S. Turan

发表

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

F. Baş, F. Darendeliler, F. Demirel, 2016, American journal of medical genetics. Part A.

Addition of orlistat to conventional treatment in adolescents with severe obesity

B. Ozkan, A. Bereket, S. Turan, 2004, European Journal of Pediatrics.

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

S. Poyrazoglu, F. Baş, F. Darendeliler, 2015, Journal of clinical research in pediatric endocrinology.

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

J. Lupski, R. Gibbs, D. Muzny, 2019, The Journal of clinical endocrinology and metabolism.

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

G. Yeşil, H. Alpay, N. Çiçek, 2019, Pediatric Nephrology.

Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients

O. Mäkitie, L. Rejnmark, M. Zillikens, 2020, Hormone Research in Paediatrics.

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

O. Mäkitie, L. Rejnmark, M. Zillikens, 2018, Nature Reviews Endocrinology.

Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder

S. Turan, 2017, Journal of clinical research in pediatric endocrinology.

The effect of economic status on height, insulin-like growth factor (IGF)-I and IGF binding protein-3 concentrations in healthy Turkish children

A. Bereket, S. Turan, G. Haklar, 2007, European Journal of Clinical Nutrition.

Effect of Zinc Supplementation on Growth Hormone Secretion, IGF-I, IGFBP-3, Somatomedin Generation, Alkaline Phosphatase, Osteocalcin and Growth in Prepubertal Children with Idiopathic Short Stature

Y. Taga, A. Bereket, S. Turan, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Does common channel length affect surgical choice in female congenital adrenal hyperplasia patients?

A. Bereket, S. Turan, Ş. Hatun, 2014, Journal of pediatric urology.

The Frequency and the Effects of 21‐Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients

F. Eren, T. Akçay, A. Bereket, 2014, Annals of human genetics.

Cathepsin K osteoporosis trials, pycnodysostosis and mouse deficiency models: Commonalities and differences

D. Brömme, S. Turan, Preety Panwar, 2016, Expert opinion on drug discovery.

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

F. Baş, F. Darendeliler, F. Demirel, 2015, Journal of clinical research in pediatric endocrinology.

Ptosis as a unique hallmark for autosomal recessive WNT1‐associated osteogenesis imperfecta

N. Elçioglu, S. Nampoothiri, S. Turan, 2019, American journal of medical genetics. Part A.

The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience

Enes Celik, A. Bereket, S. Turan, 2017, Journal of clinical research in pediatric endocrinology.

Once-Weekly Somapacitan vs Daily GH in Children With GH Deficiency: Results From a Randomized Phase 2 Trial

A. Eliakim, M. Phillip, T. Battelino, 2020, The Journal of clinical endocrinology and metabolism.

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

S. Poyrazoglu, F. Baş, F. Darendeliler, 2018, Journal of clinical research in pediatric endocrinology.

Evaluation of Diagnosis and Treatment Results in Children with Graves' Disease with Emphasis on the Pubertal Status of Patients

S. Poyrazoglu, F. Baş, T. Akçay, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Long-Term Clinical Outcome and Carrier Phenotype in Autosomal Recessive Hypophosphatemia Caused by a Novel DMP1 Mutation

O. Mäkitie, I. Kaitila, W. Cole, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Serum IGF-I and IGFBP-3 Levels of Turkish Children during Childhood and Adolescence: Establishment of Reference Ranges with Emphasis on Puberty

A. Bereket, S. Turan, G. Haklar, 2006, Hormone Research in Paediatrics.

The GNAS Complex Locus and Human Diseases Associated with Loss-of-Function Mutations or Epimutations within This Imprinted Gene

M. Bastepe, S. Turan, 2013, Hormone Research in Paediatrics.

Endocrine disrupting chemicals and bone.

S. Turan, 2021, Best practice & research. Clinical endocrinology & metabolism.

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

H. Jüppner, A. Bereket, S. Turan, 2022, Bone.

Deletion of the noncoding GNAS antisense transcript causes pseudohypoparathyroidism type Ib and biparental defects of GNAS methylation in cis.

H. Jüppner, H. Chen, M. Bastepe, 2010, The Journal of clinical endocrinology and metabolism.

Liraglutide in Children and Adolescents with Type 2 Diabetes.

