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Items: 39

1.

Acquired Chiari I malformation due to lumboperitoneal shunt: A case report and review of literature.

Hentati A, Badri M, Bahri K, Zammel I.

Surg Neurol Int. 2019 May 10;10:78. doi: 10.25259/SNI-234-2019. eCollection 2019.

2.

Successful utilization of the EMR in a multiple sclerosis clinic to support quality improvement and research initiatives at the point of care.

Claire Simon K, Hentati A, Rubin S, Franada T, Maurer D, Hillman L, Tideman S, Szela M, Meyers S, Frigerio R, Maraganore DM.

Mult Scler J Exp Transl Clin. 2018 Nov 30;4(4):2055217318813736. doi: 10.1177/2055217318813736. eCollection 2018 Oct-Dec.

3.

Bilateral Orbital Cavernous Hemangioma.

Hentati A, Matar N, Dridi H, Bouali S, Jemel H.

Asian J Neurosurg. 2018 Oct-Dec;13(4):1222-1224. doi: 10.4103/ajns.AJNS_96_17.

4.

Summaries of the papers of the 4th National Congress of the Tunisian Society of Medical Oncology attached to the 4th Maghreb Congress of Oncology.

Abbes I, Abdelhak S, Abdelhedi C, Abid K, Abidi R, Acacha E, Achour S, Achour A, Adouni O, Afrit M, Ahlem A, Akik I, Akremi M, Aloui R, Aloulou S, Ammar N, Arem S, Athimni S, Attia L, Attia M, Ayadi M, Ayadi A, Ayadi K, Ayadi H, Ayadi L, Ayadi I, Ayari J, Azzouz H, Bacha D, Bahloul R, Bahri I, Bahri M, Bakir D, Balti M, Bargaoui H, Batti R, Bayar R, Bdioui Thabet A, Beji M, Bel Hadj Hassen S, Bel Haj Ali A, Belaid I, Belaid A, Beldjiilali Y, Belkacem O, Bellamlih O, Ben Abdallah W, Ben Abdallah M, Ben Abdellah H, Ben Abderrahmen S, Ben Ahmed S, Ben Ahmed K, Ben Ayache M, Ben Ayoub W, Ben Azaiz M, Ben Azouz M, Ben Daly A, Ben Dhia S, Ben Dhiab M, Ben Dhiab T, Ben Fatma L, Ben Ghachem D, Ben Hammadi S, Ben Hassen M, Ben Hassena R, Ben Hassouna J, Ben Kridis W, Ben Leila F, Ben Mahfoudh KH, Ben Mustapha N, Ben Nasr S, Ben Othman F, Ben Rejeb M, Ben Rekaya M, Ben Rhouma S, Ben Safta Z, Ben Safta I, Ben Said A, Ben Salah M, Ben Salah H, Ben Slama S, Ben Temime R, Ben Youssef Y, Ben Zid K, Benabdella H, Benasr S, Bengueddach A, Benna M, Benna F, Bergaoui H, Berrazaga Y, Besbes M, Bhiri H, Bibi M, Blel A, Bohli M, Bouali S, Bouaouina N, Bouassida K, Bouaziz H, Boubaker J, Boudaouara T, Boudaouara Z, Boudaouara O, Boughanmi F, Boughattas W, Boughizane S, Bouguila H, Bouhani M, Bouhlel B, Boujelbane N, Boujemaa M, Boulma R, Bouraoui S, Bouriga R, Bourmech M, Bousrih C, Boussen H, Boussen N, Bouzaien F, Bouzayene F, Brahem I, Briki R, Chaabene K, Chaabouni M, Chaari H, Chabchoub I, Chachia S, Chaker K, Chamlali M, Charfi L, Charfi M, Charfi S, Charradi H, Cheffai I, Chelly B, Chelly I, Chenguel A, Cherif A, Cherif O, Chiboub A, Chouchene A, Chraiet N, Daghfous A, Daldoul A, Daoud N, Daoud J, Daoud R, Daoud E, Debaibi M, Dhaouadi S, Dhief R, Dhouib F, Dimassi S, Djebbi A, Doghri R, Doghri Y, Doudech B, Dridi M, El Amine O, El Benna H, El Khal MC, Eladeb M, Elloumi M, Elmeddeb K, Enaceur F, Ennouri S, Essoussi M, Ezzairi F, Ezzine A, Faleh R, Fallah S, Faouzi N, Fathallah