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Irene Roberts

Showing results (51-60 of 129) with videos related to

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Human Molecular Genetics|April 18, 2013
Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutationValentina S Caputo, Joana R Costa, Kalliopi Makarona, et al.
Molecular Human Reproduction|March 26, 2003
Characterization of first trimester fetal erythroblasts for non-invasive prenatal diagnosisMahesh Choolani, Keelin O'Donoghue, David Talbert, et al.
Haematologica|June 5, 2013
Age and aging in blood disorders: EHA theme of the year 2013-2014Christine Chomienne, Shaun McCann, Tony Green, et al.
Pediatrics|October 21, 2009
Prospective, observational study of outcomes in neonates with severe thrombocytopeniaSimon J Stanworth, Paul Clarke, Tim Watts, et al.
British Journal of Haematology|February 1, 2006
Correction of severe anaemia using immuno-regulated gene therapy is achieved by restoring the early erythroblast compartmentCamille Du Roure, Katalin Takács, Patrick H Maxwell, et al.
British Journal of Haematology|June 20, 2018
Guidelines for the investigation and management of Transient Leukaemia of Down SyndromeOliver Tunstall, Neha Bhatnagar, Beki James, et al.
Blood|April 10, 2010
Left ventricular hypertrophy and diastolic dysfunction in children with sickle cell disease are related to asleep and waking oxygen desaturationMark C Johnson, Fenella J Kirkham, Susan Redline, et al.
British Journal of Haematology|April 14, 2019
Impaired cellular and humoral immunity is a feature of Diamond-Blackfan anaemia; experience of 107 unselected cases in the United KingdomDeena Iskander, Irene Roberts, Clare Rees, et al.
Blood|August 12, 2008
Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutationsOliver Tunstall-Pedoe, Anindita Roy, Anastasios Karadimitris, et al.
Neurology|August 24, 2012
Recommendations for optimal ICD codes to study neurologic conditions: a systematic reviewChristine St Germaine-Smith, Amy Metcalfe, Tamara Pringsheim, et al.
Pageof 13

Showing results (51-60 of 129) with videos related to

Sort By:
Pageof 13
Human Molecular Genetics|April 18, 2013
Mechanism of Polycomb recruitment to CpG islands revealed by inherited disease-associated mutationValentina S Caputo, Joana R Costa, Kalliopi Makarona, et al.
Molecular Human Reproduction|March 26, 2003
Characterization of first trimester fetal erythroblasts for non-invasive prenatal diagnosisMahesh Choolani, Keelin O'Donoghue, David Talbert, et al.
Haematologica|June 5, 2013
Age and aging in blood disorders: EHA theme of the year 2013-2014Christine Chomienne, Shaun McCann, Tony Green, et al.
Pediatrics|October 21, 2009
Prospective, observational study of outcomes in neonates with severe thrombocytopeniaSimon J Stanworth, Paul Clarke, Tim Watts, et al.
British Journal of Haematology|February 1, 2006
Correction of severe anaemia using immuno-regulated gene therapy is achieved by restoring the early erythroblast compartmentCamille Du Roure, Katalin Takács, Patrick H Maxwell, et al.
British Journal of Haematology|June 20, 2018
Guidelines for the investigation and management of Transient Leukaemia of Down SyndromeOliver Tunstall, Neha Bhatnagar, Beki James, et al.
Blood|April 10, 2010
Left ventricular hypertrophy and diastolic dysfunction in children with sickle cell disease are related to asleep and waking oxygen desaturationMark C Johnson, Fenella J Kirkham, Susan Redline, et al.
British Journal of Haematology|April 14, 2019
Impaired cellular and humoral immunity is a feature of Diamond-Blackfan anaemia; experience of 107 unselected cases in the United KingdomDeena Iskander, Irene Roberts, Clare Rees, et al.
Blood|August 12, 2008
Abnormalities in the myeloid progenitor compartment in Down syndrome fetal liver precede acquisition of GATA1 mutationsOliver Tunstall-Pedoe, Anindita Roy, Anastasios Karadimitris, et al.
Neurology|August 24, 2012
Recommendations for optimal ICD codes to study neurologic conditions: a systematic reviewChristine St Germaine-Smith, Amy Metcalfe, Tamara Pringsheim, et al.
Pageof 13