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Nephron|March 20, 2025
Lysosomal Storage-Independent Fabry Disease Variants with α-Galactosidase A Misprocessing-Induced ER Stress and the Unfolded Protein ResponseMartina Živná, Malte Lenders, Stanislav KmochAdvances in Chronic Kidney Disease|March 13, 2017
Autosomal Dominant Tubulointerstitial Kidney DiseaseAnthony J Bleyer, Kendrah Kidd, Martina Živná, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 20, 2025
Autosomal Dominant Tubulointerstitial Kidney Disease: A ReviewAnthony J Bleyer, Kendrah O Kidd, Martina Živná, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 17, 2022
Autosomal dominant tubulointerstitial kidney disease: A reviewMartina Živná, Kendrah O Kidd, Veronika Barešová, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 9, 2017
Autosomal Dominant Tubulointerstitial Kidney Disease Due to MUC1 MutationSamuel Mon-Wei Yu, Anthony J Bleyer, Kisra Anis, et al.Clinical Nephrology|August 15, 2018
Chronic tubulointerstitial kidney disease in untreated adenine phosphoribosyl transferase (APRT) deficiency: A case reportBenjamin Cochran, Tereza Kovačíková, Kateřina Hodaňová, et al.Rheumatology (Oxford, England)|November 14, 2018
Clinical manifestations and molecular aspects of phosphoribosylpyrophosphate synthetase superactivity in femalesMarie Zikánová, Dawn Wahezi, Arielle Hay, et al.Life Science Alliance|January 22, 2022
Phenylbutyrate rescues the transport defect of the Sec61α mutations V67G and T185A for reninMark Sicking, Martina Živná, Pratiti Bhadra, et al.BMC Nephrology|November 1, 2018
Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney diseaseChristine Gast, Anthony Marinaki, Monica Arenas-Hernandez, et al.Kidney International Reports|July 18, 2025
Characterization of Monogenic Kidney Disease in Older Patients With CKDElhussein A E Elhassan, Sarah Cormican, Shohdan M Osman, et al.Pageof 3