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M Nabhan

Showing results (41-50 of 52) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 9, 2014
Soluble adhesion molecules as markers of native arteriovenous fistula thrombosis in children on uremiaFatina I Fadel, Manal F Elshamaa, Marwa M Nabhan, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|September 18, 2012
Clinical characterization and NPHP1 mutations in nephronophthisis and associated ciliopathies: a single center experienceNeveen A Soliman, Friedhelm Hildebrandt, Edgar A Otto, et al.
The Journal of Steroid Biochemistry and Molecular Biology|May 13, 2021
Whole exome sequencing and functional characterization increase diagnostic yield in siblings with a 46, XY difference of sexual development (DSD)Sofia E Luna, Daniel J Wegner, Sarah Gale, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|March 31, 2026
Clinical, biochemical, and molecular spectrum of nephropathic cystinosis: Two novel CTNS mutationsZeinab Youssef Abdallah, Rasha Helmy, Walaa S Nazim, et al.
Nephrologie & Therapeutique|February 6, 2017
Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary centerNeveen A Soliman, Marwa M Nabhan, Safaa M Abdelrahman, et al.
Journal of Medical Genetics|December 18, 2015
Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathiesMarkus Schueler, Jan Halbritter, Ian G Phelps, et al.
Orphanet Journal of Rare Diseases|November 20, 2014
Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosisMohamed A Elmonem, Samuel H Makar, Lambertus van den Heuvel, et al.
Pediatric Transplantation|November 27, 2018
Combined liver-kidney transplantation for primary hyperoxaluria type I in children: Single Center ExperienceMagd A Kotb, Alaa F Hamza, Hesham Abd El Kader, et al.
Kidney International|January 25, 2017
Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease managementAgnieszka Bierzynska, Hugh J McCarthy, Katrina Soderquest, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndromeBshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 9, 2014
Soluble adhesion molecules as markers of native arteriovenous fistula thrombosis in children on uremiaFatina I Fadel, Manal F Elshamaa, Marwa M Nabhan, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|September 18, 2012
Clinical characterization and NPHP1 mutations in nephronophthisis and associated ciliopathies: a single center experienceNeveen A Soliman, Friedhelm Hildebrandt, Edgar A Otto, et al.
The Journal of Steroid Biochemistry and Molecular Biology|May 13, 2021
Whole exome sequencing and functional characterization increase diagnostic yield in siblings with a 46, XY difference of sexual development (DSD)Sofia E Luna, Daniel J Wegner, Sarah Gale, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|March 31, 2026
Clinical, biochemical, and molecular spectrum of nephropathic cystinosis: Two novel CTNS mutationsZeinab Youssef Abdallah, Rasha Helmy, Walaa S Nazim, et al.
Nephrologie & Therapeutique|February 6, 2017
Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary centerNeveen A Soliman, Marwa M Nabhan, Safaa M Abdelrahman, et al.
Journal of Medical Genetics|December 18, 2015
Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathiesMarkus Schueler, Jan Halbritter, Ian G Phelps, et al.
Orphanet Journal of Rare Diseases|November 20, 2014
Clinical utility of chitotriosidase enzyme activity in nephropathic cystinosisMohamed A Elmonem, Samuel H Makar, Lambertus van den Heuvel, et al.
Pediatric Transplantation|November 27, 2018
Combined liver-kidney transplantation for primary hyperoxaluria type I in children: Single Center ExperienceMagd A Kotb, Alaa F Hamza, Hesham Abd El Kader, et al.
Kidney International|January 25, 2017
Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease managementAgnieszka Bierzynska, Hugh J McCarthy, Katrina Soderquest, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2026
Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndromeBshara Mansour, Katharina Lemberg, Ronen Schneider, et al.
Pageof 6