Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Zelal Bircan"'
Autor:
Ayşe Sevim Gökalp, Ayla Günlemez, Gülcan Türker, Zelal Bircan, Gamze Özsoy, Ayşe Engin Arısoy
Publikováno v:
Pediatrics International. 53:483-488
Background: The aim of the present study was to determine, using the score for neonatal acute physiology and perinatal extension II (SNAPPE-II), whether there is an association with acute renal failure (ARF) and whether it is possible to identify new
Publikováno v:
Pediatrics International. 47:95-98
Calciphylaxis (calcific uremic arteriolopathy) is a vasculopathy that is often defined in patients due to renal failure, however, some patients with calciphylaxis do not show secondary or tertiary hyperparathyroidism. It results from mural calcificat
Autor:
Veli Uysal, Zelal Bircan, Denis Ponard, Seyhun Solakoglu, Isin Kilicaslan, Demet Toprak, Gülcan Türker
Publikováno v:
Nephrology Dialysis Transplantation. 19:727-730
A 12-month-old boy presented to a local hospital with periorbital oedema and microscopic haematuria. He was pale and hypertensive and had low serum complement C3. He was treated for and followed with the diagnosis of acute post-streptococcal glomerul
Publikováno v:
The Indian Journal of Pediatrics. 77:1329-1331
The causes of hereditary nephrogenic diabetes insipidus (HNDI) are the mutations in the arginine vasopressin V2 receptor gene (AVPR2) (90%) and aquaporin 2 gene (AQP2) (10%). Although it is possible to perform mutation analysis where available, diffe
Publikováno v:
Pediatric Radiology. 40:1285-1287
A 16-year-old boy was admitted to our hospital with uncontrolled hypertension. A left renal artery aneurysm was detected on colour Doppler US and CT. Renal arteriography demonstrated the aneurysm and focal renal parenchymal areas of decreased perfusi
Publikováno v:
Pediatric Nephrology. 23:663-665
Autosomal recessive nephrogenic diabetes insipidus (ARNDI) is a rare disease usually seen in patients with consanguineous parents. We report on a case of ARNDI in a patient with non-consanguineous parents who presented with recurrent febrile attacks.
Publikováno v:
International Urology and Nephrology. 27:27-32
This prospective study was designed to investigate the most relevant radiological approach for the evaluation of urinary tract infections (UTI) in childhood. In the first 48 hours following the diagnosis of UTI, all patients underwent 99mTc dimercapt
Autor:
Bülent Kara, Zelal Bircan
Publikováno v:
Pediatrics International. 45:65-67
Background: Steroid dependency is a major problem seen after therapy for idiopathic nephrotic syndrome in childhood. Although there is consensus about the usage of cyclophosphamide (CYC) in frequent relapsers, there is still a controversy concerning
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 53(4)
The aim of the present study was to determine, using the score for neonatal acute physiology and perinatal extension II (SNAPPE-II), whether there is an association with acute renal failure (ARF) and whether it is possible to identify newborns at ris
Autor:
Nicolino, Ruperto, Seza, Ozen, Angela, Pistorio, Pavla, Dolezalova, Paul, Brogan, David A, Cabral, Ruben, Cuttica, Raju, Khubchandani, Daniel J, Lovell, Kathleen M, O'Neil, Pierre, Quartier, Angelo, Ravelli, Silvia M, Iusan, Giovanni, Filocamo, Claudia Saad, Magalhães, Erbil, Unsal, Sheila, Oliveira, Claudia, Bracaglia, Arvind, Bagga, Valda, Stanevicha, Silvia Magni, Manzoni, Polyxeni, Pratsidou, Loredana, Lepore, Graciela, Espada, Isabella, Kone-Paut, Isabelle Kone, Paut, Francesco, Zulian, Patrizia, Barone, Zelal, Bircan, Maria del Rocio, Maldonado, Ricardo, Russo, Iris, Vilca, Kjell, Tullus, Rolando, Cimaz, Gerd, Horneff, Jordi, Anton, Stella, Garay, Susan, Nielsen, Giancarlo, Barbano, Alberto, Martini
Publikováno v:
Annals of the rheumatic diseases, 69(5), 790-797. BMJ Publishing Group
OBJECTIVES: To report methodology and overall clinical, laboratory and radiographic characteristics for Henoch-Schönlein purpura (HSP), childhood polyarteritis nodosa (c-PAN), c-Wegener granulomatosis (c-WG) and c-Takayasu arteritis (c-TA) classific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca6ede8e700f734624e8c2c539660121
http://hdl.handle.net/11567/277033
http://hdl.handle.net/11567/277033