F Salachas
Overview
Explore the profile of F Salachas including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
546
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Recent Articles
1.
Georges M, Perez T, Rabec C, Jacquin L, Finet-Monnier A, Ramos C, et al.
Rev Mal Respir
. 2024 Jul;
41(8):620-637.
PMID: 39019674
Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive diaphragm weakness and deteriorating lung function. Bulbar involvement and cough weakness contribute to respiratory morbidity and mortality. ALS-related...
2.
Khamaysa M, Lefort M, Pelegrini-Issac M, Lackmy-Vallee A, Mendili M, Preuilh A, et al.
J Neurol
. 2023 Nov;
271(3):1235-1246.
PMID: 37910250
Background: Respiratory complications resulting from motor neurons degeneration are the primary cause of death in amyotrophic lateral sclerosis (ALS). Predicting the need for non-invasive ventilation (NIV) in ALS is important...
3.
Georges M, Perez T, Rabec C, Jacquin L, Finet-Monnier A, Ramos C, et al.
Respir Med Res
. 2022 Apr;
81:100901.
PMID: 35378353
Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive diaphragm weakness and deteriorating lung function. Bulbar involvement and cough weakness contribute to respiratory morbidity and mortality. ALS-related...
4.
Mongin M, Debs R, Le Forestier N, Lenglet T, Salachas F, Pradat P, et al.
Rev Neurol (Paris)
. 2020 Jul;
176(10):870-873.
PMID: 32653215
Fifteen ALS patients, with troublesome symptoms linked to masseter spasticity, benefited from BoNT-A injections in each masseter. Based on the medical records of patients, the effect of the first injection...
5.
Koutlidis R, Ayrignac X, Pradat P, Le Forestier N, Leger J, Salachas F, et al.
Neurophysiol Clin
. 2014 Sep;
44(3):267-80.
PMID: 25240560
Purpose Of The Study: Somatosensory-evoked potentials with segmental recordings were performed with the aim of distinguishing chronic inflammatory demyelinating polyneuropathy from other sensory neuropathies. Patients And Methods: Four groups of...
6.
Corcia P, Valdmanis P, Millecamps S, Lionnet C, Blasco H, Mouzat K, et al.
Neurology
. 2012 Apr;
78(19):1519-26.
PMID: 22539580
Objective: To describe the phenotype and phenotype-genotype correlations in patients with amyotrophic lateral sclerosis (ALS) with TARDBP gene mutations. Methods: French TARDBP+ patients with ALS (n = 28) were compared...
7.
Fraidakis M, Drunat S, Maisonobe T, Gerard B, Pradat P, Meininger V, et al.
Neurology
. 2012 Feb;
78(8):551-6.
PMID: 22323744
Objective: We report the cases of 2 patients with late-onset spinal muscular atrophy (SMA) type III, who were hemizygous for SMN1 deletion and carriers of novel SMN1 intragenic missense mutations,...
8.
Belzil V, Valdmanis P, Dion P, Daoud H, Kabashi E, Noreau A, et al.
Neurology
. 2009 Sep;
73(15):1176-9.
PMID: 19741216
Background: The identification of mutations in the TARDBP and more recently the identification of mutations in the FUS gene as the cause of amyotrophic lateral sclerosis (ALS) is providing the...
9.
Meininger V, Lacomblez L, Salachas F
J Neurol
. 2009 Aug;
247 Suppl 6:VI/19-22.
PMID: 19714404
Riluzole, after two significant trials, was introduced as the first standard treatment of amyotrophic lateral sclerosis (ALS) in the early 95'. After 5 years what has changed in the field...
10.
Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerriere A, Golfier V, et al.
Neurology
. 2009 May;
72(19):1669-76.
PMID: 19433740
Background: Frontotemporal dementia associated with motor neuron disease (FTD-MND) is a rare neurodegenerative disorder that may be inherited by autosomal dominant trait. No major gene has been identified but a...