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Items: 1 to 50 of 67

1.

Late activity rebound in non-active multiple sclerosis: A rare event.

Corti L, Ayrignac X, Carra Dalliere C, Charif M, de Sèze J, Biotti D, Ciron J, Labauge P.

Mult Scler. 2018 Mar 1:1352458518765670. doi: 10.1177/1352458518765670. [Epub ahead of print] No abstract available.

PMID:
29533160
2.

Reply: The expanding neurological phenotype of DNM1L-related disorders.

Gerber S, Charif M, Chevrollier A, Chaumette T, Angebault C, Kane S, Paris A, Alban J, Quiles M, Delettre C, Bonneau D, Procaccio V, Amati-Bonneau P, Reynier P, Leruez S, Calmon R, Boddaert N, Funalot B, Rio M, Bouccara D, Meunier I, Sesaki H, Kaplan J, Hamel CP, Rozet JM, Lenaers G.

Brain. 2018 Apr 1;141(4):e29. doi: 10.1093/brain/awy027. No abstract available.

PMID:
29529130
3.

AP4 deficiency: A novel form of neurodegeneration with brain iron accumulation?

Roubertie A, Hieu N, Roux CJ, Leboucq N, Manes G, Charif M, Echenne B, Goizet C, Guissart C, Meyer P, Marelli C, Rivier F, Burglen L, Horvath R, Hamel CP, Lenaers G.

Neurol Genet. 2018 Jan 24;4(1):e217. doi: 10.1212/NXG.0000000000000217. eCollection 2018 Feb.

4.

Cerebrospinal Fluid, MRI, and Florbetaben-PET in Cerebral Amyloid Angiopathy-Related Inflammation.

Renard D, Collombier L, Demattei C, Wacongne A, Charif M, Ayrignac X, Azakri S, Gaillard N, Boudousq V, Lehmann S, Menjot de Champfleur N, Thouvenot E.

J Alzheimers Dis. 2018;61(3):1107-1117. doi: 10.3233/JAD-170843.

PMID:
29254099
5.

Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults.

Charif M, Nasca A, Thompson K, Gerber S, Makowski C, Mazaheri N, Bris C, Goudenège D, Legati A, Maroofian R, Shariati G, Lamantea E, Hopton S, Ardissone A, Moroni I, Giannotta M, Siegel C, Strom TM, Prokisch H, Vignal-Clermont C, Derrien S, Zanlonghi X, Kaplan J, Hamel CP, Leruez S, Procaccio V, Bonneau D, Reynier P, White FE, Hardy SA, Barbosa IA, Simpson MA, Vara R, Perdomo Trujillo Y, Galehdari H, Deshpande C, Haack TB, Rozet JM, Taylor RW, Ghezzi D, Amati-Bonneau P, Lenaers G.

JAMA Neurol. 2018 Jan 1;75(1):105-113. doi: 10.1001/jamaneurol.2017.2065.

PMID:
29181510
6.

Mechanical Thrombectomy for Minor and Mild Stroke Patients Harboring Large Vessel Occlusion in the Anterior Circulation: A Multicenter Cohort Study.

Dargazanli C, Arquizan C, Gory B, Consoli A, Labreuche J, Redjem H, Eker O, Decroix JP, Corlobé A, Mourand I, Gaillard N, Ayrignac X, Charif M, Duhamel A, Labeyrie PE, Riquelme C, Ciccio G, Smajda S, Desilles JP, Gascou G, Lefèvre PH, Mantilla-García D, Cagnazzo F, Coskun O, Mazighi M, Riva R, Bourdain F, Labauge P, Rodesch G, Obadia M, Bonafé A, Turjman F, Costalat V, Piotin M, Blanc R, Lapergue B; ETIS REGISTRY Investigators.

Stroke. 2017 Dec;48(12):3274-3281. doi: 10.1161/STROKEAHA.117.018113. Epub 2017 Oct 31.

PMID:
29089458
7.

Mutations in DNM1L, as in OPA1, result indominant optic atrophy despite opposite effectson mitochondrial fusion and fission.

Gerber S, Charif M, Chevrollier A, Chaumette T, Angebault C, Kane MS, Paris A, Alban J, Quiles M, Delettre C, Bonneau D, Procaccio V, Amati-Bonneau P, Reynier P, Leruez S, Calmon R, Boddaert N, Funalot B, Rio M, Bouccara D, Meunier I, Sesaki H, Kaplan J, Hamel CP, Rozet JM, Lenaers G.

Brain. 2017 Oct 1;140(10):2586-2596. doi: 10.1093/brain/awx219.

