Z. Şıklar

发表

Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation.

A. Green, M. Weedon, M. O'sullivan, 2013, American journal of human genetics.

Adaptation Study of the Newest Vital Sign on Adolescents With Type 1 Diabetes and Healthy Adolescents in Turkish

Z. Şıklar, M. Berberoğlu, A. Bayindir Gümüş, 2022, Topics in Clinical Nutrition.

Incidence of Iodine Deficiency in Patients Presenting with Goitre - Discrepancy Between Clinical and Ultrasonographic Evaluation of the Thyroid: Comparison of Patients With and Without Autoimmune Thyroiditis - Clinical, Hormonal and Urinary Iodine Excretion Studies

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Latent Autoimmune Diabetes Mellitus in Children (LADC) with Autoimmune Thyroiditis and Celiac Disease

Z. Aycan, A. Ensari, Z. Şıklar, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

EVALUATION OF GLUCOSE HOMEOSTASIS IN TRANSFUSION-DEPENDENT THALASSEMIC PATIENTS

M. Ertem, Z. Şıklar, M. Berberoğlu, 2008, Pediatric hematology and oncology.

Diagnostic characteristics and metabolic risk factors of cases with polycystic ovary syndrome during adolescence.

Z. Şıklar, M. Berberoğlu, Emine Çamtosun, 2015, Journal of pediatric and adolescent gynecology.

Evaluation of Renal Function in Obese Children and Adolescents Based on Serum Cystatin C, Estimated Glomerular Filtration Rate Formulas, and Proteinuria: Which is Most Useful?

Z. Şıklar, M. Berberoğlu, Z. Özçakar, 2018, Journal of Clinical Research in Pediatric Endocrinology.

Evaluation of Thyroid Functions with Respect to Iodine Status and TRH Test in Chronic Autoimmune Thyroiditis

Z. Şıklar, M. Berberoğlu, O. Evliyaoğlu, 2011, Journal of clinical research in pediatric endocrinology.

Hashimoto encephalopathy causing drug-resistant status epilepticus treated with plasmapheresis.

Z. Şıklar, T. Kendirli, G. Deda, 2012, Pediatric neurology.

Childhood Sustained Hypercalcemia: A Diagnostic Challenge

Z. Şıklar, M. Berberoğlu, Nisa Eda Çullas İlarslan, 2017, Journal of clinical research in pediatric endocrinology.

The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders

M. Kır, K. Ceyhan, Z. Şıklar, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height

S. Poyrazoglu, F. Baş, Z. Aycan, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Is subclinical hypothyroidism increasing exogen obesity in children

C. Kırsaçlıoğlu, Z. Şıklar, Y. Dallar, 2015 .

Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche

A. Tukun, Z. Şıklar, G. Ocal, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Rare childhood tumors in a Turkish pediatric oncology center

Z. Şıklar, M. Berberoğlu, N. Taçyıldız, 2013, Indian Journal of Medical and Paediatric Oncology.

Relationships Between Osteocalcin, Glucose Metabolism, and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2012, Journal of clinical research in pediatric endocrinology.

Combined Evaluation of IGF−1 and IGFBP−3 as an Index of Efficacy and Safety in Growth Hormone Treated Patients

Z. Şıklar, M. Berberoğlu, G. Öcal,, 2009, Journal of clinical research in pediatric endocrinology.

Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty

S. Poyrazoglu, F. Baş, F. Darendeliler, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

Risk Factors for Non-Alcoholic Fatty Liver Disease in Obese Children

Z. Şıklar, M. Berberoğlu, G. Öcal,, 2009, Hormone Research in Paediatrics.

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children

E. Eren, Z. Şıklar, M. Berberoğlu, 2021, Journal of clinical research in pediatric endocrinology.

MORFAN Syndrome: An Infantile Hypoinsulinemic Hypoketotic Hypoglycemia Due to an AKT2 Mutation.

M. Tekin, G. Bademci, N. Garg, 2015, The Journal of pediatrics.

ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity

Z. Şıklar, M. Berberoğlu, T. Kendirli, 2014, Journal of clinical research in pediatric endocrinology.

Antioxidant superoxide dismutase activity in obese children

Z. Şıklar, O. Erdeve, Y. Dallar, 2004, Biological Trace Element Research.

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome

M. Tekin, N. Akar, Z. Aycan, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Hypophosphatasia associated with Pseudotumor cerebri and respiratory insufficiency

M. Kafali, Z. Şıklar, M. Berberoğlu, 2008, Indian journal of pediatrics.

Does obesity influence ventricular repolarisation in children?

