Dergiler / Journal of Clinical Research in Pediatric Endocrinology

2017 · Cilt: 9 - Sayı: 1

MakaleYazarSayfa
Non-Classical Congenital Adrenal Hyperplasia in ChildhoodSelim KURTOĞLU,Nihal HATİPOĞLU1–7
Subclinical Hypothyroidism in Danish Lean and Obese Children and AdolescentsMaria DAHL,Johanne Dam OHRT,Cilius Esmann FONVİG,Julie Tonsgaard KLOPPENBORG,Oluf PEDERSEN,Torben HANSEN,Jens-Christian HOLM8–16
Neck Circumference to Assess Obesity in Preschool ChildrenMEDA KONDOLOT,Duygu HOROZ,Serpil POYRAZOĞLU,ARDA BORLU,AHMET ÖZTÜRK,Selim KURTOĞLU,Mümtaz M. MAZICIOĞLU17–23
Role of Versican and ADAMTS-1 in Polycystic Ovary SyndromeSİBEL ÖZLER,Efser ÖZTAŞ,Aytekin TOKMAK,Merve ERGİN,Meryem Kuru PEKCAN,Başak GÜMÜŞ GÜLER,HALİL İBRAHİM YAKUT,NAFİYE YILMAZ24–30
The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood ObesityTUNCAY KÜME,Sezer ACAR,HALE ÜNVER TUHAN,GÖNÜL ÇATLI,AHMET ANIK,Özlem GÜRSOY ÇALAN,ECE BÖBER,AYHAN ABACI31–38
Comparison of Updated Weight and Height Percentiles with Previous References in 6-17-Year-Old Children in Kayseri, TurkeyGÖKMEN ZARARSIZ,BETÜL ÇİÇEK,MEDA KONDOLOT,M MÜMTAZ MAZICIOĞLU,AHMET ÖZTÜRK,Selim KURTOĞLU39–47
Association Between Endocrine Diseases and Serous Otitis Media in ChildrenMurat KOÇYİĞİT,Taliye ÇAKABAY,Safiye G ÖRTEKİN,Teoman AKÇAY,GÜVEN ÖZKAYA,Selin Üstün BEZGİN,Melek YILDIZ,Mustafa Kemal ADALI48–51
Clinical and Mutational Features of Three Chinese Children with Congenital Generalized LipodystrophyXueying SU,Ruizhu LİN,Yonglan HUANG,Huiying SHENG,Xiaofei LI,Tzer Hwu TİNG,Li LIU,Xiuzhen Lİ52–57
Age-Specific Frequencies and Characteristics of Ovarian Cysts in Children and AdolescentsHAMDİ CİHAN EMEKSİZ,Okşan DERİNÖZ,Esra Betül AKKOYUN,FARUK GÜÇLÜ PINARLI,AYSUN BİDECİ58–62
Safety and Efficacy of Stosstherapy in Nutritional RicketsDaipayan CHATTERJEE,Vikas GUPTA,Vasu SHARMA,Akshat SHARMA,Krishti CHATTERJEE63–69
Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal HyperplasiaKarin PANZER,Osayame A EKHAGUERE,Benjamin DARBRO,Jennifer COOK,Oleg A SHCHELOCHKOV70–73
Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS GeneSezgin ŞAHİN,Olaf HİORT,Susanne THİELE,SAADET OLCAY EVLİYAOĞLU,BEYHAN TÜYSÜZ74–79
Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)Gamze ÇELMELİ,DOĞA TÜRKKAHRAMAN,Yusuf ÇÜREK,Jayne HOUGHTON,Sema AKÇURİN,İffet BİRCAN80–84
Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 GeneAYLA GÜVEN,Seher POLAT85–90
A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 GeneMelikşah KESKİN,Nursel Muratoğlu ŞAHİN,Erdal KURNAZ,Elvan BAYRAMOĞLU,ŞENAY SAVAŞ ERDEVE,ZEHRA AYCAN,SEMRA ÇETİNKAYA91–94