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Expression of multiple neuregulin transcripts in postnatal rat brains.
- Published in:
- Journal of Comparative Neurology, 1994, v. 349, n. 3, p. 389, doi. 10.1002/cne.903490306
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- Publication type:
- Article
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 9, p. 3131, doi. 10.1093/brain/awae079
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- Publication type:
- Article
Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 9, p. 3826, doi. 10.1093/brain/awad095
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- Article
De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
- Published in:
- 2016
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- Publication type:
- journal article
Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene.
- Published in:
- 2015
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- Publication type:
- journal article
Blocking bad.
- Published in:
- 2015
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- Publication type:
- journal article
KCNQ2 Is a Nodal K<sup>+</sup> Channel.
- Published in:
- Journal of Neuroscience, 2004, v. 24, n. 5, p. 1236, doi. 10.1523/JNEUROSCI.4512-03.2004
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- Publication type:
- Article
Connexins Are Critical for Normal Myelination in the CNS.
- Published in:
- Journal of Neuroscience, 2003, v. 23, n. 13, p. 5963, doi. 10.1523/JNEUROSCI.23-13-05963.2003
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- Publication type:
- Article
Kv3.1b Is a Novel Component of CNS Nodes.
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- Journal of Neuroscience, 2003, v. 23, n. 11, p. 4509, doi. 10.1523/JNEUROSCI.23-11-04509.2003
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- Publication type:
- Article
The debut of a rational treatment for an inherited neuropathy?
- Published in:
- 2011
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- Publication type:
- journal article
Paranodal permeability in 'myelin mutants'.
- Published in:
- Glia, 2011, v. 59, n. 10, p. 1447, doi. 10.1002/glia.21188
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- Publication type:
- Article
Central nervous system dysfunction in a mouse model of Fa2h deficiency.
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- Glia, 2011, v. 59, n. 7, p. 1009, doi. 10.1002/glia.21172
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- Publication type:
- Article
Molecular mechanisms of inherited demyelinating neuropathies.
- Published in:
- Glia, 2008, v. 56, n. 14, p. 1578, doi. 10.1002/glia.20751
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- Publication type:
- Article
Pannexin1 is expressed by neurons and glia but does not form functional gap junctions.
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- Glia, 2007, v. 55, n. 1, p. 46, doi. 10.1002/glia.20435
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- Publication type:
- Article
Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes.
- Published in:
- Glia, 2004, v. 47, n. 4, p. 346, doi. 10.1002/glia.20043
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- Publication type:
- Article
Schwann cell caveolin-1 expression increases during myelination and decreases after axotomy.
- Published in:
- Glia, 2002, v. 38, n. 3, p. 191, doi. 10.1002/glia.10063
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- Publication type:
- Article
Disease mechanisms in inherited neuropathies.
- Published in:
- Nature Reviews Neuroscience, 2003, v. 4, n. 9, p. 714, doi. 10.1038/nrn1196
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- Publication type:
- Article
Temporal trends and yield of clinical diagnostic genetic testing in adult neurology.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 10, p. 2922, doi. 10.1002/ajmg.a.62372
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- Publication type:
- Article
Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells.
- Published in:
- Journal of Cell Biology, 2002, v. 159, n. 2, p. 361, doi. 10.1083/jcb.200207050
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- Publication type:
- Article
Notch1 control of oligodendrocyte differentiation in the spinal cord.
- Published in:
- Journal of Cell Biology, 2002, v. 158, n. 4, p. 709, doi. 10.1083/jcb.200202002
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- Publication type:
- Article
Myelination: some receptors required.
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- Journal of Cell Biology, 2002, v. 156, n. 1, p. 13, doi. 10.1083/jcb.200112017
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- Publication type:
- Article
Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations.
- Published in:
- Scientific Reports, 2017, p. 40166, doi. 10.1038/srep40166
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- Publication type:
- Article
Accelerate Clinical Trials in Charcot-Marie-Tooth Disease (ACT-CMT): A Protocol to Address Clinical Trial Readiness in CMT1A.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.930435
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- Publication type:
- Article
Regulation of fibronectin alternative splicing during peripheral nerve repair.
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- Journal of Neuroscience Research, 1999, v. 56, n. 4, p. 323, doi. 10.1002/(SICI)1097-4547(19990515)56:4<323::AID-JNR1>3.0.CO;2-6
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- Publication type:
- Article
p200, a collagen secreted by Schwann cells, is expressed in developing nerves and in adult nerves following axotomy.
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- Journal of Neuroscience Research, 1999, v. 56, n. 3, p. 284, doi. 10.1002/(SICI)1097-4547(19990501)56:3<284::AID-JNR8>3.0.CO;2-Q
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- Publication type:
- Article
Maturation-dependent apoptotic cell death of oligodendrocytes in myelin-deficient rats.
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- Journal of Neuroscience Research, 1998, v. 54, n. 5, p. 623, doi. 10.1002/(SICI)1097-4547(19981201)54:5<623::AID-JNR7>3.0.CO;2-R
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- Publication type:
- Article
Carpal tunnel syndrome in inherited neuropathies: A retrospective survey.
- Published in:
- 2018
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- Publication type:
- journal article
Prevalence and orthopedic management of foot and ankle deformities in Charcot-Marie-Tooth disease.
