T. Guran

发表

Visualization of the retinal microvasculature by targeted dye delivery.

M. Shahidi, M. Mori, R. Zeimer, 1990, Investigative ophthalmology & visual science.

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.

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.

Novel Associations in Disorders of Sex Development: Findings From the I-DSD Registry

F. Darendeliler, S. Ahmed, P. Wieacker, 2013, The Journal of clinical endocrinology and metabolism.

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.

Insulin Receptor and the Kidney: Nephrocalcinosis in Patients with Recessive INSR Mutations

D. Dunger, P. Gorden, M. Dattani, 2014, Nephron Physiology.

IRS2 variants and syndromes of severe insulin resistance

I. Barroso, R. Temple, W. Bottomley, 2009, Diabetologia.

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.

Effect of breastfeeding on serum zinc levels and growth in healthy infants.

A. B. Akcan, A. Bozaykut, G. Aydemir, 2013, Breastfeeding medicine : the official journal of the Academy of Breastfeeding Medicine.

Occlusion of retinal vessels using targeted delivery of a platelet aggregating agent.

Y. Ogura, R. Zeimer, K. Takahashi, 1993, The British journal of ophthalmology.

Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls

S. Poyrazoglu, F. Darendeliler, S. Ahmed, 2021, Sexual Development.

Association between inflammatory markers in induced sputum and clinical characteristics in children with non‐cystic fibrosis bronchiectasis

R. Ersu, E. Dağlı, B. Karadag, 2007, Pediatric pulmonology.

Frequency of Ambiguous Genitalia in 14,177 Newborns in Turkey

F. Baş, F. Darendeliler, A. Coban, 2019, Journal of the Endocrine Society.

The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene

C. Acerini, F. Darendeliler, S. Ahmed, 2016, The Journal of clinical endocrinology and metabolism.

Alendronate treatment in children with osteogenesis imperfecta.

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

Birth Weight in Different Etiologies of Disorders of Sex Development

S. Poyrazoglu, F. Darendeliler, S. Ahmed, 2015, The Journal of clinical endocrinology and metabolism.

Bone Mineral Density in Children with Non-Cystic Fibrosis Bronchiectasis

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

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

M. Korbonits, S. Poyrazoglu, F. Darendeliler, 2021, European journal of endocrinology.

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.

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.

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

A. Lenzi, M. Korbonits, F. Darendeliler, 2020, Yearbook of Paediatric Endocrinology.

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

A. Lenzi, M. Korbonits, F. Darendeliler, 2019, The Journal of clinical endocrinology and metabolism.

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

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

Primary adrenal insufficiency in children: Diagnosis and management.

T. Guran, T. Kirkgoz, 2018, Best practice & research. Clinical endocrinology & metabolism.

A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophy

M. Dattani, S. Mouilleron, G. Yeşil, 2022, American journal of medical genetics. Part A.

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

L. Looijenga, C. Acerini, F. Darendeliler, 2019, The Journal of clinical endocrinology and metabolism.

Hypercalciuria and recurrent urinary tract infections: incidence and symptoms in children over 5 years of age

H. Alpay, N. Bıyıklı, T. Guran, 2005, Pediatric Nephrology.

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

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

Steroid metabolomics for accurate and rapid diagnosis of inborn steroidogenic disorders

Michael Biehl, P. Tiňo, K. Bunte, 2017 .

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.

9 Years Follow-up of a Patient with Pituitary Form of Resistance to Thyroid Hormones Comparison of Two Treatment Periods of D-Thyroxine and Triiodothyroacetic Acid

A. Bereket, T. Guran, S. Turan,, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

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 .

Reference values for serum dehydroepiandrosterone‐sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarche

A. Bereket, T. Guran, İpek Kaplan Bulut, 2015, Clinical endocrinology.

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.

International epidemic of childhood obesity and television viewing.

T Guran, A. Bereket, A Bereket, 2011, Minerva pediatrica.

Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing

P. Hindmarsh, R. Lindsay, C. Brain, 2018, Journal of the Endocrine Society.

of the Endocrine Society Predicted Benign and Synonymous variants in CYP 11 A 1 Causes Primary Adrenal Insufficiency through

P. Hindmarsh, R. Lindsay, E. Duncan, 2018 .

Changes Over Time in Sex Assignment for Disorders of Sex Development

K. Lachlan, F. Darendeliler, A. Nordenström, 2014, Pediatrics.

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.

