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1
Ambulatory blood pressure and subclinical cardiovascular disease in patients with congenital adrenal hyperplasia: a preliminary report
Ambulatory blood pressure and subclinical cardiovascular disease in patients with congenital adrenal hyperplasia: a preliminary report
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Ambulatory blood pressure and subclinical cardiovascular disease in patients with congenital adrenal hyperplasia: a preliminary report

Akyürek, Nesibe ; Atabek, Mehmet Emre ; Eklioğlu, Beray Selver ; Alp, Hayrullah

Journal of clinical research in pediatric endocrinology, 2015-03, Vol.7 (1), p.13-18 [Periódico revisado por pares]

Turkey: Galenos Publishing House

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2
A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report
A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report
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A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report

Altıncık, Ayça ; Schlingmann, Karl Peter ; Tosun, Mahya Sultan

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.101-104 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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3
Health-Related Quality of Life and Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus
Health-Related Quality of Life and Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus
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Health-Related Quality of Life and Metabolic Control in Children and Adolescents with Type 1 Diabetes Mellitus

Caferoğlu, Zeynep ; İnanç, Neriman ; Hatipoğlu, Nihal ; Kurtoğlu, Selim

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.67-73 [Periódico revisado por pares]

Turkey: Galenos Publishing House

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4
Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports
Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports
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Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports

Calcaterra, Valeria ; Cena, Hellas ; Fonte, Maria Luisa ; De Amici, Mara ; Vandoni, Matteo ; Albanesi, Michela ; Pelizzo, Gloria

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.250-256 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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5
Higher body fat and lower fat-free mass in girls with premature adrenarche
Higher body fat and lower fat-free mass in girls with premature adrenarche
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Higher body fat and lower fat-free mass in girls with premature adrenarche

Cebeci, Ayşe Nurcan ; Taş, Ayşegül

Journal of clinical research in pediatric endocrinology, 2015-03, Vol.7 (1), p.45-48 [Periódico revisado por pares]

Turkey: Galenos Publishing House

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6
Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)
Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)
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Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

Çelmeli, Gamze ; Türkkahraman, Doğa ; Çürek, Yusuf ; Houghton, Jayne ; Akçurin, Sema ; Bircan, İffet Darendeliler,Fatma Feyza

Journal of clinical research in pediatric endocrinology, 2017-03, Vol.9 (1), p.80-84 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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7
Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene
Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene
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Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene

Deeb, Asma ; Al Suwaidi, Hana ; Ibukunoluwa, Fakunle ; Attia, Salima

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.236-240 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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8
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

Dursun, Fatma ; Mohamoud, Hussein Sheikh Ali ; Karim, Noreen ; Naeem, Muhammad ; Jelani, Musharraf ; Kırmızıbekmez, Heves

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.472-477 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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9
Prediabetes and Cardiovascular Parameters in Obese Children and Adolescents
Prediabetes and Cardiovascular Parameters in Obese Children and Adolescents
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Prediabetes and Cardiovascular Parameters in Obese Children and Adolescents

Eklioğlu, Beray Selver ; Atabek, Mehmet Emre ; Akyürek, Nesibe ; Alp, Hayrullah

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.80-85 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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10
Evaluation of Periaortic Adiposity and Metabolic Disorders in Obese Children
Evaluation of Periaortic Adiposity and Metabolic Disorders in Obese Children
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Evaluation of Periaortic Adiposity and Metabolic Disorders in Obese Children

Eklioğlu, Beray Selver ; Atabek, Mehmet Emre ; Akyürek, Nesibe ; Alp, Hayrullah

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.74-79 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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Assunto 

  1. Humans  (39)
  2. Female  (31)
  3. Male  (26)
  4. Case Report  (25)
  5. Case Studies  (25)
  6. Diagnosis  (22)
  7. Adolescent  (19)
  8. Genetic Aspects  (17)
  9. Child  (16)
  10. Case-Control Studies  (16)
  11. Original  (15)
  12. Follow-Up Studies  (12)
  13. Prognosis  (12)
  14. Gene Mutation  (10)
  15. Mutation  (10)
  16. Dna Mutational Analysis  (10)
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