W. Tamborlane, P. Hale, I. Libman, 2019, The New England journal of medicine.

Adult height in Turkish patients with Turner syndrome without growth hormone treatment.

F. Baş, F. Darendeliler, N. Elçioglu, 2008, The Turkish journal of pediatrics.

Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients HORMONERESEARCH IN PÆDIATRIC S

O. Mäkitie, R. Pignolo, H. Jüppner, 2020 .

Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross‐sectional study

Z. Aycan, N. Gungor, H. Onal, 2019, Diabetic medicine : a journal of the British Diabetic Association.

AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity

M. Fernández-Cancio, L. Audí, T. Akçay, 2014, Andrology.

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

S. Poyrazoglu, F. Baş, A. Çayır, 2020, Journal of Clinical Research in Pediatric Endocrinology.

Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia.

H. Jüppner, M. Bastepe, T. Akçay, 2010, Bone.

Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism-lack of effect of cinacalcet.

G. Hendy, D. Cole, L. Canaff, 2014, Bone.

Alendronate treatment in children with osteogenesis imperfecta.

T. Akçay, A. Bereket, S. Turan, 2008, Indian pediatrics.

The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

F. Baş, F. Darendeliler, T. Isbir, 2012, Hormone Research in Paediatrics.

Bone Mineral Density in Children with Non-Cystic Fibrosis Bronchiectasis

R. Ersu, E. Dağlı, B. Karadag, 2007, Respiration.

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

A. Bereket, S. Turan, Z. Atay, 2019, Hormone Research in Paediatrics.

The prevalence and risk factors of premature thelarche and pubarche in 4‐ to 8‐year‐old girls

A. Bereket, S. Turan, Z. Atay, 2012, Acta paediatrica.

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

S. Duan, S. Mumm, M. Whyte, 2022, JBMR plus.

Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor.

S. O’Rahilly, F. Reimann, F. Gribble, 2009, The Journal of clinical endocrinology and metabolism.

Nationwide Hypophosphatemic Rickets Cohort Study Runing Title : Nationwide Hypophosphatemic Rickets

S. Poyrazoglu, F. Baş, A. Çayır, 2019 .

Exclusion of the GNAS locus in PHP‐Ib patients with broad GNAS methylation changes: Evidence for an autosomal recessive form of PHP‐Ib?

S. Nik-Zainal, D. Feig, E. Anda, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Maternal Thyroid Dysfunction and Neonatal Thyroid Problems

H. Bilgen, E. Ozek, A. Bereket, 2013, International journal of endocrinology.

Circulating Insulin-like Growth Factor Binding Protein-4 (IGFBP-4) is not Regulated by Parathyroid Hormone and Vitamin D in vivo: Evidence from Children with Rickets

B. Özkan, T. Akçay, E. Adal, 2010, Journal of clinical research in pediatric endocrinology.

Reference data for bone speed of sound measurement by quantitative ultrasound in healthy children

A. Bereket, S. Turan, A. Omar, 2006, Archives of Osteoporosis.

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

A. Bereket, S. Turan, T. Guran, 2020, Hormone Research in Paediatrics.

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

F. Baş, Z. Aycan, B. Yuksel, 2015, The Journal of clinical endocrinology and metabolism.

Puberty and Influencing Factors in Schoolgirls Living in Istanbul: End of the Secular Trend?

A. Bereket, S. Turan, Z. Atay, 2011, Pediatrics.

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

A. Bereket, S. Turan, Omer Guran, 2021, Pediatric Research.

Is There a Change in the Presentation of Childhood Type-1 Diabetes Mellitus in the Last 15 Years? Data from a Tertiary Care Center in Turkey

Enes Celik, A. Bereket, S. Turan, 2014 .

Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

B. Özkan, T. Akçay, Y. Alanay, 2014, Orphanet Journal of Rare Diseases.

Upper segment/lower segment ratio and armspan–height difference in healthy Turkish children

A. Bereket, S. Turan, A. Omar, 2005, Acta paediatrica.

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

A. Elhan, S. Poyrazoglu, F. Baş, 2016, Journal of clinical research in pediatric endocrinology.

Effects of leukemia inhibitory receptor gene mutations on human hypothalamo–pituitary–adrenal function

A. Bereket, S. Turan, Omer Guran, 2015, Pituitary.

Osteopetrosis: Gene-based nosology and significance dysosteosclerosis.

