SLA

Maladies neuromusculaires et SLA - Hôpital de la Timone

Secrétariat :
Tél. : 04 91 38 65 79  -  04 91 38 78 75
Fax : 04 91 38 49 46
E-mail : secretariat.maladiesneuromusculaires@ap-hm.fr

 

Electroneuromyographie :
Tél. : 04 91 38 65 78

 

Hôpital de la Timone, 9ème étage

 

Equipe
medecins: 

Neurologues :

  • Pr Shahram ATTARIAN
  • Dr Annie VERSCHUEREN
  • Dr Emmanuelle CAMPANA-SALORT
  • Dr Aude-Marie GRAPPERON
  • Dr Émilien DELMONT
  • Dr Julien GALLARD
  • Dr Ludivine KOUTON


Médecins MPR :

  • Dr Virginie MILHE-DE BOVIS
  • Dr Anne DUVOCELLE


Pneumologue :

  • Dr Armelle MONNIER-FINET
Spécialités: 
Chefs de services: 
Pathologies
Pathologies: 
  • Maladies du neurone moteur dont sclérose latérale amyotrophique
  • Maladies des nerfs périphériques et neuropathies
  • Maladies de la transmission neuromusculaire
  • Maladies musculaires
Techniques et traitements
Techniques et traitements: 
  • Électroneuromyogrammes
  • Potentiels évoqués moteurs
  • Biopsies nerveuses et musculaires réalisées par le service d’anatomopathologie
Publications
Publications: 

Recherches :

 

Essais cliniques en cours :

 

  • Addition
  • ALNTTRO2-006
  • Baxalta
  • Dysferlin
  • Dyvine
  • Expret
  • Helipad
  • Igos
  • Mirocals
  • Mycopid
  • NeoGAA comete
  • Neuroinflammation
  • Nutrals
  • Obsamyl
  • Pulse

 

Essais à venir :

 

  • Eidos
  • Helios ALNTTRSC02
  • POM-003 Amicus
  • Mom-M281-004
  • Syneos ARGX-113 Myasthenia Gravis
  • 161505-extension baxalta PIDC
  • Dermatomyositis igoPro20_3007
  • Biogen 233AS301
  • Fair ALS
  • Pharm-Olam
  • Rock als

 

Publications :

 

  • Adams D, Gonzalez-Duarte A, O'Riordan WD, Yang CC, Ueda M, Kristen AV, Tournev I, Schmidt HH, Coelho T, Berk JL, Lin KP, Vita G, Attarian S, Planté-Bordeneuve V, Mezei MM, Campistol JM, Buades J, Brannagan TH 3rd, Kim BJ, Oh J, Parman Y, Sekijima Y, Hawkins PN, Solomon SD, Polydefkis M, Dyck PJ, Gandhi PJ, Goyal S, Chen J, Strahs AL, Nochur SV, Sweetser MT, Garg PP, Vaishnaw AK, Gollob JA, Suhr OB. Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis. Engl J Med. 2018 Jul 5;379(1):11-21. doi: 10.1056/NEJMoa1716153. PubMed PMID: 29972753.

  • Bas J, Delmont E, Fatehi F, Salort-Campana E, Verschueren A, Pouget J, Lefebvre MN, Grapperon AM, Attarian S. Motor unit number index correlates with disability in Charcot-Marie-Tooth disease. Clin Neurophysiol. 2018 Jul;129(7):1390-1396. doi: 10.1016/j.clinph.2018.04.359. Epub 2018 Apr 16. PubMed PMID: 29729594.

  • van Schaik IN, Mielke O; PATH study group. Intravenous versus subcutaneous immunoglobulin - Authors' reply. Lancet Neurol. 2018 May;17(5):393-394. doi: 10.1016/S1474-4422(18)30109-1. PubMed PMID: 29656738.

  • Attarian SJ, Leibel SL, Yang P, Alfano DN, Hackett BP, Cole FS, Hamvas A. Mutations in the thyroid transcription factor gene NKX2-1 result in decreased expression of SFTPB and SFTPC. Pediatr Res. 2018 Apr 11. doi: 10.1038/pr.2018.30. [Epub ahead of print] PubMed PMID: 29538355.

  • Ben Lassoued A, Fromonot J, Marlinge M, Basset N, Chefrour M, Vairo D, Couillaud J, Lopez L, Cuisset T, Boucraut J, Delmont E, Attarian S, Guieu R. Corrigendum to "A case of false positive cardiac troponin I in CANOMAD syndrome" [Int. J. Cardiol. 222 (2016) 359-360]. Int J Cardiol. 2018 May 15;259:234. doi: 10.1016/j.ijcard.2018.02.017. Epub  2018 Feb 27. PubMed PMID: 29499853.

