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Items: 1 to 50 of 52

1.

Prospective study of the additional benefit of plexus magnetic resonance imaging in the diagnosis of chronic inflammatory demyelinating polyneuropathy.

Jomier F, Bousson V, Viala K, Péréon Y, Magot A, Cauquil C, Bouhour F, Vial C, Bedat-Millet AL, Taithe F, Bresch S, Siri A, Kubis N, Lozeron P.

Eur J Neurol. 2019 Jul 26. doi: 10.1111/ene.14053. [Epub ahead of print]

PMID:
31348848
2.

Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies.

Wahbi K, Ben Yaou R, Gandjbakhch E, Anselme F, Gossios T, Lakdawala NK, Stalens C, Sacher F, Babuty D, Trochu JN, Moubarak G, Savvatis K, Porcher R, Laforêt P, Fayssoil A, Marijon E, Stojkovic T, Béhin A, Leonard-Louis S, Sole G, Labombarda F, Richard P, Metay C, Quijano-Roy S, Dabaj I, Klug D, Vantyghem MC, Chevalier P, Ambrosi P, Salort E, Sadoul N, Waintraub X, Chikhaoui K, Mabo P, Combes N, Maury P, Sellal JM, Tedrow UB, Kalman JM, Vohra J, Androulakis AFA, Zeppenfeld K, Thompson T, Barnerias C, Bécane HM, Bieth E, Boccara F, Bonnet D, Bouhour F, Boulé S, Brehin AC, Chapon F, Cintas P, Cuisset JM, Davy JM, De Sandre-Giovannoli A, Demurger F, Desguerre I, Dieterich K, Durigneux J, Echaniz-Laguna A, Eschalier R, Ferreiro A, Ferrer X, Francannet C, Fradin M, Gaborit B, Gay A, Hagège A, Isapof A, Jeru I, Juntas Morales R, Lagrue E, Lamblin N, Lascols O, Laugel V, Lazarus A, Leturcq F, Levy N, Magot A, Manel V, Martins R, Mayer M, Mercier S, Meune C, Michaud M, Minot-Myhié MC, Muchir A, Nadaj-Pakleza A, Péréon Y, Petiot P, Petit F, Praline J, Rollin A, Sabouraud P, Sarret C, Schaeffer S, Taithe F, Tard C, Tiffreau V, Toutain A, Vatier C, Walther-Louvier U, Eymard B, Charron P, Vigouroux C, Bonne G, Kumar S, Elliott P, Duboc D.

Circulation. 2019 Jul 23;140(4):293-302. doi: 10.1161/CIRCULATIONAHA.118.039410. Epub 2019 Jun 3.

PMID:
31155932
3.

LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2.

Peretti A, Perie M, Vincent D, Bouhour F, Dieterich K, Mallaret M, Duval F, Goizet C, Juntas-Morales R, Magy L, Solé G, Nollet S, Not A, Léonard-Louis S, Francou B, Leguern E, Lia AS, Magdelaine C, Latour P, Stojkovic T.

Eur J Hum Genet. 2019 Sep;27(9):1406-1418. doi: 10.1038/s41431-019-0403-8. Epub 2019 Apr 17.

PMID:
30996334
4.

FSHD1 and FSHD2 form a disease continuum.

Sacconi S, Briand-Suleau A, Gros M, Baudoin C, Lemmers RJLF, Rondeau S, Lagha N, Nigumann P, Cambieri C, Puma A, Chapon F, Stojkovic T, Vial C, Bouhour F, Cao M, Pegoraro E, Petiot P, Behin A, Marc B, Eymard B, Echaniz-Laguna A, Laforet P, Salviati L, Jeanpierre M, Cristofari G, van der Maarel SM.

Neurology. 2019 May 7;92(19):e2273-e2285. doi: 10.1212/WNL.0000000000007456. Epub 2019 Apr 12.

PMID:
30979860
5.