- Published in:
- 2018
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- Publication type:
- journal article
A Patient with neurofibromatosis type 1 and Charcot-Marie-Tooth disease type 1B.
- Published in:
- Muscle & Nerve, 2010, v. 41, n. 4, p. 555, doi. 10.1002/mus.21546
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- Publication type:
- Article
Chronic multiple paraneoplastic syndromes.
- Published in:
- 2000
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- Publication type:
- journal article
A Unique Mutation in Connexin32 Associated with Severe, Early Onset CMTX in a Heterozygous Female.
- Published in:
- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 481, doi. 10.1111/j.1749-6632.1999.tb08616.x
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- Publication type:
- Article
X-linked Charcot-Marie-Tooth Disease and Connexin32.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 36, doi. 10.1111/j.1749-6632.1999.tb08564.x
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- Publication type:
- Article
Nodes, Paranodes, and Incisures: From Form to Function.
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- Annals of the New York Academy of Sciences, 1999, v. 883, n. 1, p. 131, doi. 10.1111/j.1749-6632.1999.tb08576.x
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- Publication type:
- Article
Neuregulins as Potential Neuroprotective Agents.
- Published in:
- Annals of the New York Academy of Sciences, 1997, v. 825, n. 1, p. 348, doi. 10.1111/j.1749-6632.1997.tb48446.x
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- Publication type:
- Article
Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07718-5
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- Publication type:
- Article
Connexin32 Mutations Cause Loss of Function in Schwann Cells and Oligodendrocytes Leading to PNS and CNS Myelination Defects.
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- Journal of Neuroscience, 2009, v. 29, n. 15, p. 4736, doi. 10.1523/JNEUROSCI.0325-09.2009
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- Publication type:
- Article
Two Distinct Heterotypic Channels Mediate Gap Junction Coupling between Astrocyte and Oligodendrocyte Connexins.
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- Journal of Neuroscience, 2007, v. 27, n. 51, p. 13949, doi. 10.1523/JNEUROSCI.3395-07.2007
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- Publication type:
- Article
Genetic and Physiological Evidence That Oligodendrocyte Gap Junctions Contribute to Spatial Buffering of Potassium Released during Neuronal Activity.
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- Journal of Neuroscience, 2006, v. 26, n. 43, p. 10984, doi. 10.1523/JNEUROSCI.0304-06.2006
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- Publication type:
- Article
A Common Ankyrin-G-Based Mechanism Retains KCNQ and Na<sub>V</sub> Channels at Electrically Active Domains of the Axon.
- Published in:
- Journal of Neuroscience, 2006, v. 26, n. 10, p. 2599, doi. 10.1523/JNEUROSCI.4314-05.2006
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- Publication type:
- Article
ErbB2 Signaling in Schwann Cells Is Mostly Dispensable for Maintenance of Myelinated Peripheral Nerves and Proliferation of Adult Schwann Cells after Injury.
- Published in:
- Journal of Neuroscience, 2006, v. 26, n. 7, p. 2124, doi. 10.1523/JNEUROSCI.4594-05.2006
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- Publication type:
- Article
Both Laminin and Schwann Cell Dystroglycan Are Necessary for Proper Clustering of Sodium Channels at Nodes of Ranvier.
- Published in:
- Journal of Neuroscience, 2005, v. 25, n. 41, p. 9418, doi. 10.1523/JNEUROSCI.2068-05.2005
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- Publication type:
- Article
Prenylation-Defective Human Connexin32 Mutants Are Normally Localized and Function Equivalently to Wild-Type Connexin32 in Myelinating Schwann Cells.
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- Journal of Neuroscience, 2005, v. 25, n. 31, p. 7111, doi. 10.1523/JNEUROSCI.1319-05.2005
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- Publication type:
- Article
Altered Ion Channels in an Animal Model of Charcot-Marie-Tooth Disease Type IA.
- Published in:
- Journal of Neuroscience, 2005, v. 25, n. 6, p. 1470, doi. 10.1523/JNEUROSCI.3328-04.2005
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- Publication type:
- Article
Transgenic Expression of Human Connexin32 in Myelinating Schwann Cells Prevents Demyelination in Connexin32-Null Mice.
- Published in:
- Journal of Neuroscience, 2005, v. 25, n. 6, p. 1550, doi. 10.1523/JNEUROSCI.3082-04.2005
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- Publication type:
- Article
HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling.
- Published in:
- 2022
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- Publication type:
- journal article
Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease.
- Published in:
- Journal of Cellular & Molecular Medicine, 2008, v. 12, n. 2, p. 679, doi. 10.1111/j.1582-4934.2007.00158.x
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- Publication type:
- Article
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.
- Published in:
- Brain: A Journal of Neurology, 2009, v. 132, n. 2, p. 426, doi. 10.1093/brain/awn328
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- Publication type:
- Article
Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations.
- Published in:
- Brain: A Journal of Neurology, 2006, v. 129, n. 6, p. 1570, doi. 10.1093/brain/awl084
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- Publication type:
- Article
Schwann cell-derived periostin promotes autoimmune peripheral polyneuropathy via macrophage recruitment.
- Published in:
- 2018
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- Publication type:
- journal article
PMP22 antisense oligonucleotides reverse Charcot-Marie-Tooth disease type 1A features in rodent models.
- Published in:
- 2018
- By:
- Publication type:
- journal article