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Items: 1 to 50 of 82

1.

Eosinophilic Fasciitis and Common Variable Immunodeficiency: An Unusual Association and Literature Review.

El-Jammal T, Gerfaud-Valentin M, Durupt F, Petiot P, De Parisot A, Streichenberger N, Jamilloux Y, Sève P.

J Allergy Clin Immunol Pract. 2019 Jul 12. pii: S2213-2198(19)30566-5. doi: 10.1016/j.jaip.2019.06.014. [Epub ahead of print] No abstract available.

PMID:
31307966
2.

Charcot-Marie-Tooth (CMT)-like polyneuropathy revealing neurofibromatosis type 2: A case report and review of the literature.

Pegat A, Ducray F, Jeannin-Mayer S, Jouanneau E, Pinson S, Petiot P.

Rev Neurol (Paris). 2019 Sep - Oct;175(7-8):486-489. doi: 10.1016/j.neurol.2018.10.011. Epub 2019 Jun 17. No abstract available.

PMID:
31221421
3.

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
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.

A new MRI marker of ataxia with oculomotor apraxia.

Ronsin S, Hannoun S, Thobois S, Petiot P, Vighetto A, Cotton F, Tilikete C.

Eur J Radiol. 2019 Jan;110:187-192. doi: 10.1016/j.ejrad.2018.11.035. Epub 2018 Nov 29.

6.

Focal myositis: New insights on diagnosis and pathology.

Gallay L, Hot A, Petiot P, Thivolet-Bejui F, Maucort-Boulch D, Streichenberger N.

Neurology. 2018 Mar 20;90(12):e1013-e1020. doi: 10.1212/WNL.0000000000005160. Epub 2018 Feb 21.

PMID:
29467303
7.

Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency.

Ben Yaou R, Hubert A, Nelson I, Dahlqvist JR, Gaist D, Streichenberger N, Beuvin M, Krahn M, Petiot P, Parisot F, Michel F, Malfatti E, Romero N, Carlier RY, Eymard B, Labrune P, Duno M, Krag T, Cerino M, Bartoli M, Bonne G, Vissing J, Laforet P, Petit FM.

Neurol Genet. 2017 Dec 18;3(6):e208. doi: 10.1212/NXG.0000000000000208. eCollection 2017 Dec.

8.

Renal Involvement in Neuropathy, Ataxia, Retinitis Pigmentosa (NARP) Syndrome: A Case Report.

Lemoine S, Panaye M, Rabeyrin M, Errazuriz-Cerda E, Mousson de Camaret B, Petiot P, Juillard L, Guebre-Egziabher F.

Am J Kidney Dis. 2018 May;71(5):754-757. doi: 10.1053/j.ajkd.2017.09.020. Epub 2017 Dec 8.

PMID:
29224958
9.

Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic features.

Svahn J, Petiot P, Antoine JC, Vial C, Delmont E, Viala K, Steck AJ, Magot A, Cauquil C, Zarea A, Echaniz-Laguna A, Iancu Ferfoglia R, Gueguen A, Magy L, Léger JM, Kuntzer T, Ferraud K, Lacour A, Camdessanché JP; Francophone anti-MAG cohort Group.

J Neurol Neurosurg Psychiatry. 2018 May;89(5):499-505. doi: 10.1136/jnnp-2017-316715. Epub 2017 Oct 25.

PMID:
29070644
10.

[Thymoma and autoimmune diseases].

Jamilloux Y, Frih H, Bernard C, Broussolle C, Petiot P, Girard N, Sève P.

Rev Med Interne. 2018 Jan;39(1):17-26. doi: 10.1016/j.revmed.2017.03.003. Epub 2017 Mar 30. Review. French.

PMID:
28365191
11.

Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations.

Echaniz-Laguna A, Geuens T, Petiot P, Péréon Y, Adriaenssens E, Haidar M, Capponi S, Maisonobe T, Fournier E, Dubourg O, Degos B, Salachas F, Lenglet T, Eymard B, Delmont E, Pouget J, Juntas Morales R, Goizet C, Latour P, Timmerman V, Stojkovic T.

Hum Mutat. 2017 May;38(5):556-568. doi: 10.1002/humu.23189. Epub 2017 Feb 25.

PMID:
28144995
12.

[Unusual phenotype of myopathy associated with a new PNPLA2 mutation].

Jousserand G, Streichenberger N, Petiot P.

Med Sci (Paris). 2016 Nov;32 Hors série n°2:10-11. Epub 2016 Nov 21. French. No abstract available.

13.

Focal myositis: A review.

Devic P, Gallay L, Streichenberger N, Petiot P.

