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Items: 1 to 50 of 196

1.

Novel Antioxidant, Anti-α-Amylase, Anti-Inflammatory and Antinociceptive Water-Soluble Polysaccharides from the Aerial Part of Nitraria retusa.

Rjeibi I, Hentati F, Feriani A, Hfaiedh N, Delattre C, Michaud P, Pierre G.

Foods. 2019 Dec 26;9(1). pii: E28. doi: 10.3390/foods9010028.

2.

Structural features and rheological behavior of a water-soluble polysaccharide extracted from the seeds of Plantago ciliata Desf.

Addoun N, Boual Z, Delattre C, Ursu AV, Desbrières J, Le Cerf D, Gardarin C, Hentati F, El-Hadj MDO, Michaud P, Pierre G.

Int J Biol Macromol. 2019 Nov 13. pii: S0141-8130(19)38203-0. doi: 10.1016/j.ijbiomac.2019.11.106. [Epub ahead of print]

PMID:
31733242
3.

Quality Characteristics and Functional and Antioxidant Capacities of Algae-Fortified Fish Burgers Prepared from Common Barbel (Barbus barbus).

Hentati F, Barkallah M, Ben Atitallah A, Dammak M, Louati I, Pierre G, Fendri I, Attia H, Michaud P, Abdelkafi S.

Biomed Res Int. 2019 Oct 9;2019:2907542. doi: 10.1155/2019/2907542. eCollection 2019.

4.

Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.

Wagner M, Osborn DPS, Gehweiler I, Nagel M, Ulmer U, Bakhtiari S, Amouri R, Boostani R, Hentati F, Hockley MM, Hölbling B, Schwarzmayr T, Karimiani EG, Kernstock C, Maroofian R, Müller-Felber W, Ozkan E, Padilla-Lopez S, Reich S, Reichbauer J, Darvish H, Shahmohammadibeni N, Tafakhori A, Vill K, Zuchner S, Kruer MC, Winkelmann J, Jamshidi Y, Schüle R.

Nat Commun. 2019 Oct 21;10(1):4790. doi: 10.1038/s41467-019-12620-9.

5.

Stroke in the Middle-East and North Africa: A 2-year prospective observational study of intravenous thrombolysis treatment in the region. Results from the SITS-MENA Registry.

Al-Rukn S, Mazya M, Akhtar N, Hashim H, Mansouri B, Faouzi B, Aref H, Abdulrahman H, Kesraoui S, Hentati F, Gebelly S, Ahmed N, Wahlgren N, Abd-Allah F, Almekhlafi M, Moreira T.

Int J Stroke. 2019 Oct 8:1747493019874729. doi: 10.1177/1747493019874729. [Epub ahead of print]

PMID:
31594533
6.

Stroke in the Middle-East and North Africa: A 2-year prospective observational study of stroke characteristics in the region-Results from the Safe Implementation of Treatments in Stroke (SITS)-Middle-East and North African (MENA).

Rukn SA, Mazya MV, Hentati F, Sassi SB, Nabli F, Said Z, Faouzi B, Hashim H, Abd-Allah F, Mansouri B, Kesraoui S, Gebeily S, Abdulrahman H, Akhtar N, Ahmed N, Wahlgren N, Aref H, Almekhlafi M, Moreira T.

Int J Stroke. 2019 Oct;14(7):715-722. doi: 10.1177/1747493019830331. Epub 2019 Mar 12.

PMID:
30860454
7.

Structural characterization of water-soluble polysaccharides from Nitraria retusa fruits and their antioxidant and hypolipidemic activities.

Rjeibi I, Feriani A, Hentati F, Hfaiedh N, Michaud P, Pierre G.

Int J Biol Macromol. 2019 May 15;129:422-432. doi: 10.1016/j.ijbiomac.2019.02.049. Epub 2019 Feb 8.

PMID:
30742925
8.

