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Items: 1 to 50 of 111

1.

Novel Missense CAPN3 Mutation Responsible for Adult-Onset Limb Girdle Muscular Dystrophy with Calves Hypertrophy.

Rekik S, Sakka S, Ben Romdhan S, Farhat N, Baba Amer Y, Lehkim L, Authier FJ, Mhiri C.

J Mol Neurosci. 2019 Aug 13. doi: 10.1007/s12031-019-01383-z. [Epub ahead of print]

PMID:
31410652
2.

Shotgun proteomic analysis highlights roles of long-lived mRNAs and de novo transcribed mRNAs upon imbibition in rice embryos.

Sano N, Takebayashi Y, To A, Mhiri C, Rajjou L, Nakagami H, Kanekatsu M.

Plant Cell Physiol. 2019 Aug 2. pii: pcz152. doi: 10.1093/pcp/pcz152. [Epub ahead of print]

PMID:
31373371
3.

Myelopathy after zoster virus infection in immunocompetent patients: A case series.

Farhat N, Daoud S, Hdiji O, Sakka S, Damak M, Mhiri C.

J Spinal Cord Med. 2019 Apr 23:1-5. doi: 10.1080/10790268.2019.1607053. [Epub ahead of print]

PMID:
31013469
4.

Dyke Davidoff Masson syndrome a rare cause of schizoaffective disorder: A case report and review of the literature.

Hamza N, Hdiji O, Haj Kacem H, Farhat N, Sakka S, Dammak M, Mhiri C.

Encephale. 2019 Jun;45(3):274-275. doi: 10.1016/j.encep.2019.01.003. Epub 2019 Mar 14. No abstract available.

PMID:
30879779
5.

Vertebral solitary bone plasmacytoma in a young adult with Trisomy 21: A case report.

Bouattour N, Hdiji O, Hachicha A, Kammoun B, Sakka S, Farhat N, Hajkacem H, Kolsi F, Charfi S, Dammak M, Boudawara Z, Boudawara T, Mhiri C.

J Spinal Cord Med. 2018 Dec 17:1-4. doi: 10.1080/10790268.2018.1557866. [Epub ahead of print]

PMID:
30557097
6.

Rank-Two NMF Clustering for Glioblastoma Characterization.

Bougacha A, Njeh I, Boughariou J, Kammoun O, Ben Mahfoudh K, Dammak M, Mhiri C, Ben Hamida A.

J Healthc Eng. 2018 Oct 23;2018:1048164. doi: 10.1155/2018/1048164. eCollection 2018.

7.

Parental transposable element loads influence their dynamics in young Nicotiana hybrids and allotetraploids.

Mhiri C, Parisod C, Daniel J, Petit M, Lim KY, Dorlhac de Borne F, Kovarik A, Leitch AR, Grandbastien MA.

New Phytol. 2019 Feb;221(3):1619-1633. doi: 10.1111/nph.15484. Epub 2018 Oct 22.

PMID:
30220091
8.

A Novel SYNJ1 Mutation in a Tunisian Family with Juvenile Parkinson's Disease Associated with Epilepsy.

Ben Romdhan S, Sakka S, Farhat N, Triki S, Dammak M, Mhiri C.

J Mol Neurosci. 2018 Oct;66(2):273-278. doi: 10.1007/s12031-018-1167-2. Epub 2018 Sep 5.

PMID:
30187305
9.

LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic.

Ben Romdhan S, Farhat N, Nasri A, Lesage S, Hdiji O, Ben Djebara M, Landoulsi Z, Stevanin G, Brice A, Damak M, Gouider R, Mhiri C.

Acta Neurol Scand. 2018 Nov;138(5):425-431. doi: 10.1111/ane.12996. Epub 2018 Jul 10.

PMID:
29989150
10.

The intrathecal polyspecific antiviral immune response (MRZ reaction): A potential cerebrospinal fluid marker for multiple sclerosis diagnosis.

Feki S, Gargouri S, Mejdoub S, Dammak M, Hachicha H, Hadiji O, Feki L, Hammami A, Mhiri C, Karray H, Masmoudi H.