Neuromuscul Disord. 2016 Nov;26(11):725-733. doi: 10.1016/j.nmd.2016.08.014. Epub 2016 Aug 26. Review.

PMID:
27726926
14.

SWORD: A simplified desensitization protocol for enzyme replacement therapy in adult Pompe disease.

Gallay L, Petiot P, Durieu I, Streichenberger N, Berard F.

Neuromuscul Disord. 2016 Nov;26(11):801-804. doi: 10.1016/j.nmd.2016.07.006. Epub 2016 Jul 19.

PMID:
27637292
15.

Sporadic inclusion-body myositis: Recent advances and the state of the art in 2016.

Gallay L, Petiot P.

Rev Neurol (Paris). 2016 Oct;172(10):581-586. doi: 10.1016/j.neurol.2016.07.016. Epub 2016 Sep 9. Review.

PMID:
27616487
16.

The wide POLG-related spectrum: An integrated view.

Béreau M, Anheim M, Echaniz-Laguna A, Magot A, Verny C, Goideau-Sevrain M, Barth M, Amati-Bonneau P, Allouche S, Ayrignac X, Bédat-Millet AL, Guyant-Maréchal L, Kuntzer T, Ochsner F, Petiot P, Vial C, Omer S, Sole G, Taieb G, Carvalho N, Tio G, Kremer S, Acquaviva-Bourdain C, de Camaret BM, Tranchant C.

J Neurol Sci. 2016 Sep 15;368:70-6. doi: 10.1016/j.jns.2016.06.062. Epub 2016 Jun 29. No abstract available.

PMID:
27538604
17.

Synthesis of Highly Functionalized Triarylbismuthines by Functional Group Manipulation and Use in Palladium- and Copper-Catalyzed Arylation Reactions.

Hébert M, Petiot P, Benoit E, Dansereau J, Ahmad T, Le Roch A, Ottenwaelder X, Gagnon A.

J Org Chem. 2016 Jul 1;81(13):5401-16. doi: 10.1021/acs.joc.6b00767. Epub 2016 Jun 13.

PMID:
27231755
18.

Progressive multifocal leukoencephalopathy after liver transplantation can have favorable or unfavorable outcome.

Dumortier J, Guillaud O, Bosch A, Coppéré B, Petiot P, Roggerone S, Vukusic S, Boillot O.

Transpl Infect Dis. 2016 Aug;18(4):606-10. doi: 10.1111/tid.12554. Epub 2016 Aug 2.

PMID:
27224849
19.

Thymoma associated with autoimmune diseases: 85 cases and literature review.

Bernard C, Frih H, Pasquet F, Kerever S, Jamilloux Y, Tronc F, Guibert B, Isaac S, Devouassoux M, Chalabreysse L, Broussolle C, Petiot P, Girard N, Sève P.

Autoimmun Rev. 2016 Jan;15(1):82-92. doi: 10.1016/j.autrev.2015.09.005. Epub 2015 Sep 25. Review.

PMID:
26408958
20.

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
21.

Significant response to immune therapies in a case of subacute necrotizing myopathy and FKRP mutations.

Svahn J, Streichenberger N, Benveniste O, Menassa R, Michel L, Fayolle H, Petiot P.

Neuromuscul Disord. 2015 Nov;25(11):865-8. doi: 10.1016/j.nmd.2015.08.009. Epub 2015 Aug 21.

PMID:
26363967
22.

Severe osteomalacia mimicking progressive myopathy.

Benhamou J, Fontanges E, Streichenberger N, Petiot P.

Int J Rheum Dis. 2017 Nov;20(11):1803-1804. doi: 10.1111/1756-185X.12641. Epub 2015 May 11. No abstract available.

PMID:
25958779
23.

Somatosensory evoked potentials in the assessment of peripheral neuropathies: Commented results of a survey among French-speaking practitioners and recommendations for practice.

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.

Neurophysiol Clin. 2015 May;45(2):131-42. doi: 10.1016/j.neucli.2015.04.001. Epub 2015 May 6.

PMID:
25957985
24.

Diagnostic utility of somatosensory evoked potentials in chronic polyradiculopathy without electrodiagnostic signs of peripheral demyelination.

Devic P, Petiot P, Mauguiere F.

Muscle Nerve. 2016 Jan;53(1):78-83. doi: 10.1002/mus.24693. Epub 2015 Nov 26.

PMID:
25908550
25.

Copper-catalyzed O-arylation of N-protected 1,2-aminoalcohols using functionalized trivalent organobismuth reagents.