Optimal cultivation towards enhanced biomass and floridean starch production by Porphyridium marinum.

Ben Hlima H, Dammak M, Karkouch N, Hentati F, Laroche C, Michaud P, Fendri I, Abdelkafi S.

Int J Biol Macromol. 2019 May 15;129:152-161. doi: 10.1016/j.ijbiomac.2019.01.207. Epub 2019 Jan 31.

PMID:
30711564
9.

Stroke revealing Neuro-Behçet's disease with parenchymal and extensive vascular involvement.

Hamza N, Ben Sassi S, Nabli F, Nagi S, Mahmoud M, Ben Abdelaziz I, Hentati F.

J Neurol Sci. 2019 Mar 15;398:131-134. doi: 10.1016/j.jns.2019.01.044. Epub 2019 Jan 26. No abstract available.

PMID:
30708211
10.

Structural characterization and antioxidant activity of water-soluble polysaccharides from the Tunisian brown seaweed Cystoseira compressa.

Hentati F, Delattre C, Ursu AV, Desbrières J, Le Cerf D, Gardarin C, Abdelkafi S, Michaud P, Pierre G.

Carbohydr Polym. 2018 Oct 15;198:589-600. doi: 10.1016/j.carbpol.2018.06.098. Epub 2018 Jun 30.

PMID:
30093038
11.

Disability progression in multiple sclerosis: a Tunisian prospective cohort study.

Hentati E, Ben Sassi S, Nabli F, Mabrouk T, Zouari M, Hentati F.

Neurol Sci. 2018 May;39(5):879-884. doi: 10.1007/s10072-018-3295-4. Epub 2018 Feb 23.

PMID:
29476286
12.

Modelling Tetraselmis sp. growth-kinetics and optimizing bioactive-compound production through environmental conditions.

Dammak M, Hadrich B, Barkallah M, Hentati F, Ben Hlima H, Pichon C, Denis M, Fendri I, Michaud P, Abdelkafi S.

Bioresour Technol. 2018 Feb;249:510-518. doi: 10.1016/j.biortech.2017.10.028. Epub 2017 Oct 10.

PMID:
29078177
13.

SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.

Hammer MB, Ding J, Mochel F, Eleuch-Fayache G, Charles P, Coutelier M, Gibbs JR, Arepalli SK, Chong SB, Hernandez DG, Majounie E, Clipman S, Bouhlal Y, Nehdi H, Brice A, Hentati F, Stevanin G, Amouri R, Durr A, Singleton AB.

Neurodegener Dis. 2017;17(4-5):208-212. doi: 10.1159/000464445. Epub 2017 May 31.

14.

Effects of nutritional conditions on growth and biochemical composition of Tetraselmis sp.

Dammak M, Hadrich B, Miladi R, Barkallah M, Hentati F, Hachicha R, Laroche C, Michaud P, Fendri I, Abdelkafi S.

Lipids Health Dis. 2017 Feb 20;16(1):41. doi: 10.1186/s12944-016-0378-1.

15.

Progressive cerebellar degeneration revealing Primary Sjögren Syndrome: a case report.

Farhat E, Zouari M, Abdelaziz IB, Drissi C, Beyrouti R, Hammouda MB, Hentati F.

Cerebellum Ataxias. 2016 Oct 19;3:18. eCollection 2016.

16.

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study.

Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, Haytural H, Foroud T, Myers RH, Sassi SB, Hentati E, Nabli F, Farhat E, Amouri R, Hentati F, Farrer MJ.

Lancet Neurol. 2016 Nov;15(12):1248-1256. doi: 10.1016/S1474-4422(16)30203-4. Epub 2016 Sep 28.

PMID:
27692902
17.

Cerebral Venous Thrombosis: A Tunisian Monocenter Study on 160 Patients.

Sassi SB, Touati N, Baccouche H, Drissi C, Romdhane NB, Hentati F.