Z. Şıklar, M. Berberoğlu, S. Atalay, 2020, Cardiology in the young.

Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis

Z. Şıklar, M. Berberoğlu, A. Ikinciogullari, 2016, Journal of clinical research in pediatric endocrinology.

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

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

The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?

Z. Şıklar, M. Berberoğlu, S. Fitöz, 2012, European Journal of Pediatrics.

Does Metformin Treatment in Pediatric Population Cause Vitamin B12 Deficiency?

Ozlem Dogan, Z. Şıklar, M. Berberoğlu, 2022, Klinische Padiatrie.

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.

Plasma Amino-Terminal Propeptide of C-Type Natriuretic Peptide Concentration in Normal-Weight and Obese Children

Z. Şıklar, M. Berberoğlu, A. Alkan, 2017, Journal of clinical research in pediatric endocrinology.

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

A. Öztürk, S. Poyrazoglu, F. Baş, 2020, Journal of clinical research in pediatric endocrinology.

Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

Z. Kuloğlu, A. Kansu, Z. Şıklar, 2020, European Journal of Clinical Nutrition.

The endocrine spectrum of intracranial cysts in childhood and review of the literature

Z. Şıklar, G. Ocal, M. Berberoğlu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Is Adrenocorticotropic Hormone Deficiency Really Rare in Patients with Idiopathic Growth Hormone Deficiency and Normal Thyroid Function Tests

Z. Şıklar, G. Ocal, M. Berberoğlu, 2010, Hormone Research in Paediatrics.

A novel mutation of 5α-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment

N. Akar, Z. Aycan, Kadir Sipahi, 2010, European Journal of Pediatrics.

Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases

K. Patel, Z. Şıklar, M. Berberoğlu, 2021, Journal of clinical research in pediatric endocrinology.

Nationwide Hypophosphatemic Rickets Cohort Study Runing Title : Nationwide Hypophosphatemic Rickets

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

Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell

S. Ellard, S. Flanagan, Z. Şıklar, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

The Effectiveness of Sirolimus Treatment in Two Rare Disorders with Nonketotic Hypoinsulinemic Hypoglycemia: The Role of mTOR Pathway

Z. Şıklar, M. Berberoğlu, N. Çakar, 2020, Journal of clinical research in pediatric endocrinology.

Monogenic Diabetes Not Caused By Mutations in Mody Genes: A Very Heterogenous Group of Diabetes

S. Ellard, S. Flanagan, E. De Franco, 2017, Experimental and Clinical Endocrinology & Diabetes.

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results

Z. Aycan, A. Kansu, A. Ensari, 2010, Journal of clinical research in pediatric endocrinology.

Cardiac phenotype in familial partial lipodystrophy

H. Oral, J. Jalife, Z. Şıklar, 2021, Clinical endocrinology.

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

Z. Şıklar, M. Berberoğlu, S. Ceylaner, 2017, Journal of clinical research in pediatric endocrinology.

Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Growth Hormone Treatment: Is There Really Need for Treatment at Transition to Adulthood?

Z. Şıklar, M. Berberoğlu, Emine Çamtosun, 2018, Journal of clinical research in pediatric endocrinology.

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome

B. Tüysüz, S. Poyrazoglu, F. Baş, 2021, Journal of clinical research in pediatric endocrinology.

Early prophylactic thyroidectomy for RETmutation‐positive MEN 2B

Z. Şıklar, G. Ocal, M. Berberoğlu, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Early and severe presentation of vitamin D deficiency and nutritional rickets among hospitalized infants and the effective factors.

Z. Şıklar, Y. Dallar, H. Tezer, 2009, The Turkish journal of pediatrics.

Investigation of early puberty prevalence and time of addition thelarche to pubarche in girls with premature pubarche: two-year follow-up results

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2021, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Determining the risk of diabulimia and its relationship with diet quality and nutritional status of adolescents with type 1 diabetes

Z. Şıklar, M. Berberoğlu, A. Keser, 2021, Nutrition Clinique et Métabolisme.

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.

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

A. Elhan, Z. Aycan, F. Sadeghi, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Ori Gi Nal Ar Tic Le Ad Dress for Cor Res Pon Den Ce the Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-like Growth Factor-1 Levels

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2022 .

The Effect of Growth Hormone Therapy on Cardiac Outcomes in Noonan Syndrome: Long Term Follow-up Results

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2022, Journal of clinical research in pediatric endocrinology.

An Infantile Cushing Syndrome Due to Misuse of Topical Steroid

Z. Şıklar, Y. Dallar, I. Bostanci, 2004, Pediatric dermatology.

Superoxide dismutase activity and zinc and copper concentrations in growth retardation

Z. Şıklar, Ö. Erdeve, G. Kavas, 2007, Biological Trace Element Research.

Clinical review of 95 patients with 46,XX disorders of sex development based on the new Chicago classification.