  • Duchesne M, Danigo A, Richard L, Vallat JM, Attarian S, Gonnaud PM, Lacour A, Péréon Y, Stojkovic T, Nave KA, Bertrand V, Nabirotchkin S, Cohen D, Demiot C, Magy L. Skin Biopsy Findings in Patients With CMT1A: Baseline Data From the CLN-PXT3003-01 Study Provide New Insights Into the Pathophysiology of the Disorder. J Neuropathol Exp Neurol. 2018 Apr 1;77(4):274-281. doi: 10.1093/jnen/nly001. PubMed PMID: 29408953.

  • Van den Bergh PYK, Piéret F, Woodard JL, Attarian S, Grapperon AM, Nicolas G, Brisset M, Cassereau J, Rajabally YA, Van Parijs V, Verougstraete D, Jacquerye P, Raymackers JM, Redant C, Michel C, Delmont E; University of Louvain GBS Electrodiagnosis Study Group. Guillain-BarrÉ syndrome subtype diagnosis: A prospective multicentric  European study. Muscle Nerve. 2018 Jan 5. doi: 10.1002/mus.26056. [Epub ahead of print] PubMed PMID: 29315669.

  • Attarian S, Yu C, Anderson KE, Friedman EW. Effects of hemin and hemodialysis in a patient with acute intermittent porphyria and renal failure. Blood Adv. 2017 Jun 5;1(14):915-917. doi: 10.1182/bloodadvances.2017005660. eCollection 2017 Jun 13. PubMed PMID: 29296735; PubMed Central PMCID: PMC5737596.

  • Rajabally YA, Attarian S. Chronic inflammatory demyelinating polyneuropathy and malignancy: A systematic review. Muscle Nerve. 2018 Jun;57(6):875-883. doi: 10.1002/mus.26028. Epub 2017 Dec 20. Review. PubMed PMID: 29194677.

  • Sevy A, Grapperon AM, Salort Campana E, Delmont E, Attarian S. Detection of proximal conduction blocks using a triple stimulation technique improves the early diagnosis of Guillain-Barré syndrome. Clin Neurophysiol. 2018 Jan;129(1):127-132. doi: 10.1016/j.clinph.2017.10.035. Epub 2017 Nov 11. PubMed PMID: 29182914.

  • Attarian S, Reed L, Singh S, Shestopalov A, Singh AP, Budhathoki A, Abi-Aad S, Shah UA, Kim S, Bachiashvili K, Elrafei T, Li W, Yee C, Friedman EW. Visualization of the bone marrow biopsy needle track. Am J Hematol. 2018 Mar;93(3):E60-E61. doi: 10.1002/ajh.24985. Epub 2017 Dec 6. PubMed PMID: 29168229.

  • Ibrahim J, Grapperon AM, Manfredonia F, van den Bergh PY, Attarian S, Rajabally YA. Serial electrophysiology in Guillain-Barré syndrome: A retrospective cohort and case-by-case multicentre analysis. Acta Neurol Scand. 2018 Mar;137(3):335-340. doi: 10.1111/ane.12872. Epub 2017 Nov 21. PubMed PMID: 29164611.

  • Martinez-Martinez L, Lleixà MC, Boera-Carnicero G, Cortese A, Devaux J, Siles A, Rajabally Y, Martinez-Piñeiro A, Carvajal A, Pardo J, Delmont E, Attarian S, Diaz-Manera J, Callegari I, Marchioni E, Franciotta D, Benedetti L, Lauria G, de la Calle Martin O, Juárez C, Illa I, Querol L. Anti-NF155 chronic inflammatory demyelinating polyradiculoneuropathy strongly associates to HLA-DRB15. Neuroinflammation. 2017 Nov 16;14(1):224. doi: 10.1186/s12974-017-0996-1. PubMed PMID: 29145880; PubMed Central PMCID: PMC5691853.

  • Marion S, Béhin A, Attarian S. [GNE myopathy: proven failure of sialic acid supplementation… what's next?]. Med Sci (Paris). 2017 Nov;33 Hors série n°1:55-56. doi: 10.1051/medsci/201733s111. Epub 2017 Nov 15. French. PubMed PMID: 29139388.