Clin Appl Thromb Hemost. 2017 Nov;23(8):1005-1009. doi: 10.1177/1076029616665168. Epub 2016 Aug 31.

PMID:
27582021
18.

Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans.

Wang Y, Hersheson J, Lopez D, Hammer M, Liu Y, Lee KH, Pinto V, Seinfeld J, Wiethoff S, Sun J, Amouri R, Hentati F, Baudry N, Tran J, Singleton AB, Coutelier M, Brice A, Stevanin G, Durr A, Bi X, Houlden H, Baudry M.

Cell Rep. 2016 Jun 28;16(1):79-91. doi: 10.1016/j.celrep.2016.05.044. Epub 2016 Jun 16.

19.

Motor phenotype of LRRK2-associated Parkinson's disease: a Tunisian longitudinal study.

Nabli F, Ben Sassi S, Amouri R, Duda JE, Farrer MJ, Hentati F.

Mov Disord. 2015 Feb;30(2):253-8. doi: 10.1002/mds.26097. Epub 2014 Dec 9.

PMID:
25487881
20.

The role of SNCA and MAPT in Parkinson disease and LRRK2 parkinsonism in the Tunisian Arab-Berber population.

Trinh J, Gustavsson EK, Guella I, Vilariño-Güell C, Evans D, Encarnacion M, Sherman H, Hentati F, Farrer MJ.

Eur J Neurol. 2014 Nov;21(11):e91-2. doi: 10.1111/ene.12489. No abstract available.

PMID:
25303626
21.

LRRK2 parkinsonism in Tunisia and Norway: a comparative analysis of disease penetrance.

Hentati F, Trinh J, Thompson C, Nosova E, Farrer MJ, Aasly JO.

Neurology. 2014 Aug 5;83(6):568-9. doi: 10.1212/WNL.0000000000000675. Epub 2014 Jul 9. No abstract available.

22.

Pseudotumoral brain lesion as the presenting feature of primary Sjögren's syndrome.

Sassi SB, Nabli F, Boubaker A, Ghorbel IB, Neji S, Hentati F.

J Neurol Sci. 2014 Apr 15;339(1-2):214-6. doi: 10.1016/j.jns.2014.01.027. Epub 2014 Jan 30.

PMID:
24507949
23.

Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency.

El Euch-Fayache G, Bouhlal Y, Amouri R, Feki M, Hentati F.

Brain. 2014 Feb;137(Pt 2):402-10. doi: 10.1093/brain/awt339. Epub 2013 Dec 25.

PMID:
24369383
24.

Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism.

Trinh J, Amouri R, Duda JE, Morley JF, Read M, Donald A, Vilariño-Güell C, Thompson C, Szu Tu C, Gustavsson EK, Ben Sassi S, Hentati E, Zouari M, Farhat E, Nabli F, Hentati F, Farrer MJ.

Neurobiol Aging. 2014 May;35(5):1125-31. doi: 10.1016/j.neurobiolaging.2013.11.015. Epub 2013 Nov 22.

PMID:
24355527
25.

DNAJC13 mutations in Parkinson disease.

Vilariño-Güell C, Rajput A, Milnerwood AJ, Shah B, Szu-Tu C, Trinh J, Yu I, Encarnacion M, Munsie LN, Tapia L, Gustavsson EK, Chou P, Tatarnikov I, Evans DM, Pishotta FT, Volta M, Beccano-Kelly D, Thompson C, Lin MK, Sherman HE, Han HJ, Guenther BL, Wasserman WW, Bernard V, Ross CJ, Appel-Cresswell S, Stoessl AJ, Robinson CA, Dickson DW, Ross OA, Wszolek ZK, Aasly JO, Wu RM, Hentati F, Gibson RA, McPherson PS, Girard M, Rajput M, Rajput AH, Farrer MJ.

Hum Mol Genet. 2014 Apr 1;23(7):1794-801. doi: 10.1093/hmg/ddt570. Epub 2013 Nov 11.

