Detalhe da pesquisa
1.
Gene therapies for CMT neuropathies: from the bench to the clinic.
Curr Opin Neurol
; 2024 Jun 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38873808
2.
AAV9-mediated SH3TC2 gene replacement therapy targeted to Schwann cells for the treatment of CMT4C.
Mol Ther
; 31(11): 3290-3307, 2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37641403
3.
Charcot-Marie-Tooth neuropathies: Current gene therapy advances and the route toward translation.
J Peripher Nerv Syst
; 28(2): 150-168, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36965137
4.
Mitofusin 1 overexpression rescues the abnormal mitochondrial dynamics caused by the Mitofusin 2 K357T mutation in vitro.
J Peripher Nerv Syst
; 28(3): 329-340, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37220142
5.
NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice.
Brain
; 145(11): 3999-4015, 2022 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35148379
6.
Glial Gap Junction Pathology in the Spinal Cord of the 5xFAD Mouse Model of Early-Onset Alzheimer's Disease.
Int J Mol Sci
; 23(24)2022 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36555237
7.
AAV9-mediated Schwann cell-targeted gene therapy rescues a model of demyelinating neuropathy.
Gene Ther
; 28(10-11): 659-675, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33692503
8.
Emerging Therapies for Charcot-Marie-Tooth Inherited Neuropathies.
Int J Mol Sci
; 22(11)2021 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34205075
9.
Aberrant Mitochondrial Dynamics and Exacerbated Response to Neuroinflammation in a Novel Mouse Model of CMT2A.
Int J Mol Sci
; 22(21)2021 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34769001
10.
Gene replacement therapy in a model of Charcot-Marie-Tooth 4C neuropathy.
Brain
; 142(5): 1227-1241, 2019 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30907403
11.
Golgi-retained Cx32 mutants interfere with gene addition therapy for CMT1X.
Hum Mol Genet
; 26(9): 1622-1633, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334782
12.
Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy.
Proc Natl Acad Sci U S A
; 113(17): E2421-9, 2016 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27035961
13.
Regulatory role of oligodendrocyte gap junctions in inflammatory demyelination.
Glia
; 66(12): 2589-2603, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30325069
14.
Gene therapy targeting oligodendrocytes provides therapeutic benefit in a leukodystrophy model.
Brain
; 140(3): 599-616, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28100454
15.
Novel de novo DNMT1 gene mutation associated with hereditary sensory and autonomic neuropathy 1E (HSAN1E).
Neurol Sci
; 44(6): 2199-2201, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36746843
16.
Transgenic replacement of Cx32 in gap junction-deficient oligodendrocytes rescues the phenotype of a hypomyelinating leukodystrophy model.
Hum Mol Genet
; 24(7): 2049-64, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25524707
17.
Epidemiology of Amyotrophic Lateral Sclerosis in the Republic of Cyprus: A 25-Year Retrospective Study.
Neuroepidemiology
; 48(1-2): 79-85, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28528330
18.
Intraneural GJB1 gene delivery improves nerve pathology in a model of X-linked Charcot-Marie-Tooth disease.
Ann Neurol
; 78(2): 303-16, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26010264
19.
Differential modulation of the juxtaparanodal complex in Multiple Sclerosis.
Mol Cell Neurosci
; 67: 93-103, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26070930
20.
In the Clinic. Carpal Tunnel Syndrome.
Ann Intern Med
; 163(5): ITC1, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26322711