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Renal biopsy in children with IgA vasculitis

Brazilian Journal of Nephrology, 2022-01, Vol.44 (1), p.48-57

2022

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Urotensin-II:More Than a Mediator for Kidney

International Journal of Nephrology, 2012-01, Vol.2012 (2012), p.120-126

2012

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Increased potassium excretion in children with monosymptomatic nocturnal enuresis: could it be related to Kir 4.1- KCNJ10 gene polymorphism?

The Turkish journal of pediatrics, 2020, Vol.62 (2), p.208-214

2020

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P73 A rare case: Thrombotic thrombocytopenic purpura presenting with acute kidney injury

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A185

2019

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Renal biopsy in children with IgA vasculitis

Brazilian Journal of Nephrology, 2022-03, Vol.44 (1), p.48-57

2022

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Pediatric post‐streptococcal glomerulonephritis: Clinical and laboratory data

Pediatrics international, 2018-07, Vol.60 (7), p.645-650

2018

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Autoimmune polyglandular syndrome type 3c with ectodermal dysplasia, immune deficiency and hemolytic-uremic syndrome

Journal of clinical research in pediatric endocrinology, 2014-01, Vol.6 (1), p.47-50

2014

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Hyponatremic-hypertensive Syndrome in a 19-month-old Boy with Renovascular Hypertension

Saudi journal of kidney diseases and transplantation, 2022-02, Vol.33 (7), p.87-90

2022

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ACE Gene Polymorphism in Turkish Children with Nephrotic Syndrome

Renal failure, 2006-01, Vol.28 (5), p.401-403

2006

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Mitral annular calcification and brown tumor of the rib in a child with chronic renal failure

Pediatric nephrology (Berlin, West), 2005-05, Vol.20 (5), p.673-675

2005

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May the Best Friend be an Enemy if not Recognized Early: Hypernatremic Dehydration due to Breastfeeding

Pediatric emergency care, 2005-07, Vol.21 (7), p.445-448

2005

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A Pediatric Case Presented with Posterior Reversible Encephalopathy Due to Cystinosis: Case Report

Turkiye Klinikleri Journal of Pediatrics, 2016-05, Vol.25 (1), p.52-55

2016

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Prevalence of hypertension determined by ambulatory blood pressure monitoring (ABPM) and body composition in long-term survivors of childhood cancer

Pediatric hematology and oncology, 2018-02, Vol.35 (1), p.1-10

2018

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Evaluation of disease outcome with demographic,clinical and laboratory features of childhood-onset systemic lupus erythematosus: Single center experience

Annals of medical research, 2020-02, Vol.27 (2), p.628

2020

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Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome

Pediatric nephrology (Berlin, West), 2018-02, Vol.33 (2), p.295-303

2018

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Bartter syndrome and growth hormone deficiency: three cases

Pediatric nephrology (Berlin, West), 2012-11, Vol.27 (11), p.2145-2148

2012

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ACE gene polymorphism in Turkish children with acute post streptococcal glomerulonephritis

Turkish archives of pediatrics, 2006-09, Vol.41 (3), p.151

2006

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Angiotensin Converting Enzyme Gene Polymorphism in Children with Henoch-Schonlein Purpura

Çocuk dergisi = The journal of the pediatrics, 2013-09, Vol.13 (1), p.11-15

2013

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Barttin mutations in antenatal Bartter syndrome with sensorineural deafness

Pediatric nephrology (Berlin, West), 2006-07, Vol.21 (7), p.1056-1057

2006

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An unusual cause of pleural effusion, urinothorax in a child with urinary stone disease

Pediatric nephrology (Berlin, West), 2005-10, Vol.20 (10), p.1487-1489

2005

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Hyponatremic-hypertensive Syndrome in a 19-month-old Boy with Renovascular Hypertension

Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 2022, Vol.33, p.S87-S90

2022

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A child with Beckwith-Wiedemann syndrome and posterior urethral valves

Genetic counseling, 2005, Vol.16 (1), p.41

2005

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Changes in Osmolal Gap and Osmolality in Children with Chronic and End-Stage Renal Failure

Nephron, 2007-01, Vol.105 (2), p.p19

2007

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Barttin mutations in antenatal Bartter syndrome with sensorineural deafness

Pediatric nephrology (Berlin, Germany), 2006, Vol.21 (7), p.1056-1057

2006

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Renal biopsy in children with IgA vasculitis

Urotensin-II:More Than a Mediator for Kidney

Increased potassium excretion in children with monosymptomatic nocturnal enuresis: could it be related to Kir 4.1- KCNJ10 gene polymorphism?

P73 A rare case: Thrombotic thrombocytopenic purpura presenting with acute kidney injury

Renal biopsy in children with IgA vasculitis

Pediatric post‐streptococcal glomerulonephritis: Clinical and laboratory data

Autoimmune polyglandular syndrome type 3c with ectodermal dysplasia, immune deficiency and hemolytic-uremic syndrome

Hyponatremic-hypertensive Syndrome in a 19-month-old Boy with Renovascular Hypertension

ACE Gene Polymorphism in Turkish Children with Nephrotic Syndrome

Mitral annular calcification and brown tumor of the rib in a child with chronic renal failure

May the Best Friend be an Enemy if not Recognized Early: Hypernatremic Dehydration due to Breastfeeding

A Pediatric Case Presented with Posterior Reversible Encephalopathy Due to Cystinosis: Case Report

Prevalence of hypertension determined by ambulatory blood pressure monitoring (ABPM) and body composition in long-term survivors of childhood cancer

Evaluation of disease outcome with demographic,clinical and laboratory features of childhood-onset systemic lupus erythematosus: Single center experience

Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome

Bartter syndrome and growth hormone deficiency: three cases

ACE gene polymorphism in Turkish children with acute post streptococcal glomerulonephritis

Angiotensin Converting Enzyme Gene Polymorphism in Children with Henoch-Schonlein Purpura

Barttin mutations in antenatal Bartter syndrome with sensorineural deafness

An unusual cause of pleural effusion, urinothorax in a child with urinary stone disease

Hyponatremic-hypertensive Syndrome in a 19-month-old Boy with Renovascular Hypertension

A child with Beckwith-Wiedemann syndrome and posterior urethral valves

Changes in Osmolal Gap and Osmolality in Children with Chronic and End-Stage Renal Failure

Barttin mutations in antenatal Bartter syndrome with sensorineural deafness

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