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ŞÜKRAN POYRAZOĞLU
ŞÜKRAN POYRAZOĞLU
Unknown affiliation
Verified email at istanbul.edu.tr
Title
Cited by
Cited by
Year
Sitting height and sitting height/height ratio references for Turkish children
R Bundak, F Bas, A Furman, H Günöz, F Darendeliler, N Saka, ...
European journal of pediatrics 173, 861-869, 2014
1052014
Constitutional delay of growth and puberty: from presentation to final height
Ş Poyrazoglu, H Günöz, F Darendeliler, Ν Saka, R Bundak, F Baş
Journal of Pediatric Endocrinology and Metabolism 18 (2), 171-180, 2005
842005
Turner syndrome and associated problems in Turkish children: a multicenter study
E Yeşilkaya, A Bereket, F Darendeliler, F Baş, Ş Poyrazoğlu, BK Aydın, ...
Journal of Clinical Research in Pediatric Endocrinology 7 (1), 27, 2015
782015
Cleidocranial dysplasia: clinical, endocrinologic and molecular findings in 15 patients from 11 families
FD Bir, N Dinçkan, Y Güven, F Baş, U Altunoğlu, SS Kuvvetli, ...
European journal of medical genetics 60 (3), 163-168, 2017
442017
Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism
F Gürbüz, LD Kotan, E Mengen, Z Şıklar, M Berberoğlu, S Dökmetaş, ...
Journal of clinical research in pediatric endocrinology 4 (3), 121, 2012
372012
Klinefelter syndrome in childhood: variability in clinical and molecular findings
N Akcan, Ş Poyrazoğlu, F Baş, R Bundak, F Darendeliler
Journal of clinical research in pediatric endocrinology 10 (2), 100, 2018
352018
The growth characteristics of patients with noonan syndrome: results of three years of growth hormone treatment: a nationwide multicenter study
Z Şıklar, M Genens, Ş Poyrazoğlu, F Baş, F Darendeliler, R Bundak, ...
Journal of Clinical Research in Pediatric Endocrinology 8 (3), 305, 2016
322016
Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene
F Baş, G Toksoy, B Ergun-Longmire, ZO Uyguner, ZY Abalı, Ş Poyrazoğlu, ...
The Journal of steroid biochemistry and molecular biology 181, 88-97, 2018
302018
Incidence of type 1 diabetes in children aged below 18 years during 2013-2015 in northwest Turkey
Ş Poyrazoğlu, R Bundak, ZY Abalı, H Önal, S Sarıkaya, A Akgün, S Baş, ...
Journal of clinical research in pediatric endocrinology 10 (4), 336, 2018
282018
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 …
AD Kardelen, G Toksoy, F Baş, ZY Abalı, G Gençay, Ş Poyrazoğlu, ...
Journal of Clinical Research in Pediatric Endocrinology 10 (3), 206, 2018
272018
Two novel mutations in XYLT2 cause spondyloocular syndrome
F Taylan, Z Yavaş Abalı, N Jaentti, N Güneş, F Darendeliler, F Baş, ...
American Journal of Medical Genetics Part A 173 (12), 3195-3200, 2017
262017
Clinicopathological characteristics of papillary thyroid cancer in children with emphasis on pubertal status and association with BRAFV600E mutation
Ş Poyrazoğlu, R Bundak, F Baş, G Yeğen, Y Şanlı, F Darendeliler
Journal of clinical research in pediatric endocrinology 9 (3), 185, 2017
252017
Frequency and severity of ketoacidosis at onset of autoimmune type 1 diabetes over the past decade in children referred to a tertiary paediatric care centre: potential impact …
A Uçar, N Saka, F Baş, M Sukur, S Poyrazoğlu, F Darendeliler, R Bundak
Journal of Pediatric Endocrinology and Metabolism 26 (11-12), 1059-1065, 2013
242013
Associations of size at birth and postnatal catch-up growth status with clinical and biomedical characteristics in prepubertal girls with precocious adrenarche: preliminary results
A Uçar, M Yackobovitch-Gavan, OB Erol, E Yekeler, N Saka, F Baş, ...
The Journal of Clinical Endocrinology & Metabolism 99 (8), 2878-2886, 2014
232014
Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients
Ş Poyrazoğlu, N Saka, F Bas, P Isguven, A Dogu, S Turan, A Turan, ...
Journal of Pediatric Endocrinology and Metabolism 21 (8), 745-752, 2008
23*2008
Assessment of paediatric Hashimoto's thyroiditis using superb microvascular imaging
Z Bayramoglu, SG Kandemirli, E Caliskan, R Yilmaz, AD Kardelen, ...
Clinical Radiology 73 (12), 1059. e9-1059. e15, 2018
222018
Sonography and magnetic resonance imaging characteristics of testicular adrenal rest tumors
R Yılmaz, D Şahin, A Aghayev, OB Erol, Ş Poyrazoğlu, N Saka, E Yekeler
Polish journal of radiology 82, 583, 2017
222017
Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey
Ş Poyrazoğlu, T Akcay, İ Arslanoğlu, ME Atabek, Z Atay, M Berberoğlu, ...
Journal of clinical research in pediatric endocrinology 7 (1), 37, 2015
222015
Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height
Ş Savaş-Erdeve, S Çetinkaya, ZY Abalı, Ş Poyrazoğlu, F Baş, ...
Journal of Pediatric Endocrinology and Metabolism 30 (7), 759-766, 2017
202017
Increased arterial stiffness in young normotensive patients with Turner syndrome: associations with vascular biomarkers
A Uçar, F Öz, F Baş, H Oflaz, K Nişli, M Tuğrul, A Yetim, F Darendeliler, ...
Clinical Endocrinology 82 (5), 719-727, 2015
202015
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