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Items: 1 to 50 of 110

1.

A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis.

Aasfara J, Regragui W, Ouardi LE, Haddou EHAB, Benomar A, Yahyaoui M.

Pan Afr Med J. 2019 May 6;33:2. doi: 10.11604/pamj.2019.33.2.13327. eCollection 2019.

2.

Excessive laboratory monitoring to prevent adolescent's refeeding syndrome: opportunities for enhancement.

Ghaddar R, Chartrand J, Benomar A, Jamoulle O, Taddeo D, Frappier JY, Stheneur C.

Eat Weight Disord. 2019 Jun 5. doi: 10.1007/s40519-019-00723-7. [Epub ahead of print]

PMID:
31168728
3.

Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study.

Cheikh A, Ajaja MR, Rhazali H, Bouatia M, Benomar A, Slaoui A, Cherrah Y, Abouqal R, El Hassani A, Cheikhaoui Y.

BMC Cardiovasc Disord. 2019 May 16;19(1):117. doi: 10.1186/s12872-019-1102-7.

4.

Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.

Bouhouche A, Tibar H, Kriouale Y, Jiddane M, Smaili I, Bouslam N, Benomar A, Yahyaoui M, El Fahime E.

Case Rep Genet. 2018 Nov 15;2018:8635698. doi: 10.1155/2018/8635698. eCollection 2018.

5.

Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat.

Rahmani M, Benabdeljlil M, Bellakhdar F, Faris MEA, Jiddane M, Bayad KE, Boutbib F, Razine R, Gana R, Hassani MRE, Fatemi NE, Fikri M, Sanhaji S, Tassine H, Balrhiti IEA, Hadri SE, Kettani NE, Abbadi NE, Amor M, Moussaoui A, Semlali A, Aidi S, Benhaddou EHA, Benomar A, Bouhouche A, Yahyaoui M, Khamlichi AE, Ouahabi AE, Maaqili RE, Tibar H, Arkha Y, Melhaoui A, Benazzouz A, Regragui W.

Front Neurol. 2018 Jul 31;9:532. doi: 10.3389/fneur.2018.00532. eCollection 2018.

6.

Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients.

Tibar H, El Bayad K, Bouhouche A, Ait Ben Haddou EH, Benomar A, Yahyaoui M, Benazzouz A, Regragui W.

Front Neurol. 2018 Apr 4;9:170. doi: 10.3389/fneur.2018.00170. eCollection 2018.

7.

Stroke and syphilis: A retrospective study of 53 patients.

Ahbeddou N, El Alaoui Taoussi K, Ibrahimi A, Ait Ben Haddou EH, Regragui W, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2018 May;174(5):313-318. doi: 10.1016/j.neurol.2017.07.014. Epub 2018 Apr 7.

PMID:
29631855
8.

Association of vitamin D status with multiple sclerosis in a case-control study from Morocco.

Skalli A, Ait Ben Haddou EH, El Jaoudi R, Razine R, Mpandzou GA, Tibar H, El Fahime E, Bouslam N, Alami A, Benomar A, Hajjout K, Yahyaoui M, Bouhouche A.

Rev Neurol (Paris). 2018 Mar;174(3):150-156. doi: 10.1016/j.neurol.2017.06.030. Epub 2018 Mar 7.

PMID:
29525037
9.

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.

Bouhouche A, Tesson C, Regragui W, Rahmani M, Drouet V, Tibar H, Souirti Z, Ben El Haj R, Bouslam N, Yahyaoui M, Brice A, Benomar A, Lesage S.

Front Neurol. 2017 Oct 31;8:567. doi: 10.3389/fneur.2017.00567. eCollection 2017.

10.

Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.

Ben El Haj R, Salmi A, Regragui W, Moussa A, Bouslam N, Tibar H, Benomar A, Yahyaoui M, Bouhouche A.

PLoS One. 2017 Jul 19;12(7):e0181335. doi: 10.1371/journal.pone.0181335. eCollection 2017.

11.

LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease.

Bouhouche A, Tibar H, Ben El Haj R, El Bayad K, Razine R, Tazrout S, Skalli A, Bouslam N, Elouardi L, Benomar A, Yahyaoui M, Regragui W.

