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Author/Creator Pfeffer, Gerald

4. Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure. Issue 3 (13th March 2013)

Authors:
Pfeffer, Gerald; Barresi, Rita; Wilson, Ian J; Hardy, Steven A; Griffin, Helen; Hudson, Judith; Elliott, Hannah R; Ramesh, Aravind V; Radunovic, Aleksandar; Winer, John B; Vaidya, Sujit; Raman, Ashok; Busby, Mark; Farrugia, Maria E; Ming, Alec; Everett, Chris; Emsley, Hedley C A; Horvath, Rita; S...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 85:Issue 3(2014)
Page Start:
331
Record Type:
Journal Article
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7. A National Spinal Muscular Atrophy Registry for Real-World Evidence. (4th November 2020)

Authors:
Hodgkinson, Victoria L.; Oskoui, Maryam; Lounsberry, Joshua; M'Dahoma, Saïd; Butler, Emily; Campbell, Craig; MacKenzie, Alex; McMillan, Hugh J.; Simard, Louise; Vajsar, Jiri; Brais, Bernard; Chapman, Kristine M.; Chrestian, Nicolas; Crone, Meghan; Dobrowolski, Peter; Dojeiji, Susan; Dowling, Jame...
Journal:
Canadian journal of neurological sciences
Issue:
Volume 47:Number 6(2020)
Page Start:
810
Record Type:
Journal Article
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9. Response to Provincial Governments' Decisions Regarding Monitoring for Adults with Spinal Muscular Atrophy. (27th March 2021)

Authors:
Hodgkinson, Victoria L.; Chapman, Kristine; Izenberg, Aaron; Lochmüller, Hanns; O'Connell, Colleen; O'Ferrall, Erin K.; Oskoui, Maryam; Pfeffer, Gerald; Plamondon, Stephanie; Rodrigue, Xavier; Shoesmith, Christen; Warman-Chardon, Jodi; Brais, Bernard; Korngut, Lawrence; Schellenberg, Kerri
Journal:
Canadian journal of neurological sciences
Issue:
Volume 48:Number 2(2021)
Page Start:
201
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