The high prevalence of hereditary spastic paraplegia in Sardinia, insular Italy

The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population

(2013) Alessandro Gialluisi et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance

(2012) Josef Finsterer et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Hereditary ataxias and paraplegias in Valle ďAosta, Italy: a study of prevalence and disability

(2010) M. Leone et al.   ACTA NEUROLOGICA SCANDINAVICA

Hereditary spastic paraplegia in Western Norway

(2010) H. Skre   CLINICAL GENETICS

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study

(2009) A. K. Erichsen et al.   BRAIN

Clustering of multiple sclerosis, age of onset and gender in Sardinia

(2009) Maura Pugliatti et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

(2008) Sylvain Hanein et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia

(2008) Amir Boukhris et al.   ARCHIVES OF NEUROLOGY

The Prevalence of Hereditary Spastic Paraplegia and the Occurrence of SPG4 Mutations in Estonia

(2008) Mark Braschinsky et al.   NEUROEPIDEMIOLOGY

Y-Chromosome Based Evidence for Pre-Neolithic Origin of the Genetically Homogeneous but Diverse Sardinian Population: Inference for Association Scans

(2008) Daniela Contu et al.   PLoS One