S. Turan, 2022, Bone.

Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours

A. Bereket, S. Turan, S. Abalı, 2016, Pediatric obesity.

Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females

R. Ersu, B. Karadag, F. Karakoç, 2017, Pediatric diabetes.

Current research on pycnodysostosis.

S. Turan, 2014, Intractable & rare diseases research.

Persistent hyperglycemia in a neonate: Is it a complication of therapeutic hypothermia?

E. Özek, H. Bilgen, S. Turan, 2017, The Turkish journal of pediatrics.

Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients.

S. Poyrazoglu, F. Baş, F. Darendeliler, 2017, Journal of pediatric and adolescent gynecology.

Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes.

M. Konrad, T. Akçay, K. Schlingmann, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia : novel mutations in TRPM 6 and CLDN 16 genes

M. Konrad, T. Akçay, K. Schlingmann, 2012 .

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

A. Dağçınar, M. Sakar, A. Bereket, 2020, Calcified Tissue International.

Clinical Significance of Hypophosphatasemia in Children

A. Bereket, S. Turan, S. Baş, 2020, Calcified Tissue International.

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

S. Kitanaka, A. Bereket, S. Turan, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Prevalence of acne in primary school children and the relationship of acne with pubertal maturation

I. Altunay, S. Turan, H. Erdogan, 2014 .

Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method.

H. Kayserili, N. Şatıroğlu-Tufan, B. Tuysuz, 2007, The Tohoku journal of experimental medicine.

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

A. Çayır, Erdal Kurnaz, A. Bereket, 2021, Hormone Research in Paediatrics.

Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency

J. Lupski, S. Jhangiani, C. Hodges, 2018, Human molecular genetics.

Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children

Serpil Bas, Tulay Guran, A. Bereket, 2015, Hormone Research in Paediatrics.

Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism.

T. Walsh, M. King, J. Lupski, 2015, The Journal of clinical endocrinology and metabolism.

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatasez-scores in Different Types of Rickets

T. Akçay, İ. Gökçe, A. Bereket, 2011, Journal of clinical research in pediatric endocrinology.

Revisiting classical 3β-hydroxysteroid dehydrogenase 2 deficiency: lessons from 31 pediatric cases.

K. Storbeck, H. Onal, T. Akçay, 2020, The Journal of clinical endocrinology and metabolism.

Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hair.

R. Auchus, T. Akçay, A. Bereket, 2008, European journal of endocrinology.

An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations in MC2R (T152K) and MC1R (R160W)

L. Metherell, A. Bereket, S. Turan, 2011, The Journal of clinical endocrinology and metabolism.

Catch-up growth and discontinuation of fludrocortisone treatment in aldosterone synthase deficiency.

A. Çayır, Elvan Bayramoğlu, M. Ozbek, 2021, The Journal of clinical endocrinology and metabolism.

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

A. Bereket, S. Turan, K. Ağan, 2018, BMC Neurology.

From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network.

A. Barlier, O. Hiort, K. Freson, 2016, European journal of endocrinology.

GNAS Spectrum of Disorders

M. Bastepe, S. Turan, 2015, Current Osteoporosis Reports.

Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS.

M. Bastepe, A. Bereket, S. Turan, 2015, Bone.

A Patient with Hypopituitarism and Isochromosome 18q Mosaicism

A. Bereket, S. Turan, N. Saka, 2005, Hormone Research in Paediatrics.

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study.

S. Kurtoğlu, Z. Aycan, S. Çetinkaya, 2016, The Journal of clinical endocrinology and metabolism.

Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.

A. Grüters, H. Biebermann, H. Krude, 2014, The Journal of clinical endocrinology and metabolism.

Heterotrimeric G proteins in the control of parathyroid hormone actions.

M. Bastepe, S. Turan, Qing He, 2017, Journal of molecular endocrinology.

Dysgenesis and dysfunction of pancreas and pituitary due to FOXA2 gene defects.