PMID:
28969390
8.

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.

Salime S, Charif M, Bousfiha A, Elrharchi S, Bakhchane A, Charoute H, Kabine M, Snoussi K, Lenaers G, Barakat A.

Int J Pediatr Otorhinolaryngol. 2017 Oct;101:25-29. doi: 10.1016/j.ijporl.2017.07.024. Epub 2017 Jul 21.

PMID:
28964305
9.

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

Bousfiha A, Bakhchane A, Charoute H, Detsouli M, Rouba H, Charif M, Lenaers G, Barakat A.

Mol Biol Rep. 2017 Oct;44(5):429-434. doi: 10.1007/s11033-017-4129-9. Epub 2017 Sep 26.

PMID:
28951997
10.

MRI volumetric morphometry in vascular parkinsonism.

Dunet V, Deverdun J, Charroud C, Le Bars E, Molino F, Menjot de Champfleur S, Maury F, Charif M, Ayrignac X, Labauge P, Castelnovo G, Pinna F, Bonafe A, Geny C, Menjot de Champfleur N.

J Neurol. 2017 Jul;264(7):1511-1519. doi: 10.1007/s00415-017-8561-5. Epub 2017 Jul 1.

PMID:
28669119
11.

Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.

Zhang J, Gambin T, Yuan B, Szafranski P, Rosenfeld JA, Balwi MA, Alswaid A, Al-Gazali L, Shamsi AMA, Komara M, Ali BR, Roeder E, McAuley L, Roy DS, Manchester DK, Magoulas P, King LE, Hannig V, Bonneau D, Denommé-Pichon AS, Charif M, Besnard T, Bézieau S, Cogné B, Andrieux J, Zhu W, He W, Vetrini F, Ward PA, Cheung SW, Bi W, Eng CM, Lupski JR, Yang Y, Patel A, Lalani SR, Xia F, Stankiewicz P.

Hum Genet. 2017 Aug;136(8):1009-1011. doi: 10.1007/s00439-017-1828-1. No abstract available.

PMID:
28660352
13.

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.

Bakhchane A, Charif M, Bousfiha A, Boulouiz R, Nahili H, Rouba H, Charoute H, Lenaers G, Barakat A.

PLoS One. 2017 May 4;12(5):e0176516. doi: 10.1371/journal.pone.0176516. eCollection 2017.

14.

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.

Zhang J, Gambin T, Yuan B, Szafranski P, Rosenfeld JA, Balwi MA, Alswaid A, Al-Gazali L, Shamsi AMA, Komara M, Ali BR, Roeder E, McAuley L, Roy DS, Manchester DK, Magoulas P, King LE, Hannig V, Bonneau D, Denommé-Pichon AS, Charif M, Besnard T, Bézieau S, Cogné B, Andrieux J, Zhu W, He W, Vetrini F, Ward PA, Cheung SW, Bi W, Eng CM, Lupski JR, Yang Y, Patel A, Lalani SR, Xia F, Stankiewicz P.

Hum Genet. 2017 Apr;136(4):377-386. doi: 10.1007/s00439-017-1763-1. Epub 2017 Mar 1. Erratum in: Hum Genet. 2017 Jun 28;:.

15.

Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy.

Colin E, Daniel J, Ziegler A, Wakim J, Scrivo A, Haack TB, Khiati S, Denommé AS, Amati-Bonneau P, Charif M, Procaccio V, Reynier P, Aleck KA, Botto LD, Herper CL, Kaiser CS, Nabbout R, N'Guyen S, Mora-Lorca JA, Assmann B, Christ S, Meitinger T, Strom TM, Prokisch H; FREX Consortium, Miranda-Vizuete A, Hoffmann GF, Lenaers G, Bomont P, Liebau E, Bonneau D.

Am J Hum Genet. 2016 Sep 1;99(3):695-703. doi: 10.1016/j.ajhg.2016.06.030. Epub 2016 Aug 18.

16.

Cognitive Impairment and Basal Ganglia Functional Connectivity in Vascular Parkinsonism.

Dunet V, Deverdun J, Charroud C, Le Bars E, Molino F, Menjot de Champfleur S, Maury F, Charif M, Ayrignac X, Labauge P, Castelnovo G, Pinna F, Bonafe A, Geny C, Menjot de Champfleur N.

AJNR Am J Neuroradiol. 2016 Dec;37(12):2310-2316. Epub 2016 Jul 14.

17.

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.

Bakhchane A, Bousfiha A, Charoute H, Salime S, Detsouli M, Snoussi K, Nadifi S, Kabine M, Rouba H, Dehbi H, Roky R, Charif M, Barakat A.

