Tulay Guran
Tulay Guran
Marmara University Department of Pediatric Endocrinology and Diabetes
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Cited by
Mutations in CYP24A1 and idiopathic infantile hypercalcemia
KP Schlingmann, M Kaufmann, S Weber, A Irwin, C Goos, U John, ...
New England Journal of Medicine 365 (5), 410-421, 2011
Genes that affect brain structure and function identified by rare variant analyses of Mendelian neurologic disease
E Karaca, T Harel, D Pehlivan, SN Jhangiani, T Gambin, ZC Akdemir, ...
Neuron 88 (3), 499-513, 2015
Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatasez-scores in different types of rickets
S Turan, B Topcu, İ Gökçe, T Güran, Z Atay, A Omar, T Akçay, A Bereket
Journal of clinical research in pediatric endocrinology 3 (1), 7, 2011
Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome
R Prasad, I Hadjidemetriou, A Maharaj, E Meimaridou, F Buonocore, ...
The Journal of clinical investigation 127 (3), 942-953, 2017
Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor
T Guran, G Tolhurst, A Bereket, N Rocha, K Porter, S Turan, FM Gribble, ...
The Journal of Clinical Endocrinology & Metabolism 94 (10), 3633-3639, 2009
Rare causes of primary adrenal insufficiency: genetic and clinical characterization of a large nationwide cohort
T Guran, F Buonocore, N Saka, MN Ozbek, Z Aycan, A Bereket, F Bas, ...
The Journal of Clinical Endocrinology & Metabolism 101 (1), 284-292, 2016
Changes over time in sex assignment for disorders of sex development
Z Kolesinska, SF Ahmed, M Niedziela, J Bryce, M Molinska-Glura, ...
Pediatrics 134 (3), e710-e715, 2014
Novel associations in disorders of sex development: findings from the I-DSD Registry
K Cox, J Bryce, J Jiang, M Rodie, R Sinnott, M Alkhawari, W Arlt, L Audi, ...
The Journal of Clinical Endocrinology & Metabolism 99 (2), E348-E355, 2014
Significance of acanthosis nigricans in childhood obesity
T Guran, S Turan, T Akcay, A Bereket
Journal of paediatrics and child health 44 (6), 338-341, 2008
Puberty and influencing factors in schoolgirls living in Istanbul: end of the secular trend?
Z Atay, S Turan, T Guran, A Furman, A Bereket
Pediatrics 128 (1), e40-e45, 2011
The long-term outcome of boys with partial androgen insensitivity syndrome and a mutation in the androgen receptor gene
A Lucas-Herald, S Bertelloni, A Juul, J Bryce, J Jiang, M Rodie, R Sinnott, ...
The Journal of Clinical Endocrinology & Metabolism 101 (11), 3959-3967, 2016
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1
C Bonnard, AC Strobl, M Shboul, H Lee, B Merriman, SF Nelson, ...
Nature genetics 44 (6), 709-713, 2012
Hypercalciuria and recurrent urinary tract infections: incidence and symptoms in children over 5 years of age
NK Biyikli, H Alpay, T Guran
Pediatric nephrology 20, 1435-1438, 2005
The prevalence and risk factors of premature thelarche and pubarche in 4‐to 8‐year‐old girls
Z Atay, S Turan, T Guran, A Furman, A Bereket
Acta Paediatrica 101 (2), e71-e75, 2012
Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome
E Dikoglu, A Alfaiz, M Gorna, D Bertola, JH Chae, TJ Cho, M Derbent, ...
American journal of medical genetics Part A 167 (7), 1501-1509, 2015
Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia
S Turan, C Aydin, A Bereket, T Akcay, T Güran, BA Yaralioglu, M Bastepe, ...
Bone 46 (2), 402-409, 2010
Primary adrenal insufficiency in children: Diagnosis and management
T Kirkgoz, T Guran
Best Practice & Research Clinical Endocrinology & Metabolism 32 (4), 397-424, 2018
Exome sequencing of a primary ovarian insufficiency cohort reveals common molecular etiologies for a spectrum of disease
A Jolly, Y Bayram, S Turan, Z Aycan, T Tos, ZY Abali, B Hacihamdioglu, ...
The Journal of Clinical Endocrinology & Metabolism 104 (8), 3049-3067, 2019
Content analysis of food advertising in Turkish television
T Guran, S Turan, T Akcay, F Degirmenci, O Avci, A Asan, E Erdil, A Majid, ...
Journal of paediatrics and child health 46 (7‐8), 427-430, 2010
AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity
T Akcay, M Fernandez‐Cancio, S Turan, T Güran, L Audi, A Bereket
Andrology 2 (4), 572-578, 2014
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