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Items: 25

1.

Tolerance strategies of two Mediterranean native xerophytes under fluoride pollution in Tunisia.

Boukhris A, Laffont-Schwob I, Folzer H, Rabier J, Mezghani I, Salducci MD, Tatoni T, Chaieb M.

Environ Sci Pollut Res Int. 2018 Dec;25(34):34753-34764. doi: 10.1007/s11356-018-3431-y. Epub 2018 Oct 15.

PMID:
30324375
2.

Synthesis and crystal structure of a new magnesium phosphate Na3RbMg7(PO4)6.

Ben Hamed T, Boukhris A, Badri A, Ben Amara M.

Acta Crystallogr E Crystallogr Commun. 2017 May 5;73(Pt 6):817-820. doi: 10.1107/S2056989017006363. eCollection 2017 Jun 1.

3.

A new score for the diagnosis of acute coronary syndrome in acute chest pain with non-diagnostic ECG and normal troponin.

Boubaker H, Grissa MH, Beltaief K, Amor MH, Mdimagh Z, Boukhris A, Ben Amor M, Dridi Z, Letaief M, Bouida W, Boukef R, Najjar F, Nouira S.

Emerg Med J. 2015 Oct;32(10):764-8. doi: 10.1136/emermed-2013-203151. Epub 2015 Jan 5.

PMID:
25560250
4.

Changes in mesophyll element distribution and phytometabolite contents involved in fluoride tolerance of the arid gypsum-tolerant plant species Atractylis serratuloides Sieber ex Cass. (Asteraceae).

Boukhris A, Laffont-Schwob I, Rabier J, Salducci MD, El Kadri L, Tonetto A, Tatoni T, Chaieb M.

Environ Sci Pollut Res Int. 2015 May;22(10):7918-29. doi: 10.1007/s11356-014-3957-6. Epub 2014 Dec 17.

PMID:
25510616
5.

Screening biological traits and fluoride contents of native vegetations in arid environments to select efficiently fluoride-tolerant native plant species for in-situ phytoremediation.

Boukhris A, Laffont-Schwob I, Mezghani I, Kadri LE, Prudent P, Pricop A, Tatoni T, Chaieb M.

Chemosphere. 2015 Jan;119:217-223. doi: 10.1016/j.chemosphere.2014.06.007. Epub 2014 Jul 9.

PMID:
25014764
6.

Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia.

Boukhris A, Schule R, Loureiro JL, Lourenço CM, Mundwiller E, Gonzalez MA, Charles P, Gauthier J, Rekik I, Acosta Lebrigio RF, Gaussen M, Speziani F, Ferbert A, Feki I, Caballero-Oteyza A, Dionne-Laporte A, Amri M, Noreau A, Forlani S, Cruz VT, Mochel F, Coutinho P, Dion P, Mhiri C, Schols L, Pouget J, Darios F, Rouleau GA, Marques W Jr, Brice A, Durr A, Zuchner S, Stevanin G.

Am J Hum Genet. 2013 Jul 11;93(1):118-23. doi: 10.1016/j.ajhg.2013.05.006. Epub 2013 Jun 6.

7.

Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy.

Rekik I, Boukhris A, Ketata S, Amri M, Essid N, Feki I, Mhiri C.

Ann Indian Acad Neurol. 2013 Jan;16(1):57-61. doi: 10.4103/0972-2327.107704.

8.

Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia.

Martin E, Schüle R, Smets K, Rastetter A, Boukhris A, Loureiro JL, Gonzalez MA, Mundwiller E, Deconinck T, Wessner M, Jornea L, Oteyza AC, Durr A, Martin JJ, Schöls L, Mhiri C, Lamari F, Züchner S, De Jonghe P, Kabashi E, Brice A, Stevanin G.

Am J Hum Genet. 2013 Feb 7;92(2):238-44. doi: 10.1016/j.ajhg.2012.11.021. Epub 2013 Jan 17.

9.