Eur J Med Genet. 2016 Jun;59(6-7):325-9. doi: 10.1016/j.ejmg.2016.05.002. Epub 2016 May 8.

PMID:
27169813
18.

Cerebrospinal Fluid Alzheimer's Disease Biomarkers in Cerebral Amyloid Angiopathy-Related Inflammation.

Renard D, Wacongne A, Ayrignac X, Charif M, Fourcade G, Azakri S, Le Floch A, Bouly S, Marelli C, Arquizan C, Hirtz C, Gabelle A, Thouvenot E, Lehmann S.

J Alzheimers Dis. 2016;50(3):759-64. doi: 10.3233/JAD-150621.

PMID:
26757185
19.

Supine sleep and obstructive sleep apnea syndrome in Parkinson's disease.

Cochen De Cock V, Benard-Serre N, Driss V, Granier M, Charif M, Carlander B, Desplan M, Croisier Langenier M, Cugy D, Bayard S.

Sleep Med. 2015 Dec;16(12):1497-501. doi: 10.1016/j.sleep.2014.09.014. Epub 2015 Apr 14.

PMID:
26611947
20.

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies.

Angebault C, Guichet PO, Talmat-Amar Y, Charif M, Gerber S, Fares-Taie L, Gueguen N, Halloy F, Moore D, Amati-Bonneau P, Manes G, Hebrard M, Bocquet B, Quiles M, Piro-Mégy C, Teigell M, Delettre C, Rossel M, Meunier I, Preising M, Lorenz B, Carelli V, Chinnery PF, Yu-Wai-Man P, Kaplan J, Roubertie A, Barakat A, Bonneau D, Reynier P, Rozet JM, Bomont P, Hamel CP, Lenaers G.

Am J Hum Genet. 2015 Nov 5;97(5):754-60. doi: 10.1016/j.ajhg.2015.09.012. Epub 2015 Oct 22. Erratum in: Am J Hum Genet. 2015 Nov 5;97(5):769.

21.

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability.

Charif M, Roubertie A, Salime S, Mamouni S, Goizet C, Hamel CP, Lenaers G.

Front Genet. 2015 Oct 19;6:311. doi: 10.3389/fgene.2015.00311. eCollection 2015.

22.

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees.

Bakhchane A, Charif M, Salime S, Boulouiz R, Nahili H, Roky R, Lenaers G, Barakat A.

PLoS One. 2015 Sep 15;10(9):e0138072. doi: 10.1371/journal.pone.0138072. eCollection 2015.

23.

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

Bakhchane A, Charoute H, Nahili H, Roky R, Rouba H, Charif M, Lenaers G, Barakat A.

Gene. 2015 Dec 10;574(1):28-33. doi: 10.1016/j.gene.2015.07.075. Epub 2015 Jul 28.

PMID:
26226225
24.

Optic neuropathy, cardiomyopathy, cognitive disability in patients with a homozygous mutation in the nuclear MTO1 and a mitochondrial MT-TF variant.

Charif M, Titah SM, Roubertie A, Desquiret-Dumas V, Gueguen N, Meunier I, Leid J, Massal F, Zanlonghi X, Mercier J, Raynaud de Mauverger E, Procaccio V, Mousson de Camaret B, Lenaers G, Hamel CP.

Am J Med Genet A. 2015 Oct;167A(10):2366-74. doi: 10.1002/ajmg.a.37188. Epub 2015 Jun 10.

PMID:
26061759
25.

In vitro approach to study the synergistic effects of tobramycin and clarithromycin against Pseudomonas aeruginosa biofilms using prokaryotic or eukaryotic culture media.

Thellin O, Zorzi W, Jolois O, Elmoualij B, Duysens G, Cahay B, Streel B, Charif M, Bastin R, Heinen E, Quatresooz P.

Int J Antimicrob Agents. 2015 Jul;46(1):33-8. doi: 10.1016/j.ijantimicag.2015.02.010. Epub 2015 Mar 18.

PMID:
25963337
26.

Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability.

Angebault C, Charif M, Guegen N, Piro-Megy C, Mousson de Camaret B, Procaccio V, Guichet PO, Hebrard M, Manes G, Leboucq N, Rivier F, Hamel CP, Lenaers G, Roubertie A.

Hum Mol Genet. 2015 Jul 15;24(14):3948-55. doi: 10.1093/hmg/ddv133. Epub 2015 Apr 21.

PMID:
25901006
27.

Reversible pseudo-tumoral brain lesion in patient with focal status epilepticus.

Azakri S, Charif M, Menjot de Champfleur N, Gélisse P, Mourand I.