Efficacy and Safety of Octagam® in Patients With Chronic Inflammatory Demyelinating Polyneuropathy.

Belmokhtar C, Lozeron P, Adams D, Franques J, Lacour A, Godet E, Bataille M, Dubourg O, Angibaud G, Delmont E, Bouhour F, Corcia P, Pouget J.

Neurol Ther. 2019 Jun;8(1):69-78. doi: 10.1007/s40120-019-0132-5. Epub 2019 Mar 22.

6.

Late-onset Pompe disease in France: molecular features and epidemiology from a nationwide study.

Semplicini C, Letard P, De Antonio M, Taouagh N, Perniconi B, Bouhour F, Echaniz-Laguna A, Orlikowski D, Sacconi S, Salort-Campana E, Solé G, Zagnoli F, Hamroun D, Froissart R, Caillaud C, Laforêt P; French Pompe Study Group.

J Inherit Metab Dis. 2018 Nov;41(6):937-946. doi: 10.1007/s10545-018-0243-7. Epub 2018 Aug 28.

PMID:
30155607
7.

Safety of Intravenous Immunoglobulin (Tegeline®), Administered at Home in Patients with Autoimmune Disease: Results of a French Study.

Hachulla E, Le Masson G, Solé G, Hamidou M, Desnuelle C, Azulay JP, Besson G, Swiader L, Abad S, Antoine JC, Bouhour F, Créange A, Grenouillet M, Magy L, Marcel S, Paquet JM, Rouhart F, Ziegler F, Mathis S, Gauthier-Darnis M, Puget S.

Biomed Res Int. 2018 Mar 15;2018:8147251. doi: 10.1155/2018/8147251. eCollection 2018.

8.

Incobotulinum toxin A in Parkinson's disease with foot dystonia: A double blind randomized trial.

Rieu I, Degos B, Castelnovo G, Vial C, Durand E, Pereira B, Simonetta-Moreau M, Sangla S, Fluchère F, Guehl D, Burbaud P, Geny C, Gayraud D, Ory-Magne F, Bouhour F, Llinares E, Derost P, Marques A, Durif F.

Parkinsonism Relat Disord. 2018 Jan;46:9-15. doi: 10.1016/j.parkreldis.2017.10.009. Epub 2017 Oct 19.

PMID:
29102441
9.

Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.

Bauché S, Vellieux G, Sternberg D, Fontenille MJ, De Bruyckere E, Davoine CS, Brochier G, Messéant J, Wolf L, Fardeau M, Lacène E, Romero N, Koenig J, Fournier E, Hantaï D, Streichenberger N, Manel V, Lacour A, Nadaj-Pakleza A, Sukno S, Bouhour F, Laforêt P, Fontaine B, Strochlic L, Eymard B, Chevessier F, Stojkovic T, Nicole S.

J Neurol. 2017 Aug;264(8):1791-1803. doi: 10.1007/s00415-017-8569-x. Epub 2017 Jul 15.

PMID:
28712002
10.

Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria.

Robert-Varvat F, Jousserand G, Bouhour F, Vial C, Cintas P, Echaniz-Laguna A, Delmont E, Clavelou P, Chauplannaz G, Jomir L, Pereon Y, Leonard-Louis S, Manel V, Antoine JC, Lacour A, Camdessanche JP.

Muscle Nerve. 2018 Feb;57(2):217-221. doi: 10.1002/mus.25666. Epub 2017 Jun 11.

PMID:
28407266
11.

Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study.