A. Bereket, S. Turan, T. Guran, 2021, The Journal of clinical endocrinology and metabolism.

Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib

G. Kelsey, H. Jüppner, M. Bastepe, 2012, Proceedings of the National Academy of Sciences.

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

K. Cerit, P. Bagci, A. Bereket, 2020, Pediatric Blood & Cancer.

Extra-long Gαs Variant XLαs Protein Escapes Activation-induced Subcellular Redistribution and Is Able to Provide Sustained Signaling*

M. Bastepe, J. Vilardaga, Vanessa L. Wehbi, 2011, The Journal of Biological Chemistry.

Postnatal Establishment of Allelic Gαs Silencing as a Plausible Explanation for Delayed Onset of Parathyroid Hormone Resistance Owing to Heterozygous Gαs Disruption

Min Chen, L. Weinstein, M. Bastepe, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic cases.

H. Stewart, H. Jüppner, M. Bastepe, 2012, The Journal of clinical endocrinology and metabolism.

Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib.

H. Jüppner, M. Bastepe, T. Akçay, 2010, European journal of endocrinology.

Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years

A. Bereket, S. Turan, I. Akpınar, 2015, Journal of clinical research in pediatric endocrinology.

The diagnostic value of soluble urokinase plasminogen activator receptor (suPAR) compared to C-reactive protein (CRP) and procalcitonin (PCT) in children with systemic inflammatory response syndrome (SIRS).

I. Cinel, A. Karaaslan, A. Soysal, 2017, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

The diagnostic value of soluble urokinase plasminogen activator receptor compared with C-reactive protein and procalcitonin in children with febrile neutropenia

I. Cinel, A. Karaaslan, A. Soysal, 2016, Pediatric hematology and oncology.

The effect of the mode of delivery on neonatal thyroid function

O. Koroglu, H. Bilgen, E. Ozek, 2007, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

GCK gene mutations are a common cause of childhood‐onset MODY (maturity‐onset diabetes of the young) in Turkey

S. Ellard, G. Hysenaj, A. Bereket, 2016, Clinical endocrinology.

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

B. Aru, G. Demirel, G. Yeşil, 2019, European journal of endocrinology.

Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development

L. Looijenga, H. Stoop, K. De Bosscher, 2017, Genetics in Medicine.

Significance of acanthosis nigricans in childhood obesity

T. Akçay, A. Bereket, S. Turan, 2008, Journal of paediatrics and child health.

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

I. Gokce, A. Bereket, S. Turan, 2021, Calcified Tissue International.

Faculty Opinions recommendation of TGF-beta type II receptor phosphorylates PTH receptor to integrate bone remodelling signalling.

M. Bastepe, S. Turan, 2010 .

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

L. Teboul, S. Poyrazoglu, F. Baş, 2021, European journal of endocrinology.

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

S. Barış, A. Bereket, S. Turan, 2020, Hormone Research in Paediatrics.

Pycnodysostosis at otorhinolaryngology.

R. Ersu, S. Turan, T. Baglam, 2017, International journal of pediatric otorhinolaryngology.

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

F. Baş, E. Eren, H. Sağlam, 2018, Journal of clinical research in pediatric endocrinology.

Use of Insulin Degludec/Insulin Aspart in the Management of Diabetes Mellitus: Expert Panel Recommendations on Appropriate Practice Patterns

K. Unluhizarci, O. Topaloğlu, S. Turan, 2021, Frontiers in Endocrinology.

Clinical and hormonal profiles correlate with molecular characteristics in patients with 11β-hydroxylase deficiency.

F. Baş, F. Darendeliler, A. Çayır, 2021, The Journal of clinical endocrinology and metabolism.

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

A. Bereket, S. Turan, P. Ata, 2021, Calcified tissue international.

Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy.

T. Akçay, E. Adal, F. Dede, 2012, European journal of endocrinology.

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

S. Poyrazoglu, F. Darendeliler, S. Kurtoğlu, 2015, Journal of clinical research in pediatric endocrinology.

H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis.