26.

Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia.

Hammer MB, El Euch-Fayache G, Nehdi H, Feki M, Maamouri-Hicheri W, Hentati F, Amouri R.

J Clin Neurosci. 2014 Feb;21(2):311-5. doi: 10.1016/j.jocn.2013.04.016. Epub 2013 Oct 16.

PMID:
24139731
27.

Giant axonal neuropathy.

Hentati F, Hentati E, Amouri R.

Handb Clin Neurol. 2013;115:933-8. doi: 10.1016/B978-0-444-52902-2.00052-7. Review.

PMID:
23931822
28.

Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.

Heckman MG, Soto-Ortolaza AI, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, Elbaz A, Ferrarese C, Fiske B, Gibson JM, Gibson R, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Boczarska-Jedynak M, Jasinska-Myga B, Jeon BS, Kim YJ, Klein C, Kruger R, Kyratzi E, Lesage S, Lin CH, Lynch T, Maraganore DM, Mellick GD, Mutez E, Nilsson C, Opala G, Park SS, Petrucci S, Puschmann A, Quattrone A, Sharma M, Silburn PA, Sohn YH, Stefanis L, Tadic V, Theuns J, Tomiyama H, Uitti RJ, Valente EM, Van Broeckhoven C, van de Loo S, Vassilatis DK, Vilariño-Güell C, White LR, Wirdefeldt K, Wszolek ZK, Wu RM, Hentati F, Farrer MJ, Ross OA; Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.

Mov Disord. 2013 Oct;28(12):1740-4. doi: 10.1002/mds.25600. Epub 2013 Aug 2.

29.

STX6 rs1411478 is not associated with increased risk of Parkinson's disease.

Trinh J, Vilariño-Güell C, Donald A, Shah B, Yu I, Szu-Tu C, Aasly JO, Wu RM, Hentati F, Rajput AH, Rajput A, Farrer MJ.

Parkinsonism Relat Disord. 2013 May;19(5):563-5. doi: 10.1016/j.parkreldis.2013.01.019. Epub 2013 Feb 14.

PMID:
23415606
30.

Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity.

Hammer MB, Eleuch-Fayache G, Schottlaender LV, Nehdi H, Gibbs JR, Arepalli SK, Chong SB, Hernandez DG, Sailer A, Liu G, Mistry PK, Cai H, Shrader G, Sassi C, Bouhlal Y, Houlden H, Hentati F, Amouri R, Singleton AB.

Am J Hum Genet. 2013 Feb 7;92(2):245-51. doi: 10.1016/j.ajhg.2012.12.012. Epub 2013 Jan 17.

31.

A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia.

Ben Ammar A, Soltanzadeh P, Bauché S, Richard P, Goillot E, Herbst R, Gaudon K, Huzé C, Schaeffer L, Yamanashi Y, Higuchi O, Taly A, Koenig J, Leroy JP, Hentati F, Najmabadi H, Kahrizi K, Ilkhani M, Fardeau M, Eymard B, Hantaï D.

PLoS One. 2013;8(1):e53826. doi: 10.1371/journal.pone.0053826. Epub 2013 Jan 9. Erratum in: PLoS One. 2013;8(9). doi: 10.1371/annotation/3ff2b918-c83c-4c6f-a2e2-4d91294ec92f.

32.

Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian families.

Hammer MB, El Euch-Fayache G, Nehdi H, Saidi D, Nasri A, Nabli F, Bouhlal Y, Maamouri-Hicheri W, Hentati F, Amouri R.

Diagn Mol Pathol. 2012 Dec;21(4):241-5. doi: 10.1097/PDM.0b013e318257ad9a.

PMID:
23111195
33.

Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders.

Hammer MB, Eleuch-Fayache G, Gibbs JR, Arepalli SK, Chong SB, Sassi C, Bouhlal Y, Hentati F, Amouri R, Singleton AB.

