Search research articles
Contact Us
Filters
Showing results (1-10 of 142) with videos related to
Page
of 15
Sort By:
Neurology. Genetics
|
April 12, 2016
Next-generation sequencing still needs our generation's clinicians
A Reghan Foley, Sandra Donkervoort, Carsten G Bönnemann
Muscle & Nerve
|
April 25, 2026
Emerging Upper Extremity Muscle Ultrasound Patterns as a Diagnostic Aid in TTN-Related Myopathies
Abigail Potticary, Meghan McAnally, Sandra Donkervoort, et al.
Neuromuscular Disorders : NMD
|
August 12, 2019
214th ENMC International Workshop: Establishing an international consortium for gene discovery and clinical research for Congenital Muscle Disease, Heemskerk, the Netherlands, 6-18 October 2015
Sandra Donkervoort, James J Dowling, Jocelyn Laporte, et al.
Forensic Science International. Genetics
|
December 17, 2008
Enhancing accurate data collection in mass fatality kinship identifications: lessons learned from Hurricane Katrina
Sandra Donkervoort, Siobhan M Dolan, Michelle Beckwith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 16, 2009
The emerging role of genetics professionals in forensic kinship DNA identification after a mass fatality: lessons learned from Hurricane Katrina volunteers
Siobhan M Dolan, Devki S Saraiya, Sandra Donkervoort, et al.
Skeletal Radiology
|
June 7, 2011
Radiological features of Paget disease of bone associated with VCP myopathy
Farzin Farpour, Jamshid Tehranzadeh, Sandra Donkervoort, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
September 8, 2023
Recessive Pathogenic <i>GMPPB</i> Variants Cause a Childhood Onset Myasthenic Syndrome Responsive to Pyridostigmine
Gordon Jewett, Benjamin Beland, Shahin Khayambashi, et al.
Muscle & Nerve
|
January 10, 2017
Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase necrotizing myopathy masquerading as a muscular dystrophy in a child
Payam Mohassel, A Reghan Foley, Sandra Donkervoort, et al.
Neuromuscular Disorders : NMD
|
August 12, 2018
A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein gene
Jake Plewa, Abhilasha Surampalli, Marie Wencel, et al.
Journal of Lipid Research
|
October 9, 2009
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresis
Rebecca Schüle, Teepu Siddique, Han-Xiang Deng, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 142) with videos related to
Sort By:
Page
of 15
Neurology. Genetics
|
April 12, 2016
Next-generation sequencing still needs our generation's clinicians
A Reghan Foley, Sandra Donkervoort, Carsten G Bönnemann
Muscle & Nerve
|
April 25, 2026
Emerging Upper Extremity Muscle Ultrasound Patterns as a Diagnostic Aid in TTN-Related Myopathies
Abigail Potticary, Meghan McAnally, Sandra Donkervoort, et al.
Neuromuscular Disorders : NMD
|
August 12, 2019
214th ENMC International Workshop: Establishing an international consortium for gene discovery and clinical research for Congenital Muscle Disease, Heemskerk, the Netherlands, 6-18 October 2015
Sandra Donkervoort, James J Dowling, Jocelyn Laporte, et al.
Forensic Science International. Genetics
|
December 17, 2008
Enhancing accurate data collection in mass fatality kinship identifications: lessons learned from Hurricane Katrina
Sandra Donkervoort, Siobhan M Dolan, Michelle Beckwith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 16, 2009
The emerging role of genetics professionals in forensic kinship DNA identification after a mass fatality: lessons learned from Hurricane Katrina volunteers
Siobhan M Dolan, Devki S Saraiya, Sandra Donkervoort, et al.
Skeletal Radiology
|
June 7, 2011
Radiological features of Paget disease of bone associated with VCP myopathy
Farzin Farpour, Jamshid Tehranzadeh, Sandra Donkervoort, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
September 8, 2023
Recessive Pathogenic <i>GMPPB</i> Variants Cause a Childhood Onset Myasthenic Syndrome Responsive to Pyridostigmine
Gordon Jewett, Benjamin Beland, Shahin Khayambashi, et al.
Muscle & Nerve
|
January 10, 2017
Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase necrotizing myopathy masquerading as a muscular dystrophy in a child
Payam Mohassel, A Reghan Foley, Sandra Donkervoort, et al.
Neuromuscular Disorders : NMD
|
August 12, 2018
A cross-sectional analysis of clinical evaluation in 35 individuals with mutations of the valosin-containing protein gene
Jake Plewa, Abhilasha Surampalli, Marie Wencel, et al.
Journal of Lipid Research
|
October 9, 2009
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresis
Rebecca Schüle, Teepu Siddique, Han-Xiang Deng, et al.
Page
of 15