Ionela-Loredana Popa
Biographic Data
| ID | 8261232 |
|---|---|
| NAME | Ionela-Loredana Popa |
| GIVEN NAMES | Ionela-Loredana |
| FAMILY NAME | Popa |
| SIGNATURE | POPA I |
| AFFILIATIONS | Spitalului Clinic de Urgență pentru Copii Maria Sklodowska Curie |
| VERIFIED | No |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2023 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 0 |
WT1-Related Nephropathy in a Phenotypically Female Child
WT1-related disorders comprise a spectrum of conditions resulting from mutations or deletions of the WT1 gene. Alteration in this gene have been associated with many syndromes, including WAGR syndrome, Denys-Drash syndrome (DDS), Frasier syndrome (FS) and Meacham syndrome. We present the case of an 8-year-old phenotypically female child with symptoms of end-stage kidney disease (ESKD), hypertension and anasarca, requiring renal replacement therap…
Posterior Reversible Encephalopathy Syndrome in a Pediatric Patient with End-Stage Renal Disease
Posterior reversible encephalopathy syndrome (PRES) is a clinical and neuroimaging syndrome that can affect both children and adults and has variable etiology. It is clinically defined by headaches, consciousness disorders, seizures and visual disturbances. Early recognition (clinical and imaging) can lead to appropriate general measures to correct the underlying cause of PRES. In this paper, we report a case of PRES in an eight-year-old boy with…
No prominent works on this page.
Posterior Reversible Encephalopathy Syndrome in a Pediatric Patient with End-Stage Renal Disease
Posterior reversible encephalopathy syndrome (PRES) is a clinical and neuroimaging syndrome that can affect both children and adults and has variable etiology. It is clinically defined by headaches, consciousness disorders, seizures and visual disturbances. Early recognition (clinical and imaging) can lead to appropriate general measures to correct the underlying cause of PRES. In this paper, we report a case of PRES in an eight-year-old boy with…
WT1-Related Nephropathy in a Phenotypically Female Child
WT1-related disorders comprise a spectrum of conditions resulting from mutations or deletions of the WT1 gene. Alteration in this gene have been associated with many syndromes, including WAGR syndrome, Denys-Drash syndrome (DDS), Frasier syndrome (FS) and Meacham syndrome. We present the case of an 8-year-old phenotypically female child with symptoms of end-stage kidney disease (ESKD), hypertension and anasarca, requiring renal replacement therap…
Disease (2 works) · Internal Medicine (2 works) · Medicine (2 works) · Bioinformatics (1 work) · Biology (1 work) · Encephalopathy (1 work) · End stage renal disease (1 work) · Etiology (1 work) · Focal segmental glomerulosclerosis (1 work) · Gene (1 work)