REEP1 mutations in SPG31: frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction.

Goizet C, Depienne C, Benard G, Boukhris A, Mundwiller E, Solé G, Coupry I, Pilliod J, Martin-Négrier ML, Fedirko E, Forlani S, Cazeneuve C, Hannequin D, Charles P, Feki I, Pinel JF, Ouvrard-Hernandez AM, Lyonnet S, Ollagnon-Roman E, Yaouanq J, Toutain A, Dussert C, Fontaine B, Leguern E, Lacombe D, Durr A, Rossignol R, Brice A, Stevanin G.

Hum Mutat. 2011 Oct;32(10):1118-27. doi: 10.1002/humu.21542. Epub 2011 Sep 9.

PMID:
21618648
10.

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.

Boukhris A, Feki I, Elleuch N, Miladi MI, Boland-Augé A, Truchetto J, Mundwiller E, Jezequel N, Zelenika D, Mhiri C, Brice A, Stevanin G.

Neurogenetics. 2010 Oct;11(4):441-8. doi: 10.1007/s10048-010-0249-2. Epub 2010 Jul 1.

PMID:
20593214
11.

[A novel mutation in ATP7B gene associated with severe neurological impairment in Wilson's disease].

Elleuch N, Feki I, Turki E, Miladi MI, Boukhris A, Damak M, Mhiri C, Chappuis E, Woimant F.

Rev Neurol (Paris). 2010 May;166(5):550-2. doi: 10.1016/j.neurol.2009.10.008. Epub 2009 Dec 29. French. No abstract available.

PMID:
20036408
12.

SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.

Goizet C, Boukhris A, Maltete D, Guyant-Maréchal L, Truchetto J, Mundwiller E, Hanein S, Jonveaux P, Roelens F, Loureiro J, Godet E, Forlani S, Melki J, Auer-Grumbach M, Fernandez JC, Martin-Hardy P, Sibon I, Sole G, Orignac I, Mhiri C, Coutinho P, Durr A, Brice A, Stevanin G.

Neurology. 2009 Oct 6;73(14):1111-9. doi: 10.1212/WNL.0b013e3181bacf59.

PMID:
19805727
13.

CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.

Goizet C, Boukhris A, Durr A, Beetz C, Truchetto J, Tesson C, Tsaousidou M, Forlani S, Guyant-Maréchal L, Fontaine B, Guimarães J, Isidor B, Chazouillères O, Wendum D, Grid D, Chevy F, Chinnery PF, Coutinho P, Azulay JP, Feki I, Mochel F, Wolf C, Mhiri C, Crosby A, Brice A, Stevanin G.

Brain. 2009 Jun;132(Pt 6):1589-600. doi: 10.1093/brain/awp073. Epub 2009 May 12.

PMID:
19439420
14.

Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity.

Boukhris A, Stevanin G, Feki I, Denora P, Elleuch N, Miladi MI, Goizet C, Truchetto J, Belal S, Brice A, Mhiri C.

Clin Genet. 2009 Jun;75(6):527-36. doi: 10.1111/j.1399-0004.2009.01176.x. Epub 2009 May 5.

PMID:
19438933
15.

Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.

Denora PS, Schlesinger D, Casali C, Kok F, Tessa A, Boukhris A, Azzedine H, Dotti MT, Bruno C, Truchetto J, Biancheri R, Fedirko E, Di Rocco M, Bueno C, Malandrini A, Battini R, Sickl E, de Leva MF, Boespflug-Tanguy O, Silvestri G, Simonati A, Said E, Ferbert A, Criscuolo C, Heinimann K, Modoni A, Weber P, Palmeri S, Plasilova M, Pauri F, Cassandrini D, Battisti C, Pini A, Tosetti M, Hauser E, Masciullo M, Di Fabio R, Piccolo F, Denis E, Cioni G, Massa R, Della Giustina E, Calabrese O, Melone MA, De Michele G, Federico A, Bertini E, Durr A, Brockmann K, van der Knaap MS, Zatz M, Filla A, Brice A, Stevanin G, Santorelli FM.

