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J Raphael

Showing results (301-310 of 488) with videos related to

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Journal of Cardiothoracic and Vascular Anesthesia|August 11, 2019
Therapeutic Whole Lung Lavage for Alveolar ProteinosisSatyajeet Misra, Prasanta Kumar Das, Shakti Kumar Bal, et al.
Assessment|August 13, 1999
Reliability of the Advanced Psychodiagnostic Interpretation (API) scoring system for the Bender GestaltE J Aucone, A J Raphael, C J Golden, et al.
Nature Neuroscience|February 19, 2013
mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortexAllissa A Dillman, David N Hauser, J Raphael Gibbs, et al.
Current Oncology (Toronto, Ont.)|March 27, 2024
Barriers and Unequal Access to Timely Molecular Testing Results: Addressing the Inequities in Cancer Care Delays across CanadaStephanie Snow, Christine Brezden-Masley, Michael D Carter, et al.
Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Leukemia Research|July 22, 2008
Computational identification of CDR3 sequence archetypes among immunoglobulin sequences in chronic lymphocytic leukemiaBradley T Messmer, Benjamin J Raphael, Sarah J Aerni, et al.
Muscle & Nerve|January 1, 2017
Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathyJames B Caress, Janel O Johnson, Yevgeniya A Abramzon, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 28, 2021
Long-Term Mental Health Service Utilization Among Survivors of Testicular Cancer: A Population-Based Cohort StudyMichael J Raphael, Sumit Gupta, Xuejiao Wei, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|September 17, 2017
Stereotactic Body Radiotherapy versus Low Dose Rate Brachytherapy for Localised Prostate Cancer: a Cost-Utility AnalysisJ Helou, S Torres, H B Musunuru, et al.
Journal of Neurology|May 16, 2009
An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variantMaria Teresa Dotti, Rosaria Buccoliero, Andrew Lee, et al.
Pageof 49

Showing results (301-310 of 488) with videos related to

Sort By:
Pageof 49
Journal of Cardiothoracic and Vascular Anesthesia|August 11, 2019
Therapeutic Whole Lung Lavage for Alveolar ProteinosisSatyajeet Misra, Prasanta Kumar Das, Shakti Kumar Bal, et al.
Assessment|August 13, 1999
Reliability of the Advanced Psychodiagnostic Interpretation (API) scoring system for the Bender GestaltE J Aucone, A J Raphael, C J Golden, et al.
Nature Neuroscience|February 19, 2013
mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortexAllissa A Dillman, David N Hauser, J Raphael Gibbs, et al.
Current Oncology (Toronto, Ont.)|March 27, 2024
Barriers and Unequal Access to Timely Molecular Testing Results: Addressing the Inequities in Cancer Care Delays across CanadaStephanie Snow, Christine Brezden-Masley, Michael D Carter, et al.
Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Leukemia Research|July 22, 2008
Computational identification of CDR3 sequence archetypes among immunoglobulin sequences in chronic lymphocytic leukemiaBradley T Messmer, Benjamin J Raphael, Sarah J Aerni, et al.
Muscle & Nerve|January 1, 2017
Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathyJames B Caress, Janel O Johnson, Yevgeniya A Abramzon, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 28, 2021
Long-Term Mental Health Service Utilization Among Survivors of Testicular Cancer: A Population-Based Cohort StudyMichael J Raphael, Sumit Gupta, Xuejiao Wei, et al.
Clinical Oncology (Royal College of Radiologists (Great Britain))|September 17, 2017
Stereotactic Body Radiotherapy versus Low Dose Rate Brachytherapy for Localised Prostate Cancer: a Cost-Utility AnalysisJ Helou, S Torres, H B Musunuru, et al.
Journal of Neurology|May 16, 2009
An infantile case of Alexander disease unusual for its MRI features and a GFAP allele carrying both the p.Arg79His mutation and the p.Glu223Gln coding variantMaria Teresa Dotti, Rosaria Buccoliero, Andrew Lee, et al.
Pageof 49