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

A Soliman

Showing results (1211-1220 of 1,228) with videos related to

Pageof 123
Sort By:
Lupus|May 9, 2020
Association of interleukin-17A gene polymorphisms and susceptibility to systemic lupus erythematosus in Egyptian children and adolescents: a multi-centre studyMohamed A Elkoumi, Mayy An Allah, Faisal Y Mohamed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Lupus|January 6, 2026
Association of CTLA-4 exon 1(+49 A/G) polymorphism and susceptibility to SLE in Egyptian children and adolescentsFaika Arab, Sarah A Saleh, Dina M Ibrahim, et al.
Pediatric Pulmonology|March 7, 2020
Ficolin-1 gene (FCN1) -144 C/A polymorphism is associated with adverse outcome of severe pneumonia in the under-five Egyptian children: A multicenter studyMohamed A Elkoumi, Sawsan H Abdellatif, Faisal Y Mohamed, et al.
Pediatric Research|September 10, 2022
Vitamin D deficiency and vitamin D receptor FokI polymorphism as risk factors for COVID-19Nancy M S Zeidan, Hanan M Abd El Lateef, Dalia M Selim, et al.
The Journal of Clinical Investigation|May 5, 2011
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSaskia F Heeringa, Gil Chernin, Moumita Chaki, et al.
Nature Genetics|January 25, 2011
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrumErica E Davis, Qi Zhang, Qin Liu, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2021
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiencyStefano Vavassori, Janet Chou, Laura Eva Faletti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT familiesLea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 19, 2019
Treatment and long-term outcome in primary distal renal tubular acidosisSergio Camilo Lopez-Garcia, Francesco Emma, Stephen B Walsh, et al.
Pageof 123

Showing results (1211-1220 of 1,228) with videos related to

Sort By:
Pageof 123
Lupus|May 9, 2020
Association of interleukin-17A gene polymorphisms and susceptibility to systemic lupus erythematosus in Egyptian children and adolescents: a multi-centre studyMohamed A Elkoumi, Mayy An Allah, Faisal Y Mohamed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Lupus|January 6, 2026
Association of CTLA-4 exon 1(+49 A/G) polymorphism and susceptibility to SLE in Egyptian children and adolescentsFaika Arab, Sarah A Saleh, Dina M Ibrahim, et al.
Pediatric Pulmonology|March 7, 2020
Ficolin-1 gene (FCN1) -144 C/A polymorphism is associated with adverse outcome of severe pneumonia in the under-five Egyptian children: A multicenter studyMohamed A Elkoumi, Sawsan H Abdellatif, Faisal Y Mohamed, et al.
Pediatric Research|September 10, 2022
Vitamin D deficiency and vitamin D receptor FokI polymorphism as risk factors for COVID-19Nancy M S Zeidan, Hanan M Abd El Lateef, Dalia M Selim, et al.
The Journal of Clinical Investigation|May 5, 2011
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSaskia F Heeringa, Gil Chernin, Moumita Chaki, et al.
Nature Genetics|January 25, 2011
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrumErica E Davis, Qi Zhang, Qin Liu, et al.
The Journal of Allergy and Clinical Immunology|April 19, 2021
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiencyStefano Vavassori, Janet Chou, Laura Eva Faletti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT familiesLea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 19, 2019
Treatment and long-term outcome in primary distal renal tubular acidosisSergio Camilo Lopez-Garcia, Francesco Emma, Stephen B Walsh, et al.
Pageof 123