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Quoted phrase not found in phrase index: "Neuropathy, hereditary sensory and autonomic, type 1A"
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AAV-Mediated Gene Therapy for Glycosphingolipid Biosynthesis Deficiencies.
Yang H, Brown RH Jr, Wang D, Strauss KA, Gao G. Yang H, et al. Trends Mol Med. 2021 Jun;27(6):520-523. doi: 10.1016/j.molmed.2021.02.004. Epub 2021 Mar 10. Trends Mol Med. 2021. PMID: 33714697 Free PMC article. Review.
De novo glycosphingolipid (GSL) biosynthesis defects cause severe neurological diseases, including hereditary sensory and autonomic neuropathy type 1A (HSAN1A), GM3 synthase deficiency, and hereditary spastic paraplegia type …
De novo glycosphingolipid (GSL) biosynthesis defects cause severe neurological diseases, including hereditary sensory and a …
Experimental therapeutics in hereditary neuropathies: the past, the present, and the future.
Herrmann DN. Herrmann DN. Neurotherapeutics. 2008 Oct;5(4):507-15. doi: 10.1016/j.nurt.2008.07.001. Neurotherapeutics. 2008. PMID: 19019301 Free PMC article. Review.
Hereditary neuropathies represent approximately 40% of undiagnosed neuropathies in a tertiary clinic setting. ...Some 15% of demyelinating CMT and 70% of axonal CMT await genetic clarification. Other hereditary neuropathies include the heredi …
Hereditary neuropathies represent approximately 40% of undiagnosed neuropathies in a tertiary clinic setting. ...Some 1 …