Dogan C, De Antonio M, Hamroun D, Varet H, Fabbro M, Rougier F, Amarof K, Arne Bes MC, Bedat-Millet AL, Behin A, Bellance R, Bouhour F, Boutte C, Boyer F, Campana-Salort E, Chapon F, Cintas P, Desnuelle C, Deschamps R, Drouin-Garraud V, Ferrer X, Gervais-Bernard H, Ghorab K, Laforet P, Magot A, Magy L, Menard D, Minot MC, Nadaj-Pakleza A, Pellieux S, Pereon Y, Preudhomme M, Pouget J, Sacconi S, Sole G, Stojkovich T, Tiffreau V, Urtizberea A, Vial C, Zagnoli F, Caranhac G, Bourlier C, Riviere G, Geille A, Gherardi RK, Eymard B, Puymirat J, Katsahian S, Bassez G.

PLoS One. 2016 Feb 5;11(2):e0148264. doi: 10.1371/journal.pone.0148264. eCollection 2016.

12.

Peripheral small fiber dysfunction and neuropathic pain in patients with Morvan syndrome.

Laurencin C, André-Obadia N, Camdessanché JP, Mauguière F, Ong E, Vukusic S, Peter-Derex L, Meyronet D, Bouhour F, Vial C, Ducray F, Honnorat J, Petiot P.

Neurology. 2015 Dec 8;85(23):2076-8. doi: 10.1212/WNL.0000000000002037. Epub 2015 Sep 23. No abstract available.

PMID:
26400578
13.

Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study.

Salort-Campana E, Nguyen K, Bernard R, Jouve E, Solé G, Nadaj-Pakleza A, Niederhauser J, Charles E, Ollagnon E, Bouhour F, Sacconi S, Echaniz-Laguna A, Desnuelle C, Tranchant C, Vial C, Magdinier F, Bartoli M, Arne-Bes MC, Ferrer X, Kuntzer T, Levy N, Pouget J, Attarian S.

Orphanet J Rare Dis. 2015 Jan 21;10:2. doi: 10.1186/s13023-014-0218-1.

14.

Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution.

Deconinck N, Richard P, Allamand V, Behin A, Lafôret P, Ferreiro A, de Becdelievre A, Ledeuil C, Gartioux C, Nelson I, Carlier RY, Carlier P, Wahbi K, Romero N, Zabot MT, Bouhour F, Tiffreau V, Lacour A, Eymard B, Stojkovic T.

J Neurol Neurosurg Psychiatry. 2015 Dec;86(12):1337-46. doi: 10.1136/jnnp-2013-307245. Epub 2014 Dec 22.

PMID:
25535305
15.

Sporadic late-onset nemaline myopathy with MGUS: long-term follow-up after melphalan and SCT.

Voermans NC, Benveniste O, Minnema MC, Lokhorst H, Lammens M, Meersseman W, Delforge M, Kuntzer T, Novy J, Pabst T, Bouhour F, Romero N, Leblond V, Bergh Pv, Vekemans MC, van Engelen BG, Eymard B.

Neurology. 2014 Dec 2;83(23):2133-9. doi: 10.1212/WNL.0000000000001047. Epub 2014 Nov 5.

16.

Atrio-ventricular block requiring pacemaker in patients with late onset Pompe disease.

Sacconi S, Wahbi K, Theodore G, Garcia J, Salviati L, Bouhour F, Vial C, Duboc D, Laforêt P, Desnuelle C.

Neuromuscul Disord. 2014 Jul;24(7):648-50. doi: 10.1016/j.nmd.2014.04.005. Epub 2014 Apr 24.

PMID:
24844452
17.
18.

Development and validation of a motor function classification in patients with neuromuscular disease: the NM-score.

Vuillerot C, Rippert P, Roche S, Bérard C, Margirier F, de Lattre C, Poirot I, Berruyer A, Tiffreau V, Fournier-Mehouas M, Bouhour F, Urtizberea JA, Renders A, Ecochard R; Le groupe d’étude NM-Score.

Ann Phys Rehabil Med. 2013 Dec;56(9-10):673-86. doi: 10.1016/j.rehab.2013.10.002. Epub 2013 Oct 18.

19.

The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease.