Hum Mutat. 2009 Mar;30(3):E500-19. doi: 10.1002/humu.20945.

PMID:
19105190
16.

Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.

Goizet C, Boukhris A, Mundwiller E, Tallaksen C, Forlani S, Toutain A, Carriere N, Paquis V, Depienne C, Durr A, Stevanin G, Brice A.

Hum Mutat. 2009 Feb;30(2):E376-85. doi: 10.1002/humu.20920.

PMID:
18853458
17.

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

Hanein S, Martin E, Boukhris A, Byrne P, Goizet C, Hamri A, Benomar A, Lossos A, Denora P, Fernandez J, Elleuch N, Forlani S, Durr A, Feki I, Hutchinson M, Santorelli FM, Mhiri C, Brice A, Stevanin G.

Am J Hum Genet. 2008 Apr;82(4):992-1002. doi: 10.1016/j.ajhg.2008.03.004.

18.

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

Boukhris A, Stevanin G, Feki I, Denis E, Elleuch N, Miladi MI, Truchetto J, Denora P, Belal S, Mhiri C, Brice A.

Arch Neurol. 2008 Mar;65(3):393-402. doi: 10.1001/archneur.65.3.393.

PMID:
18332254
19.

Spastic paraplegia 15: linkage and clinical description of three Tunisian families.

Boukhris A, Feki I, Denis E, Miladi MI, Brice A, Mhiri C, Stevanin G.

Mov Disord. 2008 Feb 15;23(3):429-33.

PMID:
18098276
20.

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.

Stevanin G, Azzedine H, Denora P, Boukhris A, Tazir M, Lossos A, Rosa AL, Lerer I, Hamri A, Alegria P, Loureiro J, Tada M, Hannequin D, Anheim M, Goizet C, Gonzalez-Martinez V, Le Ber I, Forlani S, Iwabuchi K, Meiner V, Uyanik G, Erichsen AK, Feki I, Pasquier F, Belarbi S, Cruz VT, Depienne C, Truchetto J, Garrigues G, Tallaksen C, Tranchant C, Nishizawa M, Vale J, Coutinho P, Santorelli FM, Mhiri C, Brice A, Durr A; SPATAX consortium.

Brain. 2008 Mar;131(Pt 3):772-84. Epub 2007 Dec 13.

PMID:
18079167
21.

[Familial spastic paraplegia with severe amyotrophy of the hands. (Silver syndrome?)].

Feki I, Miladi MI, Elleuch N, Boukhris A, Stévanin G, Brice A, Mhiri C.

Rev Neurol (Paris). 2007 Apr;163(4):476-9. French.

PMID:
17452950
22.

[Primary pulmonary angiosarcoma].

Bouhaouala MH, Charfi MR, Fajraoui N, Bouaziz N, Boukhris A, Kilani T.

Rev Pneumol Clin. 2005 Apr;61(2):115-8. French.

PMID:
16012366
23.

[Pulmonary papillary adenoma: report of two cases].

Boukhris AA, Baccari S, Kamoun NS, Belhabib D, Horchani H, Kilani T.

Ann Pathol. 2002 Dec;22(6):497-8. French. No abstract available.

PMID:
12594401
24.

[An uncommon tumor of the lung].

Sassi SH, Boukhris AA, Sellami NK, Charfi MR, Horchani H, El Mezni F, Ben Romdhane K.

Ann Pathol. 2002 Jun;22(3):237-8. French. No abstract available.

PMID:
12410112
25.

Electron density in ammonium dihydrogen phosphate: non-uniqueness of the multipolar model in simple inorganic structures.

Pérès N, Boukhris A, Souhassou M, Gavoille G, Lecomte C.

Acta Crystallogr A. 1999 Nov 1;55(Pt 6):1038-1048.

PMID:
10927321

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