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Brain : a Journal of Neurology
|
December 20, 2021
Forecasting stroke-like episodes and outcomes in mitochondrial disease
Yi Shiau Ng, Nichola Z Lax, Alasdair P Blain, et al.
EMBO Molecular Medicine
|
April 4, 2023
Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability
Direnis Erdinc, Alejandro Rodríguez-Luis, Mahmoud R Fassad, et al.
Nature
|
September 10, 2025
Myeloid progenitor dysregulation fuels immunosuppressive macrophages in tumours
Samarth Hegde, Bruno Giotti, Brian Y Soong, et al.
Journal of Computational Chemistry
|
May 16, 2009
CHARMM: the biomolecular simulation program
B R Brooks, C L Brooks, A D Mackerell, et al.
Brain : a Journal of Neurology
|
April 15, 2014
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
Gerald Pfeffer, Gráinne S Gorman, Helen Griffin, et al.
Ebiomedicine
|
March 7, 2018
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load
Yi Shiau Ng, Nichola Z Lax, Paul Maddison, et al.
Medical Image Analysis
|
July 22, 2017
Validation, comparison, and combination of algorithms for automatic detection of pulmonary nodules in computed tomography images: The LUNA16 challenge
Arnaud Arindra Adiyoso Setio, Alberto Traverso, Thomas de Bel, et al.
ESMO Open
|
January 21, 2026
International multicenter retrospective study on pleomorphic rhabdomyosarcoma (P-RMS), a PUSH platform study: outcome of primary localized disease
C Giani, G G Baldi, S Ljevar, et al.
American Journal of Obstetrics and Gynecology
|
May 17, 2022
Gestational diabetes mellitus and COVID-19: results from the COVID-19-Related Obstetric and Neonatal Outcome Study (CRONOS)
Helmut J Kleinwechter, Katharina S Weber, Nina Mingers, et al.
ESMO Open
|
September 12, 2024
Low-grade fibromyxoid sarcoma and sclerosing epithelioid fibrosarcoma, outcome of advanced disease: retrospective study from the Ultra-Rare Sarcoma Working Group
C Giani, R A Denu, S Ljevar, et al.
Page
of 113
Search research articles
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Showing results (1111-1120 of 1,124) with videos related to
Sort By:
Page
of 113
Brain : a Journal of Neurology
|
December 20, 2021
Forecasting stroke-like episodes and outcomes in mitochondrial disease
Yi Shiau Ng, Nichola Z Lax, Alasdair P Blain, et al.
EMBO Molecular Medicine
|
April 4, 2023
Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stability
Direnis Erdinc, Alejandro Rodríguez-Luis, Mahmoud R Fassad, et al.
Nature
|
September 10, 2025
Myeloid progenitor dysregulation fuels immunosuppressive macrophages in tumours
Samarth Hegde, Bruno Giotti, Brian Y Soong, et al.
Journal of Computational Chemistry
|
May 16, 2009
CHARMM: the biomolecular simulation program
B R Brooks, C L Brooks, A D Mackerell, et al.
Brain : a Journal of Neurology
|
April 15, 2014
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
Gerald Pfeffer, Gráinne S Gorman, Helen Griffin, et al.
Ebiomedicine
|
March 7, 2018
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load
Yi Shiau Ng, Nichola Z Lax, Paul Maddison, et al.
Medical Image Analysis
|
July 22, 2017
Validation, comparison, and combination of algorithms for automatic detection of pulmonary nodules in computed tomography images: The LUNA16 challenge
Arnaud Arindra Adiyoso Setio, Alberto Traverso, Thomas de Bel, et al.
ESMO Open
|
January 21, 2026
International multicenter retrospective study on pleomorphic rhabdomyosarcoma (P-RMS), a PUSH platform study: outcome of primary localized disease
C Giani, G G Baldi, S Ljevar, et al.
American Journal of Obstetrics and Gynecology
|
May 17, 2022
Gestational diabetes mellitus and COVID-19: results from the COVID-19-Related Obstetric and Neonatal Outcome Study (CRONOS)
Helmut J Kleinwechter, Katharina S Weber, Nina Mingers, et al.
ESMO Open
|
September 12, 2024
Low-grade fibromyxoid sarcoma and sclerosing epithelioid fibrosarcoma, outcome of advanced disease: retrospective study from the Ultra-Rare Sarcoma Working Group
C Giani, R A Denu, S Ljevar, et al.
Page
of 113