GluckmanPDWilliamsCE. When and why do brain cells die?Developmental Medicine & Child Neurology1992; 34: 1010–1014
2.
SarnatHBSarnatMS. Neonatal encephalopathy following fetal distress. A clinical and electroencephalographic study. Archives of Neurology1976; 33: 696–705
3.
LeveneMIGrindulisHSandsCMooreJR. Comparison of two methods of predicting outcome in perinatal asphyxia. Lancet1986; i: 67–69
4.
WyattJSEdwardsADAzzopardiDReynoldsEOR. Magnetic resonance and near infrared spectroscopy for the investigation of perinatal hypoxic-ischaemic brain injury. Archives of Diseases of Childhood1989; 64: 953–963
5.
AzzopardiDWyattJSCadyEB. Prognosis of newborn infants with hypoxic-ischaemic brain injury assessed by phosphorus magnetic resonance spectroscopy. Pediatric Research1989; 25: 445–451
6.
RothSCEdwardsADCadyEB. Relation between cerebral oxidative metabolism following birth asphyxia and neurodevelopmental outcome at one year. Developmental Medicine & Child Neurology1992; 34: 285–295
7.
GroenendaalFVeenhovenRHvan der GrondJJansenGHWitkampTDde VriesLS. Cerebral lactate and N-acetyl aspartate/choline ratios in asphyxiated full-term neonates demonstrated in vivo using proton magnetic resonance spectroscopy. Pediatric Research1994; 35: 148–151
8.
PedenCJRutherfordMASargentoniJCoxIJBryantDJDubowitzLM. Proton spectroscopy of the neonatal brain following hypoxic-ischaemic injury. Developmental Medicine & Child Neurology1993; 35: 502–510
9.
LorekATakeiYCadyEB. Delayed cerebral energy failure following acute hypoxia-ischaemia in the newborn piglet: Continuous 48-hour studies by phosphorus magnetic resonance spectroscopy. Pediatric Research1994; 36: 699–706
10.
MehmetHYueXSquierMV. Increased apoptosis in the cingulate sulcus of newborn piglets following transient hypoxia-ischaemia is related to the degree of high energy phosphate depletion during the insult. Neuroscience Letters1994; 181: 121–125
11.
WyattJS. Near infrared spectroscopy: Investigation of perinatal brain injury. Biology of the Neonate1992; 62: 290–294
12.
EdwardsADWyattJSRichardsonECDelpyDTCopeMReynoldsEOR. Cotside measurement of cerebral blood flow in ill newborn infants by near infrared spectroscopy. Lancet1988; ii: 701–702
13.
WyattJSCopeMDelpyDTRichardsonCEEdwardsADWraySReynoldsEOR. Quantitation of cerebral blood volume in newborn human infants by near infrared spectroscopy. Journal of Applied Physiology1990; 68: 1086–1091
14.
WyattJS. Near infrared spectroscopy in asphyxial brain injury. Clinics in Perinatology1993; 20: 369–378
15.
PeeblesDMWyattJS. Near infrared spectroscopy and intrapartum fetal monitoring. Contemporary Reviews in Obstetrics & Gynaecology1993; 5: 124–129
16.
PeeblesDMEdwardsADWyattJSBishopAPCopeMDelpyDTReynoldsEOR. Changes in human fetal cerebral hemoglobin concentration and oxygenation during labor measured by near infrared spectroscopy. American Journal of Obstetrics and Gynaecology1992; 166: 1369–1373
17.
AldrichCAD'AntonaDSpencerJADWyattJS. Near infrared spectroscopy used in the assessment of intrapartum fetal cerebral oxygenation. Contemporary Reviews in Obstetrics & Gynaecology1995; 7: 71–76
18.
AldrichCJD'AntonaDWyattJSSpencerJADPeeblesDMReynoldsEOR. Fetal cerebral oxygenation measured by near infrared spectroscopy shortly before birth and acid-base status at birth. Obstetrics & Gynecology1994; 84: 861–866
19.
AldrichCJD'AntonaDSpencerJADWyattJSPeeblesDMDelpyDTReynoldsEOR. Late fetal heart rate decelerations and changes in cerebral oxygenation measured by near infrared spectroscopy during the first stage of labour. British Journal of Obstetrics & Gynaecology1995; 102: 9–13