Parkinsons Dis. 2017;2017:2412486. doi: 10.1155/2017/2412486. Epub 2017 Mar 30.

12.

A case of neurosyphilis presenting with essential-like tremor.

Tibar H, Ait Ben Haddou E, Benomar A, Yahyaoui M, Regragui W.

Rev Neurol (Paris). 2017 Mar;173(3):169-170. doi: 10.1016/j.neurol.2017.02.005. Epub 2017 Mar 18. No abstract available.

PMID:
28320518
13.

A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.

Ben El Haj R, Regragui W, Tazi-Ahnini R, Skalli A, Bouslam N, Benomar A, Yahyaoui M, Bouhouche A.

Biomed Res Int. 2016;2016:3460234. doi: 10.1155/2016/3460234. Epub 2016 Jun 20.

14.

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.

Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers DB, Vérièpe J, Androschuk A, Laurent SB, Rochefort D, Spiegelman D, Dionne-Laporte A, Szuto A, Liao M, Figlewicz DA, Bouhouche A, Benomar A, Yahyaoui M, Ouazzani R, Yoon G, Dupré N, Suchowersky O, Bolduc FV, Parker JA, Dion PA, Drapeau P, Rouleau GA, Ouled Amar Bencheikh B.

Am J Hum Genet. 2016 Jun 2;98(6):1271. doi: 10.1016/j.ajhg.2016.05.009. Epub 2016 Jun 2. No abstract available.

15.

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.

Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers DB, Vérièpe J, Androschuk A, Laurent SB, Rochefort D, Spiegelman D, Dionne-Laporte A, Szuto A, Liao M, Figlewicz DA, Bouhouche A, Benomar A, Yahyaoui M, Ouazzani R, Yoon G, Dupré N, Suchowersky O, Bolduc FV, Parker JA, Dion PA, Drapeau P, Rouleau GA, Ouled Amar Bencheikh B.

Am J Hum Genet. 2016 May 5;98(5):1038-1046. doi: 10.1016/j.ajhg.2016.04.002. Erratum in: Am J Hum Genet. 2016 Jun 2;98 (6):1271.

16.

Clinical and genetic data of Huntington disease in Moroccan patients.

Bouhouche A, Regragui W, Lamghari H, Khaldi K, Birouk N, Lytim S, Bellamine S, Kriouile Y, Bouslam N, Haddou el HA, Faris MA, Benomar A, Yahyaoui M.

Afr Health Sci. 2015 Dec;15(4):1232-8. doi: 10.4314/ahs.v15i4.23.

17.

Vitamin D deficiency and its role in neurological conditions: A review.

Mpandzou G, Aït Ben Haddou E, Regragui W, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2016 Feb;172(2):109-22. doi: 10.1016/j.neurol.2015.11.005. Epub 2016 Feb 8. Review.

PMID:
26867662
18.

[Clinical and environmental aspects of amyotrophic lateral sclerosis in moroccan population: a study of 60 cases].

Imounan F, Lahbouje S, Hsaini Y, Regragui W, Ait Ben Haddou el H, Benomar A, Bourazza A, Yahyaoui M.

Tunis Med. 2015 Jun;93(6):365-70. French.

19.

[Pathological and clinical correlations in renal AA amyloidosis: A Moroccan series of 30 cases].

Bziz A, Rouas L, Lamalmi N, Malihy A, Cherradi N, Ouzeddoun N, Bayahia R, Flayou K, Chala S, Bouclouze A, Benomar A, Abouqal R, Alhamany Z.

Nephrol Ther. 2015 Dec;11(7):543-50. doi: 10.1016/j.nephro.2015.06.007. Epub 2015 Oct 23. French.

PMID:
26608566
20.

Locked in syndrome revealing an antiphospholipid syndrome.

Aasfara J, Imounan F, Ait Ben Haddou el H, Regragui W, Benomar A, Yahyaoui M.

Tunis Med. 2015 Jan;93(1):47-8. No abstract available.

21.

Evaluation of retinal nerve fiber layer thickness measured by optical coherence tomography in Moroccan patients with multiple sclerosis.

