Lymphangiome kystique abdominal = Abdominal cystic lymphangiomaELLEUCH, Nizar; LAURIAN, Claude.STV. Sang thrombose vaisseaux. 2003, Vol 15, Num 5, pp 278-279, issn 0999-7385, 2 p.Article

Malformation vasculaire des membres et anévrisme des veines tibiales = Vascular malformations of the limbs and aneurysm of the tibial veinsELLEUCH, Nizar; LAURIAN, Claude.STV. Sang thrombose vaisseaux. 2004, Vol 16, Num 2, pp 105-106, issn 0999-7385, 2 p.Article

Corps étranger intra-artériel = Intra arterial foreign bodyELLEUCH, Nizar; GIGOU, Frédéric.STV. Sang thrombose vaisseaux. 2004, Vol 16, Num 1, pp 59-60, issn 0999-7385, 2 p.Article

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosumSTEVANIN, Giovanni; SANTORELLI, Filippo M; LOSSOS, Alexander et al.Nature genetics. 2007, Vol 39, Num 3, pp 366-372, issn 1061-4036, 7 p.Article

A novel locus for autosomal dominant uncomplicated hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3HANEIN, Sylvain; DÜRR, Alexandra; BRICE, Alexis et al.Human genetics. 2007, Vol 122, Num 3-4, pp 261-273, issn 0340-6717, 13 p.Article

Spastic paraplegia 5 : Locus refinement, candidate gene analysis and clinical descriptionKLEBE, Stephan; DURR, Alexandra; POEA-GUYON, Sandrine et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 7, pp 854-861, issn 1552-4841, 8 p.Article

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin SyndromeHANEIN, Sylvain; MARTIN, Elodie; ELLEUCH, Nizar et al.American journal of human genetics. 2008, Vol 82, Num 4, pp 992-1002, issn 0002-9297, 11 p.Article

Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia : SPG11, SPG15, and Further Genetic HeterogeneityBOUKHRIS, Amir; STEVANIN, Giovanni; BRICE, Alexis et al.Archives of neurology (Chicago). 2008, Vol 65, Num 3, pp 393-402, issn 0003-9942, 10 p.Article

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab familiesELLEUCH, Nizar; BOUSLAM, Naima; BACQ, Delphine et al.Neurogenetics (Oxford. Print). 2007, Vol 8, Num 4, pp 307-315, issn 1364-6745, 9 p.Article

Hereditary spastic paraplegia with thin corpus callosum : Reduction of the SPG11 interval and evidence for further genetic heterogeneityLOSSOS, Alexander; STEVANIN, Giovanni; SILVERSTEIN, Shira et al.Archives of neurology (Chicago). 2006, Vol 63, Num 5, pp 756-760, issn 0003-9942, 5 p.Article