Laforêt P, Laloui K, Granger B, Hamroun D, Taouagh N, Hogrel JY, Orlikowski D, Bouhour F, Lacour A, Salort-Campana E, Penisson-Besnier I, Sacconi S, Zagnoli F, Chapon F, Eymard B, Desnuelle C, Pouget J; French Pompe Registry Study Group.

Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):595-602. doi: 10.1016/j.neurol.2013.07.002. Epub 2013 Sep 3.

PMID:
24008051
20.

Absence of airway secretion accumulation predicts tolerance of noninvasive ventilation in subjects with amyotrophic lateral sclerosis.

Vandenberghe N, Vallet AE, Petitjean T, Le Cam P, Peysson S, Guérin C, Dailler F, Jay S, Cadiergue V, Bouhour F, Court-Fortune I, Camdessanche JP, Antoine JC, Philit F, Beuret P, Bin-Dorel S, Vial C, Broussolle E.

Respir Care. 2013 Sep;58(9):1424-32. doi: 10.4187/respcare.02103. Epub 2013 Jan 15.

21.

Clinical and electrophysiological characteristics of neuropathy associated with Tangier disease.

Zyss J, Béhin A, Couvert P, Bouhour F, Sassolas A, Kolev I, Denys V, Vial C, Lacour A, Carrié A, Stojkovic T.

J Neurol. 2012 Jun;259(6):1222-6. doi: 10.1007/s00415-011-6340-2. Epub 2011 Dec 17.

PMID:
22179783
22.

Quantitative assessment of skeletal muscle degeneration in patients with myotonic dystrophy type 1 using MRI.

Hiba B, Richard N, Hébert LJ, Coté C, Nejjari M, Vial C, Bouhour F, Puymirat J, Janier M.

J Magn Reson Imaging. 2012 Mar;35(3):678-85. doi: 10.1002/jmri.22849. Epub 2011 Nov 8.

PMID:
22069222
23.

[Identification and characterization of a monoclonal IgM reacting with disialylated gangliosides recognizing the CANOMAD syndrome].

Boussaïd I, Bouhour F, Vial C, Caudie C.

Ann Biol Clin (Paris). 2011 Jul-Aug;69(4):476-80. doi: 10.1684/abc.2011.0603. French.

24.

[Natural history of adult-onset eIF2B-related disorders: a multicentric survey of 24 cases].

Carra-Dalliere C, Horzinski L, Ayrignac X, Vukusic S, Rodriguez D, Mauguiere F, Peter L, Goizet C, Bouhour F, Denier C, Confavreux C, Obadia M, Blanc F, de Seze J, Sedel F, Guennoc AM, Sartori E, Laplaud D, Antoine JC, Fogli A, Boespflug-Tanguy O, Labauge P.

Rev Neurol (Paris). 2011 Nov;167(11):802-11. doi: 10.1016/j.neurol.2011.03.008. Epub 2011 Jun 14. French.

PMID:
21676421
25.

[Serum antibody profiles against gangliosides and sulfatide in peripheral neuropathies: evaluation of a new immunoassay].

Caudie C, Vial C, Petiot P, Bouhour F.

Ann Biol Clin (Paris). 2010 Nov-Dec;68(6):675-80. doi: 10.1684/abc.2010.0495. French.

26.

Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing.

Gaudon K, Pénisson-Besnier I, Chabrol B, Bouhour F, Demay L, Ben Ammar A, Bauché S, Vial C, Nicolas G, Eymard B, Hantaï D, Richard P.

J Med Genet. 2010 Dec;47(12):795-6. doi: 10.1136/jmg.2010.081034. Epub 2010 Oct 7.

27.

Lewis and Sumner syndrome following infliximab treatment in Crohn's disease: a report of 2 cases.

Nancey S, Bouhour F, Boschetti G, Magnier C, Gonneau PM, Souquet JC, Kaiserlian D, Flourie B.