  • van Schaik IN, Bril V, van Geloven N, Hartung HP, Lewis RA, Sobue G, Lawo JP, Praus M, Mielke O, Durn BL, Cornblath DR, Merkies ISJ; PATH study group. Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (PATH): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Neurol. 2018 Jan;17(1):35-46. doi: 10.1016/S1474-4422(17)30378-2. Epub 2017 Nov 6. Erratum in: Lancet Neurol. 2018 Jan;17 (1):26. Lancet Neurol. 2018 Aug;17(8):661. PubMed PMID: 29122523.

  • Rasoanandrianina H, Grapperon AM, Taso M, Girard OM, Duhamel G, Guye M, Ranjeva JP, Attarian S, Verschueren A, Callot V. Region-specific impairment of the cervical spinal cord (SC) in amyotrophic lateral sclerosis: A preliminary study using SC templates and quantitative MRI (diffusion tensor imaging/inhomogeneous magnetization transfer). NMR Biomed. 2017 Dec;30(12). doi: 10.1002/nbm.3801. Epub 2017 Sep 19. PubMed PMID: 28926131.

  • Rajabally YA, Delmont E, Hiew FL, Aubé-Nathier AC, Grapperon AM, Cassereau J, Attarian S. Prevalence, correlates and impact of pain and cramps in anti-MAG neuropathy: a multicentre European study. Eur J Neurol. 2018 Jan;25(1):135-141. doi: 10.1111/ene.13459. Epub 2017 Oct 19. PubMed PMID: 28906575.

  • Fatehi F, Salort-Campana E, Le Troter A, Lareau-Trudel E, Bydder M, Fouré A, Guye M, Bendahan D, Attarian S. Long-term follow-up of MRI changes in thigh muscles of patients with Facioscapulohumeral dystrophy: A quantitative study. PLoS One. 2017 Aug 25;12(8):e0183825. doi: 10.1371/journal.pone.0183825. eCollection 2017. PubMed PMID: 28841698; PubMed Central PMCID: PMC5571945. 

  • van Eijk JJJ, Dalton HR, Ripellino P, Madden RG, Jones C, Fritz M, Gobbi C, Melli G, Pasi E, Herrod J, Lissmann RF, Ashraf HH, Abdelrahim M, Masri OABAL, Fraga M, Benninger D, Kuntzer T, Aubert V, Sahli R, Moradpour D, Blasco-Perrin H, Attarian S, Gérolami R, Colson P, Giordani MT, Hartl J, Pischke S, Lin NX, Mclean BN, Bendall RP, Panning M, Peron JM, Kamar N, Izopet J, Jacobs BC, van Alfen N, van Engelen BGM. Clinical phenotype and outcome of hepatitis E virus-associated neuralgic amyotrophy. Neurology. 2017 Aug 29;89(9):909-917. doi: 10.1212/WNL.0000000000004297. Epub 2017 Aug 2. PubMed PMID: 28768846.

  • Attarian S, Sharma J, Kaubisch A, Zonszein J, Haigentz M Jr. Multiple Endocrine and Neoplastic Diseases After Unsuccessful Treatment of Hepatitis C With Interferon and Ribavirin. Am J Med Sci. 2017 Jul;354(1):66. doi: 10.1016/j.amjms.2016.10.001. Epub 2016 Oct 18. PubMed PMID: 28755736.

  • Nguyen K, Puppo F, Roche S, Gaillard MC, Chaix C, Lagarde A, Pierret M, Vovan C, Olschwang S, Salort-Campana E, Attarian S, Bartoli M, Bernard R, Magdinier F, Levy N. Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy. Hum Mutat. 2017 Oct;38(10):1432-1441. doi: 10.1002/humu.23304. Epub 2017 Aug 6. PubMed PMID: 28744936.

  • Mul K, Kinoshita J, Dawkins H, van Engelen B, Tupler R; FSHD Consortium. 225th ENMC international workshop:: A global FSHD registry framework, 18-20 November 2016, Heemskerk, The Netherlands. Neuromuscul Disord. 2017 Aug;27(8):782-790. doi: 10.1016/j.nmd.2017.04.004. Epub 2017 Apr 12. PubMed PMID: 28625604.

  • Franques J, Sahuc P, Dussol B, Penaranda G, Swiader L, Froissart R, Attarian S, Stavris C, Chiche L, Pouget J. Peripheral nerve involvement in Fabry's disease: Which investigations? A case series and review of the literature. Rev Neurol (Paris). 2017 Dec;173(10):650-657. doi: 10.1016/j.neurol.2017.05.007. Epub 2017 Jun 1. Review. PubMed PMID: 28579207.

