufficiency events in children with congenital adrenal hyperplasia

    Endocrine Abstracts, 2023

    DOI 10.1530/endoabs.95.p86 Source: OpenAlex

  10. Acute adrenal insufficiency related adverse events in children with congenital adrenal hyperplasia (CAH): Changes during the period 2019-2022 in I-CAH

    Endocrine Abstracts, 2023

    DOI 10.1530/endoabs.94.p16 Source: OpenAlex

  11. An international study of the association between local health care resources and acute adrenal insufficiency events in children with congenital adrenal hyperplasia

    Endocrine Abstracts, 2023

    DOI 10.1530/endoabs.94.p161 Source: OpenAlex

  12. Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

    European Journal of Medical Genetics, 2022

    DOI 10.1016/j.ejmg.2022.104654 PMID 36343887 6 citations (Europe PMC) Open-access full textSource: OpenAlex

  13. A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/B

    Bone, 2022

    DOI 10.1016/j.bone.2022.116344 PMID 35104666 Open-access full textSource: OpenAlex

  14. Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C

    Yearbook of pediatric endocrinology, 2022

    DOI 10.1530/ey.19.6.5 Source: OpenAlex

  15. A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophy

    American Journal of Medical Genetics Part A, 2022

    DOI 10.1002/ajmg.a.62888 PMID 35792517 6 citations (OpenAlex) Open-access full textSource: OpenAlex

  16. Obezite problemi olan çocuklarda kardiyopulmoner sağlamlık ve kognitif fonksiyon değişiklikleri

    Dspace Repository (Marmara Üniversitesi), 2022

    Source: OpenAlex

  17. Primary adrenal insufficiency in a patient with biallelic QRSL1 mutations

    European Journal of Endocrinology, 2022

    DOI 10.1530/eje-22-0233 PMID 35894854 5 citations (Europe PMC) Open-access full textSource: ORCID

  18. Evaluation of thyroid function and metabolic parameters in obese and overweight children: A prospective case-control study.

    Investigación Clínica, 2022

    DOI 10.54817/ic.v63n2a02 2 citations (OpenAlex) Open-access full textSource: ORCID

  19. Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high-normal testicular volume

    European Journal of Endocrinology, 2022

    DOI 10.1530/eje-21-1230 PMID 35235537 3 citations (Europe PMC) Open-access full textSource: ORCID

  20. Insights From Long-term Follow-up of a Girl With Adrenal Insufficiency and Sphingosine-1-Phosphate Lyase Deficiency

    Journal of the Endocrine Society, 2022

    DOI 10.1210/jendso/bvac020 PMID 35308304 7 citations (Europe PMC) Open-access full textSource: ORCID

  21. Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure

    European Journal of Endocrinology, 2022

    DOI 10.1530/eje-21-1085 PMID 35290211 13 citations (Europe PMC) Open-access full textSource: ORCID

  22. Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure

    OpenAlex, 2022

    DOI 10.60692/vgzrc-48f92 Source: ORCID

  23. Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure

    OpenAlex, 2022

    DOI 10.60692/35972-g6p93 Source: ORCID

  24. A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review

    Endocrine Connections, 2022

    DOI 10.1530/ec-22-0250 PMID 35904228 10 citations (Europe PMC) Open-access full textSource: ORCID

  25. Adrenal steroids reference ranges in infancy determined by LC-MS/MS

    Pediatric Research, 2022

    DOI 10.1038/s41390-021-01739-5 PMID 34556810 8 citations (Europe PMC) Source: ORCID

  26. Approaching a Newborn with Atypical Genitalia: Hints for Pediatricians

    Trends in Pediatrics, 2022

    DOI 10.4274/tp.2022.63634 Open-access full textSource: ORCID

  27. Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C

    European Journal of Endocrinology, 2022

    DOI 10.1530/eje-21-0910 PMID 34714774 3 citations (Europe PMC) Open-access full textSource: ORCID

  28. Catch-up Growth and Discontinuation of Fludrocortisone Treatment in Aldosterone Synthase Deficiency

    Journal of Clinical Endocrinology and Metabolism, 2022

    DOI 10.1210/clinem/dgab619 PMID 34415991 10 citations (Europe PMC) Open-access full textSource: ORCID

