21 results on '"Nabhan, Marwa M."'
Search Results
2. Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome
3. Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome
4. Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease
5. Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center
6. Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management
7. Cystic kidneys in fetal Walker–Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature
8. Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies
9. Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice
10. Homozygous NPHP1 deletions in Egyptian children with nephronophthisis including an infantile onset patient
11. Combined liver-kidney transplantation for primary hyperoxaluria type I in children: Single Center Experience
12. Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease
13. Clinical utility of chitotriosidase enzyme in nephropathic cystinosis
14. Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies
15. SP905CLINICAL PHENOTYPES OF POLYCYSTIC KIDNEY DISEASE IN EGYPTIAN CHILDREN
16. SP889RENAL AND RETINAL PHENOTYPING IN A COHORT OF BARDET-BIEDL SYNDROME
17. Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosis
18. Soluble adhesion molecules as markers of native arteriovenous fistula thrombosis in children on uremia
19. Clinical and ultrasonographical characterization of childhood cystic kidney diseases in Egypt
20. Clinical Characterization and NPHP1 Mutations in Nephronophthisis and Associated Ciliopathies: A Single Center Experience.
21. Combined liver‐kidney transplantation for primary hyperoxaluria type I in children: Single Center Experience.
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