Wissenschaftliche Arbeiten

Prof. Dr. Tülay Güran

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

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  1. Practice patterns and treatment outcomes of growth-promoting therapies in CAH: insights from real-world data

    Endocrine Abstracts, 2025

    DOI 10.1530/endoabs.111.oc5.6 Quelle: OpenAlex

  2. Phenotypic variation and pubertal outcomes in males and females with 46,XY partial gonadal dysgenesis

    Yearbook of pediatric endocrinology, 2025

    DOI 10.1530/ey.22.6.13 Quelle: OpenAlex

  3. Phenotypes linked to duplication upstream of SOX9: new insights into presentation and diagnosis

    Yearbook of pediatric endocrinology, 2025

    DOI 10.1530/ey.22.6.7 Quelle: OpenAlex

  4. DSD and Gender Incongruence

    Yearbook of pediatric endocrinology, 2025

    DOI 10.1530/ey.22.6.0 Quelle: OpenAlex

  5. Primary adrenal insufficiency in patients with CPOX gene mutations

    Yearbook of pediatric endocrinology, 2025

    DOI 10.1530/ey.22.6.10 Quelle: OpenAlex

  6. Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

    EBioMedicine, 2024

    DOI 10.1016/j.ebiom.2023.104941 PMID 38168586 31 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

  7. Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia

    The Journal of Clinical Endocrinology & Metabolism, 2024

    DOI 10.1210/clinem/dgae868 PMID 39700445 3 Zitationen (Europe PMC) Quelle: OpenAlex

  8. 6687 New indication for monogenic diabetes genetic testing in children – implication for routine clinical practice

    British Society for Paediatric Endocrinology and Diabetes Meeting (BSPED), 2024

    DOI 10.1136/archdischild-2024-rcpch.361 Quelle: OpenAlex

  9. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

    Endocrine, 2024

    DOI 10.1007/s12020-024-03962-6 PMID 39020240 13 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  10. Development of external genitalia during mini-puberty: Is it related to somatic growth or pubertal hormones?

    Global Pediatrics, 2024

    DOI 10.1016/j.gpeds.2024.100155 Frei zugänglicher VolltextQuelle: OpenAlex

  11. Prolactin Elevation Due to Heterophile Antibody Interference in Pituitary Deficiency

    Turkish Society of Clinical Biochemistry, 2024

    DOI 10.56615/tkbd.2024.17 Frei zugänglicher VolltextQuelle: ORCID

  12. Rare forms of congenital adrenal hyperplasia

    Clinical Endocrinology, 2024

    DOI 10.1111/cen.15009 PMID 38126084 16 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  13. Assessment of prognostic factors in pediatric adrenocortical tumors: the modified pediatric S-GRAS score in an international multicenter cohort—a work from the ENSAT-PACT working group

    European Journal of Endocrinology, 2024

    DOI 10.1093/ejendo/lvae079 PMID 38924056 11 Zitationen (Europe PMC) Quelle: ORCID

  14. International consensus on mitotane treatment in pediatric patients with adrenal cortical tumors: indications, therapy, and management of adverse effects.

    Oxford University Press (OUP), 2024

    DOI 10.17863/cam.108568 Frei zugänglicher VolltextQuelle: ORCID

  15. Evaluating breast ultrasonography as a complementary diagnostic method in girls with central precocious puberty

    Pediatric Radiology, 2024

    DOI 10.1007/s00247-024-05934-4 PMID 38717607 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  16. Lack of NAD(P)+ transhydrogenase activity in patients with primary adrenal insufficiency due to NNT variants

    European Journal of Endocrinology, 2024

    DOI 10.1093/ejendo/lvae011 PMID 38261461 4 Zitationen (Europe PMC) Quelle: ORCID

  17. Supplemental Figures of Phenotypes linked to duplication upstream of SOX9: New insights into presentation, diagnosis and management.

    figshare, 2024

    DOI 10.6084/m9.figshare.25067672.v1 Quelle: ORCID

  18. Supplemental Figures of Phenotypes linked to duplication upstream of SOX9: New insights into presentation, diagnosis and management.

    figshare, 2024

    DOI 10.6084/m9.figshare.25067672.v2 Quelle: ORCID

  19. Supplemental Figures of Phenotypes linked to duplication upstream of SOX9: New insights into presentation, diagnosis and management.

    figshare, 2024

    DOI 10.6084/m9.figshare.25067672 Quelle: ORCID

  20. Supplemental Figures of Phenotypes linked to duplication upstream of SOX9: New insights into presentation, diagnosis and management.

    figshare, 2024

    DOI 10.6084/m9.figshare.25067672.v3 Quelle: ORCID

  21. Supplemental Figures of Phenotypes linked to duplication upstream of SOX9: New insights into presentation and diagnosis

    figshare, 2024

    DOI 10.6084/m9.figshare.25067672.v6 Quelle: ORCID

  22. Supplemental Figures of Phenotypes linked to duplication upstream of SOX9: New insights into presentation and diagnosis

    figshare, 2024

    DOI 10.6084/m9.figshare.25067672.v4 Quelle: ORCID

  23. Supplemental Figures of Phenotypes linked to duplication upstream of SOX9: New insights into presentation and diagnosis

    figshare, 2024

    DOI 10.6084/m9.figshare.25067672.v5 Quelle: ORCID

  24. Supplementary Materials of Clinical and Molecular Genetic Characteristics of the Patients with Hereditary Hypophosphatemia Supplementary Documents

