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The Oncologist
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December 16, 2018
Patient-Reported Toxicities During Chemotherapy Regimens in Current Clinical Practice for Early Breast Cancer
Kirsten A Nyrop, Allison M Deal, Shlomit S Shachar, et al.
Cancer
|
May 16, 2019
Patient-reported and clinician-reported chemotherapy-induced peripheral neuropathy in patients with early breast cancer: Current clinical practice
Kirsten A Nyrop, Allison M Deal, Kathryn E Reeder-Hayes, et al.
Cancer
|
April 22, 2020
Congruence of patient- and clinician-reported toxicity in women receiving chemotherapy for early breast cancer
Kirsten A Nyrop, Allison M Deal, Bryce B Reeve, et al.
Human Mutation
|
June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants
Duyen H Pham, Melissa R Pitman, Raman Kumar, et al.
Human Molecular Genetics
|
December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder
Raman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Cancer Medicine
|
January 16, 2023
A phase II single-arm trial of memantine for prevention of cognitive decline during chemotherapy in patients with early breast cancer: Feasibility, tolerability, acceptability, and preliminary effects
Zev M Nakamura, Allison M Deal, Eliza M Park, et al.
Nature Communications
|
February 8, 2024
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 23, 2026
Novel <i>PCDH12</i> pathogenic missense variants cause neurodevelopmental disorders with ocular malformation
Jennifer Rakotomamonjy, Lucas Fares-Taie, Raman Kumar, et al.
American Journal of Human Genetics
|
July 14, 2015
THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability
Raman Kumar, Mark A Corbett, Bregje W M van Bon, et al.
NPJ Genomic Medicine
|
December 10, 2020
Missense variant contribution to USP9X-female syndrome
Lachlan A Jolly, Euan Parnell, Alison E Gardner, et al.
Page
of 24
Search research articles
Search
Showing results (211-220 of 233) with videos related to
Sort By:
Page
of 24
The Oncologist
|
December 16, 2018
Patient-Reported Toxicities During Chemotherapy Regimens in Current Clinical Practice for Early Breast Cancer
Kirsten A Nyrop, Allison M Deal, Shlomit S Shachar, et al.
Cancer
|
May 16, 2019
Patient-reported and clinician-reported chemotherapy-induced peripheral neuropathy in patients with early breast cancer: Current clinical practice
Kirsten A Nyrop, Allison M Deal, Kathryn E Reeder-Hayes, et al.
Cancer
|
April 22, 2020
Congruence of patient- and clinician-reported toxicity in women receiving chemotherapy for early breast cancer
Kirsten A Nyrop, Allison M Deal, Bryce B Reeve, et al.
Human Mutation
|
June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants
Duyen H Pham, Melissa R Pitman, Raman Kumar, et al.
Human Molecular Genetics
|
December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder
Raman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Cancer Medicine
|
January 16, 2023
A phase II single-arm trial of memantine for prevention of cognitive decline during chemotherapy in patients with early breast cancer: Feasibility, tolerability, acceptability, and preliminary effects
Zev M Nakamura, Allison M Deal, Eliza M Park, et al.
Nature Communications
|
February 8, 2024
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 23, 2026
Novel <i>PCDH12</i> pathogenic missense variants cause neurodevelopmental disorders with ocular malformation
Jennifer Rakotomamonjy, Lucas Fares-Taie, Raman Kumar, et al.
American Journal of Human Genetics
|
July 14, 2015
THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability
Raman Kumar, Mark A Corbett, Bregje W M van Bon, et al.
NPJ Genomic Medicine
|
December 10, 2020
Missense variant contribution to USP9X-female syndrome
Lachlan A Jolly, Euan Parnell, Alison E Gardner, et al.
Page
of 24