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G Sole

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Articles 42
Citations 290
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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...