J Neuroradiol. 2015 Jul;42(4):245-7. doi: 10.1016/j.neurad.2014.10.002. Epub 2014 Nov 17. No abstract available.

28.

Impulse control disorder and rapid eye movement sleep behavior disorder in Parkinson's disease.

Bayard S, Dauvilliers Y, Yu H, Croisier-Langenier M, Rossignol A, Charif M, Geny C, Carlander B, Cochen De Cock V.

Parkinsonism Relat Disord. 2014 Dec;20(12):1411-4. doi: 10.1016/j.parkreldis.2014.09.020. Epub 2014 Sep 23.

PMID:
25283069
29.

Daytime sleepiness in Parkinson's disease: a reappraisal.

Cochen De Cock V, Bayard S, Jaussent I, Charif M, Grini M, Langenier MC, Yu H, Lopez R, Geny C, Carlander B, Dauvilliers Y.

PLoS One. 2014 Sep 8;9(9):e107278. doi: 10.1371/journal.pone.0107278. eCollection 2014.

30.

Diffusion tensor imaging differentiates vascular parkinsonism from parkinsonian syndromes of degenerative origin in elderly subjects.

Deverdun J, Menjot de Champfleur S, Cabello-Aguilar S, Maury F, Molino F, Charif M, Leboucq N, Ayrignac X, Labauge P, Bonafe A, Castelnovo G, Le Bars E, Geny C, Menjot de Champfleur N.

Eur J Radiol. 2014 Nov;83(11):2074-9. doi: 10.1016/j.ejrad.2014.07.012. Epub 2014 Jul 24.

PMID:
25154005
31.

Lifelong desquamation of the hands and feet.

Grosshandler JA, El-Charif M, Shamma HN.

JAMA Dermatol. 2014 Jun;150(6):647-8. doi: 10.1001/jamadermatol.2013.9190. No abstract available.

PMID:
24760359
32.

Lack of confirmation of anti-inward rectifying potassium channel 4.1 antibodies as reliable markers of multiple sclerosis.

Nerrant E, Salsac C, Charif M, Ayrignac X, Carra-Dalliere C, Castelnovo G, Goulabchand R, Tisseyre J, Raoul C, Eliaou JF, Labauge P, Vincent T.

Mult Scler. 2014 Nov;20(13):1699-703. doi: 10.1177/1352458514531086. Epub 2014 Apr 22.

PMID:
24756568
33.

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.

Charif M, Boulouiz R, Bakhechane A, Benrahma H, Nahili H, Eloualid A, Rouba H, Kandil M, Abidi O, Lenaers G, Barakat A.

Indian J Hum Genet. 2013 Jul;19(3):331-6. doi: 10.4103/0971-6866.120828.

34.

[Natalizumab as induction therapy in multiple sclerosis].

Corlobé A, Charif M, Mania A, Outteryck O, de Sèze J, Labauge P.

Rev Neurol (Paris). 2014 Jan;170(1):2-5. doi: 10.1016/j.neurol.2013.06.004. Epub 2013 Oct 11. Review. French.

PMID:
24125463
35.

Triphenylphosphonium salts of 1,2,4-benzothiadiazine 1,1-dioxides related to diazoxide targeting mitochondrial ATP-sensitive potassium channels.

Constant-Urban C, Charif M, Goffin E, Van Heugen JC, Elmoualij B, Chiap P, Mouithys-Mickalad A, Serteyn D, Lebrun P, Pirotte B, De Tullio P.

Bioorg Med Chem Lett. 2013 Nov 1;23(21):5878-81. doi: 10.1016/j.bmcl.2013.08.091. Epub 2013 Sep 6.

PMID:
24055044
36.

Hemolytic uremic syndrome: an unusual complication of interferon-β treatment in a MS patient.

Nerrant E, Charif M, Ramay AS, Perrochia H, Patrier L, de Champfleur NM, Renard D, Labauge P.

J Neurol. 2013 Jul;260(7):1915-6. doi: 10.1007/s00415-013-6961-8. Epub 2013 May 25. No abstract available.

PMID:
23708674
37.

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.

Charif M, Bakhchane A, Abidi O, Boulouiz R, Eloualid A, Roky R, Rouba H, Kandil M, Lenaers G, Barakat A.

Gene. 2013 Jul 1;523(1):103-5. doi: 10.1016/j.gene.2013.03.123. Epub 2013 Apr 13.

PMID:
23590985
38.

Ipsilateral uveitis and optic neuritis in multiple sclerosis.

Thouvenot E, Mura F, De Verdal M, Carlander B, Charif M, Schneider C, Navarre S, Camu W.