Soufi G, AitBenhaddou E, Hajji Z, Tazrout S, Benomar A, Soufi M, Boulanouar A, Abouqal R, Yahyaoui M, Berraho A.

J Fr Ophtalmol. 2015 Jun;38(6):497-503. doi: 10.1016/j.jfo.2014.11.008. Epub 2015 Apr 18.

PMID:
25896580
22.

Measles in Morocco: epidemiological profile and impact of vaccination strategy.

Cheikh A, Ziani M, Cheikh Z, Barakat A, El Menzhi O, Braikat M, Benomar A, Cherrah Y, El Hassani A.

Adv Ther. 2015 Feb;32(2):172-83. doi: 10.1007/s12325-015-0188-2. Epub 2015 Mar 3.

PMID:
25732939
23.

Multiple sclerosis: clinical characteristics and disability progression in Moroccan children.

Ait Ben Haddou E, Alhyan M, Aasfara J, Regragui W, Ibrahimi A, Razine R, Abouqal R, Benomar A, Yahyaoui M.

J Neurol Sci. 2014 Nov 15;346(1-2):128-32. doi: 10.1016/j.jns.2014.08.008. Epub 2014 Aug 13.

PMID:
25216553
24.

Profile of idiopathic parkinson's disease in Moroccan patients.

Regragui W, Lachhab L, Razine R, Raissouni L, Rasmouni K, Imounan F, Benhaddou EHA, Abouqal R, Benomar A, Yahyaoui M.

Int Arch Med. 2014 Mar 6;7(1):10. doi: 10.1186/1755-7682-7-10.

25.

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.

Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E, Mansour L, Masri A, Kayserili H, Al-Aama JY, Abdel-Salam GMH, Karminejad A, Kara M, Kara B, Bozorgmehri B, Ben-Omran T, Mojahedi F, El Din Mahmoud IG, Bouslam N, Bouhouche A, Benomar A, Hanein S, Raymond L, Forlani S, Mascaro M, Selim L, Shehata N, Al-Allawi N, Bindu PS, Azam M, Gunel M, Caglayan A, Bilguvar K, Tolun A, Issa MY, Schroth J, Spencer EG, Rosti RO, Akizu N, Vaux KK, Johansen A, Koh AA, Megahed H, Durr A, Brice A, Stevanin G, Gabriel SB, Ideker T, Gleeson JG.

Science. 2014 Jan 31;343(6170):506-511. doi: 10.1126/science.1247363.

26.

A clinical study of non-parkinsonian tremor in Moroccan patients.

Regragui W, Lachhab L, Razine R, Ait Benhaddou EH, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2014 Jan;170(1):26-31. doi: 10.1016/j.neurol.2013.06.006. Epub 2013 Dec 7.

PMID:
24321218
27.

KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.

Dor T, Cinnamon Y, Raymond L, Shaag A, Bouslam N, Bouhouche A, Gaussen M, Meyer V, Durr A, Brice A, Benomar A, Stevanin G, Schuelke M, Edvardson S.

J Med Genet. 2014 Feb;51(2):137-42. doi: 10.1136/jmedgenet-2013-102012. Epub 2013 Dec 6.

PMID:
24319291
28.

Genetic factors and multiple sclerosis in the Moroccan population: a role for HLA class II.

Ouadghiri S, El Alaoui Toussi K, Brick C, Ait Benhaddou EH, Benseffaj N, Benomar A, El Yahyaoui M, Essakalli M.

Pathol Biol (Paris). 2013 Dec;61(6):259-63. doi: 10.1016/j.patbio.2013.05.002. Epub 2013 Jul 9.

PMID:
23849771
29.

Neurosyphilis revealed by trochlear nerve (IV) palsy.

El Alaoui Taoussi K, Serrou A, Ait Benhaddou E, Regragui W, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2013 Mar;169(3):279-80. doi: 10.1016/j.neurol.2012.09.009. Epub 2013 Feb 14. No abstract available.

PMID:
23415906
30.

CLN6 p.I154del mutation causing late infantile neuronal ceroid lipofuscinosis in a large consanguineous Moroccan family.

Bouhouche A, Regragui W, El Fahime E, Bouslam N, Tazi-Ahnini R, Melloul M, Benomar A, Yahyaoui M.

