Traumatic white matter injury and toxic leukoencephalopathies

References

• Waller A. Experiments on the section of glossopharyngeal and hypoglossal nerves of the frog and observations of the alternatives produced thereby in the structure of their primitive fibres. Philos. Trans. R. Soc. Lond. B Biol. Sci.140, 423–429 (1850).
   Google Scholar
• Serbest G, Burkhardt MF, Siman R, Raghupathi R, Saatman KE. Temporal profiles of cytoskeletal protein loss following traumatic axonal injury in mice. Neurochemic Res.32, 2006–2014 (2007).
   Google Scholar
• Shea TB, Chan WK. Regulation of neurofilament dynamics by phosphorylation. Eur. J. Neurosci.27, 1893–1901 (2008).
   Google Scholar
• Barry DM, Millecamps S, Julien JP, Garcia ML. New movements in neurofilament transport, turnover and disease. Exp. Cell Res.313, 2110–2120 (2007).
   PubMed Web of Science ®Google Scholar
• Al-Chalabi A, Miller CC. Neurofilaments and neurological disease. BioEssays25, 346–355 (2003).
   PubMed Web of Science ®Google Scholar
• Petzold A. Neurofilament phosphoforms: surrogate markers for axonal injury, degeneration and loss. J. Neurol. Sci.33, 183–198 (2005).
   Google Scholar
• Liu Q, Xie F, Siedlak SL et al. Neurofilament proteins in neurodegenerative diseases. Cell Mol. Life Sci.61, 3057–3075 (2004).
   PubMedGoogle Scholar
• Wang L, Ho C, Sun D et al. Rapid movement of axonal neurofilaments interrupted by prolonged pauses. Nat. Cell Biol.2, 137–141 (2000).
   PubMed Web of Science ®Google Scholar
• Perrot R, Berges R, Bocquet A, Eyer J. Review of the multiple aspects of neurofilament functions, and their possible contribution to neurodegeneration. Mol. Neurobiol.38, 27–65 (2008).
   PubMed Web of Science ®Google Scholar
• Nguyen MD, Lariviere RC, Julien JP. Deregulation of Cdk5 in a mouse model of ALS: toxicity alleviated by perikaryal neurofilament inclusions. Neuron30, 135–147 (2001).
   PubMed Web of Science ®Google Scholar
• De Waegh SM, Lee VM, Brady ST. Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells. Cell68, 451–463 (1992).
   PubMed Web of Science ®Google Scholar
• Grant P, Pant HC. Neurofilament protein synthesis and phosphorylation. J. Neurocytology29, 843–872 (2000).
   Google Scholar
• Strong MJ, Strong WL, Jaffe H, Traggert B, Sopper MM, Pant HC. Phosphorylation state of the native high-molecular-weight neurofilament subunit protein from cervical spinal cord in sporadic amyotrophic lateral sclerosis. J. Neurochem.76, 1315–1325 (2001).
   PubMed Web of Science ®Google Scholar
• Betts JC, Blackstock WP, Ward MA, Anderton BH. Identification of phosphorylation sites on neurofilament proteins by nanoelectrospray mass spectrometry. J. Biol. Chem.272, 12922–12927 (1997).
   Google Scholar
• Guan RJ, Khatra BS, Cohlberg JA. Phosphorylation of bovine neurofilament proteins by protein kinase FA (glycogen synthase kinase 3). J. Biol. Chem.266, 8262–8267 (1991).
   Google Scholar
• Guidato S, Tsai LH, Woodgett J, Miller CC. Differential cellular phosphorylation of neurofilament heavy side-arms by glycogen synthase kinase-3 and cyclin-dependent kinase-5. J. Neurochem.66, 1698–1706 (1996).
   Google Scholar
• Roder HM, Hoffman FJ, Schroder W. Phosphatase resistance of ERK2 brain kinase PK40erk2. J. Neurochem.64, 2203–2212 (1995).
   Google Scholar
• Roder HM, Ingram VM. Two novel kinases phosphorylate tau and the KSP site of heavy neurofilament subunits in high stoichiometric ratios. J. Neurosci.11, 3325–3343 (1991).
   PubMedGoogle Scholar
• Shetty KT, Link WT, Pant HC. cdc2-like kinase from rat spinal cord specifically phosphorylates KSPXK motifs in neurofilament proteins: isolation and characterization. Proc. Natl Acad. Sci. USA90, 6844–6848 (1993).