K, Fehri R, Feki J, Fekih M, Fendri S, Fessi Z, Fourati N, Fourati M, Frikha I, Frikha M, Gabsi A, Gadria S, Gamoudi A, Gargoura A, Gargouri W, Ghariani N, Ghazouani E, Ghorbal A, Ghorbel L, Ghorbel S, Ghozzi A, Glili A, Gmadh K, Goucha A, Gouiaa N, Gritli S, Guazzah K, Guebsi A, Guermazi Z, Guermazi F, Gueryani N, Guezguez M, Hacheni F, Hachicha M, Haddad A, Haddaoui A, Hadoussa M, Haj Mansour M, Hajjaji A, Hajji A, Hamdi A, Hamdi Y, Hammemi R, Haouet S, Hdiji A, Hechiche M, Hedfi M, Helali AJ, Henchiri H, Heni S, Hentati A, Herbegue K, Hidar S, Hlaf M, Hmida W, Hmida I, Hmida L, Hmila Ben Salem I, Hochlef M, Hsairi M, Jaffel H, Jaidane M, Jarraya H, Jebsi M, Jedidi M, Jlassi A, Jlassi H, Jmal H, Jmour O, Jouini M, Kabtni W, Kacem M, Kacem S, Kacem I, Kaid M, Kairi H, Kallel M, Kallel R, Kallel F, Kammoun H, Kamoun S, Kanoun Belajouza S, Karray W, Karrit S, Karrou M, Kchir N, Kdous S, Kehili H, Keskes H, Khairi H, Khalfallah MT, Khalifa MB, Khanfir A, Khanfir F, Khechine W, Khemiri S, Khiari H, Khlif A, Khouni H, Khrouf S, Kochbati L, Korbi I, Korbi A, Krir MW, Ksaier I, Ksantini R, Ksantini M, Ksantini F, Ktari K, Laabidi S, Laamouri B, Labidi A, Lahmar A, Lahouar R, Lamine O, Letaief F, Limaiem F, Limayem I, Limem S, Limem F, Loghmari A, M'ghirbi F, Maamouri F, Magherbi H, Mahjoub N, Mahjoub M, Mahjoubi K, Majdoub S, Makhlouf T, Makni A, Makni S, Mallat N, Manai MH, Mansouri H, Maoua M, Marghli I, Masmoudi T, Mathlouthi N, Meddeb K, Medini B, Mejri N, Merdessi A, Mesali C, Mezlini E, Mezlini A, Mezni E, Mghirbi F, Mhiri N, Mighri N, Mlika M, Mnejja W, Mnif H, Mokni M, Mokrani A, Mosbah F, Moujahed R, Mousli A, Moussa A, Mrad Dali K, Mrizak N, Msakni I, Mzabi S, Mzali R, Mzoughi Z, Naimi Z, Najjar S, Nakkouri R, Nasr C, Nasrallah D, Nasri M, Njim L, Noubigh GEF, Nouira Y, Nouri O, Omrani S, Osmane W, Ouanes Y, Ouanna N, Oubich F, Oumelreit Belamlih G, Rachdi H, Rafraf F, Rahal K, Raies H, Rammeh S, Rebaii N, Rekik W, Rekik H, Rhim MS, Rhim S, Rihab D, Rjiba R, Rziga T, Saad H, Saad A, Saadi M, Said N, Salah R, Sallemi N, Sassi A, Sassi K, Sassi Mahfoudh A, Sbika W, Sellami A, Serghini M, Sghaier S, Sh Zidi Y, Siala W, Slimane M, Slimani O, Soltani S, Souguir MK, Sridi A, Tabet Zatla A, Tajina D, Talbi G, Tbessi S, Tebra Mrad S, Temessek H, Tlili G, Toumi N, Toumi O, Toumia N, Tounsi H, Trigui E, Triki M, Triki A, Turki M, Werda I, Yahyaoui S, Yahyaoui Y, Yaich A, Yamouni M, Yazid D, Yousfi A, Zaghouani H, Zaied S, Zairi F, Zaraa S, Zehani A, Zenzri Y, Zidi A, Znaidi N, Zouari K, Zouari S, Zoukar O, Zribi A.

Tunis Med. 2017 Oct;95(10):859-964. No abstract available.

5.

[Accuracy of magnetic resonance imaging in the diagnosis of thymolipoma].

Toumi N, Harbi H, Bahloul N, Hentati A, Charfi S, Abid H, Ben Mahfoudh K.

Presse Med. 2018 Jan;47(1):97-99. doi: 10.1016/j.lpm.2017.09.024. Epub 2017 Dec 20. French. No abstract available.

PMID:
29275028
6.

[Study of correlation between radiological aspect of pulmonary hydatid cyst and postoperative course].