  • Delmont E, Manso C, Querol L, Cortese A, Berardinelli A, Lozza A, Belghazi M, Malissart P, Labauge P, Taieb G, Yuki N, Illa I, Attarian S, Devaux JJ. Autoantibodies to nodal isoforms of neurofascin in chronic inflammatory demyelinating polyneuropathy. Brain. 2017 Jul 1;140(7):1851-1858. doi: 10.1093/brain/awx124. PubMed PMID: 28575198.

  • Fatehi F, Delmont E, Grapperon AM, Salort-Campana E, Sévy A, Verschueren A, Boucraut J, Attarian S. Motor unit number index (MUNIX) in patients with anti-MAG neuropathy. Clin Neurophysiol. 2017 Jul;128(7):1264-1269. doi: 10.1016/j.clinph.2017.04.022. Epub 2017 May 9. PubMed PMID: 28545015. 

  • Gazzola S, Delmont E, Franques J, Boucraut J, Salort-Campana E, Verschueren A, Sagui E, Hubert AM, Pouget J, Attarian S. Predictive factors of efficacy of rituximab in patients with anti-MAG neuropathy. J Neurol Sci. 2017 Jun 15;377:144-148. doi: 10.1016/j.jns.2017.04.015. Epub 2017 Apr 12. PubMed PMID: 28477685.

  • Grapperon AM, Attarian S. Disorders of motor neurons manifested by hyperactivity. Rev Neurol (Paris). 2017 May;173(5):345-351. doi: 10.1016/j.neurol.2017.04.002. Epub 2017 Apr 28. Review. PubMed PMID: 28457490.

  • Jacobs BC, van den Berg B, Verboon C, Chavada G, Cornblath DR, Gorson KC, Harbo T, Hartung HP, Hughes RAC, Kusunoki S, van Doorn PA, Willison HJ; IGOS Consortium. International Guillain-Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in Guillain-Barré syndrome. J Peripher Nerv Syst. 2017 Jun;22(2):68-76. doi: 10.1111/jns.12209. PubMed PMID: 28406555.

  • Leporq B, Le Troter A, Le Fur Y, Salort-Campana E, Guye M, Beuf O, Attarian S, Bendahan D. Combined quantification of fatty infiltration, T (1)-relaxation times and T (2)*-relaxation times in normal-appearing skeletal muscle of controls and dystrophic patients. MAGMA. 2017 Aug;30(4):407-415. doi: 10.1007/s10334-017-0616-1. Epub 2017 Mar 22. PubMed PMID: 28332039.

  • Attarian S, Karami A, Ayatolahi F. Combination Therapy of Infections Caused by Injection of Paint Using Medical Laser. World J Plast Surg. 2017 Jan;6(1):120-122. PubMed PMID: 28289626; PubMed Central PMCID: PMC5339622.

  • Cerino M, Gorokhova S, Laforet P, Ben Yaou R, Salort-Campana E, Pouget J, Attarian S, Eymard B, Deleuze JF, Boland A, Behin A, Stojkovic T, Bonne G, Levy N, Bartoli M, Krahn M. Genetic Characterization of a French Cohort of GNE-mutation negative inclusion body myopathy patients with exome sequencing. Muscle Nerve. 2017 Nov;56(5):993-997. doi: 10.1002/mus.25638. Epub 2017 Apr 7. PubMed PMID: 28256728.

  • Grimaldi S, Duprat L, Grapperon AM, Verschueren A, Delmont E, Attarian S. Global motor unit number index sum score for assessing the loss of lower motor neurons in amyotrophic lateral sclerosis. Muscle Nerve. 2017 Aug;56(2):202-206. doi: 10.1002/mus.25595. Epub 2017 Apr 1. PubMed PMID: 28164325.

  • Gesquière-Dando A, Delmont E, Launay M, Boucraut J, Attarian S. Are electrophysiological features related to disability in patients with anti-MAG neuropathy? Neurophysiol Clin. 2017 Feb;47(1):75-81. doi: 10.1016/j.neucli.2017.01.002. Epub 2017 Feb 1. PubMed PMID: 28161089.

  • Wang W, Guedj M, Bertrand V, Foucquier J, Jouve E, Commenges D, Proust-Lima C, Murphy NP, Blin O, Magy L, Cohen D, Attarian S. A Rasch Analysis of the Charcot-Marie-Tooth Neuropathy Score (CMTNS) in a Cohort of Charcot-Marie-Tooth Type 1A Patients. PLoS One. 2017 Jan 17;12(1):e0169878. doi: 10.1371/journal.pone.0169878. eCollection 2017. PubMed PMID: 28095456; PubMed Central PMCID: PMC5240958.