   PubMed Web of Science ®Google Scholar
• Sihag RK, Nixon RA. Identification of Ser-55 as a major protein kinase A phosphorylation site on the 70-kDa subunit of neurofilaments. Early turnover during axonal transport. J. Biol. Chem.266, 18861–18867 (1991).
   Google Scholar
• Zhulina EB, Leermakers FA. The polymer brush model of neurofilament projections: effect of protein composition. Biophys. J.98, 462–469 (2010).
   Google Scholar
• Chang R, Kwak Y, Gebremichael Y. Structural properties of neurofilament sidearms: sequence-based modeling of neurofilament architecture. J. Mol. Biol.391, 648–660 (2009).
   Google Scholar
• Saatman KE, Graham DI, McIntosh TK. The neuronal cytoskeleton is at risk after mild and moderate brain injury. J. Neurotrauma15, 1047–1058 (1998).
   PubMed Web of Science ®Google Scholar
• Yaghmai A, Povlishock J. Traumatically induced reactive change as visualized through the use of monoclonal antibodies targeted to neurofilament subunits. J. Neuropathol. Exp. Neurol.51, 158–176 (1992).
   PubMed Web of Science ®Google Scholar
• Saatman KE, Abai B, Grosvenor A, Vorwerk CK, Smith DH, Meaney DF. Traumatic axonal injury results in biphasic calpain activation and retrograde transport impairment in mice. J. Cerebral Blood Flow Metab.23, 34–42 (2003).
   PubMedGoogle Scholar
• McCracken E, Hunter AJ, Patel S, Graham DI, Dewar D. Calpain activation and cytoskeletal protein breakdown in the corpus callosum of head-injured patients. J. Neurotrauma16, 749–761 (1999).
   PubMedGoogle Scholar
• Maxwell WL, Domleo A, McColl G, Jafari SS, Graham DI. Post-acute alterations in the axonal cytoskeleton after traumatic axonal injury. J. Neurotrauma20, 151–168 (2003).
   PubMed Web of Science ®Google Scholar
• Schirmer L, Antel JP, Brück W, Stadelmann C. Axonal loss and neurofilament phosphorylation changes accompany lesion development and clinical progression in multiple sclerosis. Brain Pathol.21, 428–440 (2011)
   PubMed Web of Science ®Google Scholar
• Gennarelli TA, Thibault LE, Adams JH, Graham DI, Thompson CJ, Marcincin RP. Diffuse axonal injury and traumatic coma in the primate. Ann. Neurol.12, 564–574 (1982).
   PubMed Web of Science ®Google Scholar
• Graham DI, Adams JH, Murray LS, Jennett B. Neuropathology of the vegetative state after head injury. Neuropsychol. Rehab.15, 198–213 (2005).
   PubMed Web of Science ®Google Scholar
• Geddes JF, Whitwell HL, Graham DI. Traumatic axonal injury: practical issues for diagnosis in medicolegal cases. Neuropathol. Applied Neurobiol.26, 105–116 (2000).
   PubMed Web of Science ®Google Scholar
• Strich SJ. Diffuse degeneration of the cerebral white matter in severe dementia following head injury. J. Neurol. Neurosurg. Psychiatry19, 163–185 (1956).
   PubMed Web of Science ®Google Scholar
• Maxwell WL, Povlishock JT, Graham DI. A mechanistic analysis of nondisruptive axonal injury: a review. J. Neurotrauma14, 419–440 (1997).
   PubMed Web of Science ®Google Scholar
• Maas AI, Marmarou A, Murray GD, Steyerberg EW. Clinical trials in traumatic brain injury: current problems and future solutions. Acta Neurochir. Suppl.89, 113–118 (2004).
   Google Scholar
• Friess SH, Ichord RN, Owens K et al. Neurobehavioral functional deficits following closed head injury in the neonatal pig. Exp. Neurol.204, 234–243 (2007).
   PubMed Web of Science ®Google Scholar
• Duhaime AC, Margulies SS, Durham SR et al. Maturation-dependent response of the piglet brain to scaled cortical impact. J. Neurosurg.93, 455–462 (2000).
   PubMed Web of Science ®Google Scholar
• Arbogast K, Margulies S. A fiber-reinforced composite model of the viscoelastic behaviour of the brainstem in shear. J. Biomechanics32, 865–870 (1999).
