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Danko Milosevic

Showing results (11-20 of 23) with videos related to

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Rheumatology International|December 15, 2012
Polyarteritis nodosa in Croatian children: a retrospective study over the last 20 yearsMarija Jelusic, Masa Vikic-Topic, Danica Batinic, et al.
Frontiers in Pediatrics|October 5, 2023
Case report: Autoimmune hemolytic anemia caused by warm and cold autoantibodies with complement activation-etiological and therapeutic issuesDaniel Turudic, Sara Dejanovic Bekic, Lucija Mucavac, et al.
Journal of Pediatric Hematology/Oncology|December 15, 2017
Genotype-phenotype Correlation of β-Thalassemia in Croatian Patients: A Specific HBB Gene MutationsJerko Vucak, Daniel Turudic, Danko Milosevic, et al.
Clinical and Experimental Rheumatology|June 29, 2013
Childhood-onset systemic lupus erythematosus in Croatia: demographic, clinical and laboratory features, and factors influencing time to diagnosisAnita Lukic, Ivan Kresimir Lukic, Ivan Malcic, et al.
Frontiers in Immunology|April 21, 2017
Analysis of Linear Antibody Epitopes on Factor H and CFHR1 Using Sera of Patients with Autoimmune Atypical Hemolytic Uremic SyndromeEszter Trojnár, Mihály Józsi, Katalin Uray, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 21, 2016
Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or NephrocalcinosisDaniela Anne Braun, Jennifer Ashley Lawson, Heon Yung Gee, et al.
American Journal of Human Genetics|May 24, 2016
Mutations in SLC26A1 Cause NephrolithiasisHeon Yung Gee, Ikhyun Jun, Daniela A Braun, et al.
Kidney International|January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosisTilman Jobst-Schwan, Verena Klämbt, Maureen Tarsio, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2025
Survey of legislative frameworks and national recommendations governing paediatric maintenance haemodialysis in EuropeEnzo Vedrine, Claus Peter Schmitt, Johan Vande Walle, et al.
European Urology Open Science|October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary TractChen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Rheumatology International|December 15, 2012
Polyarteritis nodosa in Croatian children: a retrospective study over the last 20 yearsMarija Jelusic, Masa Vikic-Topic, Danica Batinic, et al.
Frontiers in Pediatrics|October 5, 2023
Case report: Autoimmune hemolytic anemia caused by warm and cold autoantibodies with complement activation-etiological and therapeutic issuesDaniel Turudic, Sara Dejanovic Bekic, Lucija Mucavac, et al.
Journal of Pediatric Hematology/Oncology|December 15, 2017
Genotype-phenotype Correlation of β-Thalassemia in Croatian Patients: A Specific HBB Gene MutationsJerko Vucak, Daniel Turudic, Danko Milosevic, et al.
Clinical and Experimental Rheumatology|June 29, 2013
Childhood-onset systemic lupus erythematosus in Croatia: demographic, clinical and laboratory features, and factors influencing time to diagnosisAnita Lukic, Ivan Kresimir Lukic, Ivan Malcic, et al.
Frontiers in Immunology|April 21, 2017
Analysis of Linear Antibody Epitopes on Factor H and CFHR1 Using Sera of Patients with Autoimmune Atypical Hemolytic Uremic SyndromeEszter Trojnár, Mihály Józsi, Katalin Uray, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 21, 2016
Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or NephrocalcinosisDaniela Anne Braun, Jennifer Ashley Lawson, Heon Yung Gee, et al.
American Journal of Human Genetics|May 24, 2016
Mutations in SLC26A1 Cause NephrolithiasisHeon Yung Gee, Ikhyun Jun, Daniela A Braun, et al.
Kidney International|January 22, 2020
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosisTilman Jobst-Schwan, Verena Klämbt, Maureen Tarsio, et al.
Pediatric Nephrology (Berlin, Germany)|January 23, 2025
Survey of legislative frameworks and national recommendations governing paediatric maintenance haemodialysis in EuropeEnzo Vedrine, Claus Peter Schmitt, Johan Vande Walle, et al.
European Urology Open Science|October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary TractChen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.
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