Genetic studies of Russian patients with amyotrophic lateral sclerosis

Linking RNA Dysfunction and Neurodegeneration in Amyotrophic Lateral Sclerosis

(2015) Sami J. Barmada   Neurotherapeutics

Role of VEGF and VEGFR2 Receptor in Reversal of ALS-CSF Induced Degeneration of NSC-34 Motor Neuron Cell Line

(2014) K. Vijayalakshmi et al.   MOLECULAR NEUROBIOLOGY

Experimental approach to the gene therapy of motor neuron disease with the use of genes hypoxia-inducible factors

(2014) Sh. M. Ismailov et al.   RUSSIAN JOURNAL OF GENETICS

Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitor

(2014) Antonio Canosa et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing

(2013) Kevin P Kenna et al.   JOURNAL OF MEDICAL GENETICS

Familial amyotrophic lateral sclerosis in Alberta, Canada

(2013) Ted Pfister et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

(2012) Elisa Majounie et al.   LANCET NEUROLOGY

Extensive genetics of ALS: A population-based study in Italy

(2012) A. Chio et al.   NEUROLOGY

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

(2011) Ilse Gijselinck et al.   LANCET NEUROLOGY

Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

(2011) Mariely DeJesus-Hernandez et al.   NEURON

FUS/TLSgene mutations are the second most frequent cause of familial ALS in the Spanish population

(2010) Enrique Syriani et al.   Amyotrophic Lateral Sclerosis

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

(2010) Andrew C. Elden et al.   NATURE

High frequency ofTARDBPgene mutations in Italian patients with amyotrophic lateral sclerosis

(2009) Lucia Corrado et al.   HUMAN MUTATION

Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotype

(2008) D Lambrechts et al.   JOURNAL OF MEDICAL GENETICS