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Toplam kayıt 15, listelenen: 11-15
A Pheochromocytoma Case Diagnosed As Adrenal Incidentaloma
(Turkish J Pediatrics, 2017)
There are two problems that needs to be addressed in cases of an adrenal incidentaloma. The first is to decide whether the adrenal mass is benign or malignant, and the second is to determine whether the mass is hormonally ...
Predictors of Methotrexate Response in Turkish Children with Oligoarticular and Polyarticular Juvenile Idiopathic Arthritis
(Turkish J Pediatrics, 2017)
Methotrexate (MTX) is the most commonly used disease modifying antirheumatic drug in juvenile idiopathic arthritis (JIA). We aimed to define predictor factors for response to MTX in Turkish children with oligo- and ...
Management Strategies for Cln2 Disease
(Elsevier Science Inc, 2017)
CLN2 disease (neuronal ceroid lipofuscinosis type 2) is a rare, autosomal recessive, pediatric-onset, rapidly progressive neurodegenerative lysosomal storage disorder caused by tripeptidyl peptidase 1 (TPP1) enzyme deficiency, ...
Polyposis Deserves a Perfect Physical Examination for Final Diagnosis: Bannayan-Riley-Ruvalcaba Syndrome
(Turkish J Pediatrics, 2017)
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal dominant inherited polyposis syndrome characterized by macrocephaly, lipomatosis, hemangiomatosis, intestinal polyposis and pigmented macules on penis. The ...
An International Consortium Update: Pathophysiology, Diagnosis, and Treatment of Polycystic Ovarian Syndrome in Adolescence
(Karger, 2017)
This paper represents an international collaboration of paediatric endocrine and other societies (listed in the Appendix) under the International Consortium of Paediatric Endocrinology (ICPE) aiming to improve worldwide ...