Petiot P - Search Results

1

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. Auré K, et al. Among authors: petiot p. Neurology. 2013 Nov 19;81(21):1810-8. doi: 10.1212/01.wnl.0000436067.43384.0b. Epub 2013 Oct 23. Neurology. 2013. PMID: 24153443

2

[Neurological complications caused by gold salts. Nosologic report apropos of a case].

Petiot P, Charles N, Vial C, McGregor B, Aimard G, Trillet M, Bady B. Petiot P, et al. Rev Neurol (Paris). 1993;149(10):562-5. Rev Neurol (Paris). 1993. PMID: 7912843 French.

3

[Paralysis of abdominal muscles caused by Lyme disease].

Vial C, Petiot P, Latombe D, Ruel JH, Confavreux C, Trillet M, Bady B. Vial C, et al. Among authors: petiot p. Rev Neurol (Paris). 1993;149(12):810-2. Rev Neurol (Paris). 1993. PMID: 7997746 French.

4

[Calcified cerebellar metastasis of carcinoma of the uterine cervix].

Petiot P, Aimard G, Vial C, Froment JC, Saint Pierre G, Trillet M. Petiot P, et al. Rev Neurol (Paris). 1993;149(8-9):493-6. Rev Neurol (Paris). 1993. PMID: 8009150 French.

5

[Dropped head syndrome: diagnostic discussion apropos of 3 cases].

Petiot P, Vial C, de Saint Victor JF, Charles N, Carrier H, Depierre P, Bady B. Petiot P, et al. Rev Neurol (Paris). 1997 May;153(4):251-5. Rev Neurol (Paris). 1997. PMID: 9296143 Review. French.

6

Slowly progressive spinal muscular atrophy of the hands (O'Sullivan-McLeod syndrome): clinical and magnetic resonance imaging presentation.

Petiot P, Gonon V, Froment JC, Vial C, Vighetto A. Petiot P, et al. J Neurol. 2000 Aug;247(8):654-5. doi: 10.1007/pl00007808. J Neurol. 2000. PMID: 11041339 No abstract available.

7

Paraneoplastic peripheral neuropathy associated with anti-Hu antibodies. A clinical and electrophysiological study of 20 patients.

Camdessanché JP, Antoine JC, Honnorat J, Vial C, Petiot P, Convers P, Michel D. Camdessanché JP, et al. Among authors: petiot p. Brain. 2002 Jan;125(Pt 1):166-75. doi: 10.1093/brain/awf006. Brain. 2002. PMID: 11834602

8

[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.

9

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

10

[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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

109 results

Search Page

Filters