Gonadectomy In Conditions Affecting Sex Development - A Registry-Based Cohort Study.

K. Lachlan, S. Poyrazoglu, F. Darendeliler, 2021, European journal of endocrinology.

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.

Latest Insights on the Etiology and Management of Primary Adrenal Insufficiency in Children.

T. Guran, 2018 .

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.

Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome

L. Metherell, L. Guasti, H. Storr, 2017, The Journal of clinical investigation.

Familial Glucocorticoid Defificiency in a Newborn Caused by a Mutation in Melanocortin 2 Receptor: Case Report

M. N. Özbek, S. Kavurt, T. Guran, 2017 .

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.

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

W. Chung, J. Lupski, R. Gibbs, 2015, Neuron.

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.

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.

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.

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.

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

J. Lewsey, M. Korbonits, S. Poyrazoglu, 2020, The Journal of clinical endocrinology and metabolism.

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.

Prenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia

T. Guran, Z. Y. Abalı, 2021, Fertility and Reproductive Outcomes in Different Forms of Congenital Adrenal Hyperplasia.

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.

DEFINING THE DOSE, TYPE AND TIMING OF GLUCOCORTICOID AND MINERALOCORTICOID REPLACEMENT IN 256 CHILDREN AND ADULTS WITH CONGENITAL ADRENAL HYPERPLASIA (CAH) IN THE I-CAH REGISTRY

C. Acerini, F. Darendeliler, W. Bonfig, 2017 .

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

T. Guran, R. Polat, A. Ustyol, 2020, Journal of Endocrinological Investigation.

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.

Identification of a Novel Large CYP17A1 Deletion by MLPA Analysis in a Family with Classic 17α-Hydroxylase Deficiency

D. Turkkahraman, N. Krone, R. Vijzelaar, 2015, Sexual Development.

A Rare Cause of a Relatively Common Neonatal Emergency

U. Kornak, A. Say, Omer Guran, 2012, Pediatric Hematology & Oncology.

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.

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.

Cushing's Syndrome Due to a Non-Adrenal Ectopic Adrenocorticotropin-Secreting Ewing's Sarcoma in a Child

C. Canpolat, A. Bereket, T. Guran, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

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

M. Korbonits, F. Darendeliler, V. Iotova, 2019, Endocrine Abstracts.

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.

Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome

Brian J. Stevenson, A. Reymond, G. Superti-Furga, 2015, American journal of medical genetics. Part A.

Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome. (3),

L. Metherell, L. Guasti, H. Storr, 2017 .

SGPL 1 mutations cause primary adrenal insufficiency and steroid resistant nephrotic syndrome 1

L. Metherell, L. Guasti, H. Storr, 2016 .

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

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

Withdrawal of inhaled steroids in children with non‐cystic fibrosis bronchiectasis

E. Dağlı, B. Karadag, F. Karakoç, 2008, Journal of clinical pharmacy and therapeutics.

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.

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.

Comparison of oral alendronate versus prednisolone in treatment of infants with vitamin D intoxication

A. Bozaykut, A. Bereket, T. Guran, 2012, Acta paediatrica.

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.

Alopecia: Association with Resistance to Thyroid Hormones

A. Bereket, T. Guran, S. Turan,, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

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.

A rare cause of hypertension in childhood: Answers

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

Management of Rapidly Progressive Precocious Puberty in a Patient with Mosaic Turner Syndrome.

B. Özcabı, T. Guran, F. Dursun, 2021, Acta endocrinologica.

Response to the Letter to the Editor Regarding the Article: Reference values for serum dehydroepiandrosterone‐sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarche

T. Guran, 2015, Clinical endocrinology.

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.

Quantitative analysis of retinal hemodynamics using targeted dye delivery.

M. Shahidi, M. Mori, R. Zeimer, 1990, Investigative ophthalmology & visual science.

Primary adrenal insufficiency in a patient with biallelic QRSL1 mutations.

C. Pehlivanoğlu, T. Guran, Betul Karademir Yilmaz, 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.

Content analysis of food advertising in Turkish television

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

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

W. Chung, J. Lupski, R. Gibbs, 2015, Neuron.

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

D. Braslavsky, T. Guran, R. Prasad, 2020, The Journal of Steroid Biochemistry and Molecular Biology.