Inflamm Bowel Dis. 2010 Sep;16(9):1450-3. doi: 10.1002/ibd.21202. No abstract available.

PMID:
20128005
28.

Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 cases.

Labauge P, Horzinski L, Ayrignac X, Blanc P, Vukusic S, Rodriguez D, Mauguiere F, Peter L, Goizet C, Bouhour F, Denier C, Confavreux C, Obadia M, Blanc F, de Sèze J, Fogli A, Boespflug-Tanguy O.

Brain. 2009 Aug;132(Pt 8):2161-9. doi: 10.1093/brain/awp171.

PMID:
19625339
29.

[Vasculitis multiple mononeuropathies].

Vial C, Bouhour F.

Rev Prat. 2008 Nov 15;58(17):1896-9. French.

PMID:
19157205
30.

Dehydroepiandrosterone for myotonic dystrophy type 1.

Pénisson-Besnier I, Devillers M, Porcher R, Orlikowski D, Doppler V, Desnuelle C, Ferrer X, Bes MC, Bouhour F, Tranchant C, Lagrange E, Vershueren A, Uzenot D, Cintas P, Solé G, Hogrel JY, Laforêt P, Vial C, Vila AL, Sacconi S, Pouget J, Eymard B, Chevret S, Annane D.

Neurology. 2008 Aug 5;71(6):407-12. doi: 10.1212/01.wnl.0000324257.35759.40.

PMID:
18678823
31.

[Multiple phenotypic manifestations of X-linked spinobulbar muscular atrophy].

Vandenberghe N, Bouhour F, Petiot P, Gonnaud PM, Latour P, Broussolle E, Vial C.

Rev Neurol (Paris). 2009 Jan;165(1):31-7. doi: 10.1016/j.neurol.2008.06.005. Epub 2008 Jul 29. French.

PMID:
18667219
32.

Factors predicting survival following noninvasive ventilation in amyotrophic lateral sclerosis.

Peysson S, Vandenberghe N, Philit F, Vial C, Petitjean T, Bouhour F, Bayle JY, Broussolle E.

Eur Neurol. 2008;59(3-4):164-71. doi: 10.1159/000114037. Epub 2008 Jan 29.

PMID:
18230874
33.

[Chronic inflammatory demyelinating polyneuropathy and sarcoidosis: fortuitous association?].

Ducray F, Costedoat-Chalumeau N, Bouhour F, Rousset H, Vial C.

Rev Neurol (Paris). 2007 Sep;163 Spec No 1:3S85-9. French.

PMID:
18087235
34.

[Diagnostic value of the anti-IgM SGPG Elisa (Bühlmann laboratories AG) in 147 sera with a monoclonal IgM anti-MAG/SGPG antibody-associated neuropathy].

Caudie C, Bouhour F, Petiot P, Gonnaud PM, Antoine JC, Vial C.

Ann Biol Clin (Paris). 2007 Jul-Aug;65(4):369-75. French.

35.

Marked improvement of Churg-Strauss vasculitis with intravenous gamma globulins during pregnancy.

Hot A, Perard L, Coppere B, Simon M, Bouhour F, Ninet J.

Clin Rheumatol. 2007 Dec;26(12):2149-2151. doi: 10.1007/s10067-007-0628-8. Epub 2007 May 8.

PMID:
17486292
36.

[Sarcoidosis demonstrated by fluorodeoxyglucose positron emission tomography in a case of granulomatous myopathy].

Dufour JF, Billotey C, Streichenberger N, Bouhour F, Broussolle C, Sève P.

Rev Med Interne. 2007 Aug;28(8):568-70. Epub 2007 Apr 5. French.

PMID:
17445952
37.

[Steinert disease].

Bouhour F, Bost M, Vial C.

Presse Med. 2007 Jun;36(6 Pt 2):965-71. Epub 2007 Feb 7. Review. French.

38.

Granulomatous myositis: a clinical study of thirteen cases.

