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Articles from Journal of Clinical Research in Pediatric Endocrinology (September 1, 2021)

1-17 out of 17 article(s)
Title Author Type Words
A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene. Turkkahraman, Doga; Torun, Nimet Karatas; Randa, Nadide Cemre Report 2495
An Evaluation of Glucagon Injection Anxiety and Its Association with the Fear of Hypoglycemia among the Parents of Children with Type 1 Diabetes. Muradoglu, Serra; Mutlu, Gul Yesiltepe; Gokce, Tugba; Can, Ecem; Hatun, Sukru Report 5070
Analysis of the Performance of Neck Circumference to Identify Overweight and Obese Children. Viru-Loza, Manuel Andre Letter to the editor 649
Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism. Gunbey, Ceren; Ozon, Alev; Gonc, E. Nazli; Alikasifoglu, Ayfer; Karahan, Sevilay; Kandemir, Nurgun Report 5010
Brain Abscess in a Patient with Osteopetrosis: A Rare Complication. Nepesov, Merve Iseri; Kiral, Eylem; Bozan, Gurkan; Kilic, Omer; Carman, Kursat Bora; Yarar, Coskun; Report 2310
Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome. Cakir, Aydilek Dagdeviren; Bas, Firdevs; Akin, Onur; Siklar, Zeynep; Ozcabi, Bahar; Berberoglu, Meri Report 8358
Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to CYP21A2 and SCN4A Pathogenic Variants. Kontbay, Tugba; Turan, Ihsan Clinical report 2884
Evaluation of Children and Adolescents with Thyroid Nodules: A Single Center Experience. Elmaogullari, Selin; Ozalkak, Servan; Cetinkaya, Semra; Karaman, Ibrahim; Uner, Cigdem; Arda, Nilufe Report 6199
Evaluation of Growth Hormone Results in Different Diagnosis and Trend Over 10 Year of Follow-up: A Single Center Experience. Aycan, Zehra; Yilmaz, Aslihan Arasli; Yel, Servet; Savas-Erdeve, Senay; Cetinkaya, Semra Report 7602
In reply Asif M et al. Asif, Muhammad; Aslam, Muhammad Letter to the editor 529
Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia. Bayramoglu, Elvan; Keskin, Meliksah; Aycan, Zehra; Savas-Erdeve, Senay; Cetinkaya, Semra Report 5087
Midkine: Utility as a Predictor of Early Diabetic Nephropathy in Children with Type 1 Diabetes Mellitus. Metwalley, Kotb Abbass; Farghaly, Hekma Saad; Gabri, Magda Farghali; Abdel-Aziz, Safwat Mohamed; Ism Report 4717
Pre-treatment Neutropenia in Children and Adolescents with Autoimmune Hyperthyroidism. Litao, Melissa Kaori S.; Alvarez, Ana Gutierrez; Shah, Bina Report 3829
The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region. Yalcintepe, Sinem; Comlek, Fatma Ozguc; Gurkan, Hakan; Demir, Selma; Atli, Emine Ikbal; Atli, Engin; Report 6368
Traditional and New Methods of Bone Age Assessment-An Overview. Prokop-Piotrkowska, Monika; Marszalek-Dziuba, Kamila; Moszczynska, Elzbieta; Szalecki, Mieczyslaw; J Report 9421
Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin. Bizzarri, Carla; Giannone, Germana Antonella; Gervasoni, Jacopo; Benedetti, Sabina; Albanese, Federi Clinical report 3015
Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations. Gundogan, Begumhan Demir; Sagcan, Fatih; Bozdogan, Sevcan Tug; Balci, Yuksel; Daloglu, Ferah Tuncel; Report 3493

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