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Corpus callosum thickness: A predictive factor for the first drug efficiency of self-limited epilepsy with centrotemporal spikes (selects)?

Epilepsy research, 2023-02, Vol.190, p.107072-107072, Article 107072

2023

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New-Onset Vision Impairment in Children: Magnetic Resonance Imaging Findings by Age Groups

Journal of child neurology, 2024-03, Vol.39 (3-4), p.122-128

2024

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Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International journal of neuroscience, 2024-06, Vol.134 (2), p.148-152

2024

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Radiographic findings of adenoviral pneumonia in children

Clinical imaging, 2024-04, Vol.108, p.110111-110111, Article 110111

2024

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Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International journal of neuroscience, 2022-07, p.1-5

2022

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Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International journal of neuroscience, 2024-06, Vol.134 (2), p.148

2024

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Chronic non‐bacterial osteomyelitis in children: Outcomes, quality of life

Pediatrics international, 2022-01, Vol.64 (1), p.e15351-n/a

2022

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IgG4-related disease and ANCA positive vasculitis in childhood: a case-based review

Clinical rheumatology, 2021-09, Vol.40 (9), p.3817-3825

2021

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Clavicle duplication following physeal injury

Surgical and radiologic anatomy (English ed.), 2019-04, Vol.41 (4), p.373-376

2019

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Atypical Hemolytic Uremic Syndrome

Türkiye çocuk hastalıkları dergisi, 2014-11

2014

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SP897COMPARATIVE STUDY OF VOIDING UROSONOGRAPHY WITHOUT CONTRAST ENHANCEMENT AND X-RAY VOIDING CYSTOURETHEROGRAPHY FOR DIAGNOSIS OF VESICOURETERAL REFLUX IN CHILDREN

Nephrology, dialysis, transplantation, 2015-05, Vol.30 (suppl_3), p.iii672-iii673

2015

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Additional temporal bone findings on computed tomography imaging in branchio-oto-renal syndrome

The Laryngoscope, 2009-04, Vol.119 (4), p.832-832

2009

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Left renal vein entrapment in postural proteinuria: the diagnostic utility of the aortomesenteric angle

European journal of pediatrics, 2022-09, Vol.181 (9), p.3339-3343

2022

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Occipital Hypometabolism on FDG PET/CT Scan in a Child with Hodgkin’s Lymphoma

Case reports in radiology, 2016-01, Vol.2016, p.5476108-4

2016

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Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

International Journal of Neuroscience, 2022, Vol.ahead-of-print (ahead-of-print), p.1-5

2022

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Radiation Exposure in the Neonatal Intensive Care Unit in Newborns and Staff

American journal of perinatology, 2023-07, Vol.40 (10), p.1106

2023

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Can therapeutic plasma exchange be life-saving in life-threatening manganese intoxication?

Transfusion and apheresis science, 2022-08, Vol.61 (4), p.103417-103417, Article 103417

2022

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From a branchial fistula to a branchiootorenal syndrome: a case report and review of the literature

Journal of pediatric surgery, 2009-03, Vol.44 (3), p.623-625

2009

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Mineral and bone disease in african renal failure patients

Nephro-urology monthly, 2013, Vol.5 (2), p.779-80

2013

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Corpus callosum thickness: A predictive factor for the first drug efficiency of self-limited epilepsy with centrotemporal spikes (selects)?

New-Onset Vision Impairment in Children: Magnetic Resonance Imaging Findings by Age Groups

Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Radiographic findings of adenoviral pneumonia in children

Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Primary CoQ 10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Chronic non‐bacterial osteomyelitis in children: Outcomes, quality of life

IgG4-related disease and ANCA positive vasculitis in childhood: a case-based review

Clavicle duplication following physeal injury

Atypical Hemolytic Uremic Syndrome

SP897COMPARATIVE STUDY OF VOIDING UROSONOGRAPHY WITHOUT CONTRAST ENHANCEMENT AND X-RAY VOIDING CYSTOURETHEROGRAPHY FOR DIAGNOSIS OF VESICOURETERAL REFLUX IN CHILDREN

Additional temporal bone findings on computed tomography imaging in branchio-oto-renal syndrome

Left renal vein entrapment in postural proteinuria: the diagnostic utility of the aortomesenteric angle

Occipital Hypometabolism on FDG PET/CT Scan in a Child with Hodgkin’s Lymphoma

Primary CoQ10 deficiency with a severe phenotype due to the c.901 C > T (p.R301W) mutation in the COQ8A gene

Radiation Exposure in the Neonatal Intensive Care Unit in Newborns and Staff

Can therapeutic plasma exchange be life-saving in life-threatening manganese intoxication?

From a branchial fistula to a branchiootorenal syndrome: a case report and review of the literature

Mineral and bone disease in african renal failure patients

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