List of works - Nizar Elleuch

A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum

scientific article

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.

scientific article

Aortic stent migration: a rare complication after endovascular repair

scientific article published on 6 April 2014

Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.

scientific article published on 24 January 2006

Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity

scientific article

Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity

scientific article published in May 2006

Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome

scientific article

Middle aortic coarctation: a rare vascular disorder

scientific article published on 24 January 2015

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

scientific article

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

scientific article published on 18 February 2007

Popliteal pseudoaneurysm and arteriovenous fistula after acupuncture.

scientific article

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families

scientific article

Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description

article

Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity

scientific article

[Anastomotic false aneurysms after under-diaphragmatic bypasses: about 25 cases]

scientific article published on 01 October 2006

[Surgical management of extracranial carotid artery aneurysm]

scientific article published on 23 May 2012

List of works by Nizar Elleuch

A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.

Aortic stent migration: a rare complication after endovascular repair

Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.

Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity

Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity

Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome

Middle aortic coarctation: a rare vascular disorder

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Popliteal pseudoaneurysm and arteriovenous fistula after acupuncture.

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families

Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description

Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity

[Anastomotic false aneurysms after under-diaphragmatic bypasses: about 25 cases]

[Surgical management of extracranial carotid artery aneurysm]