J Neuroimmunol. 2018 Aug 15;321:66-71. doi: 10.1016/j.jneuroim.2018.05.015. Epub 2018 May 28.

PMID:
29957390
11.

[Light chain multiple myeloma revealed by a dorsal epidural compressive tumor].

Turki M, Hdiji O, Farhat N, Haj Kacem H, Dammak M, Mhiri C.

Presse Med. 2018 Feb;47(2):167-171. doi: 10.1016/j.lpm.2017.11.009. Epub 2018 Jan 17. French. No abstract available.

PMID:
29373280
12.

An Advanced MRI Multi-Modalities Segmentation Methodology Dedicated to Multiple Sclerosis Lesions Exploration and Differentiation.

Ghribi O, Sellami L, Ben Slima M, Ben Hamida A, Mhiri C, Mahfoudh KB.

IEEE Trans Nanobioscience. 2017 Dec;16(8):656-665. doi: 10.1109/TNB.2017.2763246. Epub 2017 Oct 16.

PMID:
29035222
13.

Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort.

Landoulsi Z, Benromdhan S, Ben Djebara M, Damak M, Dallali H, Kefi R, Abdelhak S, Gargouri-Berrechid A, Mhiri C, Gouider R.

BMC Med Genet. 2017 Jul 6;18(1):70. doi: 10.1186/s12881-017-0432-5.

14.

[Neuro-myelitis optica secondary to chronic lymphocytic leukemia].

Amira M, Bouzidi N, Damak M, Mhiri C.

J Fr Ophtalmol. 2017 Jun;40(6):e219-e221. doi: 10.1016/j.jfo.2016.05.013. Epub 2017 Jun 3. French. No abstract available.

15.

LTR-retrotransposons in plants: Engines of evolution.

Galindo-González L, Mhiri C, Deyholos MK, Grandbastien MA.

Gene. 2017 Aug 30;626:14-25. doi: 10.1016/j.gene.2017.04.051. Epub 2017 May 2. Review.

PMID:
28476688
16.

[Orbital apex syndrome revealing multiple myeloma].

Bouchaala W, Dammak M, Bouzidi N, Bellaj H, Gorbel M, Elloumi M, Mhiri C.

Presse Med. 2017 Apr;46(4):449-452. doi: 10.1016/j.lpm.2017.01.012. Epub 2017 Feb 21. French. No abstract available.

PMID:
28233702
17.

Ty1-copia elements reveal diverse insertion sites linked to polymorphisms among flax (Linum usitatissimum L.) accessions.

Galindo-González L, Mhiri C, Grandbastien MA, Deyholos MK.

BMC Genomics. 2016 Dec 7;17(1):1002.

18.

[A psychiatric disorder reveals a neurobrucellosis].

Feki I, Abbes W, Sakka S, Bouchhima I, Mhiri C, Masmoudi J.

Presse Med. 2016 Dec;45(12 Pt 1):1197-1200. doi: 10.1016/j.lpm.2016.09.018. Epub 2016 Nov 2. French. No abstract available.

PMID:
27816344
19.

[Impact of physical disability and concomitant emotional disturbances on post-stroke quality of life].

Charfi N, Trabelsi S, Turki M, Mâalej Bouali M, Zouari L, Dammak M, Ben Thabet J, Mhiri C, Mâalej M.

Encephale. 2017 Oct;43(5):429-434. doi: 10.1016/j.encep.2016.05.014. Epub 2016 Sep 20. French.

PMID:
27663046
20.

Highly efficient gene tagging in the bryophyte Physcomitrella patens using the tobacco (Nicotiana tabacum) Tnt1 retrotransposon.

Vives C, Charlot F, Mhiri C, Contreras B, Daniel J, Epert A, Voytas DF, Grandbastien MA, Nogué F, Casacuberta JM.

New Phytol. 2016 Nov;212(3):759-769. doi: 10.1111/nph.14152. Epub 2016 Aug 22.

21.

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation.

