Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Neveen A Soliman

Showing results (21-30 of 79) with videos related to

Pageof 8
Sort By:
Pediatric Nephrology (Berlin, Germany)|July 16, 2020
Subtle cardiac dysfunction in nephropathic cystinosis: insight from tissue Doppler imaging and 2D speckle tracking echocardiographyMohamed H Afify, Safaa M Abdelrahman, Hossam I Mohamed, et al.
Orphanet Journal of Rare Diseases|April 23, 2016
Cystinosis: a reviewMohamed A Elmonem, Koenraad R Veys, Neveen A Soliman, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Cystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literatureMarwa M Nabhan, Nour ElKhateeb, Daniela A Braun, et al.
Laboratory Medicine|June 23, 2023
Neutrophilic Myeloid-Derived Suppressor Cells and Severity in SARS-CoV-2 InfectionMona A Omar, Rabab El Hawary, Alia Eldash, et al.
JIMD Reports|January 28, 2014
Mutational Spectrum of the CTNS Gene in Egyptian Patients with Nephropathic CystinosisNeveen A Soliman, Mohamed A Elmonem, Lambertus van den Heuvel, et al.
Genetic Testing and Molecular Biomarkers|April 24, 2024
Expanding the Genetic Spectrum of <i>AGXT</i> Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type ISomayya Naguib, Lamiaa A Mansour, Neveen A Soliman, et al.
Scientific Reports|September 23, 2022
Clinical and molecular characterization of primary hyperoxaluria in EgyptNeveen A Soliman, Mohamed A Elmonem, Safaa M Abdelrahman, et al.
Nature Genetics|April 29, 2024
The Egypt Genome ProjectMohamed A Elmonem, Neveen A Soliman, Ahmed Moustafa, 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.
Pediatric Nephrology (Berlin, Germany)|April 20, 2019
Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in childrenAsaf Vivante, Orna Staretz Chacham, Shirlee Shril, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
Pediatric Nephrology (Berlin, Germany)|July 16, 2020
Subtle cardiac dysfunction in nephropathic cystinosis: insight from tissue Doppler imaging and 2D speckle tracking echocardiographyMohamed H Afify, Safaa M Abdelrahman, Hossam I Mohamed, et al.
Orphanet Journal of Rare Diseases|April 23, 2016
Cystinosis: a reviewMohamed A Elmonem, Koenraad R Veys, Neveen A Soliman, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Cystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literatureMarwa M Nabhan, Nour ElKhateeb, Daniela A Braun, et al.
Laboratory Medicine|June 23, 2023
Neutrophilic Myeloid-Derived Suppressor Cells and Severity in SARS-CoV-2 InfectionMona A Omar, Rabab El Hawary, Alia Eldash, et al.
JIMD Reports|January 28, 2014
Mutational Spectrum of the CTNS Gene in Egyptian Patients with Nephropathic CystinosisNeveen A Soliman, Mohamed A Elmonem, Lambertus van den Heuvel, et al.
Genetic Testing and Molecular Biomarkers|April 24, 2024
Expanding the Genetic Spectrum of <i>AGXT</i> Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type ISomayya Naguib, Lamiaa A Mansour, Neveen A Soliman, et al.
Scientific Reports|September 23, 2022
Clinical and molecular characterization of primary hyperoxaluria in EgyptNeveen A Soliman, Mohamed A Elmonem, Safaa M Abdelrahman, et al.
Nature Genetics|April 29, 2024
The Egypt Genome ProjectMohamed A Elmonem, Neveen A Soliman, Ahmed Moustafa, 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.
Pediatric Nephrology (Berlin, Germany)|April 20, 2019
Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in childrenAsaf Vivante, Orna Staretz Chacham, Shirlee Shril, et al.
Pageof 8