Research Topics
Genomes and Genes | Fatih OzaltinSummaryAffiliation: Hacettepe University Country: Turkey Publications
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Publications
Eye involvement in children with primary focal segmental glomerulosclerosisFatih Ozaltin
Unit of Nephrology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Sihhiye, 06100 Ankara, Turkey
Pediatr Nephrol 23:421-7. 2008..Ophthalmologic evaluation at the time of diagnosis might be beneficial to characterize further the spectrum of this possible association...
The role of apoptosis in childhood Henoch-Schonlein purpuraF Ozaltin
Hacettepe University Faculty of Medicine, Ankara, Turkey
Clin Rheumatol 22:265-7. 2003....
Disruption of PTPRO causes childhood-onset nephrotic syndromeFatih Ozaltin
Pediatric Nephrology Unit, Department of Pediatrics, Hacettepe University Faculty of Medicine, Sihhiye, Ankara, Turkey
Am J Hum Genet 89:139-47. 2011..The present study introduces mutations in PTPRO as another cause of autosomal-recessive nephrotic syndrome...
Apoptosis and proliferation in childhood acute proliferative glomerulonephritisFatih Ozaltin
Pediatric Nephrology, Department of Pediatrics, Hacettepe University Faculty of Medicine, 06100 Sihhiye, Ankara, Turkey
Pediatr Nephrol 20:1572-7. 2005..Further studies, however, are still needed to clarify the importance of these histopathological parameters...
An unusual cause of acute renal failure: renal lymphomaFatih Ozaltin
Nephrology Unit, Department of Pediatrics, Faculty of Medicine, Hacettepe University, Ankara, Turkey
Pediatr Nephrol 19:912-4. 2004....
Evaluation of intima media thickness of the common and internal carotid arteries with inflammatory markers in familial Mediterranean fever as possible predictors for atherosclerosisYelda Bilginer
Department of Pediatric Nephrology and Rheumatology, Hacettepe University Faculty of Medicine, 06100 Sihhiye, Ankara, Turkey
Rheumatol Int 28:1211-6. 2008..Further studies will enlighten whether these patients will be predisposed more to coronary artery disease...
Genetic basis of cystinosis in Turkish patients: a single-center experienceRezan Topaloglu
Dept of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara 06100, Turkey
Pediatr Nephrol 27:115-21. 2012..This study is the first molecular analysis of Turkish cystinosis patients and provides guidance for the molecular diagnosis of cystinosis in this population...
Treatment of severe Henoch-Schönlein nephritis: justifying more immunosuppressionFatma Semsa Altugan
Unit of Pediatric Nephrology and Rheumatology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey
Turk J Pediatr 51:551-5. 2009..Long-term, multicenter controlled studies are needed to verify our results...
Carotid intima-media thickness in children and young adults with renal transplant: Internal carotid artery vs. common carotid arteryYelda Bilginer
Department of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey
Pediatr Transplant 11:888-94. 2007..These changes can be detected by measuring CCA/ICA-IMT ultrasonographically. We suggest that early renal transplantation can potentially avoid long-term cardiovascular events in children with end stage kidney disease...
Right atrial thrombosis complicating renal transplantation in a childYelda Bilginer
Department of Pediatric Nephrology, Hacettepe Unviersity Faculty of Medicine, Ankara, Turkey
Pediatr Transplant 12:251-5. 2008..This report draws attention to the risks that could be associated with thrombosis in renal recipients with congenital or acquired thrombophilias and emphasizes the importance of identifying risk factors for thrombosis in these patients...
Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft functionMukaddes Kalyoncu
Department of Pediatrics, Pediatric Nephrology Unit, Hacettepe University Faculty of Medicine, Ankara, Turkey
Pediatr Transplant 10:168-71. 2006..However, no correlation was found between C0 levels and any of the above parameters. In conclusion, our data suggest that C2 levels are correlated better with dose and serum creatinine level...
Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutationEsra Baskin
Department of Pediatric Nephrology, Baskent University, Ankara, Turkey
Pediatr Nephrol 26:1157-61. 2011..Another, more likely, possibility is that the mitochondriopathy phenotype is caused by another mutation homozygous by descent in a yet unidentified recessive gene...