  29. Congenital adrenal hyperplasia and hypertension

    Endocrine Hypertension: From Basic Science to Clinical Practice, 2022

    DOI 10.1016/b978-0-323-96120-2.00015-7 5 citations (OpenAlex) Source: ORCID

  30. Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

    JBMR Plus, 2022

    DOI 10.1002/jbm4.10663 PMID 35991533 8 citations (Europe PMC) Open-access full textSource: ORCID

  31. Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Controlled and Non-compliant Patients

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2022

    DOI 10.4274/jcrpe.galenos.2021.2021.0113 PMID 34355879 4 citations (Europe PMC) Open-access full textSource: ORCID

  32. Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency

    Journal of Clinical Endocrinology and Metabolism, 2022

    DOI 10.1210/clinem/dgac016 PMID 35028661 12 citations (Europe PMC) Open-access full textSource: ORCID

  33. Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects

    Yearbook of pediatric endocrinology, 2022

    DOI 10.1530/ey.19.1.12 1 citation (OpenAlex) Source: OpenAlex

  34. Adrenal steroids reference ranges in infancy determined by LC-MS/MS

    Yearbook of pediatric endocrinology, 2022

    DOI 10.1530/ey.19.8.5 Source: OpenAlex

  35. DSD and Gender Incongruence

    Yearbook of pediatric endocrinology, 2022

    DOI 10.1530/ey.19.6 Source: OpenAlex

  36. Obez çocuklarda kardiyopulmoner egzersiz testi sonrası akut otonomik toparlanma ile dinlenik otonomik regülasyon ilişkisi

    Dspace Repository (Marmara Üniversitesi), 2022

    Source: OpenAlex

  37. Cranial MRI Abnormalities and Long-term Follow-up of the Lesions in 770 Girls With Central Precocious Puberty

    The Journal of Clinical Endocrinology & Metabolism, 2021

    DOI 10.1210/clinem/dgab190 PMID 33765130 16 citations (Europe PMC) Open-access full textSource: OpenAlex

  38. Cranial MRI abnormalities and long-term follow-up of the lesions in 770 girls with central precocious puberty

    Yearbook of pediatric endocrinology, 2021

    DOI 10.1530/ey.18.7.1 1 citation (OpenAlex) Source: OpenAlex

  39. Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features

    Calcified Tissue International, 2021

    DOI 10.1007/s00223-021-00928-y PMID 34761296 4 citations (Europe PMC) Open-access full textSource: OpenAlex

  40. A rare cause of hypercalcemia: Congenital Lactase Deficiency

    59th ESPE Annual Meeting (ESPE 2021 Online), 2021

    Source: OpenAlex

  41. A Novel Deletion Involving the First GNAS Exon Encoding Gsα Causes PHP1A Without Methylation Changes At Exon A/B

    SSRN Electronic Journal, 2021

    DOI 10.2139/ssrn.3990635 Open-access full textSource: OpenAlex

  42. Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency

    The Journal of Clinical Endocrinology & Metabolism, 2021

    DOI 10.1210/clinem/dgab225 PMID 33830237 28 citations (Europe PMC) Open-access full textSource: OpenAlex

  43. Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

    Diabetologia, 2021

    DOI 10.1007/s00125-021-05597-y PMID 34686905 20 citations (Europe PMC) Open-access full textSource: OpenAlex

  44. Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects

    The Journal of Clinical Endocrinology & Metabolism, 2021

    DOI 10.1210/clinem/dgab352 PMID 33999151 12 citations (Europe PMC) Source: ORCID

  45. Gonadectomy in conditions affecting sex development: a registry-based cohort study

    OpenAlex, 2021

    DOI 10.60692/zk9rm-nhs71 Source: ORCID

  46. Gonadectomy in conditions affecting sex development: a registry-based cohort study

    OpenAlex, 2021

    DOI 10.60692/s9t23-ha771 Source: ORCID

  47. Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature

    Calcified Tissue International, 2021

    DOI 10.1007/s00223-020-00784-2 PMID 33386952 20 citations (Europe PMC) Source: ORCID

  48. International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia: data from the I-CAH registry

    OpenAlex, 2021

    DOI 10.60692/6ea62-2kr48 Source: ORCID

  49. International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia: data from the I-CAH registry

    OpenAlex, 2021

    DOI 10.60692/q99mz-gz810 Source: ORCID

  50. Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency

    Hormone Research in Paediatrics, 2021

    DOI 10.1159/000515079 PMID 33780934 18 citations (Europe PMC) Source: ORCID