Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Renal Biopsy Prognostic Findings in Children With Atypical Hemolytic Uremic Syndrome

PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, cilt.23, sa.5, ss.362-371, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Surgical management of renovascular hypertension in children and young adults: a 13-year experience

INTERACTIVE CARDIOVASCULAR AND THORACIC SURGERY, cilt.29, sa.5, ss.746-752, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

An immunohistochemical approach to detect oncogenic CTNNB1 mutations in primary neoplastic tissues

LABORATORY INVESTIGATION, cilt.99, sa.1, ss.128-137, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, cilt.21, sa.10, ss.1857-1862, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

TURKISH ATYPICAL HEMOLYTIC UREMIC SYNDROME REGISTRY: ECULIZUMAB TREATMENT IN AHUS PATIENTS

PEDIATRIC NEPHROLOGY, cilt.33, sa.10, ss.1832, 2018 (SCI İndekslerine Giren Dergi) identifier

CLINICAL AND PATHOLOGIC CHARACTERISTICS OF GENETICALLY CONFIRMED ALPORT SYNDROME PATIENTS

PEDIATRIC NEPHROLOGY, cilt.33, sa.10, ss.1826-1827, 2018 (SCI İndekslerine Giren Dergi) identifier

LUPUS NEPHRITIS: LONG TERM FOLLOW-UP AND EFFECT OF TREATMENT ON GROWTH

PEDIATRIC NEPHROLOGY, cilt.33, sa.10, ss.1947, 2018 (SCI İndekslerine Giren Dergi) identifier

ACUTE HEMODIALYSIS EXPERIENCE IN CHILDREN WEIGHING LESS THAN 15 KG

PEDIATRIC NEPHROLOGY, cilt.33, sa.10, ss.1893, 2018 (SCI İndekslerine Giren Dergi) identifier

GASTROINTESTINAL SYSTEM INVOLVEMENT IN ATYPICAL HEMOLYTIC UREMIC SYNDROME

PEDIATRIC NEPHROLOGY, cilt.33, sa.10, ss.1843, 2018 (SCI İndekslerine Giren Dergi) identifier

Extra-Renal manifestations of atypical hemolytic uremic syndrome in children

PEDIATRIC NEPHROLOGY, cilt.33, sa.8, ss.1395-1403, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Nephropathic Cystinosis Mimicking Bartter Syndrome A Novel Mutation

IRANIAN JOURNAL OF KIDNEY DISEASES, cilt.12, sa.1, ss.61-63, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

NATURE GENETICS, cilt.49, sa.10, ss.1529-1541, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.28, sa.10, ss.3055-3065, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

CLINICAL CHARACTERISTICS OF PATIENTS WITH MTORI CONVERSION AND EFFECTS ON RENAL OUTCOME

PEDIATRIC NEPHROLOGY, cilt.32, sa.9, ss.1803, 2017 (SCI İndekslerine Giren Dergi) identifier

GENETIC AND CLINICAL CHARACTERISTICS OF PATIENTS WITH C3 GLOMERULOPATHY

PEDIATRIC NEPHROLOGY, cilt.32, sa.9, ss.1669, 2017 (SCI İndekslerine Giren Dergi) identifier

IS RAAS BLOCKADE EFFECTIVE IN NPHS2 GLOMERULOPATHY?

PEDIATRIC NEPHROLOGY, cilt.32, sa.9, ss.1661, 2017 (SCI İndekslerine Giren Dergi) identifier

Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment

PEDIATRIC NEPHROLOGY, cilt.32, sa.8, ss.1369-1375, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Loss of diacylglycerol kinase epsilon in mice causes endothelial distress and impairs glomerular Cox-2 and PGE(2) production

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, cilt.310, sa.9, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.27, sa.1, ss.63-68, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Lupus in a patient with cystinosis: is it drug induced?

