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Critical Care Medicine
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March 20, 2026
Gaps and Strategies for Management of Sepsis in Low-Resource Settings: Expert Consensus Statements Using a Delphi Method
Sheila N Myatra, Kevin M Boyer, Jorge L Hidalgo, et al.
Archives of Disease in Childhood
|
October 4, 2018
Research priorities for childhood chronic conditions: a workshop report
Pamela Lopez-Vargas, Allison Tong, Sally Crowe, et al.
The Journal of Clinical Investigation
|
May 16, 2019
Targeting VLA4 integrin and CXCR2 mobilizes serially repopulating hematopoietic stem cells
Darja Karpova, Michael P Rettig, Julie Ritchey, et al.
EMBO Molecular Medicine
|
August 2, 2022
FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorder
Christopher W Fell, Astrid Hagelkruys, Ana Cicvaric, et al.
Annals of Neurology
|
April 13, 2024
Quantitative Foot Muscle Magnetic Resonance Imaging Reliably Measures Disease Progression in Children and Adolescents with Charcot-Marie-Tooth Disease Type 1A
Carolynne M Doherty, Paige Howard, Luke F O'Donnell, et al.
Critical Care Medicine
|
June 21, 2023
The Reviewer Academy of the Society of Critical Care Medicine: Key Principles and Strategic Plan
Peta M A Alexander, Rebecca A Aslakson, Erin F Barreto, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 21, 2020
Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study
Carolyn E B McCormick, Brian C Kavanaugh, Danielle Sipsock, et al.
Molecular Autism
|
October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autism
Lambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Annals of Neurology
|
February 2, 2019
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A
Feifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2
Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Page
of 58
Search research articles
Search
Showing results (531-540 of 573) with videos related to
Sort By:
Page
of 58
Critical Care Medicine
|
March 20, 2026
Gaps and Strategies for Management of Sepsis in Low-Resource Settings: Expert Consensus Statements Using a Delphi Method
Sheila N Myatra, Kevin M Boyer, Jorge L Hidalgo, et al.
Archives of Disease in Childhood
|
October 4, 2018
Research priorities for childhood chronic conditions: a workshop report
Pamela Lopez-Vargas, Allison Tong, Sally Crowe, et al.
The Journal of Clinical Investigation
|
May 16, 2019
Targeting VLA4 integrin and CXCR2 mobilizes serially repopulating hematopoietic stem cells
Darja Karpova, Michael P Rettig, Julie Ritchey, et al.
EMBO Molecular Medicine
|
August 2, 2022
FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorder
Christopher W Fell, Astrid Hagelkruys, Ana Cicvaric, et al.
Annals of Neurology
|
April 13, 2024
Quantitative Foot Muscle Magnetic Resonance Imaging Reliably Measures Disease Progression in Children and Adolescents with Charcot-Marie-Tooth Disease Type 1A
Carolynne M Doherty, Paige Howard, Luke F O'Donnell, et al.
Critical Care Medicine
|
June 21, 2023
The Reviewer Academy of the Society of Critical Care Medicine: Key Principles and Strategic Plan
Peta M A Alexander, Rebecca A Aslakson, Erin F Barreto, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 21, 2020
Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study
Carolyn E B McCormick, Brian C Kavanaugh, Danielle Sipsock, et al.
Molecular Autism
|
October 17, 2012
Common genetic variants, acting additively, are a major source of risk for autism
Lambertus Klei, Stephan J Sanders, Michael T Murtha, et al.
Annals of Neurology
|
February 2, 2019
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A
Feifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2
Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Page
of 58