Petiot P, Dansereau J, Hébert M, Khene I, Ahmad T, Samaali S, Leroy M, Pinsonneault F, Legault CY, Gagnon A.

Org Biomol Chem. 2015 Feb 7;13(5):1322-7. doi: 10.1039/c4ob02497d.

PMID:
25501446
26.

Synthesis of highly functionalized diaryl ethers by copper-mediated O-arylation of phenols using trivalent arylbismuth reagents.

Crifar C, Petiot P, Ahmad T, Gagnon A.

Chemistry. 2014 Mar 3;20(10):2755-60. doi: 10.1002/chem.201303684. Epub 2014 Feb 12.

PMID:
24519720
27.

Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations.

Auré K, Dubourg O, Jardel C, Clarysse L, Sternberg D, Fournier E, Laforêt P, Streichenberger N, Petiot P, Gervais-Bernard H, Vial C, Bedat-Millet AL, Drouin-Garraud V, Bouillaud F, Vandier C, Fontaine B, Lombès A.

Neurology. 2013 Nov 19;81(21):1810-8. doi: 10.1212/01.wnl.0000436067.43384.0b. Epub 2013 Oct 23.

PMID:
24153443
28.

Antibodies to clustered acetylcholine receptor: expanding the phenotype.

Devic P, Petiot P, Simonet T, Stojkovic T, Delmont E, Franques J, Magot A, Vial C, Lagrange E, Nicot AS, Risson V, Eymard B, Schaeffer L.

Eur J Neurol. 2014;21(1):130-4. doi: 10.1111/ene.12270. Epub 2013 Sep 21.

PMID:
24112557
29.

[Necrotizing autoimmune myopathies].

Petiot P, Choumert A, Hamelin L, Devic P, Streichenberger N.

Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):650-5. doi: 10.1016/j.neurol.2013.07.003. Epub 2013 Aug 30. French.

PMID:
23999024
30.

Dramatic improvement after rituximab in a patient with paraneoplastic treatment-refractory Morvan syndrome associated with anti-CASPR2 antibodies.

Ong E, Viaccoz A, Ducray F, Pérol M, Cavillon G, Rogemond V, Honnorat J, Petiot P.

Eur J Neurol. 2013 Jul;20(7):e96-7. doi: 10.1111/ene.12164. No abstract available.

PMID:
23750840
31.

Myopathic camptocormia associated with myasthenia gravis.

Devic P, Choumert A, Vukusic S, Confavreux C, Petiot P.

Clin Neurol Neurosurg. 2013 Aug;115(8):1488-9. doi: 10.1016/j.clineuro.2012.11.015. Epub 2012 Dec 21. No abstract available.

PMID:
23265561
32.

Spinal Charcot-Marie-Tooth disease: a reappraisal.

Devic P, Petiot P, Mauguière F.

Muscle Nerve. 2012 Oct;46(4):604-9. doi: 10.1002/mus.23456. Review.

PMID:
22987707
33.

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.

Boyer O, Nevo F, Plaisier E, Funalot B, Gribouval O, Benoit G, Huynh Cong E, Arrondel C, Tête MJ, Montjean R, Richard L, Karras A, Pouteil-Noble C, Balafrej L, Bonnardeaux A, Canaud G, Charasse C, Dantal J, Deschenes G, Deteix P, Dubourg O, Petiot P, Pouthier D, Leguern E, Guiochon-Mantel A, Broutin I, Gubler MC, Saunier S, Ronco P, Vallat JM, Alonso MA, Antignac C, Mollet G.

N Engl J Med. 2011 Dec 22;365(25):2377-88. doi: 10.1056/NEJMoa1109122.

34.

An unusual cause of symptomatic tension-type headache: hypertrophic branchial myopathy.

Parissis DA, Petiot P, Desestret V, Demarquay G.

Neurology. 2011 Nov 8;77(19):e115; author reply e115. doi: 10.1212/WNL.0b013e318230b05c. No abstract available.

PMID:
22067972
35.

Neurological features in adult Triple-A (Allgrove) syndrome.

Vallet AE, Verschueren A, Petiot P, Vandenberghe N, Nicolino M, Roman S, Pouget J, Vial C.

J Neurol. 2012 Jan;259(1):39-46. doi: 10.1007/s00415-011-6115-9. Epub 2011 Jun 9.

PMID:
21656342
36.

[Distal hereditary motor neuropathy].

Devic P, Petiot P.

Rev Neurol (Paris). 2011 Nov;167(11):781-90. doi: 10.1016/j.neurol.2011.03.003. Epub 2011 May 6. Review. French.

PMID:
21529868
37.

An unusual cause of symptomatic tension-type headache: hypertrophic branchial myopathy.

