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S Reuter

Showing results (131-140 of 172) with videos related to

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American Journal of Human Genetics|September 3, 2016
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive MicrocephalyMartin W Breuss, Tipu Sultan, Kiely N James, et al.
American Journal of Human Genetics|July 9, 2016
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive MicrocephalyMartin W Breuss, Tipu Sultan, Kiely N James, et al.
The Journal of Antimicrobial Chemotherapy|November 26, 2005
Caspofungin treatment in severely ill, immunocompromised patients: a case-documentation study of 118 patientsA Glasmacher, O A Cornely, K Orlopp, et al.
Journal of Medical Genetics|August 31, 2016
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrumMiriam S Reuter, Angelika Riess, Ute Moog, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
JAMA Network Open|May 26, 2021
Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care SettingIris Cohn, Roozbeh Manshaei, Eriskay Liston, et al.
Infection|March 30, 2013
Delay in the administration of appropriate antimicrobial therapy in Staphylococcus aureus bloodstream infection: a prospective multicenter hospital-based cohort studyA J Kaasch, S Rieg, J Kuetscher, et al.
Circulation. Genomic and Precision Medicine|July 30, 2021
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of FallotMiriam S Reuter, Rajiv R Chaturvedi, Rebekah K Jobling, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 17, 2016
Prospective Analyses of Circulating B Cell Subsets in ABO-Compatible and ABO-Incompatible Kidney Transplant RecipientsH A Schlößer, M Thelen, G Dieplinger, et al.
Pageof 18

Showing results (131-140 of 172) with videos related to

Sort By:
Pageof 18
American Journal of Human Genetics|September 3, 2016
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive MicrocephalyMartin W Breuss, Tipu Sultan, Kiely N James, et al.
American Journal of Human Genetics|July 9, 2016
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive MicrocephalyMartin W Breuss, Tipu Sultan, Kiely N James, et al.
The Journal of Antimicrobial Chemotherapy|November 26, 2005
Caspofungin treatment in severely ill, immunocompromised patients: a case-documentation study of 118 patientsA Glasmacher, O A Cornely, K Orlopp, et al.
Journal of Medical Genetics|August 31, 2016
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrumMiriam S Reuter, Angelika Riess, Ute Moog, et al.
American Journal of Human Genetics|January 6, 2018
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence DataBrett Trost, Susan Walker, Zhuozhi Wang, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
JAMA Network Open|May 26, 2021
Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care SettingIris Cohn, Roozbeh Manshaei, Eriskay Liston, et al.
Infection|March 30, 2013
Delay in the administration of appropriate antimicrobial therapy in Staphylococcus aureus bloodstream infection: a prospective multicenter hospital-based cohort studyA J Kaasch, S Rieg, J Kuetscher, et al.
Circulation. Genomic and Precision Medicine|July 30, 2021
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of FallotMiriam S Reuter, Rajiv R Chaturvedi, Rebekah K Jobling, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 17, 2016
Prospective Analyses of Circulating B Cell Subsets in ABO-Compatible and ABO-Incompatible Kidney Transplant RecipientsH A Schlößer, M Thelen, G Dieplinger, et al.
Pageof 18