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Paul G Rothberg

Showing results (31-40 of 45) with videos related to

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British Journal of Haematology|June 19, 2015
Evolution to plasmablastic lymphoma evades CD19-directed chimeric antigen receptor T cellsAndrew G Evans, Paul G Rothberg, W Richard Burack, et al.
Diagnostic Pathology|February 20, 2013
Immunohistochemical detection of mutations in the epidermal growth factor receptor gene in lung adenocarcinomas using mutation-specific antibodiesYan Xiong, Yun Bai, Nufatt Leong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 20, 2023
Phenylalanine hydroxylase deficiency treatment and management: A systematic evidence review of the American College of Medical Genetics and Genomics (ACMG)April D Adams, Moisés Ó Fiesco-Roa, Lawrence Wong, et al.
Blood Advances|January 4, 2018
Index case of acute myeloid leukemia in a family harboring a novel <i>CEBPA</i> germ line mutationJodi Ram, Gabrielle Flamm, Marlene Balys, et al.
Developmental Medicine and Child Neurology|November 13, 2014
Standardized assessment of seizures in patients with juvenile neuronal ceroid lipofuscinosisErika F Augustine, Heather R Adams, Christopher A Beck, et al.
Developmental Medicine and Child Neurology|March 18, 2006
Standardized assessment of behavior and adaptive living skills in juvenile neuronal ceroid lipofuscinosisHeather Adams, Elisabeth A de Blieck, Jonathan W Mink, et al.
Journal of Inherited Metabolic Disease|May 11, 2011
Parent-reported benefits of flupirtine in juvenile neuronal ceroid lipofuscinosis (Batten disease; CLN3) are not supported by quantitative dataJennifer Cialone, Erika F Augustine, Nicole Newhouse, et al.
Cold Spring Harbor Molecular Case Studies|May 9, 2023
Clonal cytopenia of undetermined significance (CCUS)-associated reversion of donor-derived, transient αβ T-cell large granular clonal lymphocytosis, emerging post-transplant in a patient with a history of γδ T-cell large granular lymphocytic leukemiaSiba El Hussein, Andrew G Evans, John M Fitzsimmons, et al.
Contemporary Clinical Trials|May 1, 2013
Methodology of clinical research in rare diseases: development of a research program in juvenile neuronal ceroid lipofuscinosis (JNCL) via creation of a patient registry and collaboration with patient advocatesElisabeth A de Blieck, Erika F Augustine, Frederick J Marshall, et al.
The Journal of Molecular Diagnostics : JMD|August 21, 2016
The Spectrum of Clinical Utilities in Molecular Pathology Testing Procedures for Inherited Conditions and Cancer: A Report of the Association for Molecular PathologyLoren Joseph, Milena Cankovic, Samuel Caughron, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
British Journal of Haematology|June 19, 2015
Evolution to plasmablastic lymphoma evades CD19-directed chimeric antigen receptor T cellsAndrew G Evans, Paul G Rothberg, W Richard Burack, et al.
Diagnostic Pathology|February 20, 2013
Immunohistochemical detection of mutations in the epidermal growth factor receptor gene in lung adenocarcinomas using mutation-specific antibodiesYan Xiong, Yun Bai, Nufatt Leong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 20, 2023
Phenylalanine hydroxylase deficiency treatment and management: A systematic evidence review of the American College of Medical Genetics and Genomics (ACMG)April D Adams, Moisés Ó Fiesco-Roa, Lawrence Wong, et al.
Blood Advances|January 4, 2018
Index case of acute myeloid leukemia in a family harboring a novel <i>CEBPA</i> germ line mutationJodi Ram, Gabrielle Flamm, Marlene Balys, et al.
Developmental Medicine and Child Neurology|November 13, 2014
Standardized assessment of seizures in patients with juvenile neuronal ceroid lipofuscinosisErika F Augustine, Heather R Adams, Christopher A Beck, et al.
Developmental Medicine and Child Neurology|March 18, 2006
Standardized assessment of behavior and adaptive living skills in juvenile neuronal ceroid lipofuscinosisHeather Adams, Elisabeth A de Blieck, Jonathan W Mink, et al.
Journal of Inherited Metabolic Disease|May 11, 2011
Parent-reported benefits of flupirtine in juvenile neuronal ceroid lipofuscinosis (Batten disease; CLN3) are not supported by quantitative dataJennifer Cialone, Erika F Augustine, Nicole Newhouse, et al.
Cold Spring Harbor Molecular Case Studies|May 9, 2023
Clonal cytopenia of undetermined significance (CCUS)-associated reversion of donor-derived, transient αβ T-cell large granular clonal lymphocytosis, emerging post-transplant in a patient with a history of γδ T-cell large granular lymphocytic leukemiaSiba El Hussein, Andrew G Evans, John M Fitzsimmons, et al.
Contemporary Clinical Trials|May 1, 2013
Methodology of clinical research in rare diseases: development of a research program in juvenile neuronal ceroid lipofuscinosis (JNCL) via creation of a patient registry and collaboration with patient advocatesElisabeth A de Blieck, Erika F Augustine, Frederick J Marshall, et al.
The Journal of Molecular Diagnostics : JMD|August 21, 2016
The Spectrum of Clinical Utilities in Molecular Pathology Testing Procedures for Inherited Conditions and Cancer: A Report of the Association for Molecular PathologyLoren Joseph, Milena Cankovic, Samuel Caughron, et al.
Pageof 5