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Oncology (Williston Park, N.Y.)
|
March 1, 2014
Acr appropriateness Criteria management of vaginal cancer
Larissa J Lee, Anuja Jhingran, Elizabeth Kidd, et al.
Practical Radiation Oncology
|
October 24, 2024
The Radiosurgery Society Working Groups on GRID, LATTICE, Microbeam, and FLASH Radiotherapies: Advancements Symposium and Subsequent Progress Made
James W Snider, Nina A Mayr, Jason Molitoris, et al.
Nature Genetics
|
October 28, 2008
TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy
Alena Cízková, Viktor Stránecký, Johannes A Mayr, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
May 23, 2024
Development and benchmarking of a Deep Learning-based MRI-guided gross tumor segmentation algorithm for Radiomics analyses in extremity soft tissue sarcomas
Jan C Peeken, Lucas Etzel, Tim Tomov, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
September 10, 2021
MRI-based delta-radiomics predicts pathologic complete response in high-grade soft-tissue sarcoma patients treated with neoadjuvant therapy
Jan C Peeken, Rebecca Asadpour, Katja Specht, et al.
American Journal of Clinical Oncology
|
July 23, 2013
ACR Appropriateness Criteria® management of locoregionally advanced squamous cell carcinoma of the vulva
, Elizabeth Kidd, David Moore, et al.
American Journal of Human Genetics
|
July 16, 2013
ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy
Tobias B Haack, Robert Kopajtich, Peter Freisinger, et al.
International Journal of Radiation Oncology, Biology, Physics
|
December 18, 2023
Overview and Recommendations for Prospective Multi-institutional Spatially Fractionated Radiation Therapy Clinical Trials
Heng Li, Nina A Mayr, Robert J Griffin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 7, 2020
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia
Simone Schröder, Yun Li, Gökhan Yigit, et al.
Oxidative Medicine and Cellular Longevity
|
August 15, 2017
Combined Respiratory Chain Deficiency and <i>UQCC2</i> Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies
René G Feichtinger, Michaela Brunner-Krainz, Bader Alhaddad, et al.
Page
of 56
Search research articles
Search
Showing results (461-470 of 555) with videos related to
Sort By:
Page
of 56
Oncology (Williston Park, N.Y.)
|
March 1, 2014
Acr appropriateness Criteria management of vaginal cancer
Larissa J Lee, Anuja Jhingran, Elizabeth Kidd, et al.
Practical Radiation Oncology
|
October 24, 2024
The Radiosurgery Society Working Groups on GRID, LATTICE, Microbeam, and FLASH Radiotherapies: Advancements Symposium and Subsequent Progress Made
James W Snider, Nina A Mayr, Jason Molitoris, et al.
Nature Genetics
|
October 28, 2008
TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy
Alena Cízková, Viktor Stránecký, Johannes A Mayr, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
May 23, 2024
Development and benchmarking of a Deep Learning-based MRI-guided gross tumor segmentation algorithm for Radiomics analyses in extremity soft tissue sarcomas
Jan C Peeken, Lucas Etzel, Tim Tomov, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
September 10, 2021
MRI-based delta-radiomics predicts pathologic complete response in high-grade soft-tissue sarcoma patients treated with neoadjuvant therapy
Jan C Peeken, Rebecca Asadpour, Katja Specht, et al.
American Journal of Clinical Oncology
|
July 23, 2013
ACR Appropriateness Criteria® management of locoregionally advanced squamous cell carcinoma of the vulva
, Elizabeth Kidd, David Moore, et al.
American Journal of Human Genetics
|
July 16, 2013
ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy
Tobias B Haack, Robert Kopajtich, Peter Freisinger, et al.
International Journal of Radiation Oncology, Biology, Physics
|
December 18, 2023
Overview and Recommendations for Prospective Multi-institutional Spatially Fractionated Radiation Therapy Clinical Trials
Heng Li, Nina A Mayr, Robert J Griffin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 7, 2020
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia
Simone Schröder, Yun Li, Gökhan Yigit, et al.
Oxidative Medicine and Cellular Longevity
|
August 15, 2017
Combined Respiratory Chain Deficiency and <i>UQCC2</i> Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies
René G Feichtinger, Michaela Brunner-Krainz, Bader Alhaddad, et al.
Page
of 56