  • Duclos Y, Grapperon AM, Jouve E, Truillet R, Zemmour C, Verschueren A, Pouget J, Attarian S. Motor-evoked potential gain is a helpful test for the detection of corticospinal tract dysfunction in amyotrophic lateral sclerosis. Clin Neurophysiol. 2017 Feb;128(2):357-364. doi: 10.1016/j.clinph.2016.12.015. Epub 2016 Dec 23. PubMed PMID: 28068522.

  • Philibert M, Grapperon AM, Delmont E, Attarian S. Monitoring the short-term effect of intravenous immunoglobulins in multifocal motor neuropathy using motor unit number index. Clin Neurophysiol. 2017 Jan;128(1):235-240. doi: 10.1016/j.clinph.2016.11.012. Epub 2016 Dec 1. PubMed PMID: 27988478.

  • Delmont E, Hiew FL, Cassereau J, Aubé-Nathier AC, Grapperon AM, Attarian S, Rajabally YA. Determinants of health-related quality of life in anti-MAG neuropathy: a cross-sectional multicentre European study. J Peripher Nerv Syst. 2017 Mar;22(1):27-33. doi: 10.1111/jns.12197. PubMed PMID: 27868289.

  • Fatehi F, Salort-Campana E, Le Troter A, Bendahan D, Attarian S. Muscle MRI of facioscapulohumeral dystrophy (FSHD): A growing demand and a promising approach. Rev Neurol (Paris). 2016 Oct;172(10):566-571. doi: 10.1016/j.neurol.2016.08.002. Epub 2016 Sep 20. Review. PubMed PMID: 27663058.

  • Gaillard MC, Puppo F, Roche S, Dion C, Campana ES, Mariot V, Chaix C, Vovan C, Mazaleyrat K, Tasmadjian A, Bernard R, Dumonceaux J, Attarian S, Lévy N, Nguyen K, Magdinier F, Bartoli M. Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo-Humeral Dystrophy: a case report. BMC Med Genet. 2016 Sep 15;17(1):66. doi: 10.1186/s12881-016-0328-9. PubMed PMID: 27634379; PubMed Central PMCID: PMC5025538.

  • Bou Ali H, Salort-Campana E, Grapperon AM, Gallard J, Franques J, Sevy A, Delmont E, Verschueren A, Pouget J, Attarian S. New strategy for improving the diagnostic sensitivity of repetitive nerve stimulation in myasthenia gravis. Muscle Nerve. 2017 Apr;55(4):532-538. doi: 10.1002/mus.25374. Epub 2017 Jan 3. PubMed PMID: 27511866.

  • Ben Lassoued A, Fromonot J, Marlinge M, Basset N, Chefrour M, Vairo D, Couillaud J, Lopez L, Cuisset T, Boucraut J, Delmont E, Attarian S, Guieu R. A case of false positive cardiac troponin I in CANOMAD syndrome. Int J Cardiol. 2016 Nov 1;222:359-360. doi: 10.1016/j.ijcard.2016.07.297. Epub 2016 Aug 2. Erratum in: Int J Cardiol. 2018 Feb 27;:. PubMed PMID: 27500764.

  • Sicello M, Sevy A, Borentain P, Gérolami R, Attarian S, Colson P. Evolution of hepatitis E virus-associated meningo-polyradiculoneuropathy on ribavirin. Int J Antimicrob Agents. 2016 Sep;48(3):343-5. doi: 10.1016/j.ijantimicag.2016.06.004. Epub 2016 Jul 8. PubMed PMID: 27470489.

  • Attarian S, Vallat JM, Magy L, Funalot B, Gonnaud PM, Lacour A, Péréon Y, Dubourg O, Pouget J, Micallef J, Franques J, Lefebvre MN, Ghorab K, Al-Moussawi M, Tiffreau V, Preudhomme M, Magot A, Leclair-Visonneau L, Stojkovic T, Bossi L, Lehert P, Gilbert W, Bertrand V, Mandel J, Milet A, Hajj R, Boudiaf L, Scart-Grès C, Nabirotchkin S, Guedj M, Chumakov I, Cohen D. Erratum to: An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A. Orphanet J Rare Dis. 2016 Jul 7;11(1):92. PubMed PMID: 27387831; PubMed Central PMCID: PMC4937550.