   PubMed Web of Science ®Google Scholar
• Eucker SA, Smith C, Ralston J, Friess SH, Margulies SS. Physiological and histopathological responses following closed rotational head injury depend on direction of head motion. Exp. Neurol.227, 79–88 (2011).
   Google Scholar
• Friess SH, Ichord RN, Ralston J et al. Repeated traumatic brain injury affects composite cognitive function in piglets. J. Neurotrauma26, 1111–1121 (2009).
   PubMed Web of Science ®Google Scholar
• Gennarelli TA, Thibault LE, Tipperman R et al. Axonal injury in the optic nerve: a model simulating diffuse axonal injury in the brain. J. Neurosurg.71, 244–253 (1989).
   PubMed Web of Science ®Google Scholar
• Mohammed Sulaiman A, Denman N, Buchanan S et al. Stereology and ultrastructure of chronic phase axonal and cell soma pathology in stretch-injured central nerve fibers. J. Neurotrauma28, 383–400 (2011).
   Google Scholar
• Farkas O, Povlishock JT. Cellular and subcellular change evoked by diffuse traumatic brain injury: a complex web of change extending far beyond focal damage. Prog. Brain Research161, 43–59 (2007).
   PubMed Web of Science ®Google Scholar
• Maxwell WL, Watts C, Graham DI, Gennarelli TA. Ultrastructural evidence of axonal shearing as a result of lateral acceleration of the head in non-human primates. Acta Neuropathol.86, 136–144 (1993).
   PubMed Web of Science ®Google Scholar
• Povlishock JT, Becker DP, Cheng DLY, Vaughan GW. Axonal change in minor head injury. J. Neuropathol. Exp. Neurol.42, 225–242 (1983).
   PubMed Web of Science ®Google Scholar
• Povlishock JT, Christman CW. The pathobiology of traumatically induced axonal injury in animals and humans: a review of current thoughts. J. Neurotrauma12, 555–564 (1995).
   PubMed Web of Science ®Google Scholar
• Maxwell WL, Irvine A, Graham et al. Focal axonal injury: the early axonal response to stretch. J. Neurocytol.20, 157–164 (1991).
   Google Scholar
• Wolf JA, Stys PK, Lusardi T, Meaney D, Smith DH. Traumatic axonal injury induces calcium influx modulated by tetrodotoxin-sensitive sodium channels. J. Neurosci.21, 1923–1930 (2001).
   PubMed Web of Science ®Google Scholar
• Stirling DP, Stys PK. Mechanisms of axonal injury: internodal nanocomplexes and calcium deregulation. Trends Mol. Med.16, 160–170 (2010).
   Google Scholar
• Staal JA, Dickson TC, Gasperini R, Liu Y, Foa L, Vickers JC. Initial calcium release from intracellular stores followed by calcium dysregulation is linked to secondary axotomy following transient axonal stretch injury. J. Neurochem.112, 1147–1155 (2010).
   Google Scholar
• Maxwell WL, Graham DI. Loss of axonal microtubules and neurofilaments after stretch-injury to guinea pig optic nerve fibers. J. Neurotrauma14, 603–614 (1997).
   PubMed Web of Science ®Google Scholar
• McIntosh TK, Vink R, Noble L et al. Traumatic brain injury in the rat: characterization of a lateral fluid-percussion model. Neuroscience28, 233–244 (1989).
   PubMed Web of Science ®Google Scholar
• Morales DM, Marklund N, Lebold D et al. Experimental models of traumatic brain injury: do we really need to build a better mousetrap? Neuroscience136, 971–989 (2005).
   PubMed Web of Science ®Google Scholar
• Stone JR, Singleton RH, Povlishock JT. Intra-axonal neurofilament compaction does not evoke local axonal swelling in all traumatically injured axons. Exp. Neurol.172, 320–331 (2001).
   PubMed Web of Science ®Google Scholar
• Kelley BJ, Farkas O, Lifshitz J, Povlishock JT. Traumatic axonal injury in the perisomatic domain triggers ultrarapid secondary axotomy and Wallerian degeneration. Exp. Neurol.198, 350–360 (2006).
   PubMed Web of Science ®Google Scholar
• Adams JH, Doyle D, Ford I et al. Diffuse axonal injury in head injury: definition, diagnosis and grading. Histopathology15, 49–59 (1989).
