N. Elleuch

发表

A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3

S. Hanein, A. Dürr, P. Ribai, 2007, Human Genetics.

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

A. Durr, N. Elleuch, C. Depienne, 2006, Neurology.

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

S. Klebe, A. Durr, S. Hanein, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

M. Ruberg, A. Durr, N. Elleuch, 2007, Nature Genetics.

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

N. Elleuch, A. Brice, G. Stevanin, 2008, Archives of neurology.

Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity

N. Elleuch, A. Brice, G. Stevanin, 2009, Clinical genetics.

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

S. Klebe, A. Durr, N. Elleuch, 2006, Archives of neurology.

Sulodexide in Patients with Chronic Venous Disease of the Lower Limbs: Clinical Efficacy and Impact on Quality of Life

N. Elleuch, A.I.H. Ahmed, K. Mondher, 2016, Advances in Therapy.

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

A. Durr, M. Hutchinson, S. Hanein, 2008, American journal of human genetics.

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

S. Klebe, P. Bastien, A. Durr, 2006, Brain : a journal of neurology.

Popliteal pseudoaneurysm and arteriovenous fistula after acupuncture.

N. Elleuch, A. Khayati, B. Derbel, 2015, Journal des maladies vasculaires.

[Management of isolated iliac aneurysms: A Tunisian center experience].

N. Elleuch, H. Cheikhrouhou, A. Jemel, 2017, Journal de medecine vasculaire.

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

D. Zélénika, N. Elleuch, A. Brice, 2010, neurogenetics.

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

S. Klebe, D. Zélénika, A. Durr, 2007, Neurogenetics.

Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex

S. Tezenas du Montcel, C. Duyckaerts, A. Durr, 2018, Brain : a journal of neurology.

Purification and properties of a maltoheptaose- and maltohexaose-forming amylase produced by Bacillus subtilis US116

N. Elleuch, S. Bejar, E. Messaoud, 2004 .

Surgical management of internal carotid artery aneurysm near the skull base.

N. Elleuch, I. Frikha, T. Boudawara, 2018, Journal de medecine vasculaire.

[Surgical management of extracranial carotid artery aneurysm].

N. Elleuch, S. Ben Omrane, A. Khayati, 2012, Journal des maladies vasculaires.

[Post-traumatic carotido-jugular fistula: Case report and review of the literature].

N. Elleuch, S. Haddar, B. Hammami, 2017, Journal de medecine vasculaire.

An unusual cause of ischemia after coronary bypass grafting!!

N. Elleuch, L. Abid, S. Kammoun, 2017, Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology.

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

J. Weissenbach, J. Prud'homme, A. Dürr, 2007, Neurology.

[Transposition of the external jugular vein onto the subclavian vein in the treatment of symptomatic stenosis of the right subclavian vein].

N. Elleuch, S. Moalla, M. Gdoura, 1996, Annales de cardiologie et d'angeiologie.

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

A. Durr, M. Hutchinson, S. Hanein, 2008, American journal of human genetics.