• 19 Citations
  • 2 h-Index
20132018
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Fingerprint Dive into the research topics where Pierre-Francois Pradat is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 2 Similar Profiles
Amyotrophic Lateral Sclerosis Medicine & Life Sciences
Motor Neurons Medicine & Life Sciences
Spinal Cord Medicine & Life Sciences
Biomarkers Medicine & Life Sciences
Motor Neuron Disease Medicine & Life Sciences
Metabolomics Medicine & Life Sciences
Atrophic Muscular Disorders Medicine & Life Sciences
Atrophy Medicine & Life Sciences

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Research Output 2013 2018

  • 19 Citations
  • 2 h-Index
  • 2 Article
  • 1 Conference contribution
7 Citations (Scopus)

Extrapyramidal deficits in ALS: a combined biomechanical and neuroimaging study

Feron, M., Couillandre, A., Mseddi, E., Termoz, N., Abidi, M., Bardinet, E., Delgadillo, D., Lenglet, T., Querin, G., Welter, M. L., Le Forestier, N., Salachas, F., Bruneteau, G., del Mar Amador, M., Debs, R., Lacomblez, L., Meininger, V., Pélégrini-Issac, M., Bede, P., Pradat, P. F. & 1 othersde Marco, G., 1 Sep 2018, In : Journal of Neurology. 265, 9, p. 2125-2136 12 p.

Research output: Contribution to journalArticle

Amyotrophic Lateral Sclerosis
Neuroimaging
Gait
Basal Ganglia
Brain Stem

Altered secretion of exosomes by muscle cells: role in ALS pathogenesis

Duguez, S., Le Gall, L., Duddy, W., Martinat, C., Thorley, M., Ouandaogo, G., Loeffler, JP., Gonzales De Aguilar, JL., Butler-Brown, G., Mouly, V. & Pradat, PF., 1 Jun 2015, Unknown Host Publication. Vol. 22. p. P4129 1 p.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Open Access
File
12 Citations (Scopus)

A Rare Motor Neuron Deleterious Missense Mutation in the DPYSL3 (CRMP4) Gene is Associated with ALS

Blasco, H., Bernard-Marissal, N., Vourc'h, P., Guettard, Y. O., Sunyach, C., Augereau, O., Khederchah, J., Mouzat, K., Antar, C., Gordon, P. H., Veyrat-Durebex, C., Besson, G., Andersen, P. M., Salachas, F., Meininger, V., Camu, W., Pettmann, B., Andres, C. R., Corcia, P., Pautot, V. & 38 othersNicolas, G., Rumbach, L., Clavelou, P., Guy, N., Besson, G., Destée, A., Brunaud-Danel, V., Couratier, P., Funalot, B., Broussole, E., Vial, C., Vandenberghe, N., Camu, W., Morales, R., Pageot, N., Debouverie, M., Pittion, S., Desnuelle, C., Soriani, M. H., Lemasson, G., Meininger, V., Salachas, F., Pradat, P. F., Dib, M., Bruneteau, G., Leforestier, N., Pouget, J., Verschuren, A., Viader, F., Carluer, L., Tranchant, C., Fleury, M. C., Antoine, J. C., Camdessanche, J. P., Arne-Bes, M. C., Cintas, P., Corcia, P. & Praline, J., 1 Jul 2013, In : Human Mutation. 34, 7, p. 953-960 8 p.

Research output: Contribution to journalArticle

dihydropyrimidinase
Motor Neurons
Missense Mutation
Growth
Genes