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Glomerular Diseases
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April 24, 2023
A Genetic Risk Score Distinguishes Different Types of Autoantibody-Mediated Membranous Nephropathy
Sanjana Gupta, Mallory Lorraine Downie, Chris Cheshire, et al.
Journal of Palliative Care
|
February 16, 2026
Another Life: Palliative Virtual Reality for Experiencing the World Until the End
Sara Patuzzo Manzati, Paolo Manganotti, Giovanni de Manzoni, et al.
Cell Stem Cell
|
August 3, 2019
Modeling Monogenic Diabetes using Human ESCs Reveals Developmental and Metabolic Deficiencies Caused by Mutations in HNF1A
Fabian L Cardenas-Diaz, Catherine Osorio-Quintero, Maria A Diaz-Miranda, et al.
Haematologica
|
February 18, 2021
Identification of a novel genetic locus associated with immune-mediated thrombotic thrombocytopenic purpura
Matthew J Stubbs, Paul Coppo, Chris Cheshire, et al.
Nature Materials
|
February 3, 2009
Supramolecular control of the magnetic anisotropy in two-dimensional high-spin Fe arrays at a metal interface
Pietro Gambardella, Sebastian Stepanow, Alexandre Dmitriev, et al.
Neurology
|
June 30, 2012
A candidate gene for autoimmune myasthenia gravis
Guida Landouré, Melanie A Knight, Horia Stanescu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
July 20, 2023
A Phase II Study of Optimized Individualized Adaptive Radiotherapy for Hepatocellular Carcinoma
Daniel J Herr, Chang Wang, Mishal Mendiratta-Lala, et al.
Epidemiology (Cambridge, Mass.)
|
September 23, 2003
Assessing exposure misclassification by expert assessment in multicenter occupational studies
Andrea 't Mannetje, Joelle Fevotte, Tony Fletcher, et al.
Contemporary Clinical Trials
|
June 17, 2026
Ultra-high dose radiation for Liver metastasis using MR-guided TReatment with stereotactic Ablative Single-fraction (ULTRAS): Study protocol for a phase III randomized controlled trial
Harroun Wong, Sylvia S W Ng, Issa Mohamad, et al.
Annals of Neurology
|
February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia
Joshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Page
of 94
Search research articles
Search
Showing results (631-640 of 940) with videos related to
Sort By:
Page
of 94
Glomerular Diseases
|
April 24, 2023
A Genetic Risk Score Distinguishes Different Types of Autoantibody-Mediated Membranous Nephropathy
Sanjana Gupta, Mallory Lorraine Downie, Chris Cheshire, et al.
Journal of Palliative Care
|
February 16, 2026
Another Life: Palliative Virtual Reality for Experiencing the World Until the End
Sara Patuzzo Manzati, Paolo Manganotti, Giovanni de Manzoni, et al.
Cell Stem Cell
|
August 3, 2019
Modeling Monogenic Diabetes using Human ESCs Reveals Developmental and Metabolic Deficiencies Caused by Mutations in HNF1A
Fabian L Cardenas-Diaz, Catherine Osorio-Quintero, Maria A Diaz-Miranda, et al.
Haematologica
|
February 18, 2021
Identification of a novel genetic locus associated with immune-mediated thrombotic thrombocytopenic purpura
Matthew J Stubbs, Paul Coppo, Chris Cheshire, et al.
Nature Materials
|
February 3, 2009
Supramolecular control of the magnetic anisotropy in two-dimensional high-spin Fe arrays at a metal interface
Pietro Gambardella, Sebastian Stepanow, Alexandre Dmitriev, et al.
Neurology
|
June 30, 2012
A candidate gene for autoimmune myasthenia gravis
Guida Landouré, Melanie A Knight, Horia Stanescu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
July 20, 2023
A Phase II Study of Optimized Individualized Adaptive Radiotherapy for Hepatocellular Carcinoma
Daniel J Herr, Chang Wang, Mishal Mendiratta-Lala, et al.
Epidemiology (Cambridge, Mass.)
|
September 23, 2003
Assessing exposure misclassification by expert assessment in multicenter occupational studies
Andrea 't Mannetje, Joelle Fevotte, Tony Fletcher, et al.
Contemporary Clinical Trials
|
June 17, 2026
Ultra-high dose radiation for Liver metastasis using MR-guided TReatment with stereotactic Ablative Single-fraction (ULTRAS): Study protocol for a phase III randomized controlled trial
Harroun Wong, Sylvia S W Ng, Issa Mohamad, et al.
Annals of Neurology
|
February 21, 2013
Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia
Joshua Hersheson, Niccolo E Mencacci, Mary Davis, et al.
Page
of 94