Prof. Dr. Tülay Güran

Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Hypergonadotropic Hypogonadism in 46, XX Adolescents Without Gonadotoxic Therapy: Clinical Features and Molecular Etiologies

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

A rare cause of chronic hyponatremia in an infant: Answers

Pediatric Nephrology, 2019

DOI 10.1007/s00467-019-04337-0 PMID 31428928 Quelle: OpenAlex

A rare cause of chronic hyponatremia in an infant: Questions

Pediatric Nephrology, 2019

DOI 10.1007/s00467-019-04335-2 PMID 31428927 Quelle: OpenAlex

Evaluation of Molecular Characteristics and Steroid Metabolomics in a Large Cohort of Children with 3β-Hydroxysteroid Dehydrogenase 2 Deficiency

58th Annual ESPE Meeting (ESPE 2019), 2019

Quelle: OpenAlex

A Case Of Syndromic Hypopituitarism

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Neonatal adrenal insufficiency: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report

Türk Pediatri Arşivi, 2019

DOI 10.5152/turkpediatriars.2018.01822 PMID 31236037 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3 beta-hydroxysteroid dehydrogenase 2 deficiency

AYBU AVESIS, 2019

Quelle: OpenAlex

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

Journal of clinical research in pediatric endocrinology, 2019

DOI 10.4274/jcrpe.galenos.2018.2018.0206 PMID 30396878 20 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: Europe PMC

Adrenocortical carcinoma in atypical Beckwith‐Wiedemann syndrome due to loss of methylation at imprinting control region 2

Pediatric Blood & Cancer, 2019

DOI 10.1002/pbc.28042 PMID 31612591 11 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Persistent Müllerian Duct Syndrome: A Rare But Important Etiology of Inguinal Hernia and Cryptorchidism

Sexual Development, 2019

DOI 10.1159/000510466 PMID 32961540 7 Zitationen (OpenAlex) Quelle: OpenAlex

MON-LB061 Cushing Syndrome Due to an Adrenocortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome

Journal of the Endocrine Society, 2019

DOI 10.1210/js.2019-mon-lb061 Frei zugänglicher VolltextQuelle: OpenAlex

Cushing Syndrome due to an Adrenacortical Carcinoma in a Baby with Atypical Beckwith-Wiedemann Syndrome

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Frequency of Ambiguous Genitalia in 14,177 Newborns in Turkey

Journal of the Endocrine Society, 2019

DOI 10.1210/js.2018-00408 PMID 31139765 15 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

Clinical but Not Histological Outcomes in Males with 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis

Journal of Clinical Endocrinology and Metabolism, 2019

DOI 10.1210/jc.2018-02752 PMID 31127831 28 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature

Hormones, 2019

DOI 10.1007/s42000-019-00096-7 PMID 30747411 9 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans

European Journal of Endocrinology, 2019

DOI 10.1530/eje-19-0067 PMID 30893644 24 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

Predicted benign and synonymous variants in CYP11A1 cause primary adrenal insufficiency through missplicing

Journal of the Endocrine Society, 2019

DOI 10.1210/js.2018-00130 PMID 30620006 25 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

Response to Letter to the Editor: "clinical but Not Histological Outcomes in Males with 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis"

Journal of Clinical Endocrinology and Metabolism, 2019

DOI 10.1210/jc.2019-01413 PMID 31276168 Frei zugänglicher VolltextQuelle: ORCID

Steroid metabolomics: a rapid computational approach for accurate differentiation of inborn disorders of steroidogenesis

Endocrine Abstracts, 2019

DOI 10.1530/endoabs.63.oc10.1 1 Zitation (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Optimizing mineralocorticoid replacement therapy in patients with congenital adrenal hyperplasia and Addison's disease

Endocrine Abstracts, 2019

DOI 10.1530/endoabs.63.gp197 Quelle: OpenAlex

Global practice of glucocorticoid and mineralocorticoid treatment in children and adults with congenital adrenal hyperplasia - insights from the I-CAH registry