Indian J Pediatr. 2013 Aug;80(8):694-6. doi: 10.1007/s12098-012-0889-3. Epub 2012 Nov 22.

PMID:
23180398
31.

Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.

Tesson C, Nawara M, Salih MA, Rossignol R, Zaki MS, Al Balwi M, Schule R, Mignot C, Obre E, Bouhouche A, Santorelli FM, Durand CM, Oteyza AC, El-Hachimi KH, Al Drees A, Bouslam N, Lamari F, Elmalik SA, Kabiraj MM, Seidahmed MZ, Esteves T, Gaussen M, Monin ML, Gyapay G, Lechner D, Gonzalez M, Depienne C, Mochel F, Lavie J, Schols L, Lacombe D, Yahyaoui M, Al Abdulkareem I, Zuchner S, Yamashita A, Benomar A, Goizet C, Durr A, Gleeson JG, Darios F, Brice A, Stevanin G.

Am J Hum Genet. 2012 Dec 7;91(6):1051-64. doi: 10.1016/j.ajhg.2012.11.001. Epub 2012 Nov 21.

32.

[Atypical metastatic sites for adenocarcinoma of the lung].

Lachhab L, Fikri M, Aitbenhaddou EH, Arkha Y, Regragui W, Jiddane M, Benomar A, Yahyaoui M.

J Fr Ophtalmol. 2013 Feb;36(2):e23-6. doi: 10.1016/j.jfo.2012.03.009. Epub 2012 Oct 18. French.

PMID:
23083771
33.

Cryptococcosis in an immunocompetent pregnant woman.

Lachhab L, Rasmouni K, Ait Ben Haddou EH, Maamar M, Seffar M, Regragui W, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2013 Jan;169(1):92-3. doi: 10.1016/j.neurol.2012.04.004. Epub 2012 Jul 4. No abstract available.

PMID:
22766327
34.

Profile of multiple system atrophy in Moroccan patients attending a movement disorders outpatient clinic in Rabat university hospital.

Regragui W, Lachhab L, Razine R, Benjelloun H, Ait Benhaddou EH, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2013 Feb;169(2):121-5. doi: 10.1016/j.neurol.2012.04.006. Epub 2012 Jul 2.

PMID:
22763206
35.

Parkinsonism as first manifestation of lupus.

Lachhab L, Regragui W, Hamaz S, Ait Benhaddou EH, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2012 Dec;168(12):990-1. doi: 10.1016/j.neurol.2012.03.010. Epub 2012 Jun 14. No abstract available.

PMID:
22703613
36.

[Invasive aspergillosis in a pediatric hematology-oncology ward].

Lamalmi F, Aghrouch M, Benomar A, Tligui H, Agoumi A.

Med Mal Infect. 2012 Jun;42(6):280-2. doi: 10.1016/j.medmal.2010.03.003. Epub 2012 Jun 4. French. No abstract available.

PMID:
22673751
37.

[Quality of life and multiple sclerosis: Arabic language translation and transcultural adaptation of "MSQOL-54"].

El Alaoui Taoussi K, Ait Ben Haddou E, Benomar A, Abouqal R, Yahyaoui M.

Rev Neurol (Paris). 2012 May;168(5):444-9. doi: 10.1016/j.neurol.2011.10.011. Epub 2012 May 2. French.

PMID:
22560010
38.

An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.

Bouhouche A, Benomar A, Errguig L, Lachhab L, Bouslam N, Aasfara J, Sefiani S, Chabraoui L, El Fahime E, El Quessar A, Jiddane M, Yahyaoui M.

BMC Med Genet. 2012 Mar 21;13:18. doi: 10.1186/1471-2350-13-18.

39.

Neurological manifestations of Behçet's disease: evaluation of 40 patients treated by cyclophosphamide.

Ait Ben Haddou EH, Imounan F, Regragui W, Mouti O, Benchakroune N, Abouqal R, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2012 Apr;168(4):344-9. doi: 10.1016/j.neurol.2011.09.006. Epub 2011 Dec 1.

PMID:
22136880
40.

