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List of works by Serap Turan

1-50 of 120 results

Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor.

scientific article

Deletion of the noncoding GNAS antisense transcript causes pseudohypoparathyroidism type Ib and biparental defects of GNAS methylation in cis

scientific article

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

scientific article

Addition of orlistat to conventional treatment in adolescents with severe obesity

scientific article published in December 2004

Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatase z-scores in different types of rickets

scientific article

GNAS Spectrum of Disorders

scientific article published on June 2015

Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia

scientific article

Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruption

scientific article published on March 2014

Puberty and influencing factors in schoolgirls living in Istanbul: end of the secular trend?

scientific article

Significance of acanthosis nigricans in childhood obesity

scientific article published in June 2008

From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network

scientific article

The GNAS complex locus and human diseases associated with loss-of-function mutations or epimutations within this imprinted gene

scientific article

Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation

scientific article

Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

article by Giovanna Mantovani et al published August 2018 in Nature Reviews Endocrinology

Serum IGF-I and IGFBP-3 levels of Turkish children during childhood and adolescence: establishment of reference ranges with emphasis on puberty

scientific article published on 03 February 2006

Effect of zinc supplementation on growth hormone secretion, IGF-I, IGFBP-3, somatomedin generation, alkaline phosphatase, osteocalcin and growth in prepubertal children with idiopathic short stature

scientific article

Cathepsin K osteoporosis trials, pycnodysostosis and mouse deficiency models: Commonalities and differences

scientific article published on 22 March 2016

De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic cases

scientific article

Exclusion of the GNAS locus in PHP-Ib patients with broad GNAS methylation changes: evidence for an autosomal recessive form of PHP-Ib?

scientific article published on August 2011

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

scientific article

Content analysis of food advertising in Turkish television

scientific article

Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib.

scientific article published on 10 April 2012

Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

scientific article

Height, weight, IGF-I, IGFBP-3 and thyroid functions in prepubertal children with attention deficit hyperactivity disorder: effect of methylphenidate treatment

scientific article published on 24 March 2005

The prevalence and risk factors of premature thelarche and pubarche in 4- to 8-year-old girls

scientific article published on 23 September 2011

Current research on pycnodysostosis

scientific article published on August 1, 2014

Extra-long Gαs variant XLαs protein escapes activation-induced subcellular redistribution and is able to provide sustained signaling

scientific article published on 2 September 2011

Circulating insulin-like growth factor binding protein-4 (IGFBP-4) is not regulated by parathyroid hormone and vitamin D in vivo: evidence from children with rickets

scientific article

Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.

scientific article published on 20 December 2013

Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes

scientific article published on 09 June 2011

Upper segment/lower segment ratio and armspan-height difference in healthy Turkish children

scientific article published in April 2005

Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism-lack of effect of cinacalcet.

scientific article published on 13 April 2014

Turner syndrome and associated problems in Turkish children: a multicenter study

scientific article published on March 2015

Comparison of capillary blood ketone measurement by electrochemical method and urinary ketone in treatment of diabetic ketosis and ketoacidosis in children

scientific article

Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development

scientific article published on 26 October 2017

Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy

scientific article

An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).

scientific article

Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method

scientific article

Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in children

scientific article published on 07 February 2015

Two patients with Kabuki syndrome presenting with endocrine problems

scientific article published in February 2001

AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity

scientific article published on 16 April 2014

The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children

scientific article

Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism

scientific article published on 16 March 2015

Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus

scientific article published on 11 July 2014

Prevalence of type 1 diabetes mellitus in 6-18-yr-old school children living in Istanbul, Turkey

scientific article published on 21 March 2011

Maternal thyroid dysfunction and neonatal thyroid problems

scientific article published on 30 April 2013

The effect of economic status on height, insulin-like growth factor (IGF)-I and IGF binding protein-3 concentrations in healthy Turkish children.

scientific article published on 13 December 2006

Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hair

scientific article

Increased QT dispersion in breath-holding spells

scientific article published in June 2004

The effect of the mode of delivery on neonatal thyroid function

scientific article