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Showing results (1191-1200 of 1,318) with videos related to
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Journal of General Internal Medicine
|
July 18, 2014
RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research
Rachel Thompson, Louise Johnston, Domenica Taruscio, et al.
The Lancet. Child & Adolescent Health
|
February 6, 2022
Probiotic peanut oral immunotherapy versus oral immunotherapy and placebo in children with peanut allergy in Australia (PPOIT-003): a multicentre, randomised, phase 2b trial
Paxton Loke, Francesca Orsini, Adriana C Lozinsky, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 1, 2023
Integration of EpiSign, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re-classification of an ARID1B missense variant
Caitlin Forwood, Katie Ashton, Ying Zhu, et al.
Dementia (London, England)
|
May 29, 2023
Transforming dementia research into policy change: A case study of the multi-country STRiDE project
Wendy Weidner, Rochelle Amour, Erica Breuer, et al.
Cytotherapy
|
February 1, 2014
Third-party umbilical cord blood-derived regulatory T cells prevent xenogenic graft-versus-host disease
Simrit Parmar, Xiaoying Liu, Shawndeep S Tung, et al.
Prenatal Diagnosis
|
December 8, 2025
Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections
Natalie B Gulrajani, John Boscardin, Billie R Lianoglou, et al.
Western Journal of Nursing Research
|
September 10, 2020
Applying the Behavior Change Technique Taxonomy to Four Multicomponent Childhood Obesity Interventions
Meghan M JaKa, Caroline Wood, Sara Veblen-Mortenson, et al.
Nature Communications
|
May 31, 2020
TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca<sup>2</sup>
Brian M Woolums, Brett A McCray, Hyun Sung, et al.
American Journal of Human Genetics
|
June 30, 2015
The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease
Tudor Groza, Sebastian Köhler, Dawid Moldenhauer, et al.
Patterns (New York, N.Y.)
|
November 16, 2020
KG-COVID-19: A Framework to Produce Customized Knowledge Graphs for COVID-19 Response
Justin T Reese, Deepak Unni, Tiffany J Callahan, et al.
Page
of 132
Search research articles
Search
Showing results (1191-1200 of 1,318) with videos related to
Sort By:
Page
of 132
Journal of General Internal Medicine
|
July 18, 2014
RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research
Rachel Thompson, Louise Johnston, Domenica Taruscio, et al.
The Lancet. Child & Adolescent Health
|
February 6, 2022
Probiotic peanut oral immunotherapy versus oral immunotherapy and placebo in children with peanut allergy in Australia (PPOIT-003): a multicentre, randomised, phase 2b trial
Paxton Loke, Francesca Orsini, Adriana C Lozinsky, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 1, 2023
Integration of EpiSign, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re-classification of an ARID1B missense variant
Caitlin Forwood, Katie Ashton, Ying Zhu, et al.
Dementia (London, England)
|
May 29, 2023
Transforming dementia research into policy change: A case study of the multi-country STRiDE project
Wendy Weidner, Rochelle Amour, Erica Breuer, et al.
Cytotherapy
|
February 1, 2014
Third-party umbilical cord blood-derived regulatory T cells prevent xenogenic graft-versus-host disease
Simrit Parmar, Xiaoying Liu, Shawndeep S Tung, et al.
Prenatal Diagnosis
|
December 8, 2025
Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections
Natalie B Gulrajani, John Boscardin, Billie R Lianoglou, et al.
Western Journal of Nursing Research
|
September 10, 2020
Applying the Behavior Change Technique Taxonomy to Four Multicomponent Childhood Obesity Interventions
Meghan M JaKa, Caroline Wood, Sara Veblen-Mortenson, et al.
Nature Communications
|
May 31, 2020
TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca<sup>2</sup>
Brian M Woolums, Brett A McCray, Hyun Sung, et al.
American Journal of Human Genetics
|
June 30, 2015
The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease
Tudor Groza, Sebastian Köhler, Dawid Moldenhauer, et al.
Patterns (New York, N.Y.)
|
November 16, 2020
KG-COVID-19: A Framework to Produce Customized Knowledge Graphs for COVID-19 Response
Justin T Reese, Deepak Unni, Tiffany J Callahan, et al.
Page
of 132