Z. Aycan, A. Tukun, Z. Şıklar, 2015, Journal of pediatric and adolescent gynecology.

The Evaluation of Cases with Y-Chromosome Gonadal Dysgenesis: Clinical Experience over 18 Years

Z. Şıklar, M. Berberoğlu, Ankara University Faculty of Medicine Disorders of Sexual Development Ethics Committee, 2017, Journal of clinical research in pediatric endocrinology.

Evaluation of Different Dose HCG Treatments in Undescended Testis

Z. Şıklar, O. Erdeve, Y. Dallar, 2003 .

A novel heterozygous mutation in steroidogenic factor-1 in pubertal virilization of a 46,XY female adolescent.

Z. Şıklar, M. Berberoğlu, S. Ceylaner, 2014, Journal of pediatric and adolescent gynecology.

Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum.

Z. Aycan, M. Salih, Z. Şıklar, 2007, Pediatric endocrinology reviews : PER.

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

T. Soygür, N. Akar, Z. Şıklar, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

F. Baş, F. Darendeliler, Z. Aycan, 2015, Endocrine.

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis.

Z. Şıklar, G. Ocal, M. Berberoğlu, 2008, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations

P. Chanson, M. Polak, S. Lyonnet, 2019, Human mutation.

Characterization of GH-1 Mutations in Children with Isolated Growth Hormone Deficiency in the Turkish Population

Z. Şıklar, A. Arman, B. Dundar, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

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.

Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2016, Journal of clinical research in pediatric endocrinology.

Syndromic Disorders with Short Stature

Z. Şıklar, M. Berberoğlu, 2014, Journal of clinical research in pediatric endocrinology.

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy

S. Ellard, S. Flanagan, Z. Şıklar, 2016, Hormone Research in Paediatrics.

Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-up

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2020, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Borderline Gongenital Hypothyroidism in the Neonatal Period

Z. Şıklar, G. Tanyer, H. Tezer, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Neonatal effects of thyroid diseases in pregnancy and approach to the infant with increased TSH: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report

S. Kurtoğlu, Z. Şıklar, A. Taştekin, 2018, Turk pediatri arsivi.

Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development

H. Karabulut, Z. Aycan, Z. Şıklar, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Three cases of Wolfram syndrome with different clinical aspects

S. Ellard, S. Flanagan, Z. Şıklar, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Permanent Central Diabetes Insipidus with Complete Regression of Pituitary Stalk Enlargement After 4 Years of Follow−up

Z. Şıklar, M. Berberoğlu, S. Fitoz, 2008, Journal of clinical research in pediatric endocrinology.

Evaluation of the etiological and clinical characteristics of pediatric central diabetes insipidus

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2022, Journal of pediatric endocrinology & metabolism : JPEM.

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey

Z. Şıklar, M. Berberoğlu, 2016, Journal of clinical research in pediatric endocrinology.

The effect of colchicine on physical growth in children wıth familial mediterranean fever

M. Eki̇m, F. Yalçınkaya, Z. Şıklar, 2010, European Journal of Pediatrics.

Multiple Presentations of LRBA Deficiency: a Single-Center Experience

Z. Kuloğlu, A. Kansu, A. Ensari, 2017, Journal of Clinical Immunology.

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes

A. Hattersley, S. Ellard, H. Lango Allen, 2017, Diabetes.

Pediatric hormonal disturbances after hematopoietic stem cell transplantation

Z. Şıklar, M. Berberoğlu, 2013, Expert review of endocrinology & metabolism.

Evaluation of Efficacy of Long-term Growth Hormone Therapy in Patients with Hypochondroplasia

Z. Şıklar, M. Berberoğlu, T. Çetin, 2018, Journal of clinical research in pediatric endocrinology.

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature

H. Karabulut, Z. Şıklar, M. Berberoğlu, 2016, Journal of clinical research in pediatric endocrinology.

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

Z. Şıklar, M. Berberoğlu, S. Fitöz, 2010, Journal of clinical research in pediatric endocrinology.

Intrathyroidal Ectopic Thymus in Children

K. Ceyhan, Z. Şıklar, M. Berberoğlu, 2015, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

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.

Intramuscular Short-term ACTH Test for the Determination of Adrenal Function in Children: Safe, Effective and Reliable

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2019, Journal of Clinical Research in Pediatric Endocrinology.

Hyperprolactinemia in children and adolescents and longterm follow-up results of prolactinoma cases: a single-centre experience.

