Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Elisa, Nigro"'
Autor:
Elisa Nigro, Eyal Grunebaum, Binita Kamath, Christoph Licht, Caroline Malcolmson, Aamir Jeewa, Craig Campbell, Hugh McMillan, Pranesh Chakraborty, Mark Tarnopolsky, Hernan Gonorazky
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Spinal muscular atrophy (SMA) is a neuromuscular genetic disorder caused by the loss of lower motor neurons leading to progressive muscle weakness and atrophy. With the rise of novel therapies and early diagnosis on newborn screening (NBS), the natur
Externí odkaz:
https://doaj.org/article/0ef9cd25f9a44b1b9fee6b56324a1d81
Publikováno v:
Journal of PeriAnesthesia Nursing.
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. :1-6
Objectives: We aimed to explore the prevalence of peroneal neuropathy in children during coronavirus disease-19 (COVID-19) pandemic. Background: Since the COVID-19 outbreak, many children worldwide have experienced a dramatic lifestyle changes, inclu
Autor:
Fatima, Al Amrani, Reshma, Amin, Jackie, Chiang, Lena, Xiao, Jennifer, Boyd, Eugenia, Law, Elisa, Nigro, Lauren, Weinstock, Ana, Stosic, Hernan D, Gonorazky
Publikováno v:
Neurology: Clinical Practice. 12:279-287
Background and ObjectivesThe introduction of spinal muscular dystrophy (SMA)-modifying therapies, such as antisense oligonucleotide therapy, has changed the natural history of SMA. Most reports on treatment outcomes have focused on motor scores and r