[Multiple sclerosis associated with antiphospholipid syndrome: diagnostic and therapeutic difficulties].

Ahbeddou N, Ait Ben Haddou E, Hammi S, Slimani C, Regragui W, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2012 Jan;168(1):65-9. doi: 10.1016/j.neurol.2011.01.021. Epub 2011 Jun 14. French.

PMID:
21665238
41.

Prevalence of human papillomavirus genotype among Moroccan women during a local screening program.

Alhamany Z, El Mzibri M, Kharbach A, Malihy A, Abouqal R, Jaddi H, Benomar A, Attaleb M, Lamalmi N, Cherradi N.

J Infect Dev Ctries. 2010 Nov 24;4(11):732-9.

42.

[Neuromarketing: When marketing meet neurosciences].

Ouazzani Touhami Z, Benlafkih L, Jiddane M, Cherrah Y, El Malki HO, Benomar A.

Rev Neurol (Paris). 2011 Feb;167(2):135-40. doi: 10.1016/j.neurol.2010.07.025. Epub 2010 Oct 8. Review. French.

PMID:
20934735
43.

[Stroke revealing granulomatosis].

Raissouni L, Aitbenhaddou E, Ahbeddou N, El Alaoui KT, Slimani C, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2011 Jan;167(1):35-8. doi: 10.1016/j.neurol.2010.03.016. Epub 2010 Jun 18. French.

PMID:
20561657
44.

[Cerebral venous thrombosis and acute polyradiculoneuritis revealing systemic lupus erythematosus].

Ahbeddou N, Benomar A, Rasmouni K, Quessar A, Ouhabi H, Ait Ben Haddou E, Yahyaoui M.

Rev Neurol (Paris). 2010 Apr;166(4):458-63. doi: 10.1016/j.neurol.2009.09.005. French.

PMID:
19836814
45.

[Resistance to fluoroquinolone among Klebsiella spp strains producing extended-spectrum betalactamases isolated from urine].

Tlamçani Z, Ellaia K, Benomar A, Kabbaj H, Alaoui A, Seffar M.

Ann Biol Clin (Paris). 2009 Sep-Oct;67(5):553-6. doi: 10.1684/abc.2009.0363. French.

46.

[Interest of corticosteroids in neurological complications of celiac disease].

Ait Ben Haddou E, Errabih I, Raissouni L, Elhassani M, Benomar A, Ouazzani H, Yahyaoui M.

Rev Neurol (Paris). 2009 Dec;165(12):1103-6. doi: 10.1016/j.neurol.2009.02.005. French.

PMID:
19541334
47.

[Efficacy and safety of cyclophosphamide treatment in progressive multiple sclerosis].

Ait Ben Haddou E, Benomar A, Ahid S, Chatri H, Slimani C, Hassani M, El Alaoui Taoussi K, Abouqal R, Yahyaoui M.

Rev Neurol (Paris). 2009 Dec;165(12):1086-91. doi: 10.1016/j.neurol.2009.03.013. French.

PMID:
19520407
48.

[Pachymeningitis associated with probable Horton's disease: a case report].

Ait Benhaddou E, Zinebi A, Elhassani M, Raissouni L, Elhassani MR, Benomar A, Yahyaoui M.

Rev Neurol (Paris). 2010 Feb;166(2):253-6. doi: 10.1016/j.neurol.2009.04.007. Epub 2009 Jun 3. French.

PMID:
19497602
49.

PRNP haplotype distribution in Moroccan goats.

Serrano C, Hammouchi M, Benomar A, Lyahyai J, Ranera B, Acín C, el Hamidi M, Monzón M, Badiola JJ, Tligui N, Zaragoza P, Martín-Burriel I.

Anim Genet. 2009 Aug;40(4):565-8. doi: 10.1111/j.1365-2052.2009.01873.x. Epub 2009 Apr 2.

PMID:
19397523
50.

[Référentiel de bon usage and Thésaurus national de cancérologie digestive: analysis of non-conform prescriptions in Tenon hospital].

Debrix I, Sitbon M, Khalil A, Benomar A, Becker A, André T.

Bull Cancer. 2009 Feb;96(2):147-55. doi: 10.1684/bdc.2008.0820. French.

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