Detalhe da pesquisa
1.
Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States.
Cytotherapy
; 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38613540
2.
Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource.
Mol Genet Metab
; 138(3): 107525, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36796138
3.
Temporal trends and yield of clinical diagnostic genetic testing in adult neurology.
Am J Med Genet A
; 185(10): 2922-2928, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34075706
4.
The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population.
J Neurogenet
; 33(1): 21-26, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30724636
5.
Novel mutation in the KCNJ10 gene in three siblings with seizures, ataxia and no electrolyte abnormalities.
J Neurogenet
; 32(1): 1-5, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29191078
6.
Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone-induced demyelination.
Glia
; 65(12): 2087-2098, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28940645
7.
Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts.
J Neurol
; 271(2): 733-747, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37891417
8.
Disparities in Genetic Testing for Neurologic Disorders.
Neurology
; 102(6): e209161, 2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38447117
9.
Motor Learning and Physical Exercise in Adaptive Myelination and Remyelination.
ASN Neuro
; 14: 17590914221097510, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35635130
10.
Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development.
Front Neurol
; 12: 788168, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35185751
11.
Gap junction disorders of myelinating cells.
Rev Neurosci
; 21(5): 397-419, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21280457
12.
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.
Brain
; 132(Pt 2): 426-38, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19056803
13.
Remyelination alters the pattern of myelin in the cerebral cortex.
Elife
; 92020 05 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32459173
14.
Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins.
J Neurosci
; 27(51): 13949-57, 2007 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-18094232
15.
Gap junctions couple astrocytes and oligodendrocytes.
J Mol Neurosci
; 35(1): 101-16, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18236012
16.
Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex.
Nat Neurosci
; 21(5): 696-706, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29556025
17.
A 6-Year-Old With Leg Cramps.
Pediatrics
; 136(4): 732-9, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26371189
18.
Clinical Reasoning: A 70-year-old woman with acute-onset weakness and progressive hemiataxia.
Neurology
; 87(22): e264-e268, 2016 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-27895250
19.
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease.
Mol Cell Neurosci
; 34(4): 629-41, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17344063