Hdiji O, Turki E, Bouzidi N, Bouchhima I, Damak M, Bohlega S, Mhiri C.

J Mov Disord. 2016 May;9(2):120-3. doi: 10.14802/jmd.16003. Epub 2016 May 25.

22.

Acute aortic dissection presenting as painless paraplegia: a case report.

Hdiji O, Bouzidi N, Damak M, Mhiri C.

J Med Case Rep. 2016 Apr 5;10:99. doi: 10.1186/s13256-016-0881-z.

23.

[Atypical onset corticobasal degeneration].

Bouzidi N, Turki E, Hamza F, Hachicha H, Guermazi F, Mhiri C.

Rev Neurol (Paris). 2015 Dec;171(12):892-4. doi: 10.1016/j.neurol.2015.09.006. Epub 2015 Nov 6. French. No abstract available.

PMID:
26553822
24.

Design of novel dispirooxindolopyrrolidine and dispirooxindolopyrrolothiazole derivatives as potential antitubercular agents.

Mhiri C, Boudriga S, Askri M, Knorr M, Sriram D, Yogeeswari P, Nana F, Golz C, Strohmann C.

Bioorg Med Chem Lett. 2015 Oct 1;25(19):4308-13. doi: 10.1016/j.bmcl.2015.07.069. Epub 2015 Jul 26.

PMID:
26271585
25.

[Optic neuritis: Rare manifestation of neurobrucellosis].

Bouzidi N, Damak M, Turki E, Mhiri C.

J Fr Ophtalmol. 2015 Oct;38(8):e169-71. doi: 10.1016/j.jfo.2014.08.013. Epub 2015 Jul 6. French. No abstract available.

26.

The effect of polyploidy and hybridization on the evolution of floral colour in Nicotiana (Solanaceae).

McCarthy EW, Arnold SE, Chittka L, Le Comber SC, Verity R, Dodsworth S, Knapp S, Kelly LJ, Chase MW, Baldwin IT, Kovařík A, Mhiri C, Taylor L, Leitch AR.

Ann Bot. 2015 Jun;115(7):1117-31. doi: 10.1093/aob/mcv048. Epub 2015 May 15.

27.

Different tobacco retrotransposons are specifically modulated by the elicitor cryptogein and reactive oxygen species.

Anca IA, Fromentin J, Bui QT, Mhiri C, Grandbastien MA, Simon-Plas F.

J Plant Physiol. 2014 Oct 15;171(16):1533-40. doi: 10.1016/j.jplph.2014.07.003. Epub 2014 Jul 23.

PMID:
25128785
28.

Clinical features and disability progression in multiple sclerosis in Tunisia: do we really have a more aggressive disease course?

Sidhom Y, Damak M, Riahi A, Hizem Y, Mrissa R, Mhiri C, Gouider R.

J Neurol Sci. 2014 Aug 15;343(1-2):110-4. doi: 10.1016/j.jns.2014.05.049. Epub 2014 Jun 2.

PMID:
24980939
29.

[Paraneoplastic cerebellar degeneration as the presenting manifestation of breast carcinoma: a case report].

Chaabane K, Turki E, Zouari F, Charfi S, Guermazi M, Mhiri C.

Rev Med Interne. 2013 Nov;34(11):713-5. Epub 2013 Oct 23. French.

PMID:
24367813
30.

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.

31.

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.

32.

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.

33.

Differential dynamics of transposable elements during long-term diploidization of Nicotiana section Repandae (Solanaceae) allopolyploid genomes.

Parisod C, Mhiri C, Lim KY, Clarkson JJ, Chase MW, Leitch AR, Grandbastien MA.

PLoS One. 2012;7(11):e50352. doi: 10.1371/journal.pone.0050352. Epub 2012 Nov 21.

34.

Cerebral rheumatoid vasculitis: a case report.

Akrout R, Bendjemaa S, Fourati H, Ezzeddine M, Hachicha I, Mhiri C, Baklouti S.

J Med Case Rep. 2012 Sep 13;6:302. doi: 10.1186/1752-1947-6-302.

