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Neveen A Soliman

Showing results (41-50 of 79) with videos related to

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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.
Indian Journal of Pediatrics|February 3, 2016
Lysosomal Storage Disorders in Egyptian ChildrenMohamed A Elmonem, Iman G Mahmoud, Dina A Mehaney, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tractStefan Kohl, Jing Chen, Asaf Vivante, et al.
Journal of Medical Genetics|November 12, 2010
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategyEdgar A Otto, Gokul Ramaswami, Sabine Janssen, 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.
Nature Reviews. Nephrology|January 5, 2023
Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEuropeJaap W Groothoff, Ella Metry, Lisa Deesker, 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 Reports|November 22, 2021
Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone DiseaseAndrea G Cogal, Jennifer Arroyo, Ronak Jagdeep Shah, et al.
Kidney International|October 22, 2015
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicityDaniela A Braun, Markus Schueler, Jan Halbritter, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2014
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndromeCarolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, et al.
Pageof 8

Showing results (41-50 of 79) with videos related to

Sort By:
Pageof 8
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.
Indian Journal of Pediatrics|February 3, 2016
Lysosomal Storage Disorders in Egyptian ChildrenMohamed A Elmonem, Iman G Mahmoud, Dina A Mehaney, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tractStefan Kohl, Jing Chen, Asaf Vivante, et al.
Journal of Medical Genetics|November 12, 2010
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategyEdgar A Otto, Gokul Ramaswami, Sabine Janssen, 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.
Nature Reviews. Nephrology|January 5, 2023
Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEuropeJaap W Groothoff, Ella Metry, Lisa Deesker, 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 Reports|November 22, 2021
Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone DiseaseAndrea G Cogal, Jennifer Arroyo, Ronak Jagdeep Shah, et al.
Kidney International|October 22, 2015
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicityDaniela A Braun, Markus Schueler, Jan Halbritter, et al.
Journal of the American Society of Nephrology : JASN|October 29, 2014
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndromeCarolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, et al.
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