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axo·nop·a·thy (ak″sə-nopґə-the) [axon + -pathy] a disorder disrupting the normal functioning of the axons.Medical dictionary. 2011.
proximal axonopathy — axonopathy in which the disease process starts at the periphery and proceeds towards the center; cf. dying back … Medical dictionary
Distal axonopathy — ( aka dying back neuropathy) is a type of peripheral neuropathy that results from some metabolic or toxic derangement of peripheral nervous system (PNS) neurons.It is the most common response of nerves to metabolic or toxic disturbances, and as… … Wikipedia
distal axonopathy — the more common kind of axonopathy, in which the disease process starts centrally and proceeds towards the periphery; cf. wallerian degeneration … Medical dictionary
axonal neuropathy — axonopathy … Medical dictionary
Peripheral neuropathy — Neuropathy redirects here. For other uses, see Neuropathy (disambiguation). Not to be confused with Nephropathy. Peripheral neuropathy Classification and external resources … Wikipedia
Polyneuropathy — Classification and external resources ICD 10 G60 G64 ICD 9 … Wikipedia
Acute motor axonal neuropathy — (AMAN) is a variant of Guillain Barre Syndrome. It is characterized by acute paralysis, loss of reflexes without sensory loss. Pathologically, one can observe motor axonal degeneration with antibody mediated attacks of motor nerve and nodes of… … Wikipedia
Gluten-sensitive idiopathic neuropathies — Diagnosis of gluten sensitive neuropathies without a clear cause is on the rise. These idiopathic neuropathies were first identified by screening for anti gliadin IgG (AGA).cite journal | author = Hadjivassiliou M, Gibson A, Davies Jones GA, Lobo … Wikipedia
Malaoxon — IUPAC name diethyl 2 (dimethoxyphosphorylsulfanyl)butanedioate … Wikipedia
GDAP1 — Ganglioside induced differentiation associated protein 1, also known as GDAP1, is a human gene.cite web | title = Entrez Gene: GDAP1 ganglioside induced differentiation associated protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