Eur J Neurol. 2013 Mar;20(3):486-92. doi: 10.1111/j.1468-1331.2012.03883.x. Epub 2012 Oct 9.

34.

A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C.

Herson S, Hentati F, Rigolet A, Behin A, Romero NB, Leturcq F, Laforêt P, Maisonobe T, Amouri R, Haddad H, Audit M, Montus M, Masurier C, Gjata B, Georger C, Cheraï M, Carlier P, Hogrel JY, Herson A, Allenbach Y, Lemoine FM, Klatzmann D, Sweeney HL, Mulligan RC, Eymard B, Caizergues D, Voït T, Benveniste O.

Brain. 2012 Feb;135(Pt 2):483-92. doi: 10.1093/brain/awr342. Epub 2012 Jan 11.

PMID:
22240777
35.

Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's disease.

Ben Sassi S, Nabli F, Hentati E, Nahdi H, Trabelsi M, Ben Ayed H, Amouri R, Duda JE, Farrer MJ, Hentati F.

Parkinsonism Relat Disord. 2012 Mar;18(3):243-6. doi: 10.1016/j.parkreldis.2011.10.009. Epub 2011 Nov 6.

PMID:
22056842
36.

Translation initiator EIF4G1 mutations in familial Parkinson disease.

Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, Kreisler A, Ross OA, Nishioka K, Soto-Ortolaza AI, Cobb SA, Melrose HL, Behrouz B, Keeling BH, Bacon JA, Hentati E, Williams L, Yanagiya A, Sonenberg N, Lockhart PJ, Zubair AC, Uitti RJ, Aasly JO, Krygowska-Wajs A, Opala G, Wszolek ZK, Frigerio R, Maraganore DM, Gosal D, Lynch T, Hutchinson M, Bentivoglio AR, Valente EM, Nichols WC, Pankratz N, Foroud T, Gibson RA, Hentati F, Dickson DW, Destée A, Farrer MJ.

Am J Hum Genet. 2011 Sep 9;89(3):398-406. doi: 10.1016/j.ajhg.2011.08.009.

37.

Ataxia with vitamin E deficiency and abetalipoproteinemia.

Hentati F, El-Euch G, Bouhlal Y, Amouri R.

Handb Clin Neurol. 2012;103:295-305. doi: 10.1016/B978-0-444-51892-7.00018-8. Review. No abstract available.

PMID:
21827896
38.

VPS35 mutations in Parkinson disease.

Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, Conibear E, Wasserman WW, Aasly JO, Burkhard PR, Djaldetti R, Ghika J, Hentati F, Krygowska-Wajs A, Lynch T, Melamed E, Rajput A, Rajput AH, Solida A, Wu RM, Uitti RJ, Wszolek ZK, Vingerhoets F, Farrer MJ.

Am J Hum Genet. 2011 Jul 15;89(1):162-7. doi: 10.1016/j.ajhg.2011.06.001. Erratum in: Am J Hum Genet. 2011 Aug 12;89(2):347.

39.

Microscopic polyangiitis presenting with peripheral and central neurological manifestations.

Sassi SB, Ghorbel IB, Mizouni H, Houman MH, Hentati F.

Neurol Sci. 2011 Aug;32(4):727-9. doi: 10.1007/s10072-011-0653-x. Epub 2011 Jun 17.

PMID:
21681367
40.

Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overview.

Bouhlal Y, Amouri R, El Euch-Fayeche G, Hentati F.

Parkinsonism Relat Disord. 2011 Jul;17(6):418-22. doi: 10.1016/j.parkreldis.2011.03.005. Epub 2011 Mar 30. Review.

PMID:
21450511
41.

Computational analysis of a novel SACS gene mutation with BioExtract server.

Bouhlal Y, Jennewein DM, Anderson B, Reynoldson J, Maamouri W, Hentati F, Amouri R, Lushbough C.

