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A M Morris

Showing results (101-110 of 127) with videos related to

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Journal of Inherited Metabolic Disease|December 16, 2006
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathyA A M Morris, R E Appleton, B Power, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|March 3, 2017
Staphylococcus aureus bacteremia in immunosuppressed patients: a multicenter, retrospective cohort studyG Sasson, A D Bai, A Showler, et al.
Antimicrobial Resistance and Infection Control|September 6, 2018
Rationale and development of a business case for antimicrobial stewardship programs in acute care hospital settingsA M Morris, E Rennert-May, B Dalton, et al.
Neurology|August 29, 2007
Homoplasmy, heteroplasmy, and mitochondrial dystoniaR McFarland, P F Chinnery, E L Blakely, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|August 6, 2017
Human resources estimates and funding for antibiotic stewardship teams are urgently neededC Pulcini, C M Morel, E Tacconelli, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|November 16, 2017
Effect of an antimicrobial stewardship programme on antimicrobial utilisation and costs in patients with leukaemia: a retrospective controlled studyM So, M M Mamdani, A M Morris, et al.
Molecular Genetics and Metabolism Reports|December 6, 2023
Long-term outcomes in two adult siblings with Fucosidosis - Diagnostic odyssey and clinical manifestationsNuria Puente-Ruiz, Ian Ellis, Marsel Bregu, et al.
American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
American Journal of Human Genetics|July 9, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
Neurogenetics|October 28, 2017
Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunitsRuth I C Glasgow, Kyle Thompson, Inês A Barbosa, et al.
Pageof 13

Showing results (101-110 of 127) with videos related to

Sort By:
Pageof 13
Journal of Inherited Metabolic Disease|December 16, 2006
Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathyA A M Morris, R E Appleton, B Power, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|March 3, 2017
Staphylococcus aureus bacteremia in immunosuppressed patients: a multicenter, retrospective cohort studyG Sasson, A D Bai, A Showler, et al.
Antimicrobial Resistance and Infection Control|September 6, 2018
Rationale and development of a business case for antimicrobial stewardship programs in acute care hospital settingsA M Morris, E Rennert-May, B Dalton, et al.
Neurology|August 29, 2007
Homoplasmy, heteroplasmy, and mitochondrial dystoniaR McFarland, P F Chinnery, E L Blakely, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|August 6, 2017
Human resources estimates and funding for antibiotic stewardship teams are urgently neededC Pulcini, C M Morel, E Tacconelli, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|November 16, 2017
Effect of an antimicrobial stewardship programme on antimicrobial utilisation and costs in patients with leukaemia: a retrospective controlled studyM So, M M Mamdani, A M Morris, et al.
Molecular Genetics and Metabolism Reports|December 6, 2023
Long-term outcomes in two adult siblings with Fucosidosis - Diagnostic odyssey and clinical manifestationsNuria Puente-Ruiz, Ian Ellis, Marsel Bregu, et al.
American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
American Journal of Human Genetics|July 9, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.
Neurogenetics|October 28, 2017
Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunitsRuth I C Glasgow, Kyle Thompson, Inês A Barbosa, et al.
Pageof 13