S. Abalı

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.

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.

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.

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.

Cranial MRI abnormalities and long-term follow-up of the lesions in 770 girls with Central Precocious Puberty.

Esin Karakılıç Özturan, F. Darendeliler, A. Dağçınar, 2021, 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.

The Risk Factors for Autoimmune Thyroid Disorder in Children with Chronic Spontaneous Urticaria

S. Abalı, I. Şimşek, M. Aydogan, 2020 .

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.

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.

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.

Early Postnatal Metabolic Profile in Neonates With Different Birth Weight Status: A Pilot Study

M. Serteser, S. Beken, S. Abalı, 2021, Frontiers in Pediatrics.

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

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

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.

Effect of iron supplementation on development of iron deficiency anemia in breastfed infants.

Z. Karakaş, S. Abalı, G. Gokcay, 2012, Journal of tropical pediatrics.

Nationwide Hypophosphatemic Rickets Cohort Study Runing Title : Nationwide Hypophosphatemic Rickets

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

Comparison of two different GnRH analogs' impact on final height in girls with early puberty: Triptorelin acetate vs. leuprolide acetate.

S. Abalı, F. Bengur, S. Aka, 2020, Acta endocrinologica.

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 .

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.

Early postnatal metabolic profile in neonates with critical CHDs.

M. Serteser, S. Beken, E. Erek, 2022, Cardiology in the young.

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.

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.

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.

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

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

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.

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.

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.

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 assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography

B. Ozkan, S. Abalı, Ozlem Nalbantoglu, 2017, International Ophthalmology.

Poncet's Disease: Reactive Arthritis Due to Tuberculosis

A. Somer, N. Salman, S. Abalı, 2016 .

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.

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.

Application of complementary and alternative medicine in epileptic children at a tertiary pediatric neurology center in Turkey

B. Tatlı, Meral Özmen, B. Ekici, 2012 .

Clinical Features of Children and Adolescents at the Onset of Diabetes: A Single-center Experience

Y. Akın, S. Abalı, 2023, Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy.

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia

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

A. Yaman, S. Abalı, O. Karti, 2017, American journal of ophthalmology case reports.

A rare cause of hypertension in childhood: Answers

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

Retinal Ganglion Cell Loss in Children With Type 1 Diabetes Mellitus Without Diabetic Retinopathy.

B. Ozkan, T. Kusbeci, S. Abalı, 2017, Ophthalmic surgery, lasers & imaging retina.

Neonatal Problems and Infancy Growth of Term SGA Infants: Does “SGA” Definition Need to Be Re-evaluated?

S. Beken, S. Abalı, A. Korkmaz, 2021, Frontiers in Pediatrics.