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Co‐existence of renovascular hypertension, polyarteritis nodosa, antiphospholipid syndrome and methylenetetrahydrofolate reductase mutation

Pediatrics international, 2013-08, Vol.55 (4), p.e107-e110

2013

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Nonconvulsive status epilepticus due to drug induced neurotoxicity in chronically ill children

Brain & development (Tokyo. 1979), 2012-11, Vol.34 (10), p.824-828

2012

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Increased Serum Levels of Insulin-Like Growth Factor (IGF)-1 and IGF-Binding Protein-3 in Henoch-Schonlein Purpura

The Tohoku Journal of Experimental Medicine, 2008, Vol.214(4), pp.333-340

2008

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IgG1 deficiency and high IgA level with juvenile idiopathic arthritis

European journal of pediatrics, 2007-11, Vol.166 (11), p.1179-1180

2007

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CD19 + CD23+ B cells, CD4 + CD25+ T cells, E-selectin and interleukin-12 levels in children with steroid sensitive nephrotic syndrome

Italian journal of pediatrics, 2013-07, Vol.39 (1), p.42-42, Article 42

2013

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Hyperkalemia in children with nephrotic syndrome

Iranian journal of kidney diseases, 2013-07, Vol.7 (4), p.326

2013

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Acute renal failure in two infants due to ureteropelvic fungi balls

Pediatrics international, 2002-02, Vol.44 (1), p.112-114

2002

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Childhood vasculitides in Turkey: a nationwide survey

Clinical rheumatology, 2007-02, Vol.26 (2), p.196-200

2007

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Serum and urinary leptin and ghrelin in children with nephrotic syndrome

Neuro-endocrinology letters, 2013, Vol.34 (5), p.388-394

2013

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IGF-1, IGFBP-3, VEGF and MMP-9 levels and their potential relationship with renal functions in patients with compensatory renal growth

Clinical physiology and functional imaging, 2008-03, Vol.28 (2), p.107-112

2008

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ANTIOXIDANT STATUS IN JUVENILE IDIOPATHIC ARTHRITIS

Turkish journal of pediatrics, 2008-01, Vol.50, p.60

2008

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Antibiotic resistance in children with complicated urinary tract infection

Saudi medical journal, 2007-12, Vol.28 (12), p.1850

2007

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Plasma and urinary endothelin-1 concentrations in asphyxiated newborns [corrected]

Neuro-endocrinology letters, 2007-06, Vol.28 (3), p.284-288

2007

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Atypical hemolytic uremic syndrome associated with group A beta hemolytic streptococcus

Pediatric nephrology (Berlin, West), 2004-08, Vol.19 (8), p.943

2004

Volltextzugriff (PDF)

A patient with cystinosis presenting transient features of Bartter syndrome

Turkish journal of pediatrics, 2006-07, Vol.48 (3), p.260-262

2006

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Evaluation of the Relationship Between Mutation Type and Clinical Symptoms in Patients with Familial Mediterranean Fever

Turkish Journal of Pediatric Disease, 2013-12, Vol.7 (4), p.173-177

2013

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Triplets with growth failure, microcephaly, mental retardation, nail hypoplasia and corpus callosum agenesis: is it a variant of Coffin-Siris or a new syndrome?

Turkish journal of pediatrics, 2000-04, Vol.42 (2), p.171

2000

Volltextzugriff (PDF)

Renal involvement in the Laurence-Moon-Bardet-Biedl syndrome : report of five cases

Pediatric nephrology (Berlin, West), 1997-02, Vol.11 (1), p.31-35

1997

Volltextzugriff (PDF)

Renal function in children with hypercalciuria

Turkish journal of pediatrics, 1997-07, Vol.39 (3), p.335

1997

Volltextzugriff (PDF)

Co-existence of renovascular hypertension, polyarteritis nodosa, antiphospholipid syndrome and methylenetetrahydrofolate reductase mutation

Pediatrics International, 2013, Vol.55 (4), p.e107-e110

2013

Volltextzugriff (PDF)

N-acetyl-beta-D-glucosaminidase excretion in patients with unilateral renal agenesis or nephrectomy in childhood

Turkish journal of pediatrics, 1996-10, Vol.38 (4), p.485

1996

Volltextzugriff (PDF)

Diagnostic value of renal arteriography in polyarteritis nodosa

Turkish journal of pediatrics, 1996-01, Vol.38 (1), p.101

1996

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Diabetes insipidus in a pediatric patient with systemic lupus erythematosus. A case report

Turkish journal of pediatrics, 1997-04, Vol.39 (2), p.281

1997

Volltextzugriff (PDF)

Effect of vasoactive intestinal peptide and naloxone combination on urinary N-acetyl-beta-D-glucosaminidase level and kidney histology of rats exposed to severe hemorrhage

Pharmacology, 1993-09, Vol.47 (3), p.194

1993

Volltextzugriff (PDF)

Atypical hemolytic uremic syndrome associated with group A beta hemolytic streptococcus

Pediatric nephrology (Berlin, Germany), 2004, Vol.19 (8), p.943-4; author reply 945

2004

Volltextzugriff (PDF)

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Co‐existence of renovascular hypertension, polyarteritis nodosa, antiphospholipid syndrome and methylenetetrahydrofolate reductase mutation

Nonconvulsive status epilepticus due to drug induced neurotoxicity in chronically ill children

Increased Serum Levels of Insulin-Like Growth Factor (IGF)-1 and IGF-Binding Protein-3 in Henoch-Schonlein Purpura

IgG1 deficiency and high IgA level with juvenile idiopathic arthritis

CD19 + CD23+ B cells, CD4 + CD25+ T cells, E-selectin and interleukin-12 levels in children with steroid sensitive nephrotic syndrome

Hyperkalemia in children with nephrotic syndrome

Acute renal failure in two infants due to ureteropelvic fungi balls

Childhood vasculitides in Turkey: a nationwide survey

Serum and urinary leptin and ghrelin in children with nephrotic syndrome

IGF-1, IGFBP-3, VEGF and MMP-9 levels and their potential relationship with renal functions in patients with compensatory renal growth

ANTIOXIDANT STATUS IN JUVENILE IDIOPATHIC ARTHRITIS

Antibiotic resistance in children with complicated urinary tract infection

Plasma and urinary endothelin-1 concentrations in asphyxiated newborns [corrected]

Atypical hemolytic uremic syndrome associated with group A beta hemolytic streptococcus

A patient with cystinosis presenting transient features of Bartter syndrome

Evaluation of the Relationship Between Mutation Type and Clinical Symptoms in Patients with Familial Mediterranean Fever

Triplets with growth failure, microcephaly, mental retardation, nail hypoplasia and corpus callosum agenesis: is it a variant of Coffin-Siris or a new syndrome?

Renal involvement in the Laurence-Moon-Bardet-Biedl syndrome : report of five cases

Renal function in children with hypercalciuria

Co-existence of renovascular hypertension, polyarteritis nodosa, antiphospholipid syndrome and methylenetetrahydrofolate reductase mutation

N-acetyl-beta-D-glucosaminidase excretion in patients with unilateral renal agenesis or nephrectomy in childhood

Diagnostic value of renal arteriography in polyarteritis nodosa

Diabetes insipidus in a pediatric patient with systemic lupus erythematosus. A case report

Effect of vasoactive intestinal peptide and naloxone combination on urinary N-acetyl-beta-D-glucosaminidase level and kidney histology of rats exposed to severe hemorrhage

Atypical hemolytic uremic syndrome associated with group A beta hemolytic streptococcus

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