Le Roux K, Streichenberger N, Vial C, Petiot P, Feasson L, Bouhour F, Ninet J, Lachenal F, Broussolle C, Sève P.

Muscle Nerve. 2007 Feb;35(2):171-7.

PMID:
17068767
39.

[Electrophysiological manifestations of chronic inflammatory demyelinating polyradiculoneuropathy].

Vial C, Bouhour F.

Rev Neurol (Paris). 2006 Apr;162(4):522-6. Review. French.

PMID:
16585915
40.

[Myasthenia].

Bouhour F, Confavreux C.

Rev Prat. 2005 Nov 15;55(17):1927-32. French. No abstract available. Erratum in: Rev Prat. 2006 Feb 28;56(4):438.

PMID:
16396237
41.

[Electrophysiological examination of the cranial nerves: technical aspects and practical applications].

Vial Ch, Bouhour F.

Rev Med Liege. 2004;59 Suppl 1:82-90. Review. French.

42.

[Analysis of 12 cases of McArdle's disease diagnosed after 30 years].

Pavic M, Petiot P, Streichenberger N, Dupond JL, Drouet A, Flocard F, Bouhour F, Colin JY, Bielefeld P, Gouttard M, Maire I, Pellat J, Vital Durand D, Rousset H.

Rev Med Interne. 2003 Nov;24(11):716-20. French.

PMID:
14604748
43.

[Other uses for botulinum toxin in neurology].

Vial C, Bouhour F, de Saint Victor JF.

Rev Neurol (Paris). 2003 Sep;159(8-9):814-8. Review. French. No abstract available.

PMID:
13679728
44.

Ovarian failure related to eukaryotic initiation factor 2B mutations.

Fogli A, Rodriguez D, Eymard-Pierre E, Bouhour F, Labauge P, Meaney BF, Zeesman S, Kaneski CR, Schiffmann R, Boespflug-Tanguy O.

Am J Hum Genet. 2003 Jun;72(6):1544-50. Epub 2003 Apr 21.

45.

[ Varicella-zoster virus encephalitis mimicking herpes simplex encephalitis].

Philippeau F, Bouhour F, Salord F.

Rev Med Interne. 2001 Dec;22(12):1272-4. French. No abstract available.

PMID:
11794902
46.

[Multiple sclerosis: spontaneous course, natural history].

Vukusic S, Moreau T, Bouhour F, Adeleine P, Confavreux C.

Rev Neurol (Paris). 2001 Sep;157(8-9 Pt 1):753-6. French.

PMID:
11677394
47.

[18F]fluorodeoxyglucose positron emission tomography in the diagnosis of cancer in patients with paraneoplastic neurological syndrome and anti-Hu antibodies.

Antoine JC, Cinotti L, Tilikete C, Bouhour F, Camdessanché JP, Confavreux C, Vighetto A, Renault-Mannel V, Michel D, Honnorat J.

Ann Neurol. 2000 Jul;48(1):105-8.

PMID:
10894223
48.

[Disease-modifying treatments in multiple sclerosis].

Confavreux C, Bouhour F, Vukusic S.

Rev Prat. 1999 Nov 1;49(17):1882-9. French.

PMID:
10598505
49.

[Hypokalemic quadriplegia with distal tubular acidosis revealing a a case of primary Gougerot-Sjögren syndrome].

Raynal C, Durupt S, Durieu I, Boudray C, Bouhour F, Levrat R, Vital Durand D.

Presse Med. 1999 Nov 13;28(35):1935-7. French.

PMID:
10598150
50.

Ventral transdural herniation of the thoracic spinal cord: surgical treatment in four cases and review of literature.

Vallée B, Mercier P, Menei P, Bouhour F, Fischer C, Fournier D, Bougeard R, Diabira S, Mahla K.

Acta Neurochir (Wien). 1999;141(9):907-13. Review.

PMID:
10526071

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