Dergiler / Journal of Clinical Research in Pediatric Endocrinology

2016 · Cilt: 8 - Sayı: 1

MakaleYazarSayfa
Current Perspectives on Pseudohypoparathyroidism-New ClassificationSerap TURAN1–2
Sex Hormone-Binding Globulin in Children and AdolescentsBANU AYDIN,Stephen J. WİNTERS1–12
Disorders/Differences of Sex Development: A World of UncertaintyEric VİLAİN3–3
Automating Glycemic Management in Diabetes Mellitus with a Bionic PancreasSteven Jon RUSSELL4–4
Use of Next Generation Sequencing in Clinical Practice: The Example of Disorders/Differences of Sex DevelopmentEric VİLAİN5–5
Long-acting Growth Hormone Formulations: Structure and ActivityAlan D. ROGOL6–6
The Genetics of Growth and Growth Disorders: From the Hypothalamus to the EpiphysisMitchell E GEFFNER7–8
Turner Syndrome: Care Through the AgesAlan D. ROGOL9–9
Efficacy and Safety of Long-Acting Gonadotropin Releasing Hormone AnalogsMitchell E GEFFNER10–10
Genetic Defects Affecting Adrenal DevelopmentAllen LİPSON,Eric VİLAİN11–11
Congenital Adrenal Hyperplasia: Consensus Guidelines and BeyondMitchell E GEFFNER12–13
Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in TurkeyBerna İmge AYDOĞAN,Bağdagül YÜKSEL,MAZHAR MÜSLÜM TUNA,Mehtap Navdar BAŞARAN,Ayşen KOCAELİ AKKURT,Melek Eda ERTÖRER,KADRİYE AYDIN TEZCAN,SİBEL GÜLDİKEN,Yasin ŞİMŞEK,ZÜLEYHA CİHAN ÖZDAMAR KARACA,Merve YILMAZ,MÜJDE YAŞIM AKTÜRK,İNAN ANAFOROĞLU,MEDİNE NUR KEBAPÇI,CEVDET DURAN,Abdullah TAŞLIPINAR,MUSTAFA13–20
Screening of HHEX Mutations in Chinese Children with Thyroid DysgenesisShiguo LİU,Jian CHAİ,Guohua ZHENG,Huichao Lİ,LU Deguo,Yinlin GE21–25
Pediatric Reference Intervals for Free Thyroxine and Free Triiodothyronine by Equilibrium Dialysis-Liquid Chromatography-Tandem Mass SpectrometrySonia L. LA'ULU,Kyle J. RASMUSSEN,Joely A. STRASESKİ26–31
Relationship between Neck Circumference and Non-Alcoholic Fatty Liver Disease in Childhood ObesityNihal HATİPOĞLU,SERAP DOĞAN,M MÜMTAZ MAZICIOĞLU,Selim KURTOĞLU32–39
Alpha-Melanocyte-Stimulating Hormone and Agouti-Related Protein: Do They Play a Role in Appetite Regulation in Childhood Obesity?Aysel VEHAPOĞLU,Serdar TÜRKMEN,ŞULE TERZİOĞLU UŞAK40–47
Impact of Vitamin D Status on Cardiometabolic Complications among Children and Adolescents with Type 1 Diabetes MellitusAdnan Al SHAİKH,Abdullah M Al ZAHRANİ48–54
Assessment of Anti-Müllerian Hormone Level in Management of Adolescents with Polycystic Ovary SyndromeFatma DURSUN,AYLA GÜVEN,Metin YILDIZ55–60
Evaluation of Iodine Deficiency in Children with Attention Deficit/ Hyperactivity DisorderSaliha Kanık YÜKSEK,ZEHRA AYCAN,Özgür ÖNER61–66
Health-Related Quality of Life and Metabolic Control in Children and Adolescents with Type 1 Diabetes MellitusZEYNEP CAFEROĞLU,Neriman İNANÇ,Nihal HATİPOĞLU,Selim KURTOĞLU67–73
Evaluation of Periaortic Adiposity and Metabolic Disorders in Obese ChildrenBERAY SELVER EKLİOĞLU,MEHMET EMRE ATABEK,Nesibe AKYÜREK,Hayrullah ALP74–79
Prediabetes and Cardiovascular Parameters in Obese Children and AdolescentsBERAY SELVER EKLİOĞLU,MEHMET EMRE ATABEK,Nesibe AKYÜREK,Hayrullah ALP80–85
Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency SyndromeSeverine Van HULLE,Margarita CRAEN,Bert CALLEWAERT,Sjoerd JOUSTRA,Wilma OOSTDİJK,Monique LOSEKOOT,Jan Maarten WİT,Marc Olivier TURGEON,Daniel J. BERNARD,Jean De SCHEPPER86–91
An Adolescent Boy with Comorbid Anorexia Nervosa and Hashimoto ThyroiditisMELİS PEHLİVANTÜRK KIZILKAN,NURAY KANBUR,Sinem AKGÜL,AYFER ALİKAŞİFOĞLU92–95
Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan SyndromeDOĞUŞ VURALLI KARAOĞLAN,ELMAS NAZLI GÖNÇ,Dominique VİDAUD,ZEYNEP ALEV ÖZÖN,AYFER ALİKAŞİFOĞLU,Nurgün KANDEMİR96–100
A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case ReportSELDA AYÇA ALTINCIK,Karl Peter SCHLİNGMANN,Mahya Sultan TOSUN101–104
Coexistence of Kabuki Syndrome and Autoimmune ThyroiditisFATİH GÜRBÜZ,ÖZGE ÖZALP YÜREĞİR,Serdar CEYLANER,Ali Kemal TOPALOĞLU,BİLGİN YÜKSEL105–106
Reply; Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR GeneSAADET OLCAY EVLİYAOĞLU107–107
Averting the Legacy of Kidney Disease-Focus on Childhood “For in every adult there dwells the child that was, and in every child there lies the adult that will be.” - John Connolly, The Book of Lost ThingsJulie R INGELFINGER,Kamyar ZADEH KALANTAR,Franz SCHAEFER108–113