T. Ergun, A. Zlotogorski, V. Molho-Pessach, 2015, Acta dermato-venereologica.

Height, Weight, IGF-I, IGFBP-3 and Thyroid Functions in Prepubertal Children with Attention Deficit Hyperactivity Disorder: Effect of Methylphenidate Treatment

M. Yazgan, F. Ozbay, A. Bereket, 2005, Hormone Research in Paediatrics.

Liraglutide for Weight Management in Children and Adolescents With Prader–Willi Syndrome and Obesity

P. Hale, M. Tauber, A. Hokken-Koelega, 2022, The Journal of clinical endocrinology and metabolism.

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

A. Bereket, S. Turan, P. Ata, 2021, Calcified Tissue International.

Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet–Biedl syndrome

T. Akçay, G. Ekinci, A. Bereket, 2011, Clinical dysmorphology.

Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus

A. Bereket, S. Turan, S. Abalı, 2015, Pediatric diabetes.

A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy.

M. Khayat, R. Spiegel, S. Shalev, 2013, Gene.

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

A. Bereket, S. Turan, T. Guran, 2019, Hormone Research in Paediatrics.

Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation

H. Bilgen, E. Ozek, A. Bereket, 2020, Hormone Research in Paediatrics.

Perceptions of Prospective Teachers in Relation to Civil Cervant Selection Exam (KPSS)

S. Turan, 2008 .

T4 plus T3 Treatment in Children with Hypothyroidism and Inappropriately Elevated Thyroid-Stimulating Hormone despite Euthyroidism on T4 Treatment

T. Akçay, Goksenin Unluguzel, A. Bereket, 2010, Hormone Research in Paediatrics.

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

G. Yeşil, A. Bereket, S. Turan, 2019, Hormones.

Rapid progression of type 2 diabetes and related complications in children and young people—A literature review

T. Barrett, N. Shehadeh, M. Y. Jalaludin, 2019, Pediatric diabetes.

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study.

E. Bertini, N. Brunetti‐Pierri, M. Polak, 2020, The lancet. Diabetes & endocrinology.

From pseudohypoparathyroidism to inactivating PTH/PTHrP signaling disorder (iPPSD), a novel classification proposed by the European EuroPHP-network

A. Barlier, O. Hiort, K. Freson, 2016 .

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

A. Bereket, S. Turan, T. Guran, 2023, Journal of pediatric endocrinology & metabolism : JPEM.

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

A. Bereket, S. Turan, S. Abalı, 2013, European Journal of Pediatrics.

The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children

F. Baş, F. Darendeliler, H. Onal, 2009, European Journal of Pediatrics.

Prevalence of type 1 diabetes mellitus in 6–18‐yr‐old school children living in Istanbul, Turkey

A. Bereket, S. Turan, T. Güran, 2011, Pediatric diabetes.

A rare cause of hypertension in childhood: Answers

G. Yeşil, A. Bereket, S. Turan, 2019, Pediatric Nephrology.

Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development

L. Looijenga, H. Stoop, K. De Bosscher, 2018, Genetics in Medicine.

Recommendations for improving clinical trial design to facilitate the study of youth-onset type 2 diabetes

N. Shehadeh, D. Weghuber, M. Barrientos-Pérez, 2020, Clinical trials.

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

A. Greenfield, A. Bereket, S. Turan, 2022, European journal of endocrinology.

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

K. Cerit, J. Picard, A. Bereket, 2020, Sexual Development.

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

A. Bereket, S. Turan, T. Guran, 2021, Journal of Clinical Research in Pediatric Endocrinology.

Constitutional Growth Delay Pattern of Growth in Velo−Cardio−Facial Syndrome: Longitudinal follow up and final height of two cases

N. Özdemir, T. Akçay, Y. Yılmaz, 2008, Journal of clinical research in pediatric endocrinology.

Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf‐Yang syndrome

S. Turan, A. Arman, B. Geckinli, 2023, Clinical genetics.

Two Patients with Kabuki Syndrome Presenting with Endocrine Problems

S. Çomu, G. Alper, H. Alpay, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Content analysis of food advertising in Turkish television

T. Akçay, Abdulaziz Majid, A. Bereket, 2010, Journal of paediatrics and child health.

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A

F. Darendeliler, Z. Aycan, S. Çetinkaya, 2016 .

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

A. Bereket, S. Turan, T. Güran, 2021, Journal of clinical research in pediatric endocrinology.