Abid W, Hentati A, Jdidi J, Chaari Z, Ben Jemaa H, Elleuch N, Dammak J, Frikha I.

Rev Pneumol Clin. 2018 Feb;74(1):35-40. doi: 10.1016/j.pneumo.2017.10.002. Epub 2017 Dec 8. French.

PMID:
29229322
7.

Dendriform pulmonary ossification in a patient with mucoepidermoid carcinoma.

Triki M, Kallel R, Hentati A, Hentati Y, Mnif H, Boudawara T.

Asian Cardiovasc Thorac Ann. 2016 Jul;24(6):604-6. doi: 10.1177/0218492316653865. Epub 2016 Jun 1.

PMID:
27252231
8.

Left lung agenesis discovered by a spontaneous pneumothorax in a 20-year-old girl.

Hentati A, Neifar C, Abid W, M'saad S.

Lung India. 2016 Mar-Apr;33(2):205-7. doi: 10.4103/0970-2113.177443.

9.

[Hydatid cysts of the liver ruptured into the thorax (about five cases)].

Msaad S, Yangui I, Ketata W, Abid N, Feki W, Abid H, Hentati A, Kammoun S.

Rev Pneumol Clin. 2015 Oct;71(5):255-63. doi: 10.1016/j.pneumo.2015.03.002. Epub 2015 Jul 17. French.

PMID:
26195113
10.

Primary Burkitt lymphoma in the posterior mediastinum.

Chaari Z, Charfi S, Hentati A, Ayadi I, Abid H, Frikha I.

Asian Cardiovasc Thorac Ann. 2015 Nov;23(9):1110-2. doi: 10.1177/0218492315587817. Epub 2015 Jun 1.

PMID:
26038605
11.

Giant cystic schwannoma of the middle mediastinum with cervical extension.

Gueldich M, Hentati A, Chakroun A, Abid H, Kammoun S, M'saad S, Frikha I.

Libyan J Med. 2015 Apr 7;10:27409. doi: 10.3402/ljm.v10.27409. eCollection 2015.

12.

Giant cystic schwannoma of the middle mediastinum with cervical extension.

Gueldich M, Hentati A, Chakroun A, Abid H, Kammoun S, M'saad S, Frikha I.

Libyan J Med. 2015 Jan;10(1):27409. doi: 10.3402/ljm.v10.27409.

PMID:
28349787
13.

Live cell imaging of the nascent inactive X chromosome during the early differentiation process of naive ES cells towards epiblast stem cells.

Guyochin A, Maenner S, Chu ET, Hentati A, Attia M, Avner P, Clerc P.

PLoS One. 2014 Dec 29;9(12):e116109. doi: 10.1371/journal.pone.0116109. eCollection 2014.

14.

VZV encephalitis that developed in an immunized patient during fingolimod therapy.

Issa NP, Hentati A.

Neurology. 2015 Jan 6;84(1):99-100. doi: 10.1212/WNL.0000000000001109. Epub 2014 Nov 21. No abstract available.

PMID:
25416038
15.

[Spontaneous regression of epithelial thymic tumours].

Michel S, de Sanctis A, Hentati A, Lenoir S, Caliandro R, Gossot D.

Rev Mal Respir. 2012 May;29(5):727-30. doi: 10.1016/j.rmr.2011.08.010. Epub 2012 Apr 19. French.

PMID:
22682601
16.

Thoracoscopic partial thymectomy for untraceable mediastinal parathyroid adenomas.

Hentati A, Gossot D.

Interact Cardiovasc Thorac Surg. 2011 Nov;13(5):542-4. doi: 10.1510/icvts.2011.276337. Epub 2011 Aug 26.

PMID:
21873366
17.

Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.

Tsaousidou MK, Ouahchi K, Warner TT, Yang Y, Simpson MA, Laing NG, Wilkinson PA, Madrid RE, Patel H, Hentati F, Patton MA, Hentati A, Lamont PJ, Siddique T, Crosby AH.

Am J Hum Genet. 2008 Feb;82(2):510-5. doi: 10.1016/j.ajhg.2007.10.001. Epub 2008 Jan 18.

18.

Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class.

Yip AG, Dürr A, Marchuk DA, Ashley-Koch A, Hentati A, Rubinsztein DC, Reid E.

J Med Genet. 2003 Sep;40(9):e106. No abstract available.

19.

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, Hentati F, Siddique T.

Nat Genet. 2001 Oct;29(2):160-5.

PMID:
11586297
20.

Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.

Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, Ben Hamida M, Hentati F, Siddique T.

Neurology. 2000 Nov 14;55(9):1388-90.

PMID:
11087788
21.

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.

