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Journal of the Royal Society of Medicine
|
October 3, 2002
Breaking bad news
Marc Patterson
Journal of Inherited Metabolic Disease
|
August 27, 2020
Newborn screening: To WES or not to WES, that is the question
Eva Morava, Matthias Baumgartner, Marc Patterson, et al.
Molecular Syndromology
|
April 9, 2015
Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective
Amber Volk, Erin Conboy, Beverly Wical, et al.
Neurology
|
February 17, 2021
Teaching NeuroImages: Neuroimaging Findings in Inosine Triphosphate Pyrophosphohydrolase Deficiency
Karthik Muthusamy, Suzanne Boyer, Marc Patterson, et al.
Journal of Inherited Metabolic Disease
|
May 8, 2023
Guidelines in the JIMD: Evidence-based practice for inherited metabolic disease
Shamima Rahman, Marc Patterson, Verena Peters, et al.
Orphanet Journal of Rare Diseases
|
November 19, 2021
International consensus on clinical severity scale use in evaluating Niemann-Pick disease Type C in paediatric and adult patients: results from a Delphi Study
William Evans, Marc Patterson, Frances Platt, et al.
Journal of Inherited Metabolic Disease
|
March 1, 2022
Quo vadis now: Beyond genomics to an era of personalised medicine
Shamima Rahman, Matthias Baumgartner, Eva Morava, et al.
Journal of Inherited Metabolic Disease
|
October 1, 2015
Quo vadis: the re-definition of "inborn metabolic diseases"
Eva Morava, Shamima Rahman, Verena Peters, et al.
Journal of Inherited Metabolic Disease
|
December 15, 2015
Peer review fraud-it's not big and it's not clever
Shamima Rahman, Matthias R Baumgartner, Eva Morava, et al.
Journal of Inherited Metabolic Disease
|
August 3, 2023
Risk and potential of ChatGPT in scientific publishing
Verena Peters, Matthias Baumgartner, Sean Froese, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Journal of the Royal Society of Medicine
|
October 3, 2002
Breaking bad news
Marc Patterson
Journal of Inherited Metabolic Disease
|
August 27, 2020
Newborn screening: To WES or not to WES, that is the question
Eva Morava, Matthias Baumgartner, Marc Patterson, et al.
Molecular Syndromology
|
April 9, 2015
Whole-Exome Sequencing in the Clinic: Lessons from Six Consecutive Cases from the Clinician's Perspective
Amber Volk, Erin Conboy, Beverly Wical, et al.
Neurology
|
February 17, 2021
Teaching NeuroImages: Neuroimaging Findings in Inosine Triphosphate Pyrophosphohydrolase Deficiency
Karthik Muthusamy, Suzanne Boyer, Marc Patterson, et al.
Journal of Inherited Metabolic Disease
|
May 8, 2023
Guidelines in the JIMD: Evidence-based practice for inherited metabolic disease
Shamima Rahman, Marc Patterson, Verena Peters, et al.
Orphanet Journal of Rare Diseases
|
November 19, 2021
International consensus on clinical severity scale use in evaluating Niemann-Pick disease Type C in paediatric and adult patients: results from a Delphi Study
William Evans, Marc Patterson, Frances Platt, et al.
Journal of Inherited Metabolic Disease
|
March 1, 2022
Quo vadis now: Beyond genomics to an era of personalised medicine
Shamima Rahman, Matthias Baumgartner, Eva Morava, et al.
Journal of Inherited Metabolic Disease
|
October 1, 2015
Quo vadis: the re-definition of "inborn metabolic diseases"
Eva Morava, Shamima Rahman, Verena Peters, et al.
Journal of Inherited Metabolic Disease
|
December 15, 2015
Peer review fraud-it's not big and it's not clever
Shamima Rahman, Matthias R Baumgartner, Eva Morava, et al.
Journal of Inherited Metabolic Disease
|
August 3, 2023
Risk and potential of ChatGPT in scientific publishing
Verena Peters, Matthias Baumgartner, Sean Froese, et al.
Page
of 3