Zehra Yavaş Abalı

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

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

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.

Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards

F. Baş, F. Darendeliler, R. Bundak, 2022, Journal of clinical research in pediatric endocrinology.

Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD

S. Poyrazoglu, F. Baş, F. Darendeliler, 2022, Journal of clinical research in pediatric endocrinology.

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.

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

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

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations

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

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.

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.

Evaluation of growth, puberty, osteoporosis, and the response to long‐term bisphosphonate therapy in four patients with osteoporosis‐pseudoglioma syndrome

H. Kayserili, S. Poyrazoglu, F. Baş, 2022, American journal of medical genetics. Part A.

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.

Body mass index at the presentation of premature adrenarche is associated with components of metabolic syndrome at puberty

S. Poyrazoglu, F. Baş, F. Darendeliler, 2018, European Journal of Pediatrics.

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.

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.

A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey

F. Darendeliler, O. Neyzi, Zehra Yavaş Abalı, 2016, Journal of clinical research in pediatric endocrinology.

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.

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.

Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia

S. Abalı, K. Yararbaş, Zehra Yavaş Abalı, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

A rare cause of hypertension in childhood: Answers

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

PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency.

S. Poyrazoglu, F. Baş, F. Darendeliler, 2023, 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.

Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A Single-Center Experience

S. Poyrazoglu, F. Baş, F. Darendeliler, 2023, Turkish archives of pediatrics.

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.

A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy

S. Poyrazoglu, F. Baş, F. Darendeliler, 2023, Hormone Research in Paediatrics.

Diagnosis and management of non-CAH 46,XX disorders/differences in sex development

T. Guran, Zehra Yavaş Abalı, 2024, Frontiers in endocrinology.