Influence of Serum Amyloid A (SAA1) and SAA2 gene polymorphisms on renal amyloidosis, and on SAA/C-reactive protein values in patients with familial mediterranean fever in the Turkish populationAysin Bakkaloglu
Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey
J Rheumatol 31:1139-42. 2004..To evaluate the effect of serum amyloid A (SAA) 1 and SAA2 gene polymorphisms on SAA levels and renal amyloidosis in Turkish patients with familial Mediterranean fever (FMF)...
Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study GroupNesrin Besbas
Department of Pediatric Nephrology, Faculty of Medicine, Hacettepe University, Ankara, Turkey
Turk J Pediatr 52:255-61. 2010..Failure to achieve remission is a predictor of renal failure in children with primary FSGS. The use of immunosuppressive treatment in conjunction with prolonged steroid seems beneficial in primary FSGS in children...
Monocyte chemoattractant protein-1 and interleukin-8 levels in children with acute poststreptococcal glomerulonephritisNesrin Besbas
Department of Pediatric Nephrology, Faculty of Medicine, Hacettepe University, 06100 Sihhiye, Ankara, Turkey
Pediatr Nephrol 19:864-8. 2004..Our results emphasize the important role of locally produced chemokines in immune-mediated glomerular injury...
Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in childrenRezan Topaloglu
Department of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey
Pediatr Nephrol 25:919-25. 2010..In conclusion, the recognition of risk factors for UTI, caused by ESBL(+) bacteria in children, may aid in the identification of high-risk cases and may enable proper management of these patients...
A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosisNesrin Besbas
Department of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Sihhiye, 06100 Ankara, Turkey
Eur J Pediatr 168:1449-54. 2009..This is the first report of ARO associated with a novel recessive R561Q variant in CLCN7 gene, in which prenatal diagnosis was made...
Neuroendocrine immune system in familial Mediterranean feverRezan Topaloglu
Unit of Pediatric Nephrology and Rheumatology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey
Turk J Pediatr 52:588-93. 2010....
The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch-Schönlein purpuraFatih Ozaltin
Department of Pediatrics, Unit of Nephrology and Rheumatology, Hacettepe University Faculty of Medicine, Sihhiye, 06100, Ankara, Turkey
Clin Rheumatol 23:426-9. 2004..Positive IgA rheumatoid factor was present in only two patients with HSP. In conclusion, our results suggest that IgA ANCA may be useful to confirm the diagnosis of HSP in children...
Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpuraHande Canpinar
Department of Basic Oncology, Institute of Oncology, Hacettepe University Faculty of Medicine, Ankara, Turkey
Turk J Pediatr 52:22-7. 2010..Further studies will clarify whether tolerance to microbial antigens may have a role in the pathogenesis and course of Henoch-Schönlein purpura...
C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasmaRezan Topaloglu
Department of Pediatric Nephrology and Rheumatology, Faculty of Medicine, Hacettepe University, Ankara 06100, Turkey
Clin Rheumatol 31:1123-6. 2012..Regular fresh frozen plasma infusions to the patient have been clinically and therapeutically successful...
Successful renal transplantation in a child with ANCA-associated microscopic polyangiitisNesrin Besbas
Department of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey
Pediatr Nephrol 18:696-9. 2003..We describe here an unusual pediatric patient with MPO-ANCA-associated rapidly progressive glomerulonephritis (RPGN), emphasizing the management and outcome of the disease...
Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed childrenNesrin Besbas
Unit of Pediatric Nephrology, Hacettepe University, Ankara, Turkey
Pediatr Nephrol 18:1255-9. 2003..In conclusion, the results of this study confirm the presence of high circulating plasma leptin levels, which may be one of the many factors involved in the pathogenesis of the malnutrition in children on hemodialysis...
Bone mineral density in children with familial Mediterranean feverAli Duzova
Department of Pediatrics, Nephrology and Rheumatology Unit, Hacettepe University Faculty of Medicine, Sihhiye 06100 Ankara, Turkey
Clin Rheumatol 23:230-4. 2004..In conclusion, FMF patients had lower BMC, BMD and z-scores than a control group. We suggest that decreased BMD, BMC and z-score in FMF patients may be secondary to subclinical inflammation...
Childhood vasculitides in Turkey: a nationwide surveySeza Ozen
Department of Pediatrics, Faculty of Medicine, Hacettepe University, 06100 Ankara, Turkey
Clin Rheumatol 26:196-200. 2007..The aims of this study were to evaluate the characteristics of childhood vasculitides and to establish the first registry in Turkey, an eastern Mediterranean country with a white population...
Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumabNesrin Besbas
Department of Pediatric Nephrology, Hacettepe University Faculty of Medicine, 06100, Sihhiye, Ankara, Turkey
Pediatr Nephrol 28:155-8. 2013..Tyr1177Cys mutation. CONCLUSION: Eculizumab can be considered as an alternative to plasma therapy in the treatment of specific patients with aHUS, even in infants...
The distribution of juvenile idiopathic arthritis in the eastern Mediterranean: results from the registry of the Turkish Paediatric Rheumatology AssociationErkan Demirkaya
Gulhane Military Medical Acedemy, School of Medicine, Ankara, Turkey
Clin Exp Rheumatol 29:111-6. 2011..To analyse the demographics, main clinical and laboratory features and subtype distribution of juvenile idiopathic arthritis (JIA) in an eastern Mediterranean country, based on a multicentre registry...
CLCN5 mutation (R347X) associated with hypokalaemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent's diseaseNesrin Besbas
Hacettepe University Faculty of Medicine, Department of Pediatric, Ankara, Turkey
Nephrol Dial Transplant 20:1476-9. 2005
Endothelial dysfunction and increased responses to renal nerve stimulation in rat kidneys during rhabdomyolysis-induced acute renal failure: role of hydroxyl radicalOnur Cil
Department of Pharmacology, Faculty of Medicine, Hacettepe University, Ankara, Turkey
Ren Fail 34:211-20. 2012..These findings suggest that decreased endothelium-dependent vasodilation and augmented renal sympathetic tonus contribute to the development of renal vasoconstriction during rhabdomyolysis-induced ARF...
Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndromeRainer G Ruf
Departments of Pediatrics and Human Genetics, University of Michigan, Ann Arbor, Michigan, USA
Kidney Int 66:564-70. 2004..Sporadic mutations in the Wilms' tumor suppressor gene WT1 have been found to be present in patients with SRNS in association with Wilms' tumor (WT) and urinary or genital malformations, as well as in patients with isolated SRNS...
Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9Bettina Mucha
Department of Pediatrics, University of Michigan, Ann Arbor, 48109, USA
Pediatr Res 59:325-31. 2006..Kidney Int 66: 564-570, 2004) indicate that screening of WT1 exons 8 and 9 in patients with sporadic SRNS is sufficient to detect pathogenic WT1 mutations and may open inroads into differential therapy of SRNS...
Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)Bernward G Hinkes
Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA
Pediatrics 119:e907-19. 2007..Therefore, we analyzed all 4 of the genes jointly in a large European cohort of 89 children from 80 families with nephrotic syndrome manifesting in the first year of life and characterized genotype/phenotype correlations...
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndromeBernward Hinkes
Department of Pediatrics, University of Michigan, Ann Arbor, Michigan 48109, USA
J Am Soc Nephrol 19:365-71. 2008..Because the age of onset can vary by several years among those with identical mutations, additional factors may modify the phenotype...
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)Rasheed Gbadegesin
Departments of Pediatrics and of Human Genetics, University of Michigan, Ann Arbor, MI 48109, USA
Nephrol Dial Transplant 23:1291-7. 2008..Mutations in two other genes WT1 and LAMB2 may also cause IDMS. We therefore determine in this study the relative frequency of mutations in PLCE1, WT1 or LAMB2 as the cause of IDMS in a worldwide cohort...
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversibleBernward Hinkes
Department of Pediatrics, University of Michigan, Ann Arbor, Michigan 48109, USA
Nat Genet 38:1397-405. 2006..These findings, together with the zebrafish model of human nephrotic syndrome generated by plce1 knockdown, open new inroads into pathophysiology and treatment mechanisms of nephrotic syndrome...
Novel OCRL1 mutations in patients with the phenotype of Dent diseaseBoris Utsch
, , Erlangen, Germany
Am J Kidney Dis 48:942.e1-14. 2006..It remains to be elucidated why the various OCRL1 mutations found in patients with Dent 2 disease do not cause cataracts...
Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?Fatih Ozaltin
Clin Rheumatol 23:186-7. 2004
Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndromeYasemin Isik Balci
Eur J Pediatr 166:757-8; author reply 759. 2007