J Mol Neurosci. 2011 May;44(1):53-8. doi: 10.1007/s12031-011-9512-8. Epub 2011 Mar 17.

PMID:
21416271
42.

An independent replication of PARK16 in Asian samples.

Vilariño-Güell C, Ross OA, Aasly JO, White LR, Rajput A, Rajput AH, Lynch T, Krygowska-Wajs A, Jasinska-Myga B, Opala G, Barcikowska M, Lee MC, Hentati F, Uitti RJ, Wszolek ZK, Farrer MJ, Wu RM.

Neurology. 2010 Dec 14;75(24):2248-9. doi: 10.1212/WNL.0b013e318202031f. No abstract available.

43.

Spinal muscular atrophy due to double gene conversion event.

Maamouri W, Hammer MB, Bouhlel Y, Souilem S, Khmiri N, Nehdi H, Hentati F, Amouri R.

Int J Neurosci. 2011 Feb;121(2):107-11. doi: 10.3109/00207454.2010.529209. Epub 2010 Nov 3.

PMID:
21047176
44.

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.

Nishioka K, Vilariño-Güell C, Cobb SA, Kachergus JM, Ross OA, Hentati E, Hentati F, Farrer MJ.

Parkinsonism Relat Disord. 2010 Dec;16(10):686-7. doi: 10.1016/j.parkreldis.2010.09.007. Epub 2010 Oct 23.

45.

A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia.

Souilem S, Chebel S, Mancuso M, Petrozzi L, Siciliano G, FrihAyed M, Hentati F, Amouri R.

J Neurol Sci. 2011 Jan 15;300(1-2):187-90. doi: 10.1016/j.jns.2010.08.065. Epub 2010 Sep 29.

PMID:
20884012
46.

Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays.

H'mida-Ben Brahim D, M'zahem A, Assoum M, Bouhlal Y, Fattori F, Anheim M, Ali-Pacha L, Ferrat F, Chaouch M, Lagier-Tourenne C, Drouot N, Thibaut C, Benhassine T, Sifi Y, Stoppa-Lyonnet D, N'Guyen K, Poujet J, Hamri A, Hentati F, Amouri R, Santorelli FM, Tazir M, Koenig M.

J Neurol. 2011 Jan;258(1):56-67. doi: 10.1007/s00415-010-5682-5. Epub 2010 Aug 27.

PMID:
20798953
47.

Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa.

Jasinska-Myga B, Kachergus J, Vilariño-Güell C, Wider C, Soto-Ortolaza AI, Kefi M, Middleton LT, Ishihara-Paul L, Gibson RA, Amouri R, Yahmed SB, Sassi SB, Zouari M, El Euch G, Ross OA, Hentati F, Farrer MJ.

Mov Disord. 2010 Oct 15;25(13):2052-8. doi: 10.1002/mds.23283.

PMID:
20721913
48.

Inhibition of LRRK2 kinase activity leads to dephosphorylation of Ser(910)/Ser(935), disruption of 14-3-3 binding and altered cytoplasmic localization.

Dzamko N, Deak M, Hentati F, Reith AD, Prescott AR, Alessi DR, Nichols RJ.

Biochem J. 2010 Sep 15;430(3):405-13. doi: 10.1042/BJ20100784.

49.

Cerebral venous thrombosis presenting with cerebellar ataxia and cortical blindness.

Ben Sassi S, Mizouni H, Nabli F, Kallel L, Kefi M, Hentati F.

J Stroke Cerebrovasc Dis. 2010 Nov-Dec;19(6):507-9. doi: 10.1016/j.jstrokecerebrovasdis.2009.09.004. Epub 2010 Jun 9.

PMID:
20538479
50.

A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagia.

Souilem S, Kefi M, Mancuso M, Nesti C, Hentati F, Amouri R.

Diagn Mol Pathol. 2010 Mar;19(1):28-32. doi: 10.1097/PDM.0b013e3181b00f02.

PMID:
20186009

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