Content: : Strumpell-Lorrain disease - or familial spastic paraplegia (FSP) - is a rare hereditary neurological disorder, mainly characterized by variable degrees of stiffness and weakening of the muscles, with cognitive impairment, deafness, and ataxia in the more severe cases. We describe two female siblings with FSP programmed for cholecystectomy and subtotal colectomy, respectively, and also how we dealt with the anesthetic management in both cases and review the literature on this disease in relation to anesthesia. Keywords: Spastic Paraplegia, Hereditary, Anesthesia, Neuromuscular blockade/sugammadex
Syringomyelia is a chronic progressive degenerative disorder of the spinal cord, characterized clini...
Spinal muscular atrophy (SMA) is a rare genetic disease characterized by degeneration of spinal cord...
Contains fulltext : 81109.pdf (publisher's version ) (Closed access)Sugammadex is ...
Content: Strumpell-Lorrain disease- or familial spastic paraplegia (FSP)- is a rare hereditary neuro...
AbstractContent: Strumpell-Lorrain disease - or familial spastic paraplegia (FSP) - is a rare heredi...
CONTEÚDO: A doença de Strumpell-Lorrain, ou paraparesia espástica familiar (PEF), é uma doença hered...
Sugammadex is a modified gamma-cyclodextrin that acts by selectively encapsulating free amino-steroi...
Abstract Background Hereditary spastic paraplegia (HSP) is a rare, genetic neurodegenerative conditi...
Spinal cord disorders are induced by diseases of various categories: infectious, inflammatory, degen...
The term hereditary spastic paraplegia (HSP) embraces a clinically and genetically heterogeneous gro...
Copyright © 2011 Xiu-Fen Liu et al. This is an open access article distributed under the Creative Co...
Joubert syndrome (JS) is a rare genetic disorder that affects the cerebellum, controlling balance, a...
Contains fulltext : 79529.pdf (publisher's version ) (Closed access)Residual paral...
Contains fulltext : 81674.pdf (publisher's version ) (Closed access)A case is repo...
Contains fulltext : 81455.pdf (publisher's version ) (Closed access)Stuve Wiedeman...
Syringomyelia is a chronic progressive degenerative disorder of the spinal cord, characterized clini...
Spinal muscular atrophy (SMA) is a rare genetic disease characterized by degeneration of spinal cord...
Contains fulltext : 81109.pdf (publisher's version ) (Closed access)Sugammadex is ...
Content: Strumpell-Lorrain disease- or familial spastic paraplegia (FSP)- is a rare hereditary neuro...
AbstractContent: Strumpell-Lorrain disease - or familial spastic paraplegia (FSP) - is a rare heredi...
CONTEÚDO: A doença de Strumpell-Lorrain, ou paraparesia espástica familiar (PEF), é uma doença hered...
Sugammadex is a modified gamma-cyclodextrin that acts by selectively encapsulating free amino-steroi...
Abstract Background Hereditary spastic paraplegia (HSP) is a rare, genetic neurodegenerative conditi...
Spinal cord disorders are induced by diseases of various categories: infectious, inflammatory, degen...
The term hereditary spastic paraplegia (HSP) embraces a clinically and genetically heterogeneous gro...
Copyright © 2011 Xiu-Fen Liu et al. This is an open access article distributed under the Creative Co...
Joubert syndrome (JS) is a rare genetic disorder that affects the cerebellum, controlling balance, a...
Contains fulltext : 79529.pdf (publisher's version ) (Closed access)Residual paral...
Contains fulltext : 81674.pdf (publisher's version ) (Closed access)A case is repo...
Contains fulltext : 81455.pdf (publisher's version ) (Closed access)Stuve Wiedeman...
Syringomyelia is a chronic progressive degenerative disorder of the spinal cord, characterized clini...
Spinal muscular atrophy (SMA) is a rare genetic disease characterized by degeneration of spinal cord...
Contains fulltext : 81109.pdf (publisher's version ) (Closed access)Sugammadex is ...