LUPUS, cilt.24, sa.13, ss.1452-1454, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

NEPHROPATHIC CYSTINOSIS MIMICKING BARTTER SYNDROME: NOVEL MUTATION

PEDIATRIC NEPHROLOGY, cilt.30, sa.9, ss.1681, 2015 (SCI İndekslerine Giren Dergi) identifier

RESULTS OF TURKISH MULTICENTRIC NATIONAL CYSTINOSIS REGISTRY

PEDIATRIC NEPHROLOGY, cilt.30, sa.9, ss.1668-1669, 2015 (SCI İndekslerine Giren Dergi) identifier

Diagnostic validity of colchicine in patients with Familial Mediterranean fever

CLINICAL RHEUMATOLOGY, cilt.33, sa.7, ss.969-974, 2014 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

AMERICAN JOURNAL OF HUMAN GENETICS, cilt.94, sa.6, ss.884-890, 2014 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Post-transplant hypertension in pediatric kidney transplant recipients

PEDIATRIC NEPHROLOGY, cilt.29, sa.6, ss.1075-1080, 2014 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Primary coenzyme Q(10) (CoQ(10)) deficiencies and related nephropathies

PEDIATRIC NEPHROLOGY, cilt.29, sa.6, ss.961-969, 2014 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Genotype-phenotype associations in WT1 glomerulopathy

KIDNEY INTERNATIONAL, cilt.85, sa.5, ss.1169-1178, 2014 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Proteinuria in Frasier Syndrome

SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, cilt.141, ss.685-688, 2013 (SCI İndekslerine Giren Dergi) identifier identifier identifier

DGKE Variants Cause a Glomerular Microangiopathy That Mimics Membranoproliferative GN

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.24, sa.3, ss.377-384, 2013 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab

PEDIATRIC NEPHROLOGY, cilt.28, sa.1, ss.155-158, 2013 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Circulating suPAR in Two Cohorts of Primary FSGS

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.23, sa.12, ss.2051-2059, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

WT1 screening in nephrotic syndrome - lessons from PodoNet

PEDIATRIC NEPHROLOGY, cilt.27, sa.9, ss.1617-1618, 2012 (SCI İndekslerine Giren Dergi) identifier

PERITONEAL DIALYSIS IN CHILDREN UNDER TWO YEARS OF AGE

PEDIATRIC NEPHROLOGY, cilt.27, sa.9, ss.1799-1800, 2012 (SCI İndekslerine Giren Dergi) identifier

Rituximab in steroid-dependent and resistant nephrotic syndrome patients

PEDIATRIC NEPHROLOGY, cilt.27, sa.9, ss.1710-1711, 2012 (SCI İndekslerine Giren Dergi) identifier

ATYPICAL HUS AND ECULIZUMAB TREATMENT: EXPERIENCE OF A TERTIARY CENTER

PEDIATRIC NEPHROLOGY, cilt.27, sa.9, ss.1630, 2012 (SCI İndekslerine Giren Dergi) identifier

THE BENEFITS OF CYCLOSPORINE TREATMENT OF THE PATIENT WITH NPHS2 MUTATION

PEDIATRIC NEPHROLOGY, cilt.27, sa.9, ss.1703-1704, 2012 (SCI İndekslerine Giren Dergi) identifier

Genetic basis of cystinosis in Turkish patients: a single-center experience

PEDIATRIC NEPHROLOGY, cilt.27, sa.1, ss.115-121, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome

AMERICAN JOURNAL OF HUMAN GENETICS, cilt.89, sa.1, ss.139-147, 2011 (SCI İndekslerine Giren Dergi) identifier identifier identifier

MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis

NEW ENGLAND JOURNAL OF MEDICINE, cilt.365, sa.4, ss.295-306, 2011 (SCI İndekslerine Giren Dergi) identifier identifier

Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation

PEDIATRIC NEPHROLOGY, cilt.26, sa.7, ss.1157-1161, 2011 (SCI İndekslerine Giren Dergi) identifier identifier identifier

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

JOURNAL OF CLINICAL INVESTIGATION, cilt.121, sa.5, ss.2013-2024, 2011 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Spondyloenchondrodysplasia with Systemic Lupus Erythematosus: a report of three cases

CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.29, sa.2, ss.430, 2011 (SCI İndekslerine Giren Dergi) identifier

