Prof. Dr. Tülay Güran

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

European Journal of Endocrinology, 2021

DOI 10.1530/eje-20-1058 PMID 33780351 13 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

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

European Journal of Endocrinology, 2021

DOI 10.1530/eje-20-1249 PMID 33460392 26 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Management of rapidly progressive precocious puberty in a patient with mosaic turner syndrome

Acta Endocrinologica, 2021

DOI 10.4183/aeb.2021.101 PMID 34539916 1 citation (Europe PMC) Texte intégral en libre accèsSource : ORCID

Prenatal diagnosis and treatment in congenital adrenal hyperplasia

Fertility and Reproductive Outcomes in Different Forms of Congenital Adrenal Hyperplasia, 2021

DOI 10.1007/978-3-030-82591-1_9 2 citations (OpenAlex) Source : ORCID

Pubertal And Gonadal Outcomes In 46,XY Individuals With Partial Androgen Insensitivity Syndrome Raised As Girls

Research Square, 2021

DOI 10.21203/rs.3.rs-537865/v1 Texte intégral en libre accèsSource : ORCID

Real-World Estimates of Adrenal Insufficiency-Related Adverse Events in Children with Congenital Adrenal Hyperplasia

Journal of Clinical Endocrinology and Metabolism, 2021

DOI 10.1210/clinem/dgaa694 PMID 32995889 34 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Surgical Practice in Girls with Congenital Adrenal Hyperplasia: An International Registry Study

Sexual Development, 2021

DOI 10.1159/000517055 PMID 34350892 4 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

mTOR-Activating mutations in RRAGD are causative for kidney tubulopathy and cardiomyopathy

Journal of the American Society of Nephrology, 2021

DOI 10.1681/asn.2021030333 PMID 34607910 53 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

mTOR-activating mutations in RRAGD cause kidney tubulopathy and cardiomyopathy (KICA) syndrome

bioRxiv, 2021

DOI 10.1101/2021.03.11.434334 Texte intégral en libre accèsSource : ORCID

Is quail egg a potential endocrine disruptor

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

Source : OpenAlex

Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification

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

Source : OpenAlex

46,XY DSD due to biallelic DHX37 gene mutations

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

Source : OpenAlex

Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17[alpha]-Hydroxylase/17,20-Lyase Deficiency

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

Source : OpenAlex

Biallelic PPP2R3C mutations are associated with partial and complete gonadal dysgenesis in 46,XY and 46,XX individuals

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

Source : OpenAlex

Clinical and hormonal evolution of aldosterone synthase deficiency: Is complete remission possible?

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

Source : OpenAlex

Gonadal Outcome in 17beta-HSD deficiency and 5alpha-reductase deficiency

Pure Amsterdam UMC, 2021

Source : OpenAlex

Hyperinsulinemic hypoglycemia due to biallelic mutations in the DNAJC3 gene

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

Source : OpenAlex

Coexistence of Adrenal Insufficiency and Hypergonadotropic Hypogonadism: P450scc Deficiency

Dspace Repository (Marmara Üniversitesi), 2021

Source : OpenAlex

Broad range of phenotypes in an international cohort of 75 DSD individuals with SF-1/NR5A1 variants

Pure Amsterdam UMC, 2021

Source : OpenAlex

Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency

Çanakkale Onsekiz Mart University Institutional Repository, 2021

Source : OpenAlex

Machine Learning Quest for Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment

2021

Source : OpenAlex

Correlation of 11-oxygenated C19 androgens with the clinical and biochemical characteristics in premature adrenarche

2021

Source : OpenAlex

Çocuklarda Adrenal Hastalıkların Uzaktan Yönetimi

2021

Source : OpenAlex

Hormon analizlerinde temel laboratuar teknikleri ve cocuk endokrinoloji pratiginde kullanimi

2021

Source : OpenAlex

Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification

Dspace Repository (Marmara Üniversitesi), 2021

Texte intégral en libre accèsSource : OpenAlex

Adrenokortikal hormon profilleri: KAH dışı primer adrenal yetmezliktemolekuler etiyolojiyi öngörebilir mi?

