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Anne M Kelly

Showing results (31-40 of 43) with videos related to

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Rheumatology (Oxford, England)|November 22, 2025
A Child with CANDLE Syndrome Presenting as Seronegative Polyarthritis Following Early ChemotherapySamantha Cooray, Alexander Wilson, Emma-Louise Gerety, et al.
Blood|May 11, 2017
The effect of variation in donor platelet function on transfusion outcome: a semirandomized controlled trialAnne M Kelly, Stephen F Garner, Theodora Foukaneli, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 19, 2024
Expert United Kingdom consensus on the preservation of joint health in people with moderate and severe haemophilia A: A modified Delphi panelMike Laffan, Paul McLaughlin, Jayashree Motwani, et al.
Clinical Orthopaedics and Related Research|September 29, 2021
Is Grit Associated with Burnout and Well-being in Orthopaedic Resident and Faculty Physicians? A Multi-institution Longitudinal Study Across Training LevelsDonald H Lee, Kaitlyn Reasoner, Diane Lee, et al.
EMBO Molecular Medicine|August 28, 2024
The evolving genetic landscape of telomere biology disorder dyskeratosis congenitaHemanth Tummala, Amanda J Walne, Mohsin Badat, et al.
Blood|January 9, 2017
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopeniaSuthesh Sivapalaratnam, Sarah K Westbury, Jonathan C Stephens, et al.
Genome Medicine|May 8, 2015
Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disordersSarah K Westbury, Ernest Turro, Daniel Greene, et al.
Science Translational Medicine|March 4, 2016
A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologiesErnest Turro, Daniel Greene, Anouck Wijgaerts, et al.
Blood|February 26, 2016
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing lossSimon Stritt, Paquita Nurden, Ernest Turro, et al.
Nucleic Acids Research|November 13, 2013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype dataSebastian Köhler, Sandra C Doelken, Christopher J Mungall, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Rheumatology (Oxford, England)|November 22, 2025
A Child with CANDLE Syndrome Presenting as Seronegative Polyarthritis Following Early ChemotherapySamantha Cooray, Alexander Wilson, Emma-Louise Gerety, et al.
Blood|May 11, 2017
The effect of variation in donor platelet function on transfusion outcome: a semirandomized controlled trialAnne M Kelly, Stephen F Garner, Theodora Foukaneli, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 19, 2024
Expert United Kingdom consensus on the preservation of joint health in people with moderate and severe haemophilia A: A modified Delphi panelMike Laffan, Paul McLaughlin, Jayashree Motwani, et al.
Clinical Orthopaedics and Related Research|September 29, 2021
Is Grit Associated with Burnout and Well-being in Orthopaedic Resident and Faculty Physicians? A Multi-institution Longitudinal Study Across Training LevelsDonald H Lee, Kaitlyn Reasoner, Diane Lee, et al.
EMBO Molecular Medicine|August 28, 2024
The evolving genetic landscape of telomere biology disorder dyskeratosis congenitaHemanth Tummala, Amanda J Walne, Mohsin Badat, et al.
Blood|January 9, 2017
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopeniaSuthesh Sivapalaratnam, Sarah K Westbury, Jonathan C Stephens, et al.
Genome Medicine|May 8, 2015
Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disordersSarah K Westbury, Ernest Turro, Daniel Greene, et al.
Science Translational Medicine|March 4, 2016
A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologiesErnest Turro, Daniel Greene, Anouck Wijgaerts, et al.
Blood|February 26, 2016
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing lossSimon Stritt, Paquita Nurden, Ernest Turro, et al.
Nucleic Acids Research|November 13, 2013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype dataSebastian Köhler, Sandra C Doelken, Christopher J Mungall, et al.
Pageof 5