Z. Şıklar, M. Berberoğlu, E. Özsu, 2022, The Turkish journal of pediatrics.

Difficulties in the diagnosis and management of eight infants with secondary pseudohypoaldosteronism.

Z. Şıklar, M. Berberoğlu, Fatih Günay, 2022, The Turkish journal of pediatrics.

Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation

M. Ertem, Z. Şıklar, G. Ocal, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study

S. Poyrazoglu, F. Darendeliler, A. Bideci, 2008, Journal of clinical research in pediatric 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.

Acute reversible cardiomyopathy and heart failure in a child with acute adrenal crisis

Z. Şıklar, M. Berberoğlu, T. Kendirli, 2017, Paediatrics and international child health.

Adherence to growth hormone therapy: results of a multicenter study.

F. Baş, F. Darendeliler, Z. Aycan, 2014, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

F. Baş, Z. Aycan, S. Çetinkaya, 2013, Journal of clinical research in pediatric endocrinology.

The impact of high-fat and high-protein meal of adolescents with type 1 diabetes mellitus receiving intensive insulin therapy on postprandial blood glucose level: a randomized, crossover, breakfast study

Z. Şıklar, M. Berberoğlu, A. Keser, 2021, International Journal of Diabetes in Developing Countries.

Multiple dose IVIG treatment in neonatal immune hemolytic jaundice.

Z. Şıklar, U. Tiras, Y. Dallar, 2001, Journal of tropical pediatrics.

Central Precocious Puberty in an Infant with Sotos Syndrome and Response to Treatment

Z. Şıklar, M. Berberoğlu, S. Ceylaner, 2021, Journal of clinical research in pediatric endocrinology.

Preperitoneal fat tissue may be associated with arterial stiffness in obese adolescents.

Z. Şıklar, M. Berberoğlu, S. Fitöz, 2014, Ultrasound in medicine & biology.

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

N. Akar, Z. Şıklar, M. Berberoğlu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Fibroblast Growth Factor 21 Levels and Bone Mineral Density in Metabolically Healthy and Metabolically Unhealthy Obese Children

M. Kır, Z. Şıklar, M. Berberoğlu, 2022, Journal of clinical research in pediatric endocrinology.

The Diagnostic Value of Anti-Müllerian Hormone in Early Post Menarche Adolescent Girls with Polycystic Ovarian Syndrome.

Z. Şıklar, M. Berberoğlu, Pınar Kocaay, 2018, Journal of pediatric and adolescent gynecology.

Gastric carcinoid tumor in a 14-year old girl

Z. Kuloğlu, A. Kansu, A. Ensari, 2014, Scandinavian journal of gastroenterology.

Amiodarone-induced Thyrotoxicosis in Children and Adolescents is a Possible Outcome in Patients with Low Iodine Intake

Z. Şıklar, M. Berberoğlu, B. Hacıhamdioğlu, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters

N. Akar, Z. Şıklar, M. Berberoğlu, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Efficiency of Fluid Treatments with Different Sodium Concentration in Children with Type 1 Diabetic Ketoacidosis

Z. Şıklar, M. Berberoğlu, T. Kendirli, 2011, Journal of clinical research in pediatric endocrinology.

Treatment of autonomous ovarian follicular cyst with long-term anastrozole therapy

Z. Şıklar, G. Ocal, M. Berberoğlu, 2009, Indian journal of pediatrics.

Hajdu-Cheney Syndrome with Growth Hormone Deficiency and Neuropathy

Z. Şıklar, Y. Dallar, G. Tanyer, 2000, Journal of pediatric endocrinology & metabolism : JPEM.

Is hypertriglyceridaemia a new concept for visceral leishmaniasis?

Z. Şıklar, O. Erdeve, Yildaz Dallar, 2004, Annals of tropical paediatrics.

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

F. Baş, Z. Aycan, E. Mengen, 2018, Journal of Endocrinological Investigation.

A Rare Cause of Sleep-Disordered Breathing: ROHHAD Syndrome

Z. Şıklar, G. Özcan, N. Çobanoğlu, 2020, Frontiers in Pediatrics.

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

O. Mäkitie, B. Tüysüz, E. Héon, 2016, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Treatment Management with 18F-Fluoro-L-DOPA PET/CT Imaging of Focal Congenital Hyperinsulinemic Hypoglycemia Case

