Prof. Dr. Tülay Güran

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : OpenAlex

Abstracts of the ESPE 61 Annual Society Meeting

Hormone Research in Paediatrics, 2023

DOI 10.1159/000533803 PMID 37725926 36 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

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

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

Yearbook of pediatric endocrinology, 2023

DOI 10.1530/ey.20.4 Source : OpenAlex

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

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

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

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

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) Texte intégral en libre accèsSource : OpenAlex

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 Texte intégral en libre accèsSource : OpenAlex

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

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) Texte intégral en libre accèsSource : OpenAlex

Obezite problemi olan çocuklarda kardiyopulmoner sağlamlık ve kognitif fonksiyon değişiklikleri

Dspace Repository (Marmara Üniversitesi), 2022

Source : OpenAlex

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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

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

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) Texte intégral en libre accèsSource : ORCID

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

Approaching a Newborn with Atypical Genitalia: Hints for Pediatricians

Trends in Pediatrics, 2022

DOI 10.4274/tp.2022.63634 Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

JBMR Plus, 2022

DOI 10.1002/jbm4.10663 PMID 35991533 8 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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) Texte intégral en libre accèsSource : ORCID

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

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

DSD and Gender Incongruence

Yearbook of pediatric endocrinology, 2022

DOI 10.1530/ey.19.6 Source : OpenAlex

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

Dspace Repository (Marmara Üniversitesi), 2022

Source : OpenAlex

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) Texte intégral en libre accèsSource : OpenAlex

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

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) Texte intégral en libre accèsSource : OpenAlex

A rare cause of hypercalcemia: Congenital Lactase Deficiency

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

Source : OpenAlex

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 Texte intégral en libre accèsSource : OpenAlex

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) Texte intégral en libre accèsSource : OpenAlex

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) Texte intégral en libre accèsSource : OpenAlex

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

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

OpenAlex, 2021

DOI 10.60692/zk9rm-nhs71 Source : ORCID

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

OpenAlex, 2021

DOI 10.60692/s9t23-ha771 Source : ORCID

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

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

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

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