Petiot P - Search Results

1

[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations].

Ben Yaou R, Bécane HM, Demay L, Laforet P, Hannequin D, Bohu PA, Drouin-Garraud V, Ferrer X, Mussini JM, Ollagnon E, Petiot P, Penisson-Besnier I, Streichenberger N, Toutain A, Richard P, Eymard B, Bonne G. Ben Yaou R, et al. Among authors: petiot p. Rev Neurol (Paris). 2005 Jan;161(1):42-54. doi: 10.1016/s0035-3787(05)84972-0. Rev Neurol (Paris). 2005. PMID: 15678000 French.

2

Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France.

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. Mariani LL, et al. Ann Neurol. 2015 Dec;78(6):901-16. doi: 10.1002/ana.24519. Epub 2015 Oct 7. Ann Neurol. 2015. PMID: 26369527 Free PMC article.

3

Myasthenia gravis treatment in the elderly presents with a significant iatrogenic risk: a multicentric retrospective study.

Chanson JB, Bouhour F, Aubé-Nathier AC, Mallaret M, Vial C, Hacquard A, Petiot P, Spinazzi M, Nadaj-Pakleza A, Echaniz-Laguna A. Chanson JB, et al. Among authors: petiot p. J Neurol. 2023 Dec;270(12):5819-5826. doi: 10.1007/s00415-023-11925-6. Epub 2023 Aug 17. J Neurol. 2023. PMID: 37592137

4

A clinical pattern-based etiological diagnostic strategy for sensory neuronopathies: a French collaborative study.

Camdessanché JP, Jousserand G, Franques J, Pouget J, Delmont E, Créange A, Kuntzer T, Maisonobe T, Abba K, Antoine JC; French CIDP study group. Camdessanché JP, et al. J Peripher Nerv Syst. 2012 Sep;17(3):331-40. doi: 10.1111/j.1529-8027.2012.00411.x. J Peripher Nerv Syst. 2012. PMID: 22971095

5

Upper limb onset of hereditary transthyretin amyloidosis is common in non-endemic areas.

Théaudin M, Lozeron P, Algalarrondo V, Lacroix C, Cauquil C, Labeyrie C, Slama MS, Adam C, Guiochon-Mantel A, Adams D; French FAP Network (CORNAMYL) Study Group. Théaudin M, et al. Eur J Neurol. 2019 Mar;26(3):497-e36. doi: 10.1111/ene.13845. Epub 2018 Dec 11. Eur J Neurol. 2019. PMID: 30350904

6

[Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias].

Lesca G, Demarquay G, Llense S, Streichenberger N, Petiot P, Michel-Calemard L, Récan D, Vial C, Ollagnon-Roman E. Lesca G, et al. Among authors: petiot p. Rev Neurol (Paris). 2003 Sep;159(8-9):775-80. Rev Neurol (Paris). 2003. PMID: 13679720 French.

7

Focal myositis associated with S-1 radiculopathy: report of two cases.

Streichenberger N, Meyronet D, Fiere V, Pellissier JF, Petiot P. Streichenberger N, et al. Among authors: petiot p. Muscle Nerve. 2004 Mar;29(3):443-6. doi: 10.1002/mus.10540. Muscle Nerve. 2004. PMID: 14981746

8

[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. Drouet A, et al. Among authors: petiot p. Rev Neurol (Paris). 2008 Feb;164(2):169-76. doi: 10.1016/j.neurol.2007.08.008. Epub 2008 Feb 1. Rev Neurol (Paris). 2008. PMID: 18358876 French.

9

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. Laforêt P, et al. Among authors: petiot p. Neurology. 2008 May 27;70(22):2063-6. doi: 10.1212/01.wnl.0000313367.09469.13. Neurology. 2008. PMID: 18505979

10

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

Vandenberghe N, Bouhour F, Petiot P, Gonnaud PM, Latour P, Broussolle E, Vial C. Vandenberghe N, et al. Among authors: petiot p. Rev Neurol (Paris). 2009 Jan;165(1):31-7. doi: 10.1016/j.neurol.2008.06.005. Epub 2008 Jul 29. Rev Neurol (Paris). 2009. PMID: 18667219 French.

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