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Neveen A Soliman

Showing results (31-40 of 79) with videos related to

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Human Genetics|April 6, 2013
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathyJan Halbritter, Jonathan D Porath, Katrina A Diaz, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, 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.
Kidney International|May 17, 2016
Controversies and research agenda in nephropathic cystinosis: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies ConferenceCraig B Langman, Bruce A Barshop, Georges Deschênes, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 19, 2014
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndromeSvjetlana Lovric, Humphrey Fang, Virginia Vega-Warner, et al.
Kidney International|January 17, 2014
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Gabriel C Dworschak, Stefan Kohl, et al.
Journal of Advanced Research|June 6, 2024
Egypt Genome: Towards an African new genomic eraKhaled Amer, Neveen A Soliman, Sameh Soror, 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|November 29, 2012
High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencingJan Halbritter, Katrina Diaz, Moumita Chaki, et al.
Journal of the American Society of Nephrology : JASN|May 7, 2016
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary TractAsaf Vivante, Daw-Yang Hwang, Stefan Kohl, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
Human Genetics|April 6, 2013
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathyJan Halbritter, Jonathan D Porath, Katrina A Diaz, et al.
Kidney International Reports|September 14, 2019
ADPedKD: A Global Online Platform on the Management of Children With ADPKDStéphanie De Rechter, Detlef Bockenhauer, Lisa M Guay-Woodford, 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.
Kidney International|May 17, 2016
Controversies and research agenda in nephropathic cystinosis: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies ConferenceCraig B Langman, Bruce A Barshop, Georges Deschênes, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 19, 2014
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndromeSvjetlana Lovric, Humphrey Fang, Virginia Vega-Warner, et al.
Kidney International|January 17, 2014
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Gabriel C Dworschak, Stefan Kohl, et al.
Journal of Advanced Research|June 6, 2024
Egypt Genome: Towards an African new genomic eraKhaled Amer, Neveen A Soliman, Sameh Soror, 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|November 29, 2012
High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencingJan Halbritter, Katrina Diaz, Moumita Chaki, et al.
Journal of the American Society of Nephrology : JASN|May 7, 2016
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary TractAsaf Vivante, Daw-Yang Hwang, Stefan Kohl, et al.
Pageof 8