   PubMed Web of Science ®Google Scholar
• Blumbergs PC, Scott G, Manavis J, Wainwright H, Simpson DA, McLean AJ. Staining of amyloid precursor protein to study axonal damage in mild head injury. Lancet344, 1055–1056 (1994).
   PubMed Web of Science ®Google Scholar
• Oppenheimer DR. Microscopic lesions in the brain following head injury. J. Neurol. Neurosurg. Psychiatry31, 299–306 (1968).
   PubMed Web of Science ®Google Scholar
• Shaw NA. The neurophysiology of concussion. Prog. Neurobiol.67, 281–344 (2002).
   PubMed Web of Science ®Google Scholar
• Ommaya AK, Gennarelli TA. Cerebral concussion and traumatic unconsciousness. Correlation of experimental and clinical observations of blunt head injuries. Brain97, 633–654 (1974).
   PubMed Web of Science ®Google Scholar
• Sherriff FE, Bridges LR, Gentleman SM, Sivaloganathan S, Wilson S. Markers of axonal injury in post mortem human brain. Acta Neuropathol.88, 433–439 (1994).
   Google Scholar
• Hortobagyi T, Wise S, Hunt N et al. Traumatic axonal damage in the brain can be detected using β-APP immunohistochemistry within 35 min after head injury to human adults. Neuropathol. Appl. Neurobiol.33, 226–237 (2007).
   PubMed Web of Science ®Google Scholar
• Dolinak D, Smith C, Graham DI. Global hypoxia per se is an unusual cause of axonal injury. Acta Neuropathol.100, 553–560 (2000).
   PubMed Web of Science ®Google Scholar
• Dolinak D, Smith C, Graham DI. Hypoglycaemia is a cause of axonal injury. Neuropathol. Appl. Neurobiol.26, 448–453 (2000).
   Google Scholar
• Reichard RR, Smith C, Graham DI. The significance of β-APP immunoreactivity in forensic practice. Neuropathol. Appl. Neurobiol.31, 304–313 (2005).
   Google Scholar
• Marmarou CR, Walker SA, Davis L, Povlishock JT. Quantitative analysis of the relationship between intra-axonal neurofilament compaction and impaired axonal transport following diffuse traumatic brain injury. J. Neurotrauma22, 1066–1080 (2005).
   PubMed Web of Science ®Google Scholar
• Mac Donald CL, Dikranian K, Bayly P, Holtzman D, Brody D. Diffusion tensor imaging reliably detects experimental traumatic axonal injury and indicates approximate time of injury. J. Neurosci.27, 11869–11876 (2007).
   PubMed Web of Science ®Google Scholar
• Li J, Li XY, Feng DF, Gu L. Quantitative evaluation of microscopic injury with diffusion tensor imaging in a rat model of diffuse axonal injury. Eur. J. Neurosci.33, 933–945 (2011).
   PubMedGoogle Scholar
• Kinnunen KM, Greenwood R, Powell JH et al. White matter damage and cognitive impairment after traumatic brain injury. Brain134, 449–463 (2011).
   PubMed Web of Science ®Google Scholar
• Caeyenberghs K, Leemans A, Coxon J et al. Bimanual Coordination and Corpus Callosum Microstructure in Young Adults with Traumatic Brain Injury: a diffusion tensor imaging study. J. Neurotrauma28, 897–913 (2011).
   Google Scholar
• Beauchamp MH, Ditchfield M, Babl FE et al. Detecting traumatic brain lesions in children: CT versus MRI versus susceptibility weighted imaging (SWI). J. Neurotrauma28, 915–927 (2011).
   PubMed Web of Science ®Google Scholar
• Coleman M. Axon degeneration mechanisms: commonality amid diversity. Nat. Review Neurosci.6, 889–898 (2005).
   PubMed Web of Science ®Google Scholar
• Lunn ER, Perry VH, Brown MC, Rosen H, Gordon S. Absence of Wallerian degeneration does not hinder regeneration in peripheral nerve. Eur. J. Neurosci.1, 27–33 (1989).
   PubMed Web of Science ®Google Scholar
• Ribchester RR, Tsao JW, Barry JA, Asgari-Jirhandeh N, Perry VH, Brown MC. Persistence of neuromuscular junctions after axotomy in mice with slow Wallerian degeneration (C57BL/WldS). Eur. J. Neurosci.7, 1641–1650 (1995).
   Google Scholar
• Coleman MP, Freeman MR. Wallerian degeneration, WLDs, and Nmnat. Annu. Rev. Neurosci.33, 245–267 (2010).
   PubMedGoogle Scholar
• Gilley J, Coleman MP. Endogenous Nmnat2 is an essential survival factor for maintenance of healthy axons. PLoS Biol.8, e1000200 (2010).
   Google Scholar
• Wang J, Zhai Q, Chen Y et al. A local mechanism mediates NAD-dependent protection of axon degeneration. J. Cell Biol.170, 349–355 (2005).
   PubMed Web of Science ®Google Scholar
• Meyer zu Horste G, Miesbach TA, Muller JI et al. The Wlds transgene reduces axon loss in a Charcotx–Marie–Tooth disease 1A rat model and nicotinamide delays post-traumatic axonal degeneration. Neurobiol. Dis.42, 1–8 (2011).
   Google Scholar
• Barrientos SA, Martinez NW, Yoo S et al. Axonal degeneration is mediated by the mitochondrial permeability transition pore. J. Neurosci.31, 966–978 (2011).
   PubMed Web of Science ®Google Scholar
• Sullivan PG, Rabchevsky AG, Hicks RR, Gibson TR, Fletcher-Turner A, Scheff SW. Dose–response curve and optimal dosing regimen of cyclosporin A after traumatic brain injury in rats. Neuroscience101, 289–295 (2000).
   PubMed Web of Science ®Google Scholar
• Kilbaugh TJ, Bhandare S, Lorom DH, Saraswati M, Robertson CL, Margulies SS. Cyclosporin A preserves mitochondrial function after traumatic brain injury in the immature rat and piglet. J. Neurotrauma28(5), 763–774 (2011).
   PubMed Web of Science ®Google Scholar
• Naim MY, Friess S, Smith C et al. Folic acid enhances early functional recovery in a piglet model of pediatric head injury. Dev. Neurosci.32, 466–479 (2010).
   Google Scholar
• Filley CM, Kleinschmidt-DeMasters BK. Toxic leukoencephalopathy. N. Engl. J. Med.345, 425–432 (2001).
   PubMed Web of Science ®Google Scholar
• Buttner A. The neuropathology of drug abuse. Neuropathol. Appl. Neurobiol.37, 118–134 (2011).
   Web of Science ®Google Scholar
• Ryan A, Molloy FM, Farrell MA, Hutchinson M. Fatal toxic leukoencephalopathy: clinical, radiological, and necropsy findings in two patients. J. Neurol. Neurosurg. Psychiatry76, 1014–1016 (2005).
   Web of Science ®Google Scholar
• Kriegstein AR, Shungu DC, Millar WS et al. Leukoencephalopathy and raised brain lactate from heroin vapor inhalation (‘chasing the dragon’) Neurology53, 1765–1773 (1999).
   PubMed Web of Science ®Google Scholar
• Al-Hajri Z, Del Bigio MR. Brain damage in a large cohort of solvent abusers. Acta Neuropathol.119, 435–445 (2010).
   Google Scholar
• Rosenberg NL, Kleinschmidt-DeMasters BK, Davis KA, Dreisbach JN, Hormes JT, Filley CM. Toluene abuse causes diffuse central nervous system white matter changes. Ann. Neurol.23, 611–614 (1988).
   PubMed Web of Science ®Google Scholar
• Yücel M, Takagi M, Walterfang M, Lubman DI. Toluene misuse and long-term harms: a systematic review of the neuropsychological and neuroimaging literature. Neurosci. Biobehav. Rev.32, 910–926 (2008).
   PubMed Web of Science ®Google Scholar
• Soussain C, Ricard D, Fike JR, Mazeron JJ, Psimaras D, Delattre JY. CNS complications of radiotherapy and chemotherapy Lancet374, 1639–1651 (2009).
   PubMed Web of Science ®Google Scholar
• Han CH, Findlay MP. Chemotherapy-induced reversible posterior leucoencephalopathy syndrome. Intern. Med. J.40, 153–159 (2010).
   PubMed Web of Science ®Google Scholar
• Rubinstein LJ, Herman MM, Long TF, Wilbur JR. Disseminated necrotizing leukoencephalopathy: a complication of treated central nervous system leukemia and lymphoma. Cancer35, 291–305 (1975).
   PubMed Web of Science ®Google Scholar
• Matsubayashi J, Tsuchiya K, Matsunaga T, Mukai K. Methotrexate-related leukoencephalopathy without radiation therapy: distribution of brain lesions and pathological heterogeneity on two autopsy cases. Neuropathology29, 105–115 (2010).
