Marwa Nabhan
Marwa Nabhan
Lecturer of pediatrics
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Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management
A Bierzynska, HJ McCarthy, K Soderquest, ES Sen, E Colby, WY Ding, ...
Kidney international 91 (4), 937-947, 2017
Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies
M Schueler, J Halbritter, IG Phelps, DA Braun, EA Otto, JD Porath, ...
Journal of medical genetics 53 (3), 208-214, 2016
Clinical characterization and NPHP1 mutations in nephronophthisis and associated ciliopathies: a single center experience
NA Soliman, F Hildebrandt, EA Otto, MM Nabhan, SJ Allen, AM Badr, ...
Saudi journal of kidney diseases and transplantation: an official …, 2012
Risk factors for early dialysis dependency in autosomal recessive polycystic kidney disease
K Burgmaier, K Kunzmann, G Ariceta, C Bergmann, AK Buescher, ...
The Journal of pediatrics 199, 22-28. e6, 2018
Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosis
MA Elmonem, SH Makar, L van den Heuvel, H Abdelaziz, ...
Orphanet journal of rare diseases 9 (1), 1-10, 2014
Recent progress of the ARegPKD registry study on autosomal recessive polycystic kidney disease
K Ebner, F Schaefer, MC Liebau, LA Eid, N Ranguelov, B Adams, ...
Frontiers in pediatrics 5, 18, 2017
Combined liver‐kidney transplantation for primary hyperoxaluria type I in children: Single Center Experience
MA Kotb, AF Hamza, H Abd El Kader, M El Monayeri, DS Mosallam, N Ali, ...
Pediatric transplantation 23 (1), e13313, 2019
Cystic kidneys in fetal Walker–Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature
MM Nabhan, N ElKhateeb, DA Braun, S Eun, SN Saleem, H YungGee, ...
American Journal of Medical Genetics Part A 173 (10), 2697-2702, 2017
Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center
NA Soliman, MM Nabhan, SM Abdelrahman, H Abdelaziz, R Helmy, ...
Nephrologie & therapeutique 13 (3), 176-182, 2017
Soluble adhesion molecules as markers of native arteriovenous fistula thrombosis in children on uremia
FI Fadel, MF Elshamaa, MM Nabhan, RG Essam, N Kantoush, ...
Blood Coagulation & Fibrinolysis 25 (7), 675-682, 2014
Homozygous NPHP1 deletions in Egyptian children with nephronophthisis including an infantile onset patient
NA Soliman, F Hildebrandt, SJ Allen, EA Otto, MM Nabhan, AM Badr
Pediatric Nephrology 25 (10), 2193-2194, 2010
Fas/Fas Ligand pathways gene polymorphisms in pediatric renal allograft rejection
FI Fadel, MF Elshamaa, A Salah, M Nabhan, M Rasheed, S Kamel, ...
Transplant immunology 37, 28-34, 2016
Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice
AJ Majmundar, F Buerger, TA Forbes, V Klämbt, R Schneider, K Deutsch, ...
Science Advances 7 (1), eabe1386, 2021
Whole-exome analysis of a child with polycystic kidney disease and ventriculomegaly
MM Nabhan, H Abdelaziz, Y Xu, R El Sayed, M Santibanez-Koref, ...
Genetics and Molecular Research 14 (2), 3618-3624, 2015
Clinical and ultrasonographical characterization of childhood cystic kidney diseases in Egypt
NA Soliman, MM Nabhan, HM Bazaraa, AM Badr, M Shaheen
Renal failure 36 (5), 694-700, 2014
Left ventricular mass index and subendocardial myocardial function in children with chronic kidney disease, a transmural strain and three-dimensional echocardiographic study
AE El Tantawy, F Fadel, SM Abdelrahman, M Nabhan, R Ibrahim, ...
Cardiovascular endocrinology & metabolism 8 (4), 115, 2019
Vitamin D receptor gene polymorphisms in nephrotic syndrome children
GSM El-Saeed, MF Elshamaa, H Abdelaziz, EA Elghoroury, ...
JIPBS 5 (4), 86-93, 2018
CCR2 V64I Genotyping: Impact on end stage renal disease development, progression and renal transplantation outcome
EA Elghoroury, MF Elshamaa, FI Fadel, D Kandil, H Farouk, S Kamel, ...
JIPBS 5, 05-11, 2018
Visual acuity, fundus changes, and electroretinographic findings in Egyptian children with Bardet-Biedl syndrome
D El-Fayoumi, R Helmy, M Nabhan, N Soliman
Delta Journal of Ophthalmology 17 (1), 29, 2016
Intrafamilial Variability and Clinical Heterogeneity in Two Siblings with NPHP4 loss of Function Mutations
MM Nabhan, S Brenzinger, J Carlsson, SN Saleem, EA Otto, ...
J Mol Biomark Diagn 6 (217), 2, 2015
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Artículos 1–20