G Sole
Overview
Explore the profile of G Sole including associated specialties, affiliations and a list of published articles.
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Articles
42
Citations
290
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0
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Recent Articles
1.
Couchet E, Laborde B, Cassoudesalle H, Mathis S, Sole G, Guehl D, et al.
Rev Neurol (Paris)
. 2024 May;
180(8):766-769.
PMID: 38749790
Introduction: Dropped head syndrome (DHS) is characterized by a chin-on-chest deformity, correctable by passive neck extension. Methods: Case report. Results: A patient with a heavy nephrological history (dialyzed since 5 ...
2.
Adams D, Cintas P, Sole G, Tard C, Labeyrie C, Echaniz-Laguna A, et al.
Rev Neurol (Paris)
. 2024 Apr;
180(7):661-672.
PMID: 38643028
Objective: We aimed to describe characteristics of patients with ATTR variant polyneuropathy (ATTRv-PN) and ATTRv-mixed and assess the real-world use and safety profile of tafamidis meglumine 20mg. Methods: Thirty-eight French...
3.
Damour A, Delalande P, Cordelieres F, Lafon M, Faure M, Segovia-Kueny S, et al.
Rev Neurol (Paris)
. 2023 Aug;
179(9):983-992.
PMID: 37633734
Introduction: Patients with severe neuromuscular disease (sNMD) are considered at high risk of severe COVID-19. Muscle tissue is often replaced by fibroadipose tissue in these diseases whereas the new mRNA-based...
4.
Cintas P, Bouhour F, Cauquil C, Masingue M, Tard C, Sacconi S, et al.
Rev Neurol (Paris)
. 2023 Apr;
179(8):914-922.
PMID: 37019741
Treatment strategies in chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) must be adapted on a case-to-case basis. Validated and reproducible tools for monitoring treatment response are required at diagnosis, when initiating treatment...
5.
Sole G, Salort-Campana E, Pereon Y, Stojkovic T, Wahbi K, Cintas P, et al.
Rev Neurol (Paris)
. 2020 May;
176(6):507-515.
PMID: 32354651
In France, the epidemic phase of COVID-19 caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) began in February 2020 and resulted in the implementation of emergency measures and a...
6.
Victor J, Zanardo L, Heron-Mermin D, Poursac N, Sole G, Bordes C, et al.
Rev Med Interne
. 2018 Dec;
40(2):70-81.
PMID: 30527961
Introduction: Dermatomyositis are rare autoimmune diseases. The discovery of specific antibodies such as the anti-TIF1γ, anti-SAE1/2 and anti-NXP2 antibodies has been associated with specific clinical phenotypes. The recent development of...
7.
Jonson P, Palmio J, Johari M, Penttila S, Evila A, Nelson I, et al.
Eur J Neurol
. 2018 Feb;
25(5):790-794.
PMID: 29437287
Background And Purpose: The aim was to determine the genetic background of unknown muscular dystrophy in five French families. Methods: Twelve patients with limb girdle muscular dystrophy or distal myopathy...
8.
Oestergaard S, Stojkovic T, Dahlqvist J, Bouchet-Seraphin C, Nectoux J, Leturcq F, et al.
Neurol Genet
. 2016 Oct;
2(6):e112.
PMID: 27766311
Objective: In this study, muscle involvement assessed by MRI and levels of GMPPB and glycosylation of α-dystroglycan expression in muscle were examined in patients with limb-girdle muscular dystrophy (LGMD) type...
9.
Bereau M, Anheim M, Echaniz-Laguna A, Magot A, Verny C, Goideau-Sevrain M, et al.
J Neurol Sci
. 2016 Aug;
368:70-6.
PMID: 27538604
No abstract available.
10.
Naudion S, Moutton S, Coupry I, Sole G, Deforges J, Guerineau E, et al.
Clin Genet
. 2015 Sep;
89(3):371-7.
PMID: 26404489
Otopalatodigital spectrum disorders (OPDSD) include OPD syndromes types 1 and type 2 (OPD1, OPD2), Melnick-Needles syndrome (MNS), and frontometaphyseal dysplasia (FMD). These conditions are clinically characterized by variable skeletal dysplasia...