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Ann S Martin

Showing results (1-10 of 16) with videos related to

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Plos Currents|March 31, 2012
DuchenneConnect Registry ReportVanessa Rangel, Ann S Martin, Holly L Peay
Muscle & Nerve|October 2, 2019
Delays in diagnosis of Duchenne muscular dystrophy: An evaluation of genotypic and sociodemographic factorsKevin J Counterman, Pat Furlong, Richard T Wang, et al.
BMC Medical Research Methodology|August 11, 2019
Chart validation of an algorithm for identifying hereditary progressive muscular dystrophy in healthcare claimsXiaoxue Chen, Abiy Agiro, Ann S Martin, et al.
Journal of Neuromuscular Diseases|October 17, 2022
Associations Between Self-Reported Behavioral and Learning Concerns and DMD Isoforms in Duchenne Muscular DystrophyKevin J Counterman, Kathy Fatovic, Daniel C Good, et al.
Pediatrics|October 3, 2018
Evaluating Implementation of the Updated Care Considerations for Duchenne Muscular DystrophyKatherine S Ong, Kathi Kinnett, Rieza Soelaeman, et al.
Journal of Neuromuscular Diseases|February 16, 2024
Draft Guidance for Industry Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and Related Dystrophinopathies - Developing Potential Treatments for the Entire Spectrum of DiseaseCraig McDonald, Eric Camino, Rafael Escandon, et al.
Journal of Medical Genetics|December 11, 2024
Unveiling non-coding <i>DMD</i> variants: synergising RNA sequencing and DNA sequencing for enhanced molecular diagnosisYinghong Pan, Babi Ramesh Reddy Nallamilli, Ruby Liu, et al.
Journal of Neuromuscular Diseases|May 18, 2020
Clinical Phenotypes of DMD Exon 51 Skip Equivalent Deletions: A Systematic ReviewMegan A Waldrop, Rabah Ben Yaou, Karin K Lucas, et al.
Journal of Genetic Counseling|April 29, 2024
Genetic counseling for the dystrophinopathies-Practice resource of the National Society of Genetic CounselorsAngela M Pickart, Ann S Martin, Brianna N Gross, et al.
Human Mutation|June 17, 2018
DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtypeRichard T Wang, Florian Barthelemy, Ann S Martin, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Plos Currents|March 31, 2012
DuchenneConnect Registry ReportVanessa Rangel, Ann S Martin, Holly L Peay
Muscle & Nerve|October 2, 2019
Delays in diagnosis of Duchenne muscular dystrophy: An evaluation of genotypic and sociodemographic factorsKevin J Counterman, Pat Furlong, Richard T Wang, et al.
BMC Medical Research Methodology|August 11, 2019
Chart validation of an algorithm for identifying hereditary progressive muscular dystrophy in healthcare claimsXiaoxue Chen, Abiy Agiro, Ann S Martin, et al.
Journal of Neuromuscular Diseases|October 17, 2022
Associations Between Self-Reported Behavioral and Learning Concerns and DMD Isoforms in Duchenne Muscular DystrophyKevin J Counterman, Kathy Fatovic, Daniel C Good, et al.
Pediatrics|October 3, 2018
Evaluating Implementation of the Updated Care Considerations for Duchenne Muscular DystrophyKatherine S Ong, Kathi Kinnett, Rieza Soelaeman, et al.
Journal of Neuromuscular Diseases|February 16, 2024
Draft Guidance for Industry Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and Related Dystrophinopathies - Developing Potential Treatments for the Entire Spectrum of DiseaseCraig McDonald, Eric Camino, Rafael Escandon, et al.
Journal of Medical Genetics|December 11, 2024
Unveiling non-coding <i>DMD</i> variants: synergising RNA sequencing and DNA sequencing for enhanced molecular diagnosisYinghong Pan, Babi Ramesh Reddy Nallamilli, Ruby Liu, et al.
Journal of Neuromuscular Diseases|May 18, 2020
Clinical Phenotypes of DMD Exon 51 Skip Equivalent Deletions: A Systematic ReviewMegan A Waldrop, Rabah Ben Yaou, Karin K Lucas, et al.
Journal of Genetic Counseling|April 29, 2024
Genetic counseling for the dystrophinopathies-Practice resource of the National Society of Genetic CounselorsAngela M Pickart, Ann S Martin, Brianna N Gross, et al.
Human Mutation|June 17, 2018
DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtypeRichard T Wang, Florian Barthelemy, Ann S Martin, et al.
Pageof 2