Second edition

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Price BH, Gurvit H, Weintraud S et al. Neuropsychological patterns
and language deficits in 20 consecutive cases of autopsyconfirmed
Alzheimer’s disease. Arch Neurol 1993; 50:931–7.
Przelomski MM, O’Rourke E, Grady GF et al. Eastern equine
encephalitis in Massachusetts. Neurology 1988; 38:736–9.
Quinette P, Guillery-Giraud B, Dayan J et al. What does transient
global amnesia really mean? Review of the literature and
thorough study of 142 cases. Brain 2006; 129:1640–58.
Qunitanilla J. Psychosis due to quinidine intoxication. Am J
Psychiatry 1957; 113:1031–2.
Rabins PV, Folstein MF. Delirium and dementia: diagnostic criteria
and fatality rates. Br J Psychiatry 1982; 140:149–53.
Rabins PV, Merchant A, Nestadt G. Criteria for diagnosing
reversible dementia caused by depression: validation by 2-year
follow-up. Br J Psychiatry 1984; 144:488–92.
Rao V, Lyketsos C. Neuropsychiatric sequelae of traumatic brain
injury. Psychosomatics 2000; 41:95–103.
Rashiq S, Briewa L, Mooney M et al. Distinguishing acyclovir
neurotoxicity from encephalomyelitis. J Intern Med 1993;
234:507–11.
Raskin NH, Fishman RA. Neurologic disorders in renal failure. N
Engl J Med 1976; 294:143–8.
Raskin NH, Bredesen D, Ehrenfeld WK et al. Periodic confusion
caused by congenital extrahepatic portocaval shunt.
Neurology 1984; 34:666–9.
Ratcliffe SG, Bancroft J, Axworthy D et al. Klinefelter’s syndrome
in adolescents. Arch Dis Child 1982; 57:6–12.
Rathmell TK, Burns MA. The Laurence–Moon–Biedl syndrome
occurring in a brother and a sister. Arch Neurol Psychiatry
1938; 39:1033–42.
Rauschka H, Colsch B, Baumann N et al. Late-onset
metachromatic leukodystrophy. Genotype strongly influences
phenotype. Neurology 2006; 67:859–63.
Read AE, Laidlaw J, Sherlock S. Neuropsychiatric complications of
portocaval anastamosis. Lancet 1961; 1:961–4.
Reding M, Haycox J, Blass J. Depression in patients referred to a
dementia clinic: a three-year prospective study. Arch Neurol
1985; 42:894–6.
Reed D, Crawley J, Faro SN et al. Thallotoxicosis. J Am Med Assoc
1963; 183:516–22.
Reichenberg A, Yirmiya R, Schuld A et al. Cytokine-associated
emotional and cognitive disturbances in humans. Arch Gen
Psychiatry 2001; 58:445–52.
Reider-Grosswasser I, Bornstein N. CT and MRI in late-onset
metachromatic leukodystrophy. Acta Neurol Scand 1987;
75:64–9.
Rennick PM, Perez-Borja C, Rodin EA. Transient mental deficits
associated with recurrent prolonged epileptic clouded state.
Epilepsia 1969; 10:397–405.
Revesz T, Hawkins CP, du Boulay EPGH et al. Pathological findings
correlated with magnetic resonance imaging in subcortical
arteriosclerotic encephalopathy (Binswanger’s disease). J
Neurol Neurosurg Psychiatry 1989; 52:1337–44.
Reynolds EH, Rothfeld P, Pincus JH. Neurological disease
associated with folate deficiency. BMJ 1973; 2:398–400.
Richardson EP. Progressive multifocal leukencephalopathy. N Engl
J Med 1961; 265:815–23.
References 203
Richardson JC, Chambers RA, Heywood PM. Encephalopathies of
anoxia and hypoxemia. Arch Neurol 1959; 1:178–90.
Richter RW, Shimojyo S. Neurologic sequelae of Japanese B
encephalitis. Neurology 1961; 1:553–9.
Riley DE, Lang AE, Lewis A et al. Cortical-basal ganglionic
degeneration. Neurology 1990; 40:1203–12.
Rinne JO, Lee MS, Thompson PD et al. Corticobasal degeneration:
a clinical study of 36 cases. Brain 1994; 117:1183–96.
Ristic AJ, Vojvodic N, Jankovic S et al. The frequency of reversible
parkinsonism and cognitive decline associated with valproate
treatment: a study of 364 patients with different types of
epilepsy. Epilepsia 2006; 47:2183–5.
Robbins TW, James M, Lance TW et al. Cognitive performance in
multiple system atrophy. Brain 1992; 115:271–91.
Robertson EE. Progressive bulbar paralysis showing heredofamilial
incidence and intellectual impairment. Arch Neurol Psychiatry
1953; 69:197–207.
Robinson WP, Bottani A, Yagang X. Molecular, cytogenetic, and
clinical investigations of Prader–Willi syndrome patients. Am J
Hum Genet 1992; 49:1219–34.
Rodriguez ME, Artieda J, Zubieta JL et al. Reflex myoclonus in
olivopontocerebellar atrophy. J Neurol Neurosurg Psychiatry
1994; 57:316–19.
Romanul FCA, Radvany J, Rosales RK. Whipple’s disease confined
to the brain: a case confirmed clinically and pathologically. J
Neurol Neurosurg Psychiatry 1977; 40:901–9.
Roos R, Cajdusek DC, Gibbs CJ. The clinical characteristics of
transmissible Creutzfeldt–Jakob disease. Brain 1973; 96:1–20.
Rosa A, Demiati M, Cartz L et al. Marchiafava–Bignami disease,
syndrome of interhemispheric disconnection, and right handed
agraphia in a left-hander. Arch Neurol 1991; 48:986–8.
Rose FC, Symonds CP. Persistent memory defect following
encephalitis. Brain 1960; 83:195–212.
Rosebush P, Stewart T. A prognostic analysis of 24 episodes of
neuroleptic malignant syndrome. Am J Psychiatry 1989;
146:717–25.
Rosenbaum M, Lewis M, Piker P et al. Convulsive seizures in
delirium tremens. Arch Neurol Psychiatry 1941; 45:486–93.
Rosenberg NL, Kleineschmidt-DeMasters BK, Davis KA et al.
Toluene abuse causes diffuse central nervous system white
matter changes. Ann Neurol 1988; 23:611–14.
Rosman NP, Pearce J. The brain in multiple neurofibromatosis
(Von Recklinghausen’s disease): a suggested neuropathological
basis for the associated mental defect. Brain 1967;
90:829–37.
Ross AT, Dickerson WW. Tuberous sclerosis. Arch Neurol Psychiatry
1943; 50:233–57.
Roth A. Familial eunuchoidism: the Laurence–Moon–Biedl
syndrome. J Urol 1947; 57:427–42.
Roy-Byrne PR, Weingartner H, Bierer LM et al. Effortful and
automatic cognitive processes in depression. Arch Gen
Psychiatry 1986; 43:265–7.
Rozdilsky B, Cummings JN, Huston AF. Hallervorden–Spatz
disease: late infantile and adult types, report of two cases.
Acta Neuropathol 1968; 10:1–16.
Rubinstein LJ, Urich H. Meningo-encephalitis of Behçet’s disease:
case report with pathological findings. Brain 1963; 86:151–60.