    figshare, 2024

    DOI 10.6084/m9.figshare.26489875.v2 Quelle: ORCID

  25. Supplementary Materials of Clinical and Molecular Genetic Characteristics of the Patients with Hereditary Hypophosphatemia Supplementary Documents

    figshare, 2024

    DOI 10.6084/m9.figshare.26489875.v3 Quelle: ORCID

  26. Supplementary Materials of Clinical and Molecular Genetic Characteristics of the Patients with Hereditary Hypophosphatemia

    figshare, 2024

    DOI 10.6084/m9.figshare.26489875 Quelle: ORCID

  27. Supplementary Materials of Clinical and Molecular Genetic Characteristics of the Patients with Hereditary Hypophosphatemia

    figshare, 2024

    DOI 10.6084/m9.figshare.26489875.v1 Quelle: ORCID

  28. Bone Phenotype is Always Present But Androgen Excess is Less Frequently Seen in PAPSS2 Deficiency

    Journal of clinical research in pediatric endocrinology, 2024

    DOI 10.4274/jcrpe.galenos.2023.2023-12-10 PMID 38084048 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  29. Severe adrenal insufficiency in six neonates with normal newborn screening for CAH

    Clinical endocrinology, 2024

    DOI 10.1111/cen.15080 PMID 38796770 1 Zitation (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  30. International consensus on mitotane treatment in pediatric patients with adrenal cortical tumors: indications, therapy, and management of adverse effects

    European journal of endocrinology, 2024

    DOI 10.1093/ejendo/lvae038 PMID 38552173 15 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  31. Multi-Stakeholder Opinion Statement on the Care of Individuals Born with Differences of Sex Development: Common Ground and Opportunities for Improvement

    Hormone Research in Paediatrics, 2024

    DOI 10.1159/000536296 PMID 38310850 28 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  32. Diagnosis and management of non-CAH 46,XX disorders/differences in sex development

    Frontiers in Endocrinology, 2024

    DOI 10.3389/fendo.2024.1354759 PMID 38812815 12 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  33. Temporal Trends in Acute Adrenal Insufficiency Events in Children With Congenital Adrenal Hyperplasia During 2019-2022

    Journal of the Endocrine Society, 2024

    DOI 10.1210/jendso/bvae145 PMID 39258010 5 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  34. Factors influencing survival in sphingosine phosphate lyase insufficiency syndrome: a retrospective cross-sectional natural history study of 76 patients

    Orphanet Journal of Rare Diseases, 2024

    DOI 10.1186/s13023-024-03311-w PMID 39334450 6 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  35. 8568 Prevalence of Raised Blood Pressure in Individuals With 46,XY DSD: an I-DSD Registry study

    Journal of the Endocrine Society, 2024

    DOI 10.1210/jendso/bvae163.1743 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  36. Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy, and Myopathy (GDRM)

    Springer eBooks, 2024

    DOI 10.1007/978-3-319-66816-1_1321-1 Quelle: OpenAlex

  37. Glucocorticoid replacement therapy in congenital adrenal hyperplasia and its associations with growth outcomes - real world data analysis from an international cohort of 1500 patients

    Endocrine Abstracts, 2024

    DOI 10.1530/endoabs.103.oc5.5 Quelle: OpenAlex

  38. 8568 Prevalence of Raised Blood Pressure in Individuals With 46,XY DSD: an I-DSD Registry study

    Journal of the Endocrine Society, 2024

    DOI 10.1210/jendso/bvae163.1656 Frei zugänglicher VolltextQuelle: OpenAlex

  39. Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature

    Hormone Research in Paediatrics, 2023

    DOI 10.1159/000529070 PMID 36630941 1 Zitation (Europe PMC) Quelle: OpenAlex

  40. Evaluation of cardiopulmonary fitness and cognitive functions in children with obesity

    Dspace Repository (Marmara Üniversitesi), 2023

    Quelle: OpenAlex

  41. Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 Years

    Journal of clinical research in pediatric endocrinology, 2023

    DOI 10.4274/jcrpe.galenos.2023.2022-11-16 PMID 36700465 5 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

  42. Development of external genitalia during mini-puberty: is it related to somatic growth or reproductive hormones?

    European Journal of Pediatrics, 2023

    DOI 10.1007/s00431-023-05393-3 PMID 38133811 4 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

  43. Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study

    Oxford University Press, 2023

    DOI 10.5167/uzh-254821 Quelle: ORCID

  44. Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study

    OpenAlex, 2023

    DOI 10.60692/c9m3c-sqg25 Quelle: ORCID

  45. Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study

    OpenAlex, 2023

    DOI 10.60692/fnfht-d4219 Quelle: ORCID

  46. Development of external genitalia during minipuberty: Is it related to somatic growth or hormones?

    Research Square, 2023

    DOI 10.21203/rs.3.rs-3390089/v1 Frei zugänglicher VolltextQuelle: ORCID

  47. Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study

    European journal of endocrinology, 2023

    DOI 10.1093/ejendo/lvad143 PMID 37837609 10 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  48. Introduction

    Hormone Research in Paediatrics, 2023

    DOI 10.1159/000519896 PMID 34583362 Quelle: ORCID

  49. Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty

    Journal of Pediatric Endocrinology and Metabolism, 2023

    DOI 10.1515/jpem-2022-0645 PMID 36883204 7 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

  50. Non-hormonal Clitoromegaly due to Clitoral Priapism Caused by Appendicitis/Appendectomy

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2023

    DOI 10.4274/jcrpe.galenos.2021.2021-8-4 PMID 34866370 2 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID