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P Corcia

Showing results (81-90 of 102) with videos related to

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Molecular Neurobiology|January 12, 2018
Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to NeurodegenerationC Maurel, A Dangoumau, S Marouillat, et al.
Journal of Child Neurology|April 6, 1999
Neuropsychologic and adaptive functioning in adolescents and young adults shunted for congenital hydrocephalusC Hommet, C Billard, P Gillet, et al.
European Journal of Clinical Nutrition|April 20, 2017
A decrease in blood cholesterol after gastrostomy could impact survival in ALSH Blasco, F Patin, S Molinier, et al.
Neurobiology of Disease|April 10, 2018
Age-dependent neurodegeneration and organelle transport deficiencies in mutant TDP43 patient-derived neurons are independent of TDP43 aggregationN Kreiter, A Pal, X Lojewski, et al.
Neurology|November 13, 2002
SMN1 gene study in three families in which ALS and spinal muscular atrophy co-existP Corcia, J Khoris, P Couratier, et al.
European Journal of Neurology|June 23, 2015
Biological follow-up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosisF Patin, P Corcia, B Madji Hounoum, et al.
Revue Neurologique|May 8, 2009
[Update on fundamental and clinical research in amyotrophic lateral sclerosis]P-F Pradat, J-P Camdessanché, L Carluer, et al.
Scientific Reports|December 17, 2017
Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALSH Blasco, C Veyrat-Durebex, C Bocca, et al.
Revue Neurologique|September 21, 2023
French National Protocol for genetic of amyotrophic lateral sclerosisP Corcia, P Vourc'h, E Bernard, et al.
Journal of Biomedical Informatics|December 16, 2014
Comparative analysis of targeted metabolomics: dominance-based rough set approach versus orthogonal partial least square-discriminant analysisH Blasco, J Błaszczyński, J C Billaut, et al.
Pageof 11

Showing results (81-90 of 102) with videos related to

Sort By:
Pageof 11
Molecular Neurobiology|January 12, 2018
Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to NeurodegenerationC Maurel, A Dangoumau, S Marouillat, et al.
Journal of Child Neurology|April 6, 1999
Neuropsychologic and adaptive functioning in adolescents and young adults shunted for congenital hydrocephalusC Hommet, C Billard, P Gillet, et al.
European Journal of Clinical Nutrition|April 20, 2017
A decrease in blood cholesterol after gastrostomy could impact survival in ALSH Blasco, F Patin, S Molinier, et al.
Neurobiology of Disease|April 10, 2018
Age-dependent neurodegeneration and organelle transport deficiencies in mutant TDP43 patient-derived neurons are independent of TDP43 aggregationN Kreiter, A Pal, X Lojewski, et al.
Neurology|November 13, 2002
SMN1 gene study in three families in which ALS and spinal muscular atrophy co-existP Corcia, J Khoris, P Couratier, et al.
European Journal of Neurology|June 23, 2015
Biological follow-up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosisF Patin, P Corcia, B Madji Hounoum, et al.
Revue Neurologique|May 8, 2009
[Update on fundamental and clinical research in amyotrophic lateral sclerosis]P-F Pradat, J-P Camdessanché, L Carluer, et al.
Scientific Reports|December 17, 2017
Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALSH Blasco, C Veyrat-Durebex, C Bocca, et al.
Revue Neurologique|September 21, 2023
French National Protocol for genetic of amyotrophic lateral sclerosisP Corcia, P Vourc'h, E Bernard, et al.
Journal of Biomedical Informatics|December 16, 2014
Comparative analysis of targeted metabolomics: dominance-based rough set approach versus orthogonal partial least square-discriminant analysisH Blasco, J Błaszczyński, J C Billaut, et al.
Pageof 11