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Erratum to: A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement.
- Published in:
- 2021
- By:
- Publication type:
- journal article
A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Conduction Block in PMP22 Deficiency.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 2, p. 600, doi. 10.1523/JNEUROSCI.4264-09.2010
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- Publication type:
- Article
Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 12, p. 3551
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- Publication type:
- Article
Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice.
- Published in:
- 2012
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- Publication type:
- journal article
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
- Published in:
- 2012
- By:
- Publication type:
- journal article
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot–Marie–Tooth disease type 1B.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 7, p. 2032, doi. 10.1093/brain/aws140
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- Publication type:
- Article
Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside.
- Published in:
- Brain: A Journal of Neurology, 2005, v. 128, n. 5, p. 1168, doi. 10.1093/brain/awh483
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- Publication type:
- Article
Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 1, p. 69, doi. 10.1002/acn3.50965
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- Publication type:
- Article
Myelin protein zero mutations and the unfolded protein response in Charcot Marie Tooth disease type 1B.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 4, p. 445, doi. 10.1002/acn3.543
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- Publication type:
- Article
PMP22 exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E.
- Published in:
- Annals of Clinical & Translational Neurology, 2017, v. 4, n. 4, p. 236, doi. 10.1002/acn3.395
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- Publication type:
- Article
Schwann cell transcript biomarkers for hereditary neuropathy skin biopsies.
- Published in:
- 2019
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- Publication type:
- journal article
Genotype determines phenotype in experimental Lyme borreliosis.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 3, p. 361
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- Publication type:
- Article
Distinct pathogenic processes between Fig4-deficient motor and sensory neurons.
- Published in:
- European Journal of Neuroscience, 2011, v. 33, n. 8, p. 1401, doi. 10.1111/j.1460-9568.2011.07651.x
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- Publication type:
- Article
Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice.
- Published in:
- Molecular Neurobiology, 2022, v. 59, n. 7, p. 4159, doi. 10.1007/s12035-022-02838-y
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- Publication type:
- Article
Featured Cover.
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- Journal of the Peripheral Nervous System, 2021, v. 26, p. i, doi. 10.1111/jns.12475
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- Publication type:
- Article
Hereditary neuropathies: A pathological perspective.
- Published in:
- Journal of the Peripheral Nervous System, 2021, v. 26, p. S42, doi. 10.1111/jns.12467
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- Publication type:
- Article