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B Hammer

Showing results (481-490 of 518) with videos related to

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American Journal of Public Health|November 8, 2023
Employee Cardiometabolic Risk Following a Cluster-Randomized Workplace Intervention From the Work, Family and Health Network, 2009-2013Lisa F Berkman, Erin L Kelly, Leslie B Hammer, et al.
Journal of Occupational Health Psychology|December 8, 2017
Caring for the elderly at work and home: Can a randomized organizational intervention improve psychological health?Ellen Ernst Kossek, Rebecca J Thompson, Katie M Lawson, et al.
Epilepsia|April 28, 2023
IRF2BPL as a novel causative gene for progressive myoclonus epilepsyElena Gardella, Roberto Michelucci, Hanne M Christensen, et al.
Journal of Occupational and Environmental Medicine|May 15, 2020
Education and Training to Build Capacity in Total Worker Health®: Proposed Competencies for an Emerging FieldLee S Newman, Joshua G Scott, Adele Childress, et al.
Arthritis Care & Research|October 24, 2013
Defining enthesitis in spondyloarthritis by ultrasound: results of a Delphi process and of a reliability reading exerciseL Terslev, E Naredo, A Iagnocco, et al.
The Journal of Rheumatology|February 3, 2019
OMERACT Definitions for Ultrasonographic Pathologies and Elementary Lesions of Rheumatic Disorders 15 Years OnGeorge A Bruyn, Annamaria Iagnocco, Esperanza Naredo, et al.
Rheumatology (Oxford, England)|September 15, 2010
Current state of musculoskeletal ultrasound training and implementation in Europe: results of a survey of experts and scientific societiesEsperanza Naredo, Maria A D'Agostino, Philip G Conaghan, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
Epilepsia|October 16, 2020
Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 geneSara Matricardi, Paola De Liso, Elena Freri, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Pageof 52

Showing results (481-490 of 518) with videos related to

Sort By:
Pageof 52
American Journal of Public Health|November 8, 2023
Employee Cardiometabolic Risk Following a Cluster-Randomized Workplace Intervention From the Work, Family and Health Network, 2009-2013Lisa F Berkman, Erin L Kelly, Leslie B Hammer, et al.
Journal of Occupational Health Psychology|December 8, 2017
Caring for the elderly at work and home: Can a randomized organizational intervention improve psychological health?Ellen Ernst Kossek, Rebecca J Thompson, Katie M Lawson, et al.
Epilepsia|April 28, 2023
IRF2BPL as a novel causative gene for progressive myoclonus epilepsyElena Gardella, Roberto Michelucci, Hanne M Christensen, et al.
Journal of Occupational and Environmental Medicine|May 15, 2020
Education and Training to Build Capacity in Total Worker Health®: Proposed Competencies for an Emerging FieldLee S Newman, Joshua G Scott, Adele Childress, et al.
Arthritis Care & Research|October 24, 2013
Defining enthesitis in spondyloarthritis by ultrasound: results of a Delphi process and of a reliability reading exerciseL Terslev, E Naredo, A Iagnocco, et al.
The Journal of Rheumatology|February 3, 2019
OMERACT Definitions for Ultrasonographic Pathologies and Elementary Lesions of Rheumatic Disorders 15 Years OnGeorge A Bruyn, Annamaria Iagnocco, Esperanza Naredo, et al.
Rheumatology (Oxford, England)|September 15, 2010
Current state of musculoskeletal ultrasound training and implementation in Europe: results of a survey of experts and scientific societiesEsperanza Naredo, Maria A D'Agostino, Philip G Conaghan, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
Epilepsia|October 16, 2020
Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 geneSara Matricardi, Paola De Liso, Elena Freri, et al.
American Journal of Human Genetics|January 22, 2013
Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticityMonia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, et al.
Pageof 52