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Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

Journal of endocrinological investigation, 2019-04, Vol.42 (4), p.453-470

2019

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Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

European journal of clinical nutrition, 2020-08, Vol.74 (8), p.1173-1180

2020

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Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations

The journal of clinical endocrinology and metabolism, 2005-03, Vol.90 (3), p.1323-1331

2005

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1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A376-A377

2012

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Corona mortis: An anatomic study in seven cadavers and an endoscopic study in 28 patients

Surgical endoscopy, 2001, Vol.15 (1), p.72-75

2001

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A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism

Genetic counseling, 2014-01, Vol.25 (3), p.331

2014

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Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

Journal of Pediatric Endocrinology and Metabolism, 2008-08, Vol.21 (8), p.781-788

2008

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Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Journal of bone and mineral research, 2016-08, Vol.31 (8), p.1577-1585

2016

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Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b

The journal of clinical endocrinology and metabolism, 2005-07, Vol.90 (7), p.4260-4266

2005

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Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Journal of Pediatric Endocrinology and Metabolism, 2006-05, Vol.19 (5), p.741

2006

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Effect of CO2 insufflation on bacteremia and bacterial translocation in an animal model of peritonitis

Surgical endoscopy, 1999-08, Vol.13 (8), p.801-803

1999

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Isolated central diabetes insipidus in a newborn with congenital toxoplasmosis

Journal of Pediatric Endocrinology and Metabolism, 2006-02, Vol.19 (2), p.173-176

2006

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Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac disease

Journal of Pediatric Endocrinology and Metabolism, 2004-11, Vol.17 (11), p.1565

2004

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Mutations of the 5α-Steroid Reductase Type 2 Gene in Six Turkish Patients from Unrelated Families and a Large Pedigree of an Isolated Turkish Village

Journal of Pediatric Endocrinology and Metabolism, 2002, Vol.15 (4)

2002

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Dissecting Molecular and Circuit Mechanisms for Inhibition and Delayed Response of ASI Neurons during Nociceptive Stimulus

Cell reports (Cambridge), 2018-11, Vol.25 (7), p.1885-1897.e9

2018

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Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency

Journal of molecular medicine (Berlin, Germany), 2002-07, Vol.80 (7), p.406-411

2002

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Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Genes & development, 2003-03, Vol.17 (6), p.711-716

2003

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Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients

Journal of Pediatric Endocrinology and Metabolism, 2001-09, Vol.14 (8), p.1113-1118

2001

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"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Experimental and clinical endocrinology & diabetes, 2009-07, Vol.117 (7), p.312-315

2009

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Clinical characteristics of 46,XX males with congenital adrenal hyperplasia

Yearbook of Paediatric Endocrinology, 2021-09

2021

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MLP012 Hypophosphatasia associated with pseudotumour cerebri and respiratory insufficiency

European journal of paediatric neurology, 2007, Vol.11, p.70-70

2007

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Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Experimental and clinical endocrinology & diabetes, 2009-06, Vol.117 (6), p.301-304

2009

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Alterations in serum growth hormone (GH)/GH dependent ternary complex components (IGF-I, IGFBP-3, ALS, IGF-I/IGFBP-3 molar ratio) and the influence of these alterations on growth pattern in female rhythmic gymnasts

Journal of Pediatric Endocrinology and Metabolism, 2004-06, Vol.17 (6), p.895

2004

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Corona mortis: An anatomic study in seven cadavers and an endoscopic study in 28 patients

Surgical endoscopy, 2004-09, Vol.18 (9), p.1402-1402

2004

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Genotype–phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

Nutritional status and body composition in children with inflammatory bowel disease: a prospective, controlled, and longitudinal study

Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations

1321 The Management of Central Diabetes Insipidus in Neonatal Intensive Care Unit: Experience of Eight Cases

High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients

Corona mortis: An anatomic study in seven cadavers and an endoscopic study in 28 patients

A novel mutation in the calcium sensing receptor gene in a neonate with severe hyperparathyroidism

Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey

Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum

Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b

Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in children

Effect of CO2 insufflation on bacteremia and bacterial translocation in an animal model of peritonitis

Isolated central diabetes insipidus in a newborn with congenital toxoplasmosis

Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac disease

Mutations of the 5α-Steroid Reductase Type 2 Gene in Six Turkish Patients from Unrelated Families and a Large Pedigree of an Isolated Turkish Village

Dissecting Molecular and Circuit Mechanisms for Inhibition and Delayed Response of ASI Neurons during Nociceptive Stimulus

Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency

Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients

"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundice

Clinical characteristics of 46,XX males with congenital adrenal hyperplasia

MLP012 Hypophosphatasia associated with pseudotumour cerebri and respiratory insufficiency

Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesis

Alterations in serum growth hormone (GH)/GH dependent ternary complex components (IGF-I, IGFBP-3, ALS, IGF-I/IGFBP-3 molar ratio) and the influence of these alterations on growth pattern in female rhythmic gymnasts

Corona mortis: An anatomic study in seven cadavers and an endoscopic study in 28 patients

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