User profiles for Gonul Parmaksiz
gönül parmaksızBaşkent Üniversitesinde Çocuk Nefroloji uzmanı Verified email at baskent.edu.tr Cited by 358 |
Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
Background ADCK4-related glomerulopathy is an important differential diagnosis in adolescents
with steroid-resistant nephrotic syndrome (SRNS) and/or chronic kidney disease (CKD) …
with steroid-resistant nephrotic syndrome (SRNS) and/or chronic kidney disease (CKD) …
Role of new biomarkers for predicting renal scarring in vesicoureteral reflux: NGAL, KIM-1, and L-FABP
Background Reflux nephropathy is the most serious complication of vesicoureteral reflux (VUR).
The aim of this study was to assess the role of urinary levels of neutrophil-gelatinase-…
The aim of this study was to assess the role of urinary levels of neutrophil-gelatinase-…
Urinary NGAL, KIM-1 and L-FABP concentrations in antenatal hydronephrosis
Introduction The clinical tests currently in use for obstructive nephropathy (such as renal
ultrasonography, differential radionuclide renal scans and urinary creatinine concentration data) …
ultrasonography, differential radionuclide renal scans and urinary creatinine concentration data) …
Case of large placental chorioangioma associated with diffuse neonatal hemangiomatosis
…, H Karabiber, M Yuksel, G Parmaksiz… - Pediatric and …, 2004 - journals.sagepub.com
Chorioangioma is the most frequent nontrophoblastic tumor of the placenta with a incidence
ranging from 0.01 to 1.3%. Vascular anomalies of the placenta coincidental with infantile …
ranging from 0.01 to 1.3%. Vascular anomalies of the placenta coincidental with infantile …
[HTML][HTML] Diagnostic importance of 3D CT images in Klippel-Feil syndrome with multiple skeletal anomalies: a case report
…, H Karabiber, KZ Yuksel, G Parmaksiz - Korean Journal of …, 2005 - ncbi.nlm.nih.gov
We present here the case of a 12-year-old boy who had Klippel-Feil syndrome with renal,
cardiac and multiple skeletal anomalies, and we show the relevent three-dimensional …
cardiac and multiple skeletal anomalies, and we show the relevent three-dimensional …
Hypothalamic hamartoma associated with a craniopharyngeal canal
…, T Yildirim, L Sener, G Parmaksiz… - American journal …, 2005 - Am Soc Neuroradiology
Hypothalamic hamartoma is a rare congenital lesion. We present the case of a 7-year-old
girl who suffered from precocious puberty, the cause of which was diagnosed by using MR …
girl who suffered from precocious puberty, the cause of which was diagnosed by using MR …
Can RDW be used as a screening test for subclinical inflammation in children with FMF? Is RDW related to MEFV gene mutations?
G Parmaksız, ZA Noyan - Clinical rheumatology, 2023 - Springer
Objective Subclinical inflammation, an insidious feature of familial Mediterranean fever (FMF),
can lead to life-threatening amyloidosis. We aimed to investigate acute phase reactants …
can lead to life-threatening amyloidosis. We aimed to investigate acute phase reactants …
An overlooked association of brachial plexus palsy: diaphragmatic paralysis
…, KU Ozkan, M Garipardic, G Parmaksiz - Acta paediatrica …, 2004 - airitilibrary.com
Diaphragmatic paralysis in newborns is related to brachial plexus palsy. It can be overlooked
if thorough examination isn't done. We present a two-weeks-old baby with a birth weight of …
if thorough examination isn't done. We present a two-weeks-old baby with a birth weight of …
Outcome of immunosuppression in children with IgA vasculitis–related nephritis
…, M Pańczyk-Tomaszewska, G Parmaksiz… - Nephrology Dialysis …, 2024 - academic.oup.com
Background Immunoglobulin A vasculitis with nephritis (IgAVN) is the most common vasculitis
in children. Due to a lack of evidence, treatment recommendations are based on expert …
in children. Due to a lack of evidence, treatment recommendations are based on expert …
Could plasma based therapies still be considered in selected cases with atypical hemolytic uremic syndrome?
…, E Atayar, A Delibas, G Parmaksiz… - Turkish Journal of …, 2021 - avesis.hacettepe.edu.tr
Background. Atypical hemolytic uremic syndrome (aHUS) occurs due to defective regulation
of the alternative complement pathway (ACP) on vascular endothelial cells. Plasma based …
of the alternative complement pathway (ACP) on vascular endothelial cells. Plasma based …