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Hans Hartmann

Showing results (41-50 of 83) with videos related to

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Transplant International : Official Journal of the European Society for Organ Transplantation|January 6, 2015
Early kidney transplantation improves neurocognitive outcome in patients with severe congenital chronic kidney diseaseHans Hartmann, Nicola Hawellek, Mirja Wedekin, et al.
European Radiology|October 8, 2011
Patterns in early diffusion-weighted MRI in children with haemolytic uraemic syndrome and CNS involvementFrank Donnerstag, Xiaoqi Ding, Lars Pape, et al.
Neuropediatrics|April 1, 2021
Pitfalls in Genetic Diagnostics: Why Phenotyping is EssentialJanina Gburek-Augustat, Jan-Christoph Schoene-Bake, Eva Bültmann, et al.
BMC Infectious Diseases|January 23, 2017
Common and uncommon neurological manifestations of neuroborreliosis leading to hospitalizationPhilipp Schwenkenbecher, Refik Pul, Ulrich Wurster, et al.
Clinical Chemistry|January 21, 2006
Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB geneAnibh M Das, Sabine Illsinger, Thomas Lücke, et al.
Epilepsia Open|October 25, 2022
Medical treatment in infants and young children with epilepsy: Off-label use of antiseizure medications. Survey Report of ILAE Task Force Medical Therapies in ChildrenJo Sourbron, Stéphane Auvin, Alexis Arzimanoglou, et al.
Oxidative Medicine and Cellular Longevity|April 24, 2014
L-arginine/NO pathway is altered in children with haemolytic-uraemic syndrome (HUS)Nele Kirsten Kanzelmeyer, Lars Pape, Kristine Chobanyan-Jürgens, et al.
Archives of Neurology|July 12, 2012
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutationsAlexander Schmidt, Kishore R Kumar, Katharina Redyk, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRIKaan Boztug, Xiao-Qi Ding, Hans Hartmann, et al.
Neuropediatrics|December 1, 2021
Clinical and Genetic Aspects of Juvenile Onset Pompe DiseaseJohanna Holzwarth, Nadja Minopoli, Charlotte Pfrimmer, et al.
Pageof 9

Showing results (41-50 of 83) with videos related to

Sort By:
Pageof 9
Transplant International : Official Journal of the European Society for Organ Transplantation|January 6, 2015
Early kidney transplantation improves neurocognitive outcome in patients with severe congenital chronic kidney diseaseHans Hartmann, Nicola Hawellek, Mirja Wedekin, et al.
European Radiology|October 8, 2011
Patterns in early diffusion-weighted MRI in children with haemolytic uraemic syndrome and CNS involvementFrank Donnerstag, Xiaoqi Ding, Lars Pape, et al.
Neuropediatrics|April 1, 2021
Pitfalls in Genetic Diagnostics: Why Phenotyping is EssentialJanina Gburek-Augustat, Jan-Christoph Schoene-Bake, Eva Bültmann, et al.
BMC Infectious Diseases|January 23, 2017
Common and uncommon neurological manifestations of neuroborreliosis leading to hospitalizationPhilipp Schwenkenbecher, Refik Pul, Ulrich Wurster, et al.
Clinical Chemistry|January 21, 2006
Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB geneAnibh M Das, Sabine Illsinger, Thomas Lücke, et al.
Epilepsia Open|October 25, 2022
Medical treatment in infants and young children with epilepsy: Off-label use of antiseizure medications. Survey Report of ILAE Task Force Medical Therapies in ChildrenJo Sourbron, Stéphane Auvin, Alexis Arzimanoglou, et al.
Oxidative Medicine and Cellular Longevity|April 24, 2014
L-arginine/NO pathway is altered in children with haemolytic-uraemic syndrome (HUS)Nele Kirsten Kanzelmeyer, Lars Pape, Kristine Chobanyan-Jürgens, et al.
Archives of Neurology|July 12, 2012
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutationsAlexander Schmidt, Kishore R Kumar, Katharina Redyk, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRIKaan Boztug, Xiao-Qi Ding, Hans Hartmann, et al.
Neuropediatrics|December 1, 2021
Clinical and Genetic Aspects of Juvenile Onset Pompe DiseaseJohanna Holzwarth, Nadja Minopoli, Charlotte Pfrimmer, et al.
Pageof 9