A5056742014- Liver Disease Diagnosis and Treatment
- Liver Disease and Transplantation
- Diet, Metabolism, and Disease
- Pediatric Urology and Nephrology Studies
- Urological Disorders and Treatments
- Esophageal and GI Pathology
- Congenital Diaphragmatic Hernia Studies
- Tracheal and airway disorders
- Urinary Tract Infections Management
- Genetic Syndromes and Imprinting
- Vascular Malformations and Hemangiomas
- Diabetes Management and Research
- Chronic Kidney Disease and Diabetes
- Blood groups and transfusion
- Neurosurgical Procedures and Complications
- Dialysis and Renal Disease Management
- Pediatric Hepatobiliary Diseases and Treatments
- Epilepsy research and treatment
- Pharmacological Effects and Toxicity Studies
- Fatty Acid Research and Health
- Kidney Stones and Urolithiasis Treatments
- Liver Diseases and Immunity
- Lipid metabolism and biosynthesis
- Metabolism and Genetic Disorders
- Acute Kidney Injury Research
Aristotle University of Thessaloniki
2021-2025
Papageorgiou General Hospital
2021-2025
Birmingham Women’s and Children’s NHS Foundation Trust
2024
Moutafi, Maria; Ververi, Athina; Papadopoulou-Legbelou, Kyriaki; Gkiourtzis, Nikolaos; Fotoulaki, Mataftsi, Asimina Author Information
Abstract Mitochondrial myopathy is a severe metabolic related to nuclear or mitochondrial DNA dysfunction. We present rare case of myopathy, presented with multiple episodes proximal muscle weakness, lactic acidosis, and rhabdomyolysis (CPK 319,990 U/L, acid 22.31 mmol/L, GFR 3.82 mL/min/1.73m 2 ). She was hospitalized in the pediatric intensive care unit due acute kidney injury, elevated blood pressure, deterioration respiratory cardiac function. Investigation for inherited disorders showed...
Journal of Neonatal Surgery is a peer-reviewed and open-access electronic journal. Only few journals are being published on especially from developing country, which justifies the need new journal this subject.
A 12-year-old boy was transferred to our pediatric department from a rural hospital for fever, cough, and vomiting associated with thrombocytopenia, non-immune hemolytic anemia, acute kidney injury, leading the diagnosis of uremic syndrome (HUS). nasopharyngeal swab lower respiratory sample detected
This prospective study aimed to evaluate the characteristics and findings of children who presented with acute pyelonephritis (APN) determine independent risk factors for kidney scarring.
Sir, Pediatric-onset multiple sclerosis (POMS) is a demyelinating disease manifesting in children aged <18 years and represents 3–5% of all (MS) cases.[12] The association between intracranial hypertension dates back to 1994.[3] A wide range pathological conditions from sinusitis brain lesions can lead increased pressure (ICP) pediatric patients.[4] Although ICP has been reported adult MS, there only one such case MS.[35] In the present article, we report previously healthy child that...
We describe a 2-month-old female infant with macroglossia, macrosomia, omphalocele, neonatal hypoglycemia, earlobe creases, low nasal bridge, midface retrusion, syndromic facies and multiple cutaneous hepatic hemangiomas (HH). Genetic evaluation confirmed the diagnosis of Beckwith-Wiedemann Syndrome (BWS) mosaic uniparental disomy 11 as underlying genetic mechanism suggested by partial hypermethylation H19/IGF2:IG-DMR hypomethylation KCNQ1OT1:TSS-DMR on chromosome 11p15.5. Pediatric...