Desestret V, Demarquay G, de Saint Victor JF, Petiot P.

Neurology. 2011 Feb 1;76(5):488. doi: 10.1212/WNL.0b013e31820a0d4b. No abstract available.

PMID:
21282597
38.

[Diagnostic pitfalls in carpal tunnel syndrome].

Petiot P, Bernard E.

Rev Neurol (Paris). 2011 Jan;167(1):64-71. doi: 10.1016/j.neurol.2010.08.009. Epub 2010 Dec 28. Review. French.

PMID:
21190705
39.

[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.

40.

Synthesis of a new hydrophilic poly(ethylene glycol)-ionic liquid and its application in peptide synthesis.

Petiot P, Charnay C, Martinez J, Puttergill L, Galindo F, Lamaty F, Colacino E.

Chem Commun (Camb). 2010 Dec 14;46(46):8842-4. doi: 10.1039/c0cc02402c. Epub 2010 Oct 18.

PMID:
20953493
41.

Respiratory onset in an ALS family with L144F SOD1 mutation.

Corcia P, Petiot P, Stevic Z, Vourc'h P, Morales R, Gordon PH, Pageot N, Andres C, Camu W.

J Neurol Neurosurg Psychiatry. 2011 Jul;82(7):747-9. doi: 10.1136/jnnp.2009.197558. Epub 2010 Jun 20.

PMID:
20562451
42.

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7.

Ben Ammar A, Petit F, Alexandri N, Gaudon K, Bauché S, Rouche A, Gras D, Fournier E, Koenig J, Stojkovic T, Lacour A, Petiot P, Zagnoli F, Viollet L, Pellegrini N, Orlikowski D, Lazaro L, Ferrer X, Stoltenburg G, Paturneau-Jouas M, Hentati F, Fardeau M, Sternberg D, Hantaï D, Richard P, Eymard B.

J Neurol. 2010 May;257(5):754-66. doi: 10.1007/s00415-009-5405-y. Epub 2009 Dec 11.

PMID:
20012313
43.

Dysferlin deficiency treated like refractory polymyositis.

Vinit J, Samson M Jr, Gaultier JB, Laquerriere A, Ollagnon E, Petiot P, Marie I, Levesque H, Rousset H.

Clin Rheumatol. 2010 Jan;29(1):103-6. doi: 10.1007/s10067-009-1273-1.

PMID:
19730931
44.

The pattern and diagnostic criteria of sensory neuronopathy: a case-control study.

Camdessanché JP, Jousserand G, Ferraud K, Vial C, Petiot P, Honnorat J, Antoine JC.

Brain. 2009 Jul;132(Pt 7):1723-33. doi: 10.1093/brain/awp136. Epub 2009 Jun 8.

45.

[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
46.

Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe disease.

Laforêt P, Petiot P, Nicolino M, Orlikowski D, Caillaud C, Pellegrini N, Froissart R, Petitjean T, Maire I, Chabriat H, Hadrane L, Annane D, Eymard B.

Neurology. 2008 May 27;70(22):2063-6. doi: 10.1212/01.wnl.0000313367.09469.13.

PMID:
18505979
47.

[Unilateral presentation of X-linked myotubular myopathy (XLMTM) in two out of three female carriers in a family with no affected male].

Drouet A, Ollagnon-Roman E, Streichenberger N, Biancalana V, Cossée M, Guilloton L, Petiot P.

Rev Neurol (Paris). 2008 Feb;164(2):169-76. doi: 10.1016/j.neurol.2007.08.008. Epub 2008 Feb 1. French.

PMID:
18358876
48.

[Electrophysiological diagnosis of inflammatory neuropathies].

Petiot P.

Rev Neurol (Paris). 2007 Sep;163 Spec No 1:3S36-44. Review. French.

PMID:
18087228
49.

Acute neurological deterioration in ovarioleukodystrophy related to EIF2B mutations: pregnancy with oocyte donation is a potentially precipitating factor.

Peter L, Niel F, Catenoix H, Jung J, Demarquay G, Petiot P, Rudigoz RC, Boespflug-Tanguy O, Ryvlin P, Mauguière F.

Eur J Neurol. 2008 Jan;15(1):94-7. Epub 2007 Nov 14.

PMID:
18005052
50.

Successful treatment with rituximab in a patient with mental nerve neuropathy in primary Sjögren's syndrome.

Sève P, Gachon E, Petiot P, Stankovic K, Charhon A, Broussolle C.

Rheumatol Int. 2007 Dec;28(2):175-7. Epub 2007 Jul 20.

PMID:
17641898

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