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Cranial MRI Abnormalities and Long-term Follow-up of the Lesions in 770 Girls With Central Precocious Puberty

The journal of clinical endocrinology and metabolism, 2021-07, Vol.106 (7), p.e2557-e2566

2021

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Liraglutide in Children and Adolescents with Type 2 Diabetes

The New England journal of medicine, 2019-08, Vol.381 (7), p.637-646

2019

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Endocrine disrupting chemicals and bone

Best Practice & Research Clinical Endocrinology & Metabolism, 2021-09, Vol.35 (5), p.101495, Article 101495

Turan, Serap

2021

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Osteopetrosis: Gene-based nosology and significance Dysosteosclerosis

Bone (New York, N.Y.), 2023-02, Vol.167, p.116615-116615, Article 116615

Turan, Serap

2023

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

The journal of clinical endocrinology and metabolism, 2016-01, Vol.101 (1), p.284-292

2016

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Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature

Calcified tissue international, 2021-05, Vol.108 (5), p.576-586

2021

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Use of Insulin Degludec/Insulin Aspart in the Management of Diabetes Mellitus: Expert Panel Recommendations on Appropriate Practice Patterns

Frontiers in endocrinology (Lausanne), 2021-03, Vol.12, p.616514-616514

2021

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Letter to the Editor: Dysosteosclerosis related to the unique mutation in SLC29A3

Bone (New York, N.Y.), 2019-11, Vol.128, p.115057-115057, Article 115057

Turan, Serap

2019

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Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features

Calcified tissue international, 2022-04, Vol.110 (4), p.441-450

2022

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Ptosis as a unique hallmark for autosomal recessive WNT1‐associated osteogenesis imperfecta

American journal of medical genetics. Part A, 2019-06, Vol.179 (6), p.908-914

2019

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Clinical Significance of Hypophosphatasemia in Children

Calcified tissue international, 2020-06, Vol.106 (6), p.608-615

2020

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Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers

Pediatric nephrology (Berlin, West), 2020-03, Vol.35 (3), p.405-407

2020

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GNAS Spectrum of Disorders

Current osteoporosis reports, 2015-06, Vol.13 (3), p.146-158

2015

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A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

Calcified tissue international, 2020-07, Vol.107 (1), p.96-103

2020

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Recommendations for improving clinical trial design to facilitate the study of youth-onset type 2 diabetes

Clinical trials (London, England), 2020-02, Vol.17 (1), p.87-98

2020

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

Acta Paediatrica, 2012-02, Vol.101 (2), p.e71-e75

2012

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Rare cause of severe hypertension in an adolescent boy presenting with short stature: Questions

Pediatric nephrology (Berlin, West), 2020-03, Vol.35 (3), p.403-404

2020

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Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Controlled and Non-compliant Patients

Journal of clinical research in pediatric endocrinology, 2022-03, Vol.14 (1), p.10-16

2022

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Non-hormonal Clitoromegaly due to Clitoral Priapism Caused by Appendicitis/Appendectomy

Journal of clinical research in pediatric endocrinology, 2023-09, Vol.15 (3), p.324-328

2023

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Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z-scores in Different Types of Rickets

Journal of clinical research in pediatric endocrinology, 2011-03, Vol.3 (1), p.7-11

2011

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Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route

Journal of pediatric endocrinology & metabolism : JPEM, 2020-04, Vol.33 (4), p.557

2020

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Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 Years

Journal of clinical research in pediatric endocrinology, 2023-06, Vol.15 (2), p.154-159

2023

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Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder

Journal of clinical research in pediatric endocrinology, 2017-12, Vol.9 (Suppl 2), p.58-68

Turan, Serap

2017

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Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

JBMR plus, 2022-08, Vol.6 (8), p.e10663-n/a

2022

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

Orphanet journal of rare diseases, 2014-04, Vol.9 (1), p.60-60, Article 60

2014

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Cranial MRI Abnormalities and Long-term Follow-up of the Lesions in 770 Girls With Central Precocious Puberty

Liraglutide in Children and Adolescents with Type 2 Diabetes

Endocrine disrupting chemicals and bone

Osteopetrosis: Gene-based nosology and significance Dysosteosclerosis

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

Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature

Use of Insulin Degludec/Insulin Aspart in the Management of Diabetes Mellitus: Expert Panel Recommendations on Appropriate Practice Patterns

Letter to the Editor: Dysosteosclerosis related to the unique mutation in SLC29A3

Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features

Ptosis as a unique hallmark for autosomal recessive WNT1‐associated osteogenesis imperfecta

Clinical Significance of Hypophosphatasemia in Children

Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers

GNAS Spectrum of Disorders

A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

Recommendations for improving clinical trial design to facilitate the study of youth-onset type 2 diabetes

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

Rare cause of severe hypertension in an adolescent boy presenting with short stature: Questions

Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Controlled and Non-compliant Patients

Non-hormonal Clitoromegaly due to Clitoral Priapism Caused by Appendicitis/Appendectomy

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z-scores in Different Types of Rickets

Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route

Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 Years

Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity

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

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