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Refinado por: Nome da Publicação: Journal Of Clinical Research In Pediatric Endocrinology remover idioma: Turco remover
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1
Alpha-Melanocyte-Stimulating Hormone and Agouti-Related Protein: Do They Play a Role in Appetite Regulation in Childhood Obesity?
Alpha-Melanocyte-Stimulating Hormone and Agouti-Related Protein: Do They Play a Role in Appetite Regulation in Childhood Obesity?
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Alpha-Melanocyte-Stimulating Hormone and Agouti-Related Protein: Do They Play a Role in Appetite Regulation in Childhood Obesity?

Vehapoglu, Aysel ; Turkmen, Serdar ; Terzioglu, Sule

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.40-47 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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2
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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3
An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto Thyroiditis
An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto Thyroiditis
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An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto Thyroiditis

Pehlivantürk Kızılkan, Melis ; Kanbur, Nuray ; Akgül, Sinem ; Alikaşifoğlu, Ayfer

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.92-95 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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4
Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population
Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population
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Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

Sun, Ying ; Yuan, Yi ; Yang, Hua ; Li, Jingjie ; Feng, Tian ; Ouyang, Yongri ; Jin, Tianbo ; Liu, Ming

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.405-410 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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5
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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6
Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates
Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates
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Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

Korkut, Sabriye ; Baştuğ, Osman ; Raygada, Margarita ; Hatipoğlu, Nihal ; Kurtoğlu, Selim ; Kendirci, Mustafa ; Lyssikatos, Charalampos ; Stratakis, Constantine A

Journal of clinical research in pediatric endocrinology, 2016-12, Vol.8 (4), p.468-471 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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7
Correlation of Brain Neuropeptide (Nesfatin-1 and Orexin-A) Concentrations with Anthropometric and Biochemical Parameters in Malnourished Children
Correlation of Brain Neuropeptide (Nesfatin-1 and Orexin-A) Concentrations with Anthropometric and Biochemical Parameters in Malnourished Children
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Correlation of Brain Neuropeptide (Nesfatin-1 and Orexin-A) Concentrations with Anthropometric and Biochemical Parameters in Malnourished Children

Ustabaş Kahraman, Feyza ; Vehapoğlu, Aysel ; Özgen, İlker Tolga ; Terzioğlu, Şule ; Cesur, Yaşar ; Dündaröz, Ruşen

Journal of clinical research in pediatric endocrinology, 2015-09, Vol.7 (3), p.197-202 [Periódico revisado por pares]

Turkey: Galenos Publishing House

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8
Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant
Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant
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Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant

Üstyol, Ala ; Atabek, Mehmet Emre ; Taylor, Norman ; Yeung, Matthew Chun-Wing ; Chan, Angel O K

Journal of clinical research in pediatric endocrinology, 2016-09, Vol.8 (3), p.356-359 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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9
Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome
Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome
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Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome

Van Hulle, Severine ; Craen, Margarita ; Callewaert, Bert ; Joustra, Sjoerd ; Oostdijk, Wilma ; Losekoot, Monique ; Wit, Jan Maarten ; Turgeon, Marc Olivier ; Bernard, Daniel J ; De Schepper, Jean

Journal of clinical research in pediatric endocrinology, 2016-03, Vol.8 (1), p.86-91 [Periódico revisado por pares]

Turkey: Galenos Yayinevi Tic. Ltd

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10
Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients
Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients
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Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients

Sarajlija, Adrijan ; Milenkovic, Tatjana ; Djordjevic, Maja ; Mitrovic, Katarina ; Todorovic, Sladjana ; Kecman, Bozica ; Hussain, Khalid

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.228-231 [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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