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Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteria.
Robert-Varvat F, Jousserand G, Bouhour F, Vial C, Cintas P, Echaniz-Laguna A, Delmont E, Clavelou P, Chauplannaz G, Jomir L, Pereon Y, Leonard-Louis S, Manel V, Antoine JC, Lacour A, Camdessanche JP. Robert-Varvat F, et al. Among authors: jousserand g. Muscle Nerve. 2018 Feb;57(2):217-221. doi: 10.1002/mus.25666. Epub 2017 Jun 11. Muscle Nerve. 2018. PMID: 28407266
Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation.
Camdessanché JP, Belzil VV, Jousserand G, Rouleau GA, Créac'h C, Convers P, Antoine JC. Camdessanché JP, et al. Among authors: jousserand g. Orphanet J Rare Dis. 2011 Feb 5;6:4. doi: 10.1186/1750-1172-6-4. Orphanet J Rare Dis. 2011. PMID: 21294910 Free PMC article.
Trismus as the first symptom of amyotrophic lateral sclerosis.
Cisse FA, Dubois-Boissier MD, Jousserand G, Antoine JC, Camdessanche JP. Cisse FA, et al. Among authors: jousserand g. Amyotroph Lateral Scler. 2012 Sep;13(5):475-6. doi: 10.3109/17482968.2012.677047. Epub 2012 Jun 7. Amyotroph Lateral Scler. 2012. PMID: 22670882
[Unusual phenotype of myopathy associated with a new PNPLA2 mutation].
Jousserand G, Streichenberger N, Petiot P. Jousserand G, et al. Med Sci (Paris). 2016 Nov;32 Hors série n°2:10-11. doi: 10.1051/medsci/201632s203. Epub 2016 Nov 21. Med Sci (Paris). 2016. PMID: 27869069 Free article. French. No abstract available.
Brain immunohistopathological study in a patient with anti-NMDAR encephalitis.
Camdessanché JP, Streichenberger N, Cavillon G, Rogemond V, Jousserand G, Honnorat J, Convers P, Antoine JC. Camdessanché JP, et al. Among authors: jousserand g. Eur J Neurol. 2011 Jun;18(6):929-31. doi: 10.1111/j.1468-1331.2010.03180.x. Epub 2010 Aug 16. Eur J Neurol. 2011. PMID: 20722705
13 results