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Clinical Kidney Journal|June 4, 2021
Characteristics of patients with coexisting DNAJB9-associated fibrillary glomerulonephritis and IgA nephropathySamar M Said, Alejandro Best Rocha, Anthony M Valeri, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 21, 2017
Appendicular Biopsy in Total Colonic Aganglionosis: A Histologically Challenging and Inadvisable PracticeSuravi Mohanty, Usha Kini, Kanishka Das, et al.
Kidney International|July 6, 2020
DNAJB9-positive monotypic fibrillary glomerulonephritis is not associated with monoclonal gammopathy in the vast majority of patientsSamar M Said, Nelson Leung, Mariam Priya Alexander, et al.
Kidney International|March 21, 2016
The clinicopathologic characteristics and outcome of atypical anti-glomerular basement membrane nephritisSamih H Nasr, A Bernard Collins, Mariam Priya Alexander, et al.
Indian Journal of Pathology & Microbiology|August 10, 2020
Guidelines for various laboratory sections in view of COVID-19: Recommendations from the Indian Association of Pathologists and MicrobiologistsVatsala Misra, Ranjan Agrawal, Harendra Kumar, et al.
Kidney International|November 6, 2025
Dual-antigen membranous nephropathySamih H Nasr, Tiffany N Caza, Christopher P Larsen, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 11, 2020
Osmotic Nephrosis and Acute Kidney Injury Associated With SGLT2 Inhibitor Use: A Case ReportGautam Phadke, Amit Kaushal, Dean R Tolan, et al.
Clinical Genetics|April 20, 2019
The clinical presentation caused by truncating CHD8 variantsSofia Douzgou, Hui Wen Liang, Kay Metcalfe, et al.
Kidney International Reports|November 17, 2017
Negative Staining for COL4A5 Correlates With Worse Prognosis and More Severe Ultrastructural Alterations in Males With Alport SyndromeSamar M Said, Mary E Fidler, Anthony M Valeri, et al.
Human Molecular Genetics|January 4, 2011
NOTCH, a new signaling pathway implicated in holoprosencephalyValérie Dupé, Lucie Rochard, Sandra Mercier, et al.
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