نتایج جستجو برای: hereditary spastic paraplegia

تعداد نتایج: 94252  

Journal: :European journal of neurology 2017
M Krenn G Zulehner C Hotzy J Rath E Stogmann M Wagner T B Haack T M Strom A Zimprich F Zimprich

BACKGROUND AND PURPOSE Hereditary spastic paraplegia is a clinically and genetically heterogeneous group of rare, inherited disorders causing an upper motor neuron syndrome with (complex) or without (pure) additional neurological symptoms. Mutations in the KIF1A gene have already been associated with recessive and dominant forms of hereditary spastic paraplegia (SPG30) in a few cases. METHODS...

Journal: :Journal of rehabilitation medicine 2015
Mark de Niet Susanne T de Bot Bart P C van de Warrenburg Vivian Weerdesteyn Alexander C Geurts

OBJECTIVE Although calf muscle spasticity is often treated with botulinum toxin type-A, the effects on balance and gait are ambiguous. Hereditary spastic paraplegia is characterized by progressive spasticity and relatively mild muscle weakness of the lower limbs. It is therefore a good model to evaluate the functional effects of botulinum toxin type-A. DESIGN Explorative pre-post intervention...

2010
Antonio Orlacchio Carla Babalini Antonella Borreca Clarice Patrono Roberto Massa Sarenur Basaran Renato P. Munhoz Ekaterina A. Rogaeva Peter H. St George-Hyslop Giorgio Bernardi Toshitaka Kawarai

The mutation of the spatacsin gene is the single most common cause of autosomal recessive hereditary spastic paraplegia with thin corpus callosum. Common clinical, pathological and genetic features between amyotrophic lateral sclerosis and hereditary spastic paraplegia motivated us to investigate 25 families with autosomal recessive juvenile amyotrophic lateral sclerosis and long-term survival ...

2015
Rita-Eva Varga Mukhran Khundadze Markus Damme Sandor Nietzsche Birgit Hoffmann Tobias Stauber Nicole Koch J. Christopher Hennings Patricia Franzka Antje K. Huebner Michael M. Kessels Christoph Biskup Thomas J. Jentsch Britta Qualmann Thomas Braulke Ingo Kurth Christian Beetz Christian A. Hübner Gregory A. Cox

Hereditary spastic paraplegia (HSP) is characterized by a dying back degeneration of corticospinal axons which leads to progressive weakness and spasticity of the legs. SPG11 is the most common autosomal-recessive form of HSPs and is caused by mutations in SPG11. A recent in vitro study suggested that Spatacsin, the respective gene product, is needed for the recycling of lysosomes from autolyso...

2017
Zafar Iqbal Siri L Rydning Iselin M Wedding Jeanette Koht Lasse Pihlstrøm Aina H Rengmark Sandra P Henriksen Chantal M E Tallaksen Mathias Toft

Hereditary ataxia and spastic paraplegia are heterogeneous monogenic neurodegenerative disorders. To date, a large number of individuals with such disorders remain undiagnosed. Here, we have assessed molecular diagnosis by gene panel sequencing in 105 early and late-onset hereditary ataxia and spastic paraplegia probands, in whom extensive previous investigations had failed to identify the gene...

Journal: :Brain : a journal of neurology 2010
Christoph S Clemen Karthikeyan Tangavelou Karl-Heinz Strucksberg Steffen Just Linda Gaertner Hanna Regus-Leidig Maria Stumpf Jens Reimann Roland Coras Reginald O Morgan Maria-Pilar Fernandez Andreas Hofmann Stefan Müller Benedikt Schoser Franz-Georg Hanisch Wolfgang Rottbauer Ingmar Blümcke Stephan von Hörsten Ludwig Eichinger Rolf Schröder

Mutations of the human valosin-containing protein gene cause autosomal-dominant inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. We identified strumpellin as a novel valosin-containing protein binding partner. Strumpellin mutations have been shown to cause hereditary spastic paraplegia. We demonstrate that strumpellin is a ubiquitously expressed protein...

2015
YANMIN SONG YUNHAI LIU NING ZHANG LILI LONG

The aim of the present study was to conduct a familial investigation and provide a genetic diagnosis to a family presenting with spastic paraplegia and clinically diagnosed with hereditary spastic paraplegia (HSP). Blood samples were obtained from the family, and mutations in the gene causing spinocerebellar ataxia type 3 (SCA3)/Machado-Joseph disease (MJD), known as MJD1, were analyzed using t...

Journal: :Current Biology 2004
Robert M. Gould Scott T. Brady

Studies with animal models are providing new insights into the pathology of hereditary spastic paraplegia, particularly how mutations in multiple, converging pathways can lead to this family of neuropathies.

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