A. Cebeci

发表

Higher Body Fat and Lower Fat-Free Mass in Girls with Premature Adrenarche

A. Tas, A. Cebeci, 2015, Journal of clinical research in pediatric endocrinology.

Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

C. Wouters, Y. Crow, L. Adès, 2016, Journal of Clinical Immunology.

Gonadotropin releasing hormone analog treatment in children with congenital adrenal hyperplasia complicated by central precocious puberty

Suna Hancili, Ayla Güven, A. Cebeci, 2014, Hormones.

Mutation of SGK3, a novel regulator of renal phosphate transport, causes autosomal dominant hypophosphatemic rickets.

M. Zou, Yufei Shi, E. Cavalier, 2019, The Journal of clinical endocrinology and metabolism.

The debate on the link between subclinical hypothyroidism and childhood migraine: is initial endocrinological evaluation necessary for children with migraine?

B. Ekici, A. Cebeci, 2015, Acta Neurologica Belgica.

A Rare Cause of Autistic Regression in a Boy with Down Syndrome: Hashimoto Encephalopathy

B. Ekici, A. Cebeci, Feyza Kutlu, 2021, Journal of pediatric neurosciences.

Remission with Cabergoline in Adolescent Boys with Cushing’s Disease

Ayla Güven, F. Baltacioglu, A. Cebeci, 2013, Journal of clinical research in pediatric endocrinology.

The role of IL-18 in Th1/Th2 balance in children.

İ. Arslanoğlu, M. Erguven, A. Cebeci, 2006, Allergy and asthma proceedings.

A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome.

H. Kaymakçalan, A. Ercan-Sencicek, W. Dong, 2022, Anatolian journal of cardiology.

Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

C. Wouters, Y. Crow, L. Adès, 2016, Journal of Clinical Immunology.

Dietary therapies for childhood epilepsy

B. Tatlı, B. Ekici, A. Cebeci, 2014 .

3M Syndrome: A Report of Four Cases in Two Families

Ayla Güven, A. Cebeci, 2011, Journal of clinical research in pediatric endocrinology.

Impact of eating habits and nutritional status on children with autism spectrum disorder

B. Tatlı, B. Ekici, A. Cebeci, 2020, Journal of Taibah University Medical Sciences.

Profile of Hypothyroidism in Down’s Syndrome

Ayla Güven, M. Yıldız, A. Cebeci, 2013, Journal of clinical research in pediatric endocrinology.

Clinical features and management of diabetic ketoacidosis in different age groups of children: children less than 5 years of age are at higher risk of metabolic decompensation

A. Guven, M. Yıldız, A. Cebeci, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

C. Wouters, Y. Crow, L. Adès, 2016, Journal of Clinical Immunology.

Prediction of Toll-Like Receptor Gene Family in Asian Sea Bass

A. Cebeci, Asiye Nur Saltan, Kumar Sahayaraju, 2020 .

Perinephric adipose tissue thickness in relation to blood pressure, plasma apelin and C-reactive protein levels in obese adolescents.

A. Guven, A. Cebeci, L. İ. Kuru, 2016, Minerva endocrinologica.

Epilepsy treatment by sacrificing vitamin D

B. Ekici, A. Cebeci, 2014, Expert review of neurotherapeutics.

Hoffmann’s syndrome and pituitary hyperplasia in an adolescent secondary to Hashimoto thyroiditis

Ayla Güven, Cem Mesçi, A. Cebeci, 2013, Journal of pediatric endocrinology & metabolism : JPEM.

Developmental Defects of the Thyroid Gland: Relationship with Advanced Maternal Age

Ayla Güven, M. Yıldız, A. Cebeci, 2012, Journal of clinical research in pediatric endocrinology.

Should Patients with Down Syndrome be Screened for Testicular Microlithiasis?

M. Ozdemir, A. Cebeci, A. Aslanger, 2014, European Journal of Pediatric Surgery.

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism

S. Ellard, S. Flanagan, Ayla Güven, 2016, Journal of clinical research in pediatric endocrinology.

Hoffmann ' and pituitary hyperplasia in an adolescent secondary to Hashimoto thyroiditis

Cem Mesçi, A. Cebeci, S. Saltık, 2013 .

The debate on the link between subclinical hypothyroidism and childhood migraine: is initial endocrinological evaluation necessary for children with migraine?

B. Ekici, A. Cebeci, 2015, Acta Neurologica Belgica.

A rare endocrine manifestation of Down syndrome: central precocious puberty: three cases report

Ayla Güven, A. Cebeci, 2020 .

Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

A. Çayır, B. Cavdarli, K. Hussain, 2020, Journal of clinical research in pediatric endocrinology.

Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

C. Wouters, Y. Crow, L. Adès, 2016, Journal of Clinical Immunology.

Clinical Remission in a Patient with Congenital Hyperinsulinism due to Paternally Inherited Two Novel Mutations in KCJN11 Gene

S. Ellard, J. Houghton, A. Cebeci, 2014 .