Çanakkale Onsekiz Mart University AVESIS, 2021

Source : OpenAlex

Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route

Journal of Pediatric Endocrinology and Metabolism, 2020

DOI 10.1515/jpem-2019-0466 PMID 32049653 3 citations (Europe PMC) Source : OpenAlex

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants

Journal of Clinical Research in Pediatric Endocrinology, 2020

DOI 10.4274/jcrpe.galenos.2020.2019.0182 PMID 32157855 23 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases

The Journal of Clinical Endocrinology & Metabolism, 2020

DOI 10.1210/clinem/dgaa022 PMID 31950145 20 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

The Spectrum From Classic to Non-Classic 11β-Hydroxylase Deficiency

SSRN Electronic Journal, 2020

DOI 10.2139/ssrn.3712924 Texte intégral en libre accèsSource : OpenAlex

Real-World Estimates of Adrenal Insufficiency–Related Adverse Events in Children With Congenital Adrenal Hyperplasia

OpenAlex, 2020

DOI 10.60692/3atsn-v2s62 Source : ORCID

Real-World Estimates of Adrenal Insufficiency–Related Adverse Events in Children With Congenital Adrenal Hyperplasia

OpenAlex, 2020

DOI 10.60692/byzs3-33592 Source : ORCID

A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

Calcified Tissue International, 2020

DOI 10.1007/s00223-020-00694-3 PMID 32337609 14 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

A broad range of symptoms in allgrove syndrome: single center experience in Southeast Anatolia

Journal of Endocrinological Investigation, 2020

DOI 10.1007/s40618-019-01099-2 PMID 31435881 9 citations (Europe PMC) Source : ORCID

Clinical Significance of Hypophosphatasemia in Children

Calcified Tissue International, 2020

DOI 10.1007/s00223-020-00677-4 PMID 32088736 3 citations (Europe PMC) Source : ORCID

Fibroblast Growth Factor-23 and Matrix Extracellular Phosphoglycoprotein Levels in Healthy Children and, Pregnant and Puerperal Women

Hormone Research in Paediatrics, 2020

DOI 10.1159/000506477 PMID 32187608 3 citations (Europe PMC) Source : ORCID

Low DHEAS Concentration in a Girl Presenting with Short Stature and Premature Pubarche: A Novel PAPSS2 Gene Mutation

Hormone Research in Paediatrics, 2020

DOI 10.1159/000502114 PMID 31461705 8 citations (Europe PMC) Source : ORCID

Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty

Hormone Research in Paediatrics, 2020

DOI 10.1159/000505329 PMID 31972562 8 citations (Europe PMC) Source : ORCID

Plasma renin measurements are unrelated to mineralocorticoid replacement dose in patients with primary adrenal insufficiency

Journal of Clinical Endocrinology and Metabolism, 2020

DOI 10.1210/clinem/dgz055 PMID 31613957 40 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers

Pediatric Nephrology, 2020

DOI 10.1007/s00467-019-04352-1 PMID 31529157 5 citations (Europe PMC) Source : ORCID

Rare cause of severe hypertension in an adolescent boy presenting with short stature: Questions

Pediatric Nephrology, 2020

DOI 10.1007/s00467-019-04351-2 PMID 31529153 1 citation (Europe PMC) Source : ORCID

Restoration of Height after 11 Years of Letrozole Treatment in 11β-Hydroxylase Deficiency

Hormone Research in Paediatrics, 2020

DOI 10.1159/000501456 PMID 31454824 6 citations (Europe PMC) Source : ORCID

Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction

Journal of Steroid Biochemistry and Molecular Biology, 2020

DOI 10.1016/j.jsbmb.2020.105730 PMID 32682944 24 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Plasma renin measurements are unrelated to mineralocorticoid replacement dose in patients with primary adrenal insufficiency

Yearbook of pediatric endocrinology, 2020

DOI 10.1530/ey.17.8.17 2 citations (OpenAlex) Source : OpenAlex

Clinical but not histological outcomes in males with 45,X/46,XY mosaicism vary depending on reason for diagnosis

Yearbook of pediatric endocrinology, 2020

DOI 10.1530/ey.17.6.12 Source : OpenAlex

KAH Dışı Primer Adrenal Yetmezlik Tanısında Maliyet-Etkin Moleküler Tanı Yaklaşımı

Çanakkale Onsekiz Mart University AVESIS, 2020

Source : OpenAlex

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease

The Journal of Clinical Endocrinology & Metabolism, 2019

DOI 10.1210/jc.2019-00248 PMID 31042289 71 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

Journal of Clinical Research in Pediatric Endocrinology, 2019

DOI 10.4274/jcrpe.galenos.2019.2019.0098 PMID 31514490 11 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

A rare cause of hypertension in childhood: Answers

Pediatric Nephrology, 2019

DOI 10.1007/s00467-019-04329-0 PMID 31541304 3 citations (Europe PMC) Source : OpenAlex

A rare cause of hypertension in childhood: Questions

Pediatric Nephrology, 2019

DOI 10.1007/s00467-019-04326-3 PMID 31541303 Source : OpenAlex