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Markus Ries

Showing results (31-40 of 96) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2017
A cross-sectional quantitative analysis of the natural history of Farber disease: an ultra-orphan condition with rheumatologic and neurological cardinal disease featuresMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 6, 2005
Long-term therapy with agalsidase alfa for Fabry disease: safety and effects on renal function in a home infusion settingRaphael Schiffmann, Markus Ries, Margaret Timmons, et al.
Disaster Medicine and Public Health Preparedness|June 21, 2019
Disasters in Germany and France: An Analysis of the Emergency Events Database From a Pediatric PerspectiveMarkus Ries, Matthias Zielonka, Noah Ries, et al.
Journal of Inherited Metabolic Disease|June 22, 2019
Ultra-orphan lysosomal storage diseases: A cross-sectional quantitative analysis of the natural history of alpha-mannosidosisMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2017
Quantitative clinical characteristics of 53 patients with MPS VII: a cross-sectional analysisMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Studies in Health Technology and Informatics|August 10, 2012
An EMR based cancer diary - utilisation and initial usability evaluation of a new cancer data visualization toolMarkus Ries, Henriette Golcher, Hans-Ulrich Prokosch, et al.
Journal of Inherited Metabolic Disease|January 30, 2019
Quantitative natural history characterization in a cohort of 142 published cases of patients with galactosialidosis-A cross-sectional studyTomáš Sláma, Sven F Garbade, Stefan Kölker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
A cross-sectional quantitative analysis of the natural history of free sialic acid storage disease-an ultra-orphan multisystemic lysosomal storage disorderMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
American Journal of Medical Genetics. Part A|July 12, 2025
Unraveling the Genomic Architecture of Supernumerary (Iso-)Dicentric Chromosomes in Dup15q Syndrome: Insight From a Systematic Literature-Based StudySebastian Burkart, Markus Ries, Verena Romero, et al.
Pediatric Nephrology (Berlin, Germany)|April 23, 2022
Missing trial results: analysis of the current publication rate of studies in pediatric dialysis from 2003 to 2020Christian Patry, Alexander Fichtner, Britta Höcker, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2017
A cross-sectional quantitative analysis of the natural history of Farber disease: an ultra-orphan condition with rheumatologic and neurological cardinal disease featuresMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 6, 2005
Long-term therapy with agalsidase alfa for Fabry disease: safety and effects on renal function in a home infusion settingRaphael Schiffmann, Markus Ries, Margaret Timmons, et al.
Disaster Medicine and Public Health Preparedness|June 21, 2019
Disasters in Germany and France: An Analysis of the Emergency Events Database From a Pediatric PerspectiveMarkus Ries, Matthias Zielonka, Noah Ries, et al.
Journal of Inherited Metabolic Disease|June 22, 2019
Ultra-orphan lysosomal storage diseases: A cross-sectional quantitative analysis of the natural history of alpha-mannosidosisMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2017
Quantitative clinical characteristics of 53 patients with MPS VII: a cross-sectional analysisMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Studies in Health Technology and Informatics|August 10, 2012
An EMR based cancer diary - utilisation and initial usability evaluation of a new cancer data visualization toolMarkus Ries, Henriette Golcher, Hans-Ulrich Prokosch, et al.
Journal of Inherited Metabolic Disease|January 30, 2019
Quantitative natural history characterization in a cohort of 142 published cases of patients with galactosialidosis-A cross-sectional studyTomáš Sláma, Sven F Garbade, Stefan Kölker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
A cross-sectional quantitative analysis of the natural history of free sialic acid storage disease-an ultra-orphan multisystemic lysosomal storage disorderMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
American Journal of Medical Genetics. Part A|July 12, 2025
Unraveling the Genomic Architecture of Supernumerary (Iso-)Dicentric Chromosomes in Dup15q Syndrome: Insight From a Systematic Literature-Based StudySebastian Burkart, Markus Ries, Verena Romero, et al.
Pediatric Nephrology (Berlin, Germany)|April 23, 2022
Missing trial results: analysis of the current publication rate of studies in pediatric dialysis from 2003 to 2020Christian Patry, Alexander Fichtner, Britta Höcker, et al.
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