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Hereditary spastic paraplegia caused by a mutation in the VCP gene.

published in: Brain

date of publication: 2012-09-18

language: English

main subject: hereditary spastic paraplegia

Cites articles 15

Date

Title

Authors

2011-03-11

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

Maria Rita Passos-Bueno
2011-08-31

Novel p.Ile151Val mutation in VCP in a patient of African American descent with sporadic ALS

Zbigniew K Wszolek
2011-09-03

The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis

Jogeshwar Mukherjee
2010-09-09

Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases

Andreas Hofmann, Benedikt Schoser, Stephan von Hörsten, Reginald O Morgan, Maria Pilar Fernández-Fernández, Ludwig Eichinger
2010-06-01

An evaluation of neurophysiological criteria used in the diagnosis of motor neuron disease

Pamela Shaw
2010-12-09

Exome sequencing reveals VCP mutations as a cause of familial ALS

Michael Benatar, Gabriella Restagno, Adriano Chiò, Sampath Arepalli, John Q. Trojanowski, Rossella Spataro, Maria Martinez-Lage, Jessica Mandrioli, Stefania Battistini, Sonja Scholz, Andrea Calvo, Mario Sabatelli, J Paul Taylor, Gabriele Mora, Maria Rosaria Monsurrò, Maura Brunetti, Giuseppe Borghero, Bryan Traynor, Dena G. Hernandez, Leo McCluskey, Patrizia Sola
2010-03-23

Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings
2009-11

The Arp2/3 activator WASH controls the fission of endosomes through a large multiprotein complex

Alexis Gautreau
2008-01-01

An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene

Mario Sabatelli, Giorgio Tasca, Massimiliano Mirabella
2008-02-01

Roles of VCP in human neurodegenerative disorders
2008-04-12

Spastin oligomerizes into a hexamer and the mutant spastin (E442Q) redistribute the wild-type spastin into filamentous microtubule
2006-06-21

Valosin-containing protein gene mutations: clinical and neuropathologic features.
2006-09-19

Pathological consequences of VCP mutations on human striated muscle.

Andreas Hofmann, Dietmar R. Thal, Hanns Lochmüller, Erich Wanker, Benedikt Schoser, Annett Böddrich, Outi Kämäräinen
2005-10-24

Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene

Alexander Zimprich, Christine Mannhalter
2004-04

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

Michael P. Whyte, Steven Mumm

Article - wd:Q48370935

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