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Showing results (561-570 of 651) with videos related to

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American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|November 3, 2010
Cleaned, ready-to-use, reusable electrocardiographic lead wires as a source of pathogenic microorganismsNancy M Albert, Kelly Hancock, Terri Murray, et al.
Neuropediatrics|June 15, 2006
The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotinD Friebel, M von der Hagen, E R Baumgartner, et al.
Journal of Periodontology|March 16, 2002
Evaluation of pluronic polyols as carriers for grafting materials: study in rat calvaria defectsEdward B Fowler, Michael F Cuenin, Steven D Hokett, et al.
The Journal of Heart Transplantation|July 1, 1987
Cardiac sarcoidosis: response to steroids and transplantationH A Valantine, H D Tazelaar, J Macoviak, et al.
British Heart Journal|June 1, 1984
Single lead atrial synchronised pacing in patients with cardiogenic shock after acute myocardial infarctionM B Fowler, J C Crick, D I Tayler, et al.
The Pediatric Infectious Disease Journal|June 2, 2009
Cytomegalovirus shedding and delayed sensorineural hearing loss: results from longitudinal follow-up of children with congenital infectionLauren Stancik Rosenthal, Karen B Fowler, Suresh B Boppana, et al.
Pediatric Research|May 1, 1997
Five patients with a biotin-responsive defect in holocarboxylase formation: evaluation of responsiveness to biotin therapy in vivo and comparative biochemical studies in vitroT Suormala, B Fowler, M Duran, et al.
Circulation|November 1, 1987
Changes in Doppler echocardiographic indexes of left ventricular function as potential markers of acute cardiac rejectionH A Valantine, M B Fowler, S A Hunt, et al.
The Pediatric Infectious Disease Journal|December 30, 2016
Congenital Cytomegalovirus Infection and Permanent Hearing Loss in Rural North Indian ChildrenLalit Dar, Divya Namdeo, Pankaj Kumar, et al.
The New England Journal of Medicine|September 19, 1985
Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial diseaseG H Boers, A G Smals, F J Trijbels, et al.
Pageof 66

Showing results (561-570 of 651) with videos related to

Sort By:
Pageof 66
American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|November 3, 2010
Cleaned, ready-to-use, reusable electrocardiographic lead wires as a source of pathogenic microorganismsNancy M Albert, Kelly Hancock, Terri Murray, et al.
Neuropediatrics|June 15, 2006
The first case of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency responsive to biotinD Friebel, M von der Hagen, E R Baumgartner, et al.
Journal of Periodontology|March 16, 2002
Evaluation of pluronic polyols as carriers for grafting materials: study in rat calvaria defectsEdward B Fowler, Michael F Cuenin, Steven D Hokett, et al.
The Journal of Heart Transplantation|July 1, 1987
Cardiac sarcoidosis: response to steroids and transplantationH A Valantine, H D Tazelaar, J Macoviak, et al.
British Heart Journal|June 1, 1984
Single lead atrial synchronised pacing in patients with cardiogenic shock after acute myocardial infarctionM B Fowler, J C Crick, D I Tayler, et al.
The Pediatric Infectious Disease Journal|June 2, 2009
Cytomegalovirus shedding and delayed sensorineural hearing loss: results from longitudinal follow-up of children with congenital infectionLauren Stancik Rosenthal, Karen B Fowler, Suresh B Boppana, et al.
Pediatric Research|May 1, 1997
Five patients with a biotin-responsive defect in holocarboxylase formation: evaluation of responsiveness to biotin therapy in vivo and comparative biochemical studies in vitroT Suormala, B Fowler, M Duran, et al.
Circulation|November 1, 1987
Changes in Doppler echocardiographic indexes of left ventricular function as potential markers of acute cardiac rejectionH A Valantine, M B Fowler, S A Hunt, et al.
The Pediatric Infectious Disease Journal|December 30, 2016
Congenital Cytomegalovirus Infection and Permanent Hearing Loss in Rural North Indian ChildrenLalit Dar, Divya Namdeo, Pankaj Kumar, et al.
The New England Journal of Medicine|September 19, 1985
Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial diseaseG H Boers, A G Smals, F J Trijbels, et al.
Pageof 66