35.

Maize genetic diversity and association mapping using transposable element insertion polymorphisms.

Zerjal T, Rousselet A, Mhiri C, Combes V, Madur D, Grandbastien MA, Charcosset A, Tenaillon MI.

Theor Appl Genet. 2012 May;124(8):1521-37. doi: 10.1007/s00122-012-1807-9. Epub 2012 Feb 18.

PMID:
22350086
36.

Relationship between muscular strength, gait and postural parameters in multiple sclerosis.

Yahia A, Ghroubi S, Mhiri C, Elleuch MH.

Ann Phys Rehabil Med. 2011 May;54(3):144-55. doi: 10.1016/j.rehab.2011.02.004. Epub 2011 Mar 9. English, French.

37.

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
38.

[Multiple arterial thrombosis in Behçet's disease].

Kallel A, Miladi MI, Marzouk S, Feki I, Bahloul Z, Mhiri C.

Rev Med Interne. 2010 Jun;31(6):e1-4. doi: 10.1016/j.revmed.2009.05.012. Epub 2010 Apr 1. French.

PMID:
20362364
39.

Mobilization of retrotransposons in synthetic allotetraploid tobacco.

Petit M, Guidat C, Daniel J, Denis E, Montoriol E, Bui QT, Lim KY, Kovarik A, Leitch AR, Grandbastien MA, Mhiri C.

New Phytol. 2010 Apr;186(1):135-47. doi: 10.1111/j.1469-8137.2009.03140.x. Epub 2010 Jan 13.

40.

[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
41.

Potential impact of stress activated retrotransposons on genome evolution in a marine diatom.

Maumus F, Allen AE, Mhiri C, Hu H, Jabbari K, Vardi A, Grandbastien MA, Bowler C.

BMC Genomics. 2009 Dec 22;10:624. doi: 10.1186/1471-2164-10-624.

42.

Impact of transposable elements on the organization and function of allopolyploid genomes.

Parisod C, Alix K, Just J, Petit M, Sarilar V, Mhiri C, Ainouche M, Chalhoub B, Grandbastien MA.

New Phytol. 2010 Apr;186(1):37-45. doi: 10.1111/j.1469-8137.2009.03096.x. Epub 2009 Dec 7. Review.

43.

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
44.

LTR-retrotransposons Tnt1 and T135 markers reveal genetic diversity and evolutionary relationships of domesticated peppers.

Tam SM, Lefebvre V, Palloix A, Sage-Palloix AM, Mhiri C, Grandbastien MA.

Theor Appl Genet. 2009 Oct;119(6):973-89. doi: 10.1007/s00122-009-1102-6. Epub 2009 Jul 19.

PMID:
19618162
45.

[Benign intracranial hypertension induced by doxycycline].

Ghozzi H, Khemokhem Hammami B, Hammami S, Affes H, Miledi I, Ayedi L, Sahnoun Z, Dorra S, Mhiri C, Ben Jemaa M, Mounir Zeghal K.

Tunis Med. 2008 May;86(5):510-1. French. No abstract available.

PMID:
19469312
46.

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
47.

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
48.

[Cardiac involvement in Steinert myotonic dystrophy].

Miladi MI, Charfeddine H, Feki I, Turki E, Elleuch N, Trabelsi I, Krichène S, Kammoun S, Mhiri C.

Rev Med Interne. 2009 Jul;30(7):573-7. doi: 10.1016/j.revmed.2009.01.017. Epub 2009 Mar 14. French.

PMID:
19286286
49.

[Papillary fibroelastoma of mitral leaflet revealed by a cerebrovascular accident. Case report].

Ben Jmaa H, Masmoudi S, Hadj Kacem A, Abdennadher M, Mhiri C, Trabelsi I, Kammoun S, Chikhrouhou H, Frikha I.

Ann Cardiol Angeiol (Paris). 2009 Feb;58(1):53-6. doi: 10.1016/j.ancard.2008.05.010. Epub 2008 Jun 6. French.

PMID:
18707673
50.

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.

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