The bone and mineral disorder of children undergoing chronic peritoneal dialysis

KIDNEY INTERNATIONAL, cilt.78, sa.12, ss.1295-1304, 2010 (SCI İndekslerine Giren Dergi) identifier identifier

Neuroendocrine immune system in familial Mediterranean fever

TURKISH JOURNAL OF PEDIATRICS, cilt.52, sa.6, ss.588-593, 2010 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.5, sa.9, ss.1655-1662, 2010 (SCI İndekslerine Giren Dergi) identifier identifier identifier

New syndrome - Situs inversus totalis with cystic dysplasia of kidneys, pancreas and bowing

CLINICAL DYSMORPHOLOGY, cilt.19, sa.3, ss.173-174, 2010 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis

EUROPEAN JOURNAL OF PEDIATRICS, cilt.168, sa.12, ss.1449-1454, 2009 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Treatment of severe Henoch-Schonlein nephritis: justifying more immunosuppression

TURKISH JOURNAL OF PEDIATRICS, cilt.51, sa.6, ss.551-555, 2009 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

NEPHROLOGY DIALYSIS TRANSPLANTATION, cilt.23, sa.11, ss.3527-3533, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

NEPHROLOGY DIALYSIS TRANSPLANTATION, cilt.23, sa.4, ss.1291-1297, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Right atrial thrombosis complicating renal transplantation in a child

PEDIATRIC TRANSPLANTATION, cilt.12, sa.2, ss.251-255, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.19, sa.2, ss.365-371, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome

EUROPEAN JOURNAL OF PEDIATRICS, cilt.166, sa.7, ss.757-758, 2007 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Childhood vasculitides in Turkey: a nationwide survey

CLINICAL RHEUMATOLOGY, cilt.26, sa.2, ss.196-200, 2007 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Novel OCRL1 mutations in patients with the phenotype of dent disease

AMERICAN JOURNAL OF KIDNEY DISEASES, cilt.48, sa.6, ss.942-954, 2006 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Serum IgD concentrations in patients with ataxia telangiectasia and with selective IgA deficiency

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, cilt.116, sa.3, ss.246, 1998 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

PEPTIDE BIOMARKER SIGNATURES IN STEROID-RESISTANT NEPHROTIC SYNDROME

55th Congress of the European-Renal-Association (ERA) and European-Dialysis-and-Transplantation-Association (EDTA), Copenhagen, Danimarka, 24 - 27 Mayıs 2018, cilt.33 identifier

Çocuk ve genç erişkinlerde renovasküler hipertansiyonda cerrahi tedaviler.

18. Ulusal Vasküler ve Endovasküler Cerrahi Kongresi 9. Ulusal Fleboloji Kongresi, Girne, Kıbrıs (Kktc), 9 - 12 Aralık 2017

Çocuk ve Genç Erişkinlerde Renovasküler Hipertansiyonda Cerrahi Tedavi

18. Ulusal Vasküler ve Endovasküler Cerrahi Kongresi, Türkiye, 9 - 12 Kasım 2017

SMARCAL1 SCREENING IN NEPHROTIC SYNDROME - LESSONS FROM PODONET

53rd ERA-EDTA Congress, Vienna, Avusturya, 21 - 24 Mayıs 2016, cilt.31, ss.353-354 identifier

NORMAL 25-HYDROXYVITAMIN D LEVELS ARE ASSOCIATED WITH LESS PROTEINURIA AND ATTENUATE RENAL FAILURE PROGRESSION IN CHILDREN WITH CHRONIC KIDNEY DISEASE

52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 - 31 Mayıs 2015, cilt.30 identifier

CONVERSION TO SIROLIMUS IN PEDIATRIC RENAL TRANSPLANT RECIPIENTS

50th European-Renal-Association - European-Dialysis-and-Transplant-Association Congress, İstanbul, Türkiye, 18 - 21 Mayıs 2013, cilt.28, ss.294 identifier

Eye involvement in children with primary FSGS

44th ERA-EDTA Congress, Barcelona, İspanya, 22 - 24 Haziran 2007, cilt.22, ss.292 identifier