  • Runnqvist E, Bonnard M, Gauvin HS, Attarian S, Trébuchon A, Hartsuiker RJ, Alario FX. Internal modeling of upcoming speech: A causal role of the right posterior cerebellum in non-motor aspects of language production. Cortex. 2016 Aug;81:203-14. doi: 10.1016/j.cortex.2016.05.008. Epub 2016 May 21. PubMed PMID: 27249802.

  • Béhin A, Acquaviva-Bourdain C, Souvannanorath S, Streichenberger N, Attarian  S, Bassez G, Brivet M, Fouilhoux A, Labarre-Villa A, Laquerrière A, Pérard L, Kaminsky P, Pouget J, Rigal O, Vanhulle C, Eymard B, Vianey-Saban C, Laforêt P. Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease. Rev Neurol (Paris). 2016 Mar;172(3):231-41. doi: 10.1016/j.neurol.2015.11.008. Epub 2016 Mar 30. PubMed PMID: 27038534.

  • Rajabally YA, Adams D, Latour P, Attarian S. Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses. J Neurol Neurosurg Psychiatry. 2016 Oct;87(10):1051-60. doi: 10.1136/jnnp-2015-310835. Epub 2016 Mar 23. Review. PubMed PMID: 27010614.

  • Delmont E, Benvenutto A, Grimaldi S, Duprat L, Philibert M, Pouget J, Grapperon AM, Salort-Campana E, Sévy A, Verschueren A, Attarian S. Motor unit number index (MUNIX): Is it relevant in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)? Clin Neurophysiol. 2016 Mar;127(3):1891-4. doi: 10.1016/j.clinph.2015.12.002. Epub 2015 Dec 12. PubMed PMID: 26750580.

  • Fatehi F, Nafissi S, Urtizberea JA, Blanck-Labelle V, Lévy N, Krahn M, Dbouk MB, Attarian S. Dysferlinopathy in Iran: Clinical and genetic report. J Neurol Sci. 2015 Dec 15;359(1-2):256-9. doi: 10.1016/j.jns.2015.11.009. Epub 2015 Nov 11. PubMed PMID: 26671124.

  • Mariani LL, Lozeron P, Théaudin M, Mincheva Z, Signate A, Ducot B, Algalarrondo V, Denier C, Adam C, Nicolas G, Samuel D, Slama MS, Lacroix C, Misrahi M, Adams D; French Familial Amyloid Polyneuropathies Network (CORNAMYL) Study Group. Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France. Ann Neurol. 2015 Dec;78(6):901-16. doi: 10.1002/ana.24519. Epub 2015 Oct 7. PubMed PMID: 26369527; PubMed Central PMCID: PMC4738459.

  • Béhin A, Salort-Campana E, Wahbi K, Richard P, Carlier RY, Carlier P, Laforêt P, Stojkovic T, Maisonobe T, Verschueren A, Franques J, Attarian S, Maues de Paula A, Figarella-Branger D, Bécane HM, Nelson I, Duboc D, Bonne G, Vicart P, Udd B, Romero N, Pouget J, Eymard B. Myofibrillar myopathies: State of the art, present and future challenges. Rev Neurol (Paris). 2015 Oct;171(10):715-29. doi: 10.1016/j.neurol.2015.06.002. Epub 2015 Sep 3. Review. PubMed PMID: 26342832.

  • Verschueren A, Gallard J, Boucraut J, Honnorat J, Pouget J, Attarian S. Paraneoplastic subacute lower motor neuron syndrome associated with solid cancer. J Neurol Sci. 2015 Nov 15;358(1-2):413-6. doi: 10.1016/j.jns.2015.08.014. Epub 2015 Aug 12. PubMed PMID: 26323521.

  • Lareau-Trudel E, Le Troter A, Ghattas B, Pouget J, Attarian S, Bendahan D, Salort-Campana E. Muscle Quantitative MR Imaging and Clustering Analysis in Patients with Facioscapulohumeral Muscular Dystrophy Type 1. PLoS One. 2015 Jul 16;10(7):e0132717. doi: 10.1371/journal.pone.0132717. eCollection 2015. PubMed PMID: 26181385; PubMed Central PMCID: PMC4504465.

  • Attarian S, Libutti SK, Chuy J. ACTH-Producing Pancreatic Neuroendocrine Tumor Presenting with Severe Hypokalemic Alkalosis: A Case Report. J Gastrointest Cancer. 2016 Jun;47(2):217-20. doi: 10.1007/s12029-015-9740-1. PubMed PMID: 26073616.

