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Critical Care Medicine|August 13, 2005

Randomized, controlled clinical trial of point-of-care limited ultrasonography assistance of central venous cannulation: the Third Sonography Outcomes Assessment Program (SOAP-3) TrialTruman J Milling, John Rose, William M Briggs, et al.

Open Access Emergency Medicine : OAEM|February 28, 2020

The Impact of a Concierge Medicine Model on Door to Doctor Time and Patient Flow in an Urban Emergency DepartmentAsher L Mandel, Thomas Bove, Amisha D Parekh, et al.

Clinical Genetics|June 4, 2014

COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?A M McInerney-Leo, E L Duncan, P J Leo, et al.

The Plant Journal : for Cell and Molecular Biology|April 12, 2000

Defective splicing of the first nad4 intron is associated with lack of several complex I subunits in the Nicotiana sylvestris NMS1 nuclear mutantJ Brangeon, M Sabar, S Gutierres, et al.

The Annals of Thoracic Surgery|September 9, 2014

Aortic valve replacement in octogenarians with prior cardiac surgeryTomasz A Timek, Zaahir Turfe, Robert L Hooker, et al.

Pediatric Diabetes|February 9, 2018

Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinismS R Johnson, P J Leo, A M McInerney-Leo, et al.

Genes and Immunity|November 27, 2015

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitisP C Robinson, P J Leo, J J Pointon, et al.

Clinical Genetics|December 11, 2014

Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophiesA M McInerney-Leo, J E Harris, P J Leo, et al.

Environment International|June 26, 2025

Multi-site study of communities with PFAS-contaminated drinking water: Methods, demographics, and PFAS serum concentrationsMarian Pavuk, John L Adgate, Scott M Bartell, et al.

Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 9, 2020

Comparison of sporadic and familial behavioral variant frontotemporal dementia (FTD) in a North American cohortHilary W Heuer, P Wang, K Rascovsky, et al.

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

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You have reached the last page of results.This site can display upto 50 results.

Critical Care Medicine|August 13, 2005

Randomized, controlled clinical trial of point-of-care limited ultrasonography assistance of central venous cannulation: the Third Sonography Outcomes Assessment Program (SOAP-3) TrialTruman J Milling, John Rose, William M Briggs, et al.

Open Access Emergency Medicine : OAEM|February 28, 2020

The Impact of a Concierge Medicine Model on Door to Doctor Time and Patient Flow in an Urban Emergency DepartmentAsher L Mandel, Thomas Bove, Amisha D Parekh, et al.

Clinical Genetics|June 4, 2014

COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?A M McInerney-Leo, E L Duncan, P J Leo, et al.

The Plant Journal : for Cell and Molecular Biology|April 12, 2000

Defective splicing of the first nad4 intron is associated with lack of several complex I subunits in the Nicotiana sylvestris NMS1 nuclear mutantJ Brangeon, M Sabar, S Gutierres, et al.

The Annals of Thoracic Surgery|September 9, 2014

Aortic valve replacement in octogenarians with prior cardiac surgeryTomasz A Timek, Zaahir Turfe, Robert L Hooker, et al.

Pediatric Diabetes|February 9, 2018

Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinismS R Johnson, P J Leo, A M McInerney-Leo, et al.

Genes and Immunity|November 27, 2015

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitisP C Robinson, P J Leo, J J Pointon, et al.

Clinical Genetics|December 11, 2014

Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophiesA M McInerney-Leo, J E Harris, P J Leo, et al.

Environment International|June 26, 2025

Multi-site study of communities with PFAS-contaminated drinking water: Methods, demographics, and PFAS serum concentrationsMarian Pavuk, John L Adgate, Scott M Bartell, et al.

Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 9, 2020

Comparison of sporadic and familial behavioral variant frontotemporal dementia (FTD) in a North American cohortHilary W Heuer, P Wang, K Rascovsky, et al.

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