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Russell J Butterfield

Showing results (11-20 of 73) with videos related to

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The Journal of Pediatrics|July 14, 2020
Cost-Effectiveness of Nusinersen and Universal Newborn Screening for Spinal Muscular AtrophyAli Jalali, Erin Rothwell, Jeffrey R Botkin, et al.
Molecular Therapy. Methods & Clinical Development|February 28, 2025
Subacute liver injury in two young infants following gene replacement therapy for spinal muscular atrophyCassie Ables, Catalina Jaramillo, E Lynne Wood, et al.
The American Journal of Pathology|October 29, 2004
Gender, age, and season at immunization uniquely influence the genetic control of susceptibility to histopathological lesions and clinical signs of experimental allergic encephalomyelitis: implications for the genetics of multiple sclerosisCory Teuscher, Janice Y Bunn, Parley D Fillmore, et al.
International Journal of Neonatal Screening|July 25, 2024
A Five-Year Review of Newborn Screening for Spinal Muscular Atrophy in the State of Utah: Lessons LearnedKristen N Wong, Melissa McIntyre, Sabina Cook, et al.
Neuromuscular Disorders : NMD|January 18, 2026
Facioscapulohumeral muscular dystrophy diagnosed in childhood: a muscular dystrophy surveillance, tracking and research network cohortTahereh Neyaz, Kristin M Conway, Yining Yang, et al.
Cardiology in the Young|May 17, 2018
DMD mutation and LTBP4 haplotype do not predict onset of left ventricular dysfunction in Duchenne muscular dystrophyCharlotte S Van Dorn, Michael D Puchalski, Hsin-Yi Weng, et al.
Neuromuscular Disorders : NMD|November 23, 2024
Respiratory function and evaluation in individuals with facioscapulohumeral muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking and Research NetworkKatherine D Mathews, Jonathan Suhl, Kristin M Conway, et al.
Neuromuscular Disorders : NMD|March 26, 2009
A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22Russell J Butterfield, Deepa Ramachandran, Sandra J Hasstedt, et al.
Muscle & Nerve|November 19, 2016
Physical function and mobility in children with congenital myotonic dystrophyEvan M Pucillo, Deanna L Dibella, Man Hung, et al.
Genetics|March 29, 2003
Sex-specific quantitative trait loci govern susceptibility to Theiler's murine encephalomyelitis virus-induced demyelinationRussell J Butterfield, Randall J Roper, Dominic M Rhein, et al.
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
The Journal of Pediatrics|July 14, 2020
Cost-Effectiveness of Nusinersen and Universal Newborn Screening for Spinal Muscular AtrophyAli Jalali, Erin Rothwell, Jeffrey R Botkin, et al.
Molecular Therapy. Methods & Clinical Development|February 28, 2025
Subacute liver injury in two young infants following gene replacement therapy for spinal muscular atrophyCassie Ables, Catalina Jaramillo, E Lynne Wood, et al.
The American Journal of Pathology|October 29, 2004
Gender, age, and season at immunization uniquely influence the genetic control of susceptibility to histopathological lesions and clinical signs of experimental allergic encephalomyelitis: implications for the genetics of multiple sclerosisCory Teuscher, Janice Y Bunn, Parley D Fillmore, et al.
International Journal of Neonatal Screening|July 25, 2024
A Five-Year Review of Newborn Screening for Spinal Muscular Atrophy in the State of Utah: Lessons LearnedKristen N Wong, Melissa McIntyre, Sabina Cook, et al.
Neuromuscular Disorders : NMD|January 18, 2026
Facioscapulohumeral muscular dystrophy diagnosed in childhood: a muscular dystrophy surveillance, tracking and research network cohortTahereh Neyaz, Kristin M Conway, Yining Yang, et al.
Cardiology in the Young|May 17, 2018
DMD mutation and LTBP4 haplotype do not predict onset of left ventricular dysfunction in Duchenne muscular dystrophyCharlotte S Van Dorn, Michael D Puchalski, Hsin-Yi Weng, et al.
Neuromuscular Disorders : NMD|November 23, 2024
Respiratory function and evaluation in individuals with facioscapulohumeral muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking and Research NetworkKatherine D Mathews, Jonathan Suhl, Kristin M Conway, et al.
Neuromuscular Disorders : NMD|March 26, 2009
A novel form of juvenile recessive ALS maps to loci on 6p25 and 21q22Russell J Butterfield, Deepa Ramachandran, Sandra J Hasstedt, et al.
Muscle & Nerve|November 19, 2016
Physical function and mobility in children with congenital myotonic dystrophyEvan M Pucillo, Deanna L Dibella, Man Hung, et al.
Genetics|March 29, 2003
Sex-specific quantitative trait loci govern susceptibility to Theiler's murine encephalomyelitis virus-induced demyelinationRussell J Butterfield, Randall J Roper, Dominic M Rhein, et al.
Pageof 8