Z. Aycan, Ç. Soydal, Z. Şıklar, 2020 .

Pathophysiology of critical illness hyperglycemia in children

Z. Şıklar, M. Berberoğlu, T. Kendirli, 2013, Journal of pediatric endocrinology & metabolism : JPEM.

Diurnal variation of height in children

Z. Şıklar, Y. Dallar, G. Tanyer, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

Zinc treatment affects superoxide dismutase activity in growth retardation

Z. Şıklar, Y. Dallar, G. Kavas, 2007, Biological Trace Element Research.

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

S. Poyrazoglu, A. Topaloğlu, L. D. Kotan, 2012, Journal of Clinical Research in Pediatric Endocrinology.

A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course

S. Ellard, S. Flanagan, K. Hussain, 2015, Journal of clinical research in pediatric endocrinology.

Clinical Characteristics and Treatment Outcomes of Children with Primary Osteoporosis

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2023, Turkish archives of pediatrics.

Hypocalcemic seizure due to congenital rickets in the first day of life.

Z. Şıklar, G. Ocal, M. Berberoğlu, 2007, The Turkish journal of pediatrics.

Response to Growth Hormone with Respect to Pubertal Status on Increased Dose in Idiopathic Growth Hormone Deficiency: An Analysis of Turkish Children in the KIGS Database (Pfizer International Growth Study)

F. Baş, A. Bideci, Z. Şıklar, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Managing precocious puberty: A necessity for psychiatric evaluation.

Z. Şıklar, B. Kılıç, Rahime Duygu Temelturk, 2021, Asian journal of psychiatry.

Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age

Z. Şıklar, M. Berberoğlu, B. Atasay, 2009, Journal of clinical research in pediatric endocrinology.

Evaluation of Final Height and Parentally Adjusted Height Deficit in Isolated Growth Hormone Deficient Children With or Without Short Parents

Z. Şıklar, M. Berberoğlu, G. Öcal,, 2009 .

Two Siblings with Isolated GH Deficiency Due to Loss−of−Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation

S. Amselem, M. Legendre, Z. Şıklar, 2010, Journal of clinical research in pediatric endocrinology.

Case Report: Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties

Z. Şıklar, M. Berberoğlu, A. Ikinciogullari, 2011, Journal of clinical research in pediatric endocrinology.

Long−Term Follow−Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5

O. Hiort, Z. Şıklar, M. Berberoğlu, 2010, Journal of clinical research in pediatric endocrinology.

Mitotically Active Follicular Nodule in Early Childhood: A Case Report with A Novel Mutation in the Thyroglobulin Gene.

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2022, Journal of clinical research in pediatric endocrinology.

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome

M. Weedon, S. Ellard, M. Wabitsch, 2020, Wellcome open research.

Functional Ovarian Hyperandrogenism and Polycystic Ovary Syndrome in Prepubertal Girls with Obesity and/or Premature Pubarche

Z. Şıklar, G. Ocal, M. Berberoğlu, 2007, Journal of pediatric endocrinology & metabolism : JPEM.

Synchronous Occurrence of Papillary Carcinoma in the Thyroid Gland and Thyroglossal Duct in an Adolescent with Congenital Hypothyroidism

M. Kır, Z. Şıklar, M. Berberoğlu, 2012, Journal of clinical research in pediatric endocrinology.

“Maternal/Neonatal” Iodine Status in Patients with Prolonged Physiological Jaundice

Z. Şıklar, M. Berberoğlu, G. Öcal,, 2008, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Clinic Heterogeneity and Management of Pediatric Patients With Germline RET Proto-oncogene Mutation: Single-center Experience.

Z. Şıklar, M. Berberoğlu, H. Di̇nçaslan, 2023, Journal of pediatric hematology/oncology.

Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphism (-675 4G/SG) Associated with Obesity and Vascular Risk in Children

N. Akar, Z. Şıklar, M. Berberoğlu, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

Evaluation of Abnormal Uterine Bleeding in Adolescents: Single Center Experience

Z. Aycan, Z. Şıklar, M. Berberoğlu, 2023, Journal of Clinical Research in Pediatric Endocrinology.

Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

S. Ellard, Z. Şıklar, M. Berberoğlu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Response to Anastrozole Treatment in a Case with Peutz-Jeghers Syndrome and a Large Cell Calcifying Sertoli Cell Tumor

T. Soygür, Z. Kuloğlu, A. Kansu, 2017, Journal of clinical research in pediatric endocrinology.

High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients.

B. Keskinkılıc, Ş. Savaş-Erdeve, S. Çetinkaya, 2024, Journal of endocrinological investigation.

Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasia

Z. Aycan, S. Çetinkaya, Z. Şıklar, 2023, Clinical endocrinology.

Management of endocrinological problems in children on home invasive mechanical ventilation.

Z. Şıklar, 2023, Pediatric pulmonology.