Hentati A, Ouahchi K, Pericak-Vance MA, Nijhawan D, Ahmad A, Yang Y, Rimmler J, Hung W, Schlotter B, Ahmed A, Ben Hamida M, Hentati F, Siddique T.

Neurogenetics. 1998 Dec;2(1):55-60.

PMID:
9933301
22.

Familial amyotrophic lateral sclerosis.

Siddique T, Nijhawan D, Hentati A.

J Neural Transm Suppl. 1997;49:219-33. Review.

PMID:
9266431
23.

A novel mutation in the sterol 27-hydroxylase gene of a Pakistani family with autosomal recessive cerebrotendinous xanthomatosis.

Ahmed MS, Afsar S, Hentati A, Ahmad A, Pasha J, Juneja T, Hung WY, Ahmad A, Choudhri A, Saya S, Siddique T.

Neurology. 1997 Jan;48(1):258-60.

PMID:
9008528
24.

Molecular genetic basis of familial ALS.

Siddique T, Nijhawan D, Hentati A.

Neurology. 1996 Oct;47(4 Suppl 2):S27-34; discussion S34-5. Review.

PMID:
8858048
25.

Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.

Isozumi K, DeLong R, Kaplan J, Deng HX, Iqbal Z, Hung WY, Wilhelmsen KC, Hentati A, Pericak-Vance MA, Siddique T.

Hum Mol Genet. 1996 Sep;5(9):1377-82.

PMID:
8872481
26.

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.

Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T.

Neurology. 1996 Jun;46(6):1507-14. Review.

PMID:
8649538
27.

Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency.

Hentati A, Deng HX, Hung WY, Nayer M, Ahmed MS, He X, Tim R, Stumpf DA, Siddique T, Ahmed.

Ann Neurol. 1996 Mar;39(3):295-300.

PMID:
8602747
28.

Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis.

Deng HX, Tainer JA, Mitsumoto H, Ohnishi A, He X, Hung WY, Zhao Y, Juneja T, Hentati A, Siddique T.

Hum Mol Genet. 1995 Jun;4(6):1113-6. No abstract available.

PMID:
7655471
29.

Familial amyotrophic lateral sclerosis.

Siddique T, Hentati A.

Clin Neurosci. 1995-1996;3(6):338-47. Review.

PMID:
9021255
30.

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.

Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S, et al.

Hum Mol Genet. 1994 Oct;3(10):1867-71.

PMID:
7849714
31.

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T.

Hum Mol Genet. 1994 Aug;3(8):1263-7.

PMID:
7987300
32.

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C, et al.

Nat Genet. 1994 Jul;7(3):425-8.

PMID:
7920663
33.

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation.

Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, Alexander DD, Caliendo J, Hentati A, Kwon YW, Deng HX, et al.

Science. 1994 Jun 17;264(5166):1772-5. Erratum in: Science 1995 Jul 14;269(5221):149.

PMID:
8209258
34.

Report and abstracts of the Third International Workshop on Human Chromosome 2 Mapping 1994. Aarhus, Denmark, June 24-26, 1994.

Spurr NK, Barton H, Bashir R, Bryson GM, Bushby K, Cox S, Gringrich JC, Hentati A, Hildebrandt F, Kao FT, et al.

Cytogenet Cell Genet. 1994;67(4):215-44. No abstract available.

PMID:
7924452
35.

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase.

Deng HX, Hentati A, Tainer JA, Iqbal Z, Cayabyab A, Hung WY, Getzoff ED, Hu P, Herzfeldt B, Roos RP, et al.

Science. 1993 Aug 20;261(5124):1047-51.

PMID:
8351519
36.

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX, et al.

Nature. 1993 Mar 4;362(6415):59-62. Erratum in: Nature. 1993 Jul 22;364(6435):362.

PMID:
8446170
37.

Dinucleotide repeat polymorphism at the human erythroid alpha spectrin (SPTA1) locus.

Hentati A, Hu P, Asgharzadeh S, Siddique T.

Hum Mol Genet. 1992 Jun;1(3):218. No abstract available.

PMID:
1339473
38.

Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease.

Hentati A, Lamy C, Melki J, Zuber M, Munnich A, de Recondo J.

Genomics. 1992 Jan;12(1):155-7.

PMID:
1733853
39.

A molecular genetic approach to amyotrophic lateral sclerosis.

Siddique T, Hu P, Hentati A, Deng G, Hung WY, McInnis MG, Warren AC, Rimmler J, Antonarakis S, Pericak-Vance MA.

Int J Neurol. 1991-1992;25-26:60-9. Review.

PMID:
11980064

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