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Page 1
Comment on: Inaugural dropped head syndrome and camptocormia in inflammatory myopathies: a retrospective study: Reply.
Robert M, Lessard LER, Bouhour F, Petiot P, Fenouil T, Svahn J, Fiscus J, Fabien N, Perard L, Robinson P, Durieu I, Coury F, Streichenberger N, Hot A, Gallay L. Robert M, et al. Among authors: petiot p. Rheumatology (Oxford). 2024 Apr 2;63(4):e144-e145. doi: 10.1093/rheumatology/kead422. Rheumatology (Oxford). 2024. PMID: 37647649 No abstract available.
[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. Pavic M, et al. Among authors: petiot p. Rev Med Interne. 2003 Nov;24(11):716-20. doi: 10.1016/s0248-8663(03)00219-4. Rev Med Interne. 2003. PMID: 14604748 French.
[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.
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. Ben Ammar A, et al. Among authors: petiot p. J Neurol. 2010 May;257(5):754-66. doi: 10.1007/s00415-009-5405-y. Epub 2009 Dec 11. J Neurol. 2010. PMID: 20012313
Neurological features in adult Triple-A (Allgrove) syndrome.
Vallet AE, Verschueren A, Petiot P, Vandenberghe N, Nicolino M, Roman S, Pouget J, Vial C. Vallet AE, et al. Among authors: petiot p. J Neurol. 2012 Jan;259(1):39-46. doi: 10.1007/s00415-011-6115-9. Epub 2011 Jun 9. J Neurol. 2012. PMID: 21656342
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. Laforêt P, et al. Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):595-602. doi: 10.1016/j.neurol.2013.07.002. Epub 2013 Sep 3. Rev Neurol (Paris). 2013. PMID: 24008051
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. Devic P, et al. Among authors: petiot p. Eur J Neurol. 2014;21(1):130-4. doi: 10.1111/ene.12270. Epub 2013 Sep 21. Eur J Neurol. 2014. PMID: 24112557
109 results