  • Mandel J, Bertrand V, Lehert P, Attarian S, Magy L, Micallef J, Chumakov I, Scart-Grès C, Guedj M, Cohen D. A meta-analysis of randomized double-blind clinical trials in CMT1A to assess the change from baseline in CMTNS and ONLS scales after one year of treatment. Orphanet J Rare Dis. 2015 Jun 13;10:74. doi: 10.1186/s13023-015-0293-y. PubMed PMID: 26070802; PubMed Central PMCID: PMC4482281.

  • Taieb G, Grapperon AM, Duclos Y, Franques J, Labauge P, Renard D, Yuki N, Attarian S. Proximal conduction block in the pharyngeal-cervical-brachial variant of Guillain-Barré syndrome. Muscle Nerve. 2015 Dec;52(6):1102-6. doi: 10.1002/mus.24729. Epub 2015 Jul 2. PubMed PMID: 26044970.

  • Bensoussan L, Jouvion A, Kerzoncuf M, Delarque A, Theodoridou E, Milhe de Bovis V, Thefenne L, Attarian S, Viton JM. Orthopaedic shoes along with physical therapy was effective in Charcot-Marie-Tooth patient over 10 years. Prosthet Orthot Int. 2016 Oct;40(5):636-42. doi: 10.1177/0309364615584657. Epub 2015 May 26. PubMed PMID: 26015326.

  • Morizot-Koutlidis R, André-Obadia N, Antoine JC, Attarian S, Ayache SS, Azabou E, Benaderette S, Camdessanché JP, Cassereau J, Convers P, d'Anglejean J, Delval A, Durand MC, Etard O, Fayet G, Fournier E, Franques J, Gavaret M, Guehl D, Guerit JM, Krim E, Kubis N, Lacour A, Lozeron P, Mauguière F, Merle PE, Mesrati F, Mutschler V, Nicolas G, Nordine T, Pautot V, Péréon Y, Petiot P, Pouget J, Praline J, Salhi H, Trébuchon A, Tyvaert L, Vial C, Zola JM, Zyss J, Lefaucheur JP. Somatosensory evoked potentials in the assessment of peripheral neuropathies: Commented results of a survey among French-speaking practitioners and recommendations for practice. Neurophysiol Clin. 2015 May;45(2):131-42. doi: 10.1016/j.neucli.2015.04.001. Epub 2015 May 6. PubMed PMID: 25957985.

  • Sevy A, Cerino M, Gorokhova S, Dionnet E, Mathieu Y, Verschueren A, Franques J, Maues de Paula A, Figarella-Branger D, Lagarde A, Desvignes JP, Béroud C, Attarian S, Levy N, Bartoli M, Krahn M, Campana-Salort E, Pouget J. Improving molecular diagnosis of distal myopathies by targeted next-generation sequencing. J Neurol Neurosurg Psychiatry. 2016 Mar;87(3):340-2. doi: 10.1136/jnnp-2014-309663. Epub 2015 Mar 17. PubMed PMID: 25783436.

  • Gesquière-Dando A, Attarian S, Maues De Paula A, Pouget J, Salort-Campana E. Fibromyalgia-like symptoms associated with irritable bowel syndrome: A challenging diagnosis of late-onset Pompe disease. Muscle Nerve. 2015 Aug;52(2):300-4. doi: 10.1002/mus.24618. Epub 2015 Jun 18. PubMed PMID: 25703594. 

  • Ribot-Ciscar E, Milhe-De Bovis V, Aimonetti JM, Lapeyssonnie B, Campana-Salort E, Pouget J, Attarian S. Functional impact of vibratory proprioceptive assistance in patients with facioscapulohumeral muscular dystrophy. Muscle Nerve. 2015 Nov;52(5):780-7. doi: 10.1002/mus.24605. Epub 2015 Sep 3. PubMed PMID: 25678042.

  • Puppo F, Dionnet E, Gaillard MC, Gaildrat P, Castro C, Vovan C, Bertaux K, Bernard R, Attarian S, Goto K, Nishino I, Hayashi Y, Magdinier F, Krahn M, Helmbacher F, Bartoli M, Lévy N. Identification of variants in the 4q35 gene FAT1 in patients with a facioscapulohumeral dystrophy-like phenotype. Hum Mutat. 2015 Apr;36(4):443-53. doi:  10.1002/humu.22760. Epub 2015 Mar 19. PubMed PMID: 25615407.

  • 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. Low penetrance in facioscapulohumeral muscular dystrophy type 1 with large pathological D4Z4 alleles: a cross-sectional multicenter study. Orphanet J Rare Dis. 2015 Jan 21;10:2. doi: 10.1186/s13023-014-0218-1. PubMed PMID: 25603992; PubMed Central PMCID: PMC4320820.

