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Articles from Journal of Clinical Research in Pediatric Endocrinology (March 1, 2019)

1-17 out of 17 article(s)
Title Author Type Words
Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort. Touzon, Maria Sol; Garrido, Natalia Perez; Marino, Roxana; Ramirez, Pablo; Costanzo, Mariana; Guerci Report 5807
Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency. Dorr, Helmuth G.; Penger, Theresa; Albrecht, Andrea; Marx, Michaela; Volkl, Thomas M.K. Report 2969
Congenital Hyperinsulinism and Evolution to Sulfonylurea-responsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation. Isik, Emregul; Demirbilek, Huseyin; Houghton, Jayne A.; Ellard, Sian; Flanagan, Sarah E.; Hussain, K Report 3773
Editorial: Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey. Bereket, Abdullah Editorial 2312
Effect of Telehealth System on Glycemic Control in Children and Adolescents with Type 1 Diabetes. Doger, Esra; Bozbulut, Rukiye; Acar, A. Sebnem Soysal; Ercan, Sebnem; Ugurlu, Aylin Kilinc; Akbas, E Report 3865
Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia. Metwalley, Kotb Abbass; Farghaly, Hekma Saad; Abdelhamid, Abdelrahman Report 6600
ERRATUM. Correction notice 139
Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful?. Salman, Dilsah Onerli; Siklar, Zeynep; Ilarslan, Eda Nisa Cullas; Ozcakar, Z. Birsin; Kocaay, Pinar; Report 6143
Extreme Premature Small for Gestational Age Infants Have Appropriate Catch-up Growth at Term Equivalence Compared with Extreme Premature Appropriate for Gestational Age Infants. Ng, Sze May; Pintus, Donatella; Turner, Mark A. Report 3611
Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A. Dursun, Fatma; Ozgurhan, Gamze; Kirmizibekmez, Heves; Keskin, Ece; Hacihamdioglu, Bulent Report 4563
Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey. Ekinci, Rabia Miray Kisla; Gurbuz, Fatih; Balci, Sibel; Bisgin, Atil; Tastan, Mehmet; Yuksel, Bilgin Report 2698
Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner Syndrome. Siller, Alejandro F.; Shimony, Alex; Shinawi, Marwan; Amarillo, Ina; Dehner, Louis P.; Semenkovich, Report 3611
Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment. Kurtoglu, Selim; Ozdemir, Ahmet; Hatipoglu, Nihal Report 6250
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants. Guran, Tulay; Tezel, Basak; Gurbuz, Fatih; Eklioglu, Beray Selver; Hatipoglu, Nihal; Kara, Cengiz; S Report 7853
Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015. Qelmeli, Gamze; Curek, Yusuf; Gulten, Ziimrut Arslan; Yardimsever, Mehmet; Koyun, Mustafa; Akfurin, Report 3959
Severe Neonatal Cholestasis as an Early Presentation of McCune-Albright Syndrome. Coles, Nicole; Comeau, Ian; Munoz, Tatiana; Harrington, Jennifer; Mendoza-Londono, Roberto; Schulze, Report 2228
SLC30A8 Gene rs13266634 C/T Polymorphism in Children with Type 1 Diabetes in Tamil Nadu, India. Thirunavukkarasu, Ramasamy; Asirvatham, Arthur Joseph; Chitra, Ayyappan; Jayalakshmi, Mariakuttikan Report 3492

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