Mult Scler Int. 2012;2012:372361. doi: 10.1155/2012/372361. Epub 2012 Nov 19.

39.

The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.

Charif M, Bounaceur S, Abidi O, Nahili H, Rouba H, Kandil M, Boulouiz R, Barakat A.

Mol Biol Rep. 2012 Dec;39(12):11011-6. doi: 10.1007/s11033-012-2003-3. Epub 2012 Oct 8.

PMID:
23053991
40.

Association of spermatogenic failure with the b2/b3 partial AZFc deletion.

Eloualid A, Rhaissi H, Reguig A, Bounaceur S, El Houate B, Abidi O, Charif M, Louanjli N, Chadli E, Barakat A, Bashamboo A, McElreavey K, Rouba H.

PLoS One. 2012;7(4):e34902. doi: 10.1371/journal.pone.0034902. Epub 2012 Apr 13.

41.

Association of the MTHFR A1298C variant with unexplained severe male infertility.

Eloualid A, Abidi O, Charif M, El Houate B, Benrahma H, Louanjli N, Chadli E, Ajjemami M, Barakat A, Bashamboo A, McElreavey K, Rhaissi H, Rouba H.

PLoS One. 2012;7(3):e34111. doi: 10.1371/journal.pone.0034111. Epub 2012 Mar 23.

42.

Suggested immobilization test for diagnosis of restless legs syndrome in Parkinson's disease.

De Cock VC, Bayard S, Yu H, Grini M, Carlander B, Postuma R, Charif M, Dauvilliers Y.

Mov Disord. 2012 May;27(6):743-9. doi: 10.1002/mds.24969. Epub 2012 Mar 21.

PMID:
22437899
43.

[Leptomeningeal melanocytosis: a fatal course of a benign tumor].

Grini-Mazouzi M, Thouvenot E, Sabaah M, Rigau V, Charif M.

Rev Neurol (Paris). 2012 May;168(5):461-3. doi: 10.1016/j.neurol.2011.08.021. Epub 2012 Mar 7. French. No abstract available.

PMID:
22405462
44.

[Anti-GAD antibodies in paraneoplastic cerebellar ataxia associated with limbic encephalitis and autonomic dysfunction].

Carra-Dalliere C, Thouvenot E, Bonafé A, Ducray F, Touchon J, Charif M.

Rev Neurol (Paris). 2012 Apr;168(4):363-6. doi: 10.1016/j.neurol.2011.07.018. Epub 2012 Mar 7. French.

PMID:
22405456
45.

Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.

Charif M, Abidi O, Boulouiz R, Nahili H, Rouba H, Kandil M, Delprat B, Lenaers G, Barakat A.

Biochem Biophys Res Commun. 2012 Mar 23;419(4):643-7. doi: 10.1016/j.bbrc.2012.02.066. Epub 2012 Feb 20.

PMID:
22382023
46.

Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.

Abidi O, Knari S, Sefri H, Charif M, Senechal A, Hamel C, Rouba H, Zaghloul K, El Kettani A, Lenaers G, Barakat A.

Mol Vis. 2011;17:3541-7. Epub 2011 Dec 30.

47.

Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.

Benrahma H, Arfa I, Charif M, Bounaceur S, Eloualid A, Boulouiz R, Nahili H, Abidi O, Rouba H, Chadli A, Oudghiri M, Farouqui A, Abdelhak S, Barakat A.

J Community Health. 2011 Dec;36(6):943-8. doi: 10.1007/s10900-011-9393-3.

PMID:
21442339
48.

Susac's syndrome, a rare, potentially severe or lethal neurological disease.

Saux A, Niango G, Charif M, Morales R, Mura F, Bonafe A, Mourand I.

J Neurol Sci. 2010 Oct 15;297(1-2):71-3. doi: 10.1016/j.jns.2010.07.020. Epub 2010 Aug 17.

PMID:
20723912
49.

Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.

Nahili H, Charif M, Boulouiz R, Bounaceur S, Benrahma H, Abidi O, Chafik A, Rouba H, Kandil M, Barakat A.

Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1071-4. doi: 10.1016/j.ijporl.2010.06.008. Epub 2010 Jul 15.

PMID:
20637512
50.

[Meningomyeloradiculitis in an immunocompetent patient].

Carra Dalliere C, Thouvenot E, Baptista G, Le Moing V, Charif M.

Rev Neurol (Paris). 2010 Aug-Sep;166(8-9):741-4. doi: 10.1016/j.neurol.2010.01.006. Epub 2010 Mar 6. French.

PMID:
20207385

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