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Age of Obesity Onset could be the First Indicator of Future Metabolic Complications Preliminary Data of Prospective Multicenter Study

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

A 46, XX Patient with 21-OHD Diagnosed During the Etiologic Workup of Male Infertility

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Exploring trends in the glucocorticoid and mineralocorticoid treatment of congenital adrenal hyperplasia by analysing data from the I-CAH registry

Endocrine Abstracts, 2019

DOI 10.1530/endoabs.66.oc1.1 Quelle: OpenAlex

A Real-Life Experience with a New Insulin Co-Formulation Degludec/Aspart for one Year in Poorly Controlled Children and Adolescents with Type 1 Diabetes

58th Annual ESPE Meeting (ESPE 2019), 2019

Quelle: OpenAlex

SGPL1 deficiency leads to accumulation of sphingolipid species and downregulation of key enzymes within the steroidogenic pathway

Endocrine Abstracts, 2019

DOI 10.1530/endoabs.66.oc4.8 Quelle: OpenAlex

SGPL1 Deficiency Leads to Downregulation of Key Enzymes Within the Steroidogenic Pathway

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Influence of salt supplementation on drug therapy in children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency aged 0-3 years: Update on a retrospective multicentre analysis using the I-CAH registry

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

A rare cause of hypophosphatemia: Raine Syndrome

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Simplifying the Interpretation of Steroid Metabolome Data by a Machine-Learning Approach

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Evaluation of Brain Mri Lesions in 381 Girls with Central Precocious Puberty

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

A Rare Cause of 46, XX ovotesticular DSD: Tetragametic Gonadal Chimerism

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

A Rare Cause of SRY (-) 46, XX DSD: Aromatase Deficiency

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty

Dspace Repository (Marmara Üniversitesi), 2019

Frei zugänglicher VolltextQuelle: OpenAlex

Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3?-hydroxysteroid dehydrogenase 2 deficiency

Trakya University's Institutional Open Access System (Trakya University), 2019

Quelle: OpenAlex

Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey

Journal of Clinical Research in Pediatric Endocrinology, 2018

DOI 10.4274/jcrpe.0025 PMID 29789274 8 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

Nationwide Hypophosphatemic Rickets Study

Trakya University's Institutional Open Access System (Trakya University), 2018

Frei zugänglicher VolltextQuelle: OpenAlex

Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

Bursa Uludag University - AVESIS, 2018

Quelle: OpenAlex

Nationwide Hypophosphatemic Rickets Study

Bursa Uludag University - AVESIS, 2018

Quelle: OpenAlex

A RARE CAUSE OF CHRONIC HYPONATREMIA IN AN INFANT: ALDOSTERONE SYNTHASE TYPE-2 DEFICIENCY

Pediatric Nephrology, 2018

Quelle: OpenAlex

Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

Journal of Endocrinological Investigation, 2018

DOI 10.1007/s40618-018-0940-y PMID 30132287 21 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants

Journal of Clinical Research in Pediatric Endocrinology, 2018

DOI 10.4274/jcrpe.0117 PMID 30111524 18 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex

Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology

Dspace Repository (Marmara Üniversitesi), 2018

Frei zugänglicher VolltextQuelle: OpenAlex

Comprehensive Genetic Testing Shows One in FiveChildren with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology.

Kocaeli Üniversitesi - AVESİS, 2018

Quelle: OpenAlex

Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism

EBioMedicine, 2018

DOI 10.1016/j.ebiom.2018.09.024 PMID 30266295 11 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency

BMC Neurology, 2018

DOI 10.1186/s12883-018-1049-9 PMID 29685115 4 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID

A patient with proopiomelanocortin deficiency: An increasingly important diagnosis to make

JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2018

DOI 10.4274/jcrpe.4638 PMID 28739551 13 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: ORCID