   Google Scholar
• Moore-Maxwell CA, Datto MB, Hulette CM. Chemotherapy-induced toxic leukoencephalopathy causes a wide range of symptoms: a series of four autopsies. Mod. Pathol.17, 241–247 (2004).
   Google Scholar
• Filley CM. Toxic leukoencephalopathy. Clin. Neuropharmacol.22, 249–260 (1999).
   Google Scholar
• Schultheiss TE, Kun LE, Ang KK, Stephens LC. Radiation response of the central nervous system. Int. J. Radiat. Oncol. Biol. Phys.31, 1093–1112 (1995).
   PubMed Web of Science ®Google Scholar
• Burger P, Mahaley MS Jr, Dudka L. The morphologic effects of radiation administered therapeutically for intracranial gliomas. Cancer44, 1256–1272 (1979).
   PubMed Web of Science ®Google Scholar
• Yoneoka Y, Satoh M, Akiyama K, Sano K, Fujii Y, Tanaka R. An experimental study of radiation-induced cognitive dysfunction in an adult rat model. Br. J. Radiol.72, 1196–1201 (1999).
   PubMed Web of Science ®Google Scholar
• Panagiotakos G, Alshamy G, Chan B et al. Long-term impact of radiation on the stem cell and oligodendrocyte precursors in the brain. PLoS One2, e588 (2007).
   PubMed Web of Science ®Google Scholar
• Peña LA, Fuks Z, Kolesnick RN. Radiation-induced apoptosis of endothelial cells in the murine central nervous system: protection by fibroblast growth factor and sphingomyelinase deficiency. Cancer Res.60, 321–327 (2000).
   PubMed Web of Science ®Google Scholar
• Ginsberg MD, Myers RE, McDonagh BF. Experimental carbon monoxide encephalopathy in the primate. II. Clinical aspects, neuropathology, and physiologic correlation. Arch. Neurol.30, 201–216 (1974).
   Google Scholar
• Weaver LK. Carbon monoxide poisoning. N. Engl. J. Med.360, 1217–1225 (2009).
   PubMed Web of Science ®Google Scholar
• Alonso JR, Cardellach F, Lopez S, Casademont J, Miro O. Carbon monoxide specifically inhibits cytochrome c oxidase of human mitochondrial respiratory chain. Pharmacol. Toxicol.93, 142–146 (2003).
   PubMedGoogle Scholar
• Piantadosi CA, Zhang J, Levin ED, Folz RJ, Schmechel DE. Apoptosis and delayed neuronal damage after carbon monoxide poisoning in the rat. Exp. Neurol.147, 103–114 (1997).
   PubMed Web of Science ®Google Scholar
• Okeda R, Song S-Y, Funta N, Higashino F. An experimental study of the pathogenesis of Grinker’s myelinopathy in carbon monoxide intoxication. Acta Neuropathol.59, 200–206 (1983).
   Google Scholar
• Thom SR. Carbon monoxide pathophysiology and treatment. In: Physiology and Medicine of Hyperbaric Oxygen Therapy. Neuman TS, Thom SR (Eds). Saunders Elsevier, PA, USA, 321–347 (2008).
   Google Scholar
• Thom SR, Taber RL, Mendiguren II, Clark JM, Hardy KR, Fisher AB. Delayed neuropsychologic sequelae following carbon monoxide poisoning: prevention by treatment with hyperbaric oxygen. Ann. Emerg. Med.25, 474–480 (1995).
   PubMed Web of Science ®Google Scholar
• Weaver LK, Hopkins RO, Chan KJ et al. Hyperbaric oxygen for acute carbon monoxide poisoning. N. Engl. J. Med.347, 1057–1067 (2002).
   PubMed Web of Science ®Google Scholar
• Thom SR. Antagonism of carbon monoxide-mediated brain lipid per- oxidation by hyperbaric oxygen. Toxicol. Appl. Pharmacol.105, 340–344 (1990).
   PubMed Web of Science ®Google Scholar
• Hopkins RO, Weaver LK, Valentine KJ, Mower C, Churchill S, Carlquist J. Apolipoprotein E genotype and response of carbon monoxide poisoning to hyperbaric oxygen treatment. Am. J. Respir. Crit. Care Med.176, 1001–1006 (2007).
   PubMedGoogle Scholar