(no͝or′ō-ăk′sə-nəl, -ăk-sŏn′əl)
Of, relating to, or being the axon of a neuron.
References in periodicals archive ?
2008) Neuroaxonal dystrophy caused by group VIA phospholipase [A.
Some of the NBIA disorders include aceruloplasminemia, fatty acid hydroxylase-associated neurodegeneration, infantile neuroaxonal dystrophy, Kufor-Rakeb syndrome, neuroaxonal dystrophy, neuroferritinopathy.
Some also showed synapse-like structures, and one showed neuroaxonal and Schwannian-like features.
NAA is believed to be a marker of neuroaxonal cell density and viability and its decrease signifies neuronal injury.
Pope Benedict also blessed 18-month-old Alexander Frame, who has an incurable genetic disorder called neuroaxonal dystrophy.
NAA and N-acetylaspartylglutamate (tNAA) are markers of neuroaxonal integrity and have been found to decline with neuronal damage and loss.
New topics include infantile neuroaxonal dystrophy, neuronal migration disorders, meningococcal vaccines, pneumococcal meningitis, rivastigmine, Pervasive Developmental Disorders, and TORCH Disorders.
PLA2G2A Cancer colo-rectal esporadico PLA2G2C No definido PLA2G2D No definido PLA2G2E No definido PLA2G2F No definido PLA2G3 No definido PLA2G4A No definido PLA2G4B No definido PLA2G4C No definido PLA2G4D No definido PLA2G4E No definido PLA2G4F No definido PLA2G6A Distrofia neuroaxonal infantil, neurodegeneracion con acumulacion cerebral de hierro, Sindrome de Karak PLA2G6B No definido PLA2G7 Disminucion en (variedad inflamacion secretoria intestinal inflamatoria) (Ej.
Por otro lado, respecto al tratamiento neuroprotector, algunos agentes, como los bloqueadores de canales de calcio, antagonistas NMDA, antagonistas FNT alfa e inhibidores de la produccion de radicales libres de oxigeno parecen bloquear potencialmente las vias que conducen a injuria neuroaxonal.
The work, supported by the children's medical research charity WellChild, has also uncovered a genetic mutation, which causes Infantile Neuroaxonal Dystrophy that slowly degenerates the nerves throughout a child's body and ultimately results in death.
Neuroaxonal dystrophy due to lysosomal [alpha]-N-acetyl-galactosaminidase deficiency.
The study demonstrated patients who received COPAXONE([R]) improved in their cerebral neuroaxonal integrity relative to patients treated with placebo.