Şenay Savaş-Erdeve

发表

Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience

Z. Aycan, S. Çetinkaya, I. Karaman, 2020, Journal of clinical research in pediatric endocrinology.

Clinical follow-up data and the rate of development of precocious and rapidly progressive puberty in patients with premature thelarche

Z. Aycan, S. Çetinkaya, Şenay Savaş-Erdeve, 2018, 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.

Role of Ischemia Modified Albumin Serum Levels as an Oxidative Stress Marker in Children with Diabetic Ketoacidosis.

S. Çetinkaya, S. Neşelioğlu, Ö. Erel, 2019, Combinatorial chemistry & high throughput screening.

Low hemoglobin A1c levels in a patient with diabetic ketoacidosis: Fulminant type 1 diabetes mellitus.

Z. Aycan, S. Çetinkaya, Melikşah Keskin, 2018, The Turkish journal of pediatrics.

Treatment experience and long-term follow-up data in two severe neonatal hyperparathyroidism cases

Erdal Kurnaz, Z. Aycan, S. Çetinkaya, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

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

Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets

Z. Aycan, S. Çetinkaya, Elif Sağsak, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

The use of pamidronate for acute vitamin D intoxication, clinical experience with three cases

Z. Aycan, S. Çetinkaya, Elif Sağsak, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

AMH levels in girls with various pubertal problems

Z. Aycan, S. Çetinkaya, Elif Sağsak, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Do the Anti-Müllerian Hormone Levels of Adolescents with Polycystic Ovary Syndrome, Those Who Are at Risk for Developing Polycystic Ovary Syndrome, and Those Who Exhibit Isolated Oligomenorrhea Differ from Those of Adolescents with Normal Menstrual Cycles?

Z. Aycan, S. Çetinkaya, Elif Sağsak, 2016, Hormone Research in Paediatrics.

Status of Central Precocious Puberty Cases at the Onset of Coronavirus Disease 2019 Pandemic: A Single-Center Experience

S. Çetinkaya, Melikşah Keskin, Nursel Sahin, 2022, Turkish archives of pediatrics.

Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia

Z. Aycan, Elvan Bayramoğlu, S. Çetinkaya, 2021, Journal of clinical research in pediatric endocrinology.

Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation

Ç. Kasapkara, S. Ceylaner, S. Şenel, 2020, Journal of clinical research in pediatric endocrinology.

A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood.

Erdal Kurnaz, Z. Aycan, S. Çetinkaya, 2016, The Turkish journal of pediatrics.

Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report.

A. Karaman, Z. Aycan, S. Çetinkaya, 2016, The Turkish journal of pediatrics.

Detection of the SRY gene in patients with Turner Syndrome.

Erdal Kurnaz, Z. Aycan, Ş. Savaş-Erdeve, 2019, Journal of gynecology obstetrics and human reproduction.

17βHSD-3 enzyme deficiency due to novel mutations in the HSD17B3 gene diagnosed in a neonate

Z. Aycan, S. Çetinkaya, K. Karaer, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Is Chromosomal Study Necessary for Girls with Inguinal Hernia?

Erdal Kurnaz, Z. Aycan, Şenay Savaş-Erdeve, 2016, Journal of clinical and diagnostic research : JCDR.

Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis.

A. Karaman, Erdal Kurnaz, Z. Aycan, 2016, The Turkish journal of pediatrics.

Clinical presentations, metabolic abnormalities and end-organ complications in patients with familial partial lipodystrophy.

G. Yaylali, T. Atik, H. Onay, 2017, Metabolism: clinical and experimental.

Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty

Erdal Kurnaz, Z. Aycan, Nursel Muratoğlu Şahin, 2018, Journal of clinical research in pediatric endocrinology.

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.

Efficacy and safety of Saccharomyces boulardii in amebiasis-associated diarrhea in children.

Y. Dallar, Şenay Savaş-Erdeve, Songül Gökay, 2009, Turkish Journal of Pediatrics.

Cases Referred from the Turkish National Screening Program: Frequency of Congenital Hypothyroidism and Etiological Distribution

Z. Aycan, S. Çetinkaya, Şenay Savaş-Erdeve, 2019, Journal of Clinical Research in Pediatric Endocrinology.

Evaluation of permanent and transient congenital hypothyroidism in cases referred from National Neonatal Screening Program

Z. Aycan, S. Çetinkaya, Şenay Savaş-Erdeve, 2022, Journal of paediatrics and child health.

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.

An Uncommon Cause of Hypoglycemia: Insulin Autoimmune Syndrome

Z. Aycan, S. Çetinkaya, V. Baş, 2014, Hormone Research in Paediatrics.

Clinical and genetic characterisation of a series of patients with triple A syndrome

P. Duminuco, Erdal Kurnaz, Z. Aycan, 2018, European Journal of Pediatrics.

17α-Hydroylase/17,20-lyase deficiency related to P.Y27*(c.81C>A) mutation in CYP17A1 gene

Z. Aycan, S. Çetinkaya, Elif Sağsak, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

The first childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis.

Erdal Kurnaz, Z. Aycan, S. Çetinkaya, 2016, Turkish Journal of Pediatrics.

A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome.

Ş. Savaş-Erdeve, T. Doganci, O. Sakamoto, 2009, The Turkish journal of pediatrics.

Pituitary hyperplasia mimicking pituitary macroadenoma in two adolescent patients with long-standing primary hypothyroidism: case reports and review of literature.

T. Şimşek, B. Erdoğmuş, E. Şimşek, 2009, 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.

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.

Evaluation of the pathophysiological role of Fetuin A levels in adolescents with polycystic ovary syndrome

Erdal Kurnaz, Z. Aycan, Elvan Bayramoğlu, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

SHOX gene deletion screening by FISH in children with short stature and Madelung deformity and their characteristics

Erdal Kurnaz, Z. Aycan, S. Çetinkaya, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism

Erdal Kurnaz, Z. Aycan, S. Çetinkaya, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

Co-Existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis: A Single-Center Study

Z. Aycan, Ş. Savaş-Erdeve, Melikşah Keskin, 2016, Hormone Research in Paediatrics.

Stress Induced Hyperglycemia in Early Childhood as a Clue for the Diagnosis of NEUROD1-MODY.

Ş. Savaş-Erdeve, S. Çetinkaya, Şenay Savaş-Erdeve, 2022, Journal of clinical research in pediatric endocrinology.

Antimüllerian Hormone Levels of Infants with Premature Thelarche

Erdal Kurnaz, Z. Aycan, Nursel Muratoğlu Şahin, 2019, Journal of clinical research in pediatric endocrinology.

Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

S. Poyrazoglu, F. Baş, Z. Aycan, 2022, European Journal of Medical Genetics.

A girl with steroid cell ovarian tumor misdiagnosed as non-classical congenital adrenal hyperplasia.

Z. Aycan, S. Çetinkaya, I. Karaman, 2013, The Turkish journal of pediatrics.

Efficacy and safety of Saccharomyces boulardii in amebiasis-associated diarrhea in children.

Ş. Savaş-Erdeve, Y. Dallar, Şenay Savaş-Erdeve, 2009, The Turkish journal of pediatrics.

3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience.

Z. Aycan, S. Çetinkaya, Melikşah Keskin, 2023, European journal of medical genetics.

Z. Aycan, S. Çetinkaya, Elif Sağsak, 2016, Hormone Research in Paediatrics.