  • Attarian S, Franques J, Elisabeth J, Trébuchon A, Duclos Y, Wybrecht D, Verschueren A, Salort-Campana E, Pouget J. Triple-stimulation technique improves the diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy. Muscle Nerve. 2015 Apr;51(4):541-8. doi: 10.1002/mus.24352. Epub 2015 Jan 9. PubMed PMID: 25571892.

  • Attarian S, Vallat JM, Magy L, Funalot B, Gonnaud PM, Lacour A, Péréon Y, Dubourg O, Pouget J, Micallef J, Franques J, Lefebvre MN, Ghorab K, Al-Moussawi M, Tiffreau V, Preudhomme M, Magot A, Leclair-Visonneau L, Stojkovic T, Bossi L, Lehert P, Gilbert W, Bertrand V, Mandel J, Milet A, Hajj R, Boudiaf L, Scart-Grès C, Nabirotchkin S, Guedj M, Chumakov I, Cohen D. An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A. Orphanet J Rare Dis. 2014 Dec 18;9:199. doi: 10.1186/s13023-014-0199-0. Erratum in: Orphanet J Rare Dis. 2016;11(1):92. PubMed PMID: 25519680; PubMed Central PMCID: PMC4311411.

  • Wakerley BR, Uncini A, Yuki N; GBS Classification Group; GBS Classification Group. Guillain-Barré and Miller Fisher syndromes--new diagnostic classification. Nat Rev Neurol. 2014 Sep;10(9):537-44. doi: 10.1038/nrneurol.2014.138. Epub 2014 Jul 29. Review. Erratum in: Nat Rev Neurol. 2014 Nov;10(11):612. PubMed PMID: 25072194.

  • Gaillard MC, Roche S, Dion C, Tasmadjian A, Bouget G, Salort-Campana E, Vovan C, Chaix C, Broucqsault N, Morere J, Puppo F, Bartoli M, Levy N, Bernard R, Attarian S, Nguyen K, Magdinier F. Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers. Neurology. 2014 Aug 19;83(8):733-42. doi: 10.1212/WNL.0000000000000708. Epub 2014 Jul 16. PubMed PMID: 25031281.

  • Attarian S, Tran LC, Moore A, Stanton G, Meyer E, Moore RP. The neurodevelopmental impact of neonatal morphine administration. Brain Sci. 2014 Apr 25;4(2):321-34. doi: 10.3390/brainsci4020321. PubMed PMID: 24961764; PubMed Central PMCID: PMC4101480.

  • Lagarde S, Tabouret E, Matta M, Franques J, Attarian S, Pouget J, Maues De Paula A, Figarella-Branger D, Dory-Lautrec P, Chinot O, Barrié M. Primary neurolymphomatosis diagnosis and treatment: a retrospective study. J Neurol Sci. 2014 Jul 15;342(1-2):178-81. doi: 10.1016/j.jns.2014.04.030. Epub 2014 May 1. PubMed PMID: 24831985.

  • Seguier J, Serratrice J, Lachaud A, Belenotti P, Benyamine A, Verschueren A, Boucraut J, Attarian S, Weiller PJ. [Abdominal pain in progressive encephalomyelitis with rigidity]. Rev Med Interne. 2015 Apr;36(4):283-6. doi: 10.1016/j.revmed.2013.12.019. Epub 2014 Jan 21. French. PubMed PMID: 24461686.

  • Lenglet T, Lacomblez L, Abitbol JL, Ludolph A, Mora JS, Robberecht W, Shaw PJ, Pruss RM, Cuvier V, Meininger V; Mitotarget study group. A phase II-III trial of olesoxime in subjects with amyotrophic lateral sclerosis. Eur J Neurol. 2014 Mar;21(3):529-36. doi: 10.1111/ene.12344. Epub 2014 Jan 21. PubMed PMID: 24447620.

  • Grapperon AM, Verschueren A, Duclos Y, Confort-Gouny S, Soulier E, Loundou AD, Guye M, Cozzone PJ, Pouget J, Ranjeva JP, Attarian S. Association between structural and functional corticospinal involvement in amyotrophic lateral sclerosis assessed by diffusion tensor MRI and triple stimulation technique. Muscle Nerve. 2014 Apr;49(4):551-7. doi: 10.1002/mus.23957. Epub 2014 Feb 26. PubMed PMID: 23873504.
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