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Patrick G Gallagher

Showing results (81-90 of 172) with videos related to

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Blood Cells, Molecules & Diseases|January 1, 2021
Functional characterization of a novel SLC40A1 Arg88Ile mutation in a kindred with familial iron overload treated by phlebotomyJihad Womack, Abitha Sukumaran, Xiuqi Li, et al.
The Journal of Pediatrics|February 15, 2026
Neonatal Sepsis from 2014-2024: The Resurgence of Gram-Negative RodsNoa Fleiss, Thomas S Murray, Richard S Feinn, et al.
The Journal of Pediatrics|April 29, 2015
Neonatal sepsis 2004-2013: the rise and fall of coagulase-negative staphylococciMatthew J Bizzarro, Veronika Shabanova, Robert S Baltimore, et al.
Infection Control and Hospital Epidemiology|April 6, 2004
Conjunctival colonization of infants hospitalized in a neonatal intensive care unit: a longitudinal analysisCraig H Raskind, Barbara E Sabo, Deborah A Callan, et al.
Blood|November 15, 2008
An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cellsPatrick G Gallagher, Douglas G Nilson, Laurie A Steiner, et al.
Haematologica|June 5, 2014
Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locusHannah Bogardus, Vincent P Schulz, Yelena Maksimova, et al.
Journal of Cardiothoracic and Vascular Anesthesia|March 30, 2016
CASE 5-2016Complex Congenital Cardiac Surgery in an Adult Patient With Hereditary Spherocytosis: Avoidance of Massive Hemolysis Associated With Extracorporeal Circulation in the Presence of Red Blood Cell FragilityJennifer M Hargrave, Michelle J Capdeville, Andra E Duncan, et al.
Pediatric Blood & Cancer|May 4, 2011
Bi-allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemiaStephanie A Massaro, Renu Bajaj, Farzana D Pashankar, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 24, 2011
Perinatal onset mevalonate kinase deficiencyLaurie A Steiner, Richard A Ehrenkranz, Steven M Peterec, et al.
The Journal of Biological Chemistry|January 24, 2013
Identification of biologically relevant enhancers in human erythroid cellsMack Y Su, Laurie A Steiner, Hannah Bogardus, et al.
Pageof 18

Showing results (81-90 of 172) with videos related to

Sort By:
Pageof 18
Blood Cells, Molecules & Diseases|January 1, 2021
Functional characterization of a novel SLC40A1 Arg88Ile mutation in a kindred with familial iron overload treated by phlebotomyJihad Womack, Abitha Sukumaran, Xiuqi Li, et al.
The Journal of Pediatrics|February 15, 2026
Neonatal Sepsis from 2014-2024: The Resurgence of Gram-Negative RodsNoa Fleiss, Thomas S Murray, Richard S Feinn, et al.
The Journal of Pediatrics|April 29, 2015
Neonatal sepsis 2004-2013: the rise and fall of coagulase-negative staphylococciMatthew J Bizzarro, Veronika Shabanova, Robert S Baltimore, et al.
Infection Control and Hospital Epidemiology|April 6, 2004
Conjunctival colonization of infants hospitalized in a neonatal intensive care unit: a longitudinal analysisCraig H Raskind, Barbara E Sabo, Deborah A Callan, et al.
Blood|November 15, 2008
An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cellsPatrick G Gallagher, Douglas G Nilson, Laurie A Steiner, et al.
Haematologica|June 5, 2014
Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locusHannah Bogardus, Vincent P Schulz, Yelena Maksimova, et al.
Journal of Cardiothoracic and Vascular Anesthesia|March 30, 2016
CASE 5-2016Complex Congenital Cardiac Surgery in an Adult Patient With Hereditary Spherocytosis: Avoidance of Massive Hemolysis Associated With Extracorporeal Circulation in the Presence of Red Blood Cell FragilityJennifer M Hargrave, Michelle J Capdeville, Andra E Duncan, et al.
Pediatric Blood & Cancer|May 4, 2011
Bi-allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemiaStephanie A Massaro, Renu Bajaj, Farzana D Pashankar, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 24, 2011
Perinatal onset mevalonate kinase deficiencyLaurie A Steiner, Richard A Ehrenkranz, Steven M Peterec, et al.
The Journal of Biological Chemistry|January 24, 2013
Identification of biologically relevant enhancers in human erythroid cellsMack Y Su, Laurie A Steiner, Hannah Bogardus, et al.
Pageof 18