Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Caroline, Rouaux"'
Autor:
Marina Hernan-Godoy, Caroline Rouaux
Publikováno v:
Cells, Vol 13, Iss 11, p 967 (2024)
The etiology of the neurodegenerative disease amyotrophic lateral sclerosis (ALS) is complex and considered multifactorial. The majority of ALS cases are sporadic, but familial cases also exist. Estimates of heritability range from 8% to 61%, indicat
Externí odkaz:
https://doaj.org/article/360ab2caade549c9b2595e423c399c16
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease that affects selected cortical and spinal neuronal populations, leading to progressive paralysis and death. A growing body of evidences suggests that the disease may origi
Externí odkaz:
https://doaj.org/article/8a1ed8a5b50042f1995609ace847b0c7
Publikováno v:
Brain Sciences, Vol 11, Iss 3, p 369 (2021)
Amyotrophic lateral sclerosis (ALS) is a devastating and fatal neurodegenerative disease arising from the combined degeneration of upper motor neurons (UMN) in the motor cortex, and lower motor neurons (LMN) in the brainstem and spinal cord. This dua
Externí odkaz:
https://doaj.org/article/93db53e0b6864c3fbde7d3d58396af1b
Autor:
Jelena, Scekic-Zahirovic, Mathieu, Fischer, Geoffrey, Stuart-Lopez, Thibaut, Burg, Johan, Gilet, Sylvie, Dirrig-Grosch, Christine, Marques, Marie-Christine, Birling, Pascal, Kessler, Caroline, Rouaux
Publikováno v:
Progress in neurobiology. 200
Amyotrophic lateral sclerosis (ALS) arises from the combined degeneration of motor neurons (MN) and corticospinal neurons (CSN). Recent clinical and pathological studies suggest that ALS might start in the motor cortex and spread along the corticofug
Autor:
Hajer El Oussini, Christine Marques, Gina Picchiarelli, Stéphane Dieterlé, Luc Dupuis, Caroline Rouaux, Jelena Scekic-Zahirovic, Sylvie Dirrig-Grosch, Jérôme Sinniger, Pauline Vercruysse
Publikováno v:
Annals of Neurology. 82:444-456
Objective: Spasticity occurs in a wide range of neurological diseases, including neurodegenerative diseases, after trauma or after stroke and is characterized by increased reflexes leading to muscle hypertonia. Spasticity is a painful symptom and can
Autor:
Thibaut Burg, Mathieu Fischer, Geoffrey Stuart-Lopez, Jelena Scekic-Zahirovic, Caroline Rouaux, Marie-Christine Birling, Pascal Kessler
While clinical evidence of combined degeneration of the bulbar and spinal motor neurons (MN) together with the corticospinal neurons (CSN) is required to diagnose Amyotrophic Lateral Sclerosis (ALS), preclinical studies have mostly concentrated on MN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5741b61951a43f25ccac06df44b66983
https://doi.org/10.1101/2020.01.09.900944
https://doi.org/10.1101/2020.01.09.900944
Publikováno v:
Annals of Neurology
Autor:
Thibaut, Burg, Charlotte, Bichara, Jelena, Scekic-Zahirovic, Mathieu, Fischer, Geoffrey, Stuart-Lopez, Aurore, Brunet, François, Lefebvre, Matilde, Cordero-Erausquin, Caroline, Rouaux
Publikováno v:
Annals of neurology. 88(4)
Recent studies carried out on amyotrophic lateral sclerosis patients suggest that the disease might initiate in the motor cortex and spread to its targets along the corticofugal tracts. In this study, we aimed to test the corticofugal hypothesis of a
Autor:
Mathieu Fischer, Matilde Cordero-Erausquin, Caroline Rouaux, Geoffrey Stuart-Lopez, François Lefebvre, Jelena Scekic-Zahirovic, Thibaut Burg, Charlotte Bichara
Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease of adulthood that affects voluntary motricity and rapidly leads to full paralysis and death. ALS arises from the combined degeneration of motoneurons in the spinal cord and brai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a02577a749dc0432dd419180f3ca250d
Autor:
Christine Marques, Thibaut Burg, Mathieu Fischer, Aurore Brunet, Jelena Scekic-Zahirovic, Céline Keime, Caroline Rouaux
Publikováno v:
bioRxiv
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease clinically defined as the combined degeneration of corticospinal and corticobulbar neurons (CSN), and bulbar and spinal motor neurons (MN). A growing body of evidence poin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85006e2e126f63766dd781ddd3045987