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Genes
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January 21, 2022
Investigating the Genetic Profile of the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia (ALS-FTD) Continuum in Patients of Diverse Race, Ethnicity and Ancestry
Maysen Mesaros, Steven Lenz, Woobeen Lim, et al.
Neurology. Genetics
|
February 12, 2020
Incidence of pathogenic, likely pathogenic, and uncertain ALS variants in a clinic cohort
Jennifer Roggenbuck, Marilly Palettas, Leah Vicini, et al.
Journal of Genetic Counseling
|
October 21, 2016
Patients with Amyotrophic Lateral Sclerosis Have High Interest in and Limited Access to Genetic Testing
Karin N Wagner, Haikady Nagaraja, Dawn C Allain, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
April 2, 2019
Lack of consensus in ALS genetic testing practices and divergent views between ALS clinicians and patients
Holly Klepek, Haikady Nagaraja, Stephen A Goutman, et al.
European Journal of Human Genetics : EJHG
|
November 5, 2024
Genetic testing for monogenic forms of motor neuron disease/amyotrophic lateral sclerosis in unaffected family members
Jade Howard, Amina Chaouch, Andrew G L Douglas, et al.
Annals of Clinical and Translational Neurology
|
September 11, 2023
Evidence-based consensus guidelines for ALS genetic testing and counseling
Jennifer Roggenbuck, Breda H F Eubank, Joshua Wright, et al.
The Journal of Molecular Diagnostics : JMD
|
May 3, 2002
A 39-bp deletion polymorphism in PTEN in African American individuals: implications for molecular diagnostic testing
Xiao-Ping Zhou, Heather Hampel, Jennifer Roggenbuck, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
August 2, 2024
The Answer ALS return of results study: Answering the duty to disclose
Jennifer Roggenbuck, Mackenzie Kaschalk, Rory Eustace, et al.
Molecular Genetics & Genomic Medicine
|
December 22, 2017
Patients with sporadic and familial amyotrophic lateral sclerosis found value in genetic testing
Karin N Wagner, Haikady N Nagaraja, Dawn C Allain, et al.
Frontiers in Neurology
|
July 17, 2020
Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders
Alayne P Meyer, Jennifer Roggenbuck, Samantha LoRusso, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Genes
|
January 21, 2022
Investigating the Genetic Profile of the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia (ALS-FTD) Continuum in Patients of Diverse Race, Ethnicity and Ancestry
Maysen Mesaros, Steven Lenz, Woobeen Lim, et al.
Neurology. Genetics
|
February 12, 2020
Incidence of pathogenic, likely pathogenic, and uncertain ALS variants in a clinic cohort
Jennifer Roggenbuck, Marilly Palettas, Leah Vicini, et al.
Journal of Genetic Counseling
|
October 21, 2016
Patients with Amyotrophic Lateral Sclerosis Have High Interest in and Limited Access to Genetic Testing
Karin N Wagner, Haikady Nagaraja, Dawn C Allain, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
April 2, 2019
Lack of consensus in ALS genetic testing practices and divergent views between ALS clinicians and patients
Holly Klepek, Haikady Nagaraja, Stephen A Goutman, et al.
European Journal of Human Genetics : EJHG
|
November 5, 2024
Genetic testing for monogenic forms of motor neuron disease/amyotrophic lateral sclerosis in unaffected family members
Jade Howard, Amina Chaouch, Andrew G L Douglas, et al.
Annals of Clinical and Translational Neurology
|
September 11, 2023
Evidence-based consensus guidelines for ALS genetic testing and counseling
Jennifer Roggenbuck, Breda H F Eubank, Joshua Wright, et al.
The Journal of Molecular Diagnostics : JMD
|
May 3, 2002
A 39-bp deletion polymorphism in PTEN in African American individuals: implications for molecular diagnostic testing
Xiao-Ping Zhou, Heather Hampel, Jennifer Roggenbuck, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
August 2, 2024
The Answer ALS return of results study: Answering the duty to disclose
Jennifer Roggenbuck, Mackenzie Kaschalk, Rory Eustace, et al.
Molecular Genetics & Genomic Medicine
|
December 22, 2017
Patients with sporadic and familial amyotrophic lateral sclerosis found value in genetic testing
Karin N Wagner, Haikady N Nagaraja, Dawn C Allain, et al.
Frontiers in Neurology
|
July 17, 2020
Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders
Alayne P Meyer, Jennifer Roggenbuck, Samantha LoRusso, et al.
Page
of 4