Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.


The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

13 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
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.
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
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
Novel XK mutation in a McLeod patient diagnosed after heart transplant.
Laurencin C, Sebbag L, Jousserand G, Demontes M, Campean L, Thivolet-Bejui F, Lebre AS, Thobois S. Laurencin C, et al. Among authors: jousserand g. Clin Neurol Neurosurg. 2018 May;168:64-66. doi: 10.1016/j.clineuro.2018.02.039. Epub 2018 Mar 1. Clin Neurol Neurosurg. 2018. PMID: 29524658 No abstract available.
[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.
13 results