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Archives of Neurology|June 15, 2011
Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosisHussein Daoud, Véronique Belzil, Sandra Martins, et al.Neurobiology of Aging|February 25, 2012
Analysis of the SORT1 gene in familial amyotrophic lateral sclerosisVéronique V Belzil, Catherine André-Guimont, Marie-Renée Atallah, et al.The Journal of Innovations in Cardiac Rhythm Management|August 11, 2022
Establishing Safe Working Parameters for Radiofrequency Ablation In Vitro Using Acoustic Sensing, Probability Mapping, and Catheter Contact AngleWadih El Khoury, Joseph Al Aaraj, Anthony Gebran, et al.European Journal of Medical Genetics|August 12, 2015
Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegiaHussein Daoud, Eleni Merkouri Papadima, Bouchra Ouled Amar Bencheikh, et al.Archives of Neurology|January 12, 2011
Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosisHussein Daoud, Paul N Valdmanis, Francois Gros-Louis, et al.Journal of Medical Genetics|September 23, 2018
Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratoryLandry Nfonsam, Shelley Ordorica, Mahdi Ghani, et al.Gene|April 28, 2015
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patientsPaloma Gonzalez-Perez, Ute Woehlbier, Ru-Ju Chian, et al.Journal of Medical Genetics|January 29, 2013
Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadismHussein Daoud, Martine Tétreault, William Gibson, et al.The Journal of Molecular Diagnostics : JMD|April 28, 2019
Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic LaboratoriesMahdi Ghani, Landry Nfonsam, Erinija Pranckeviciene, et al.Archives of Neurology|September 12, 2012
C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementiaHussein Daoud, Hamid Suhail, Mike Sabbagh, et al.Pageof 7