Table of contents

Research Article

• Hereditary deficiency of ferroxidase (aka caeruloplasmin) (1 November, 1996)

  J I Logan
• Epidemiology of the epilepsies. (1 November, 1996)

  J W Sander, S D Shorvon
• Arachnoid cyst of the middle crania fossa, disclosed by bleeding. (1 November, 1996)

  A De Recondo, S Merran
• Transcranial Doppler ultrasonography in the detection of venous to arterial shunting in acute stroke and transient ischaemic attacks. (1 November, 1996)

  M Yeung, K A Khan, A Shuaib
• Prevalence and correlates of neuropsychological deficits in amyotrophic lateral sclerosis. (1 November, 1996)

  P J Massman, J Sims, N Cooke, L J Haverkamp, V Appel, S H Appel
• Acute lumbosacral polyradiculopathy due to cytomegalovirus in advanced HIV disease: CSF findings in 17 patients. (1 November, 1996)

  R F Miller, J D Fox, P Thomas, J C Waite, Y Sharvell, B G Gazzard, M J Harrison, N S Brink
• Paravertebral muscles in disease of the cervical spine. (1 November, 1996)

  S B Wharton, K K Chan, J D Pickard, J R Anderson
• Thomas Sydenham (1624-89). (1 November, 1996)

  L F Haas
• Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation. (1 November, 1996)

  L Schöls, G Amoiridis, J T Epplen, M Langkafel, H Przuntek, O Riess
• Electroclinical features of idiopathic generalised epilepsy with persisting absences in adult life. (1 November, 1996)

  R Michelucci, G Rubboli, D Passarelli, P Riguzzi, L Volpi, L Parmeggiani, R Rizzi, E Gardella, C A Tassinari
• Cognitive impairment after acute encephalitis: comparison of herpes simplex and other aetiologies. (1 November, 1996)

  L Hokkanen, E Poutiainen, L Valanne, O Salonen, M Iivanainen, J Launes
• Two domains of anosognosia in Alzheimer's disease. (1 November, 1996)

  S E Starkstein, L Sabe, E Chemerinski, L Jason, R Leiguarda
• Piecemeal deglutition and dysphagia limit in normal subjects and in patients with swallowing disorders. (1 November, 1996)

  C Ertekin, I Aydoğdu, N Yüceyar
• Three cases of symptom change in Tourette's syndrome and obsessive-compulsive disorder associated with paediatric cerebral malignancies. (1 November, 1996)

  B S Peterson, R A Bronen, C C Duncan
• Hereditary caeruloplasmin deficiency: clinicopathological study of a patient. (1 November, 1996)

  T Kawanami, T Kato, M Daimon, M Tominaga, H Sasaki, K Maeda, S Arai, Y Shikama, T Katagiri
• Increased writing activity in neurological conditions: a review and clinical study. (1 November, 1996)

  P van Vugt, P Paquier, L Kees, P Cras
• Interferon-gamma activated calcium influx in peripheral blood lymphocytes from patients with primary and secondary progressive multiple sclerosis. (1 November, 1996)

  G Martino, E Brambilla, M Filippi, V Martinelli, B Colombo, M Rodegher, G Comi, L M Grimaldi
• The CYP2D6B allele is not overrepresented in a population of German patients with idiopathic Parkinson's disease. (1 November, 1996)

  T Gasser, B Müller-Myhsok, A Supala, E Zimmer, G Wieditz, Z K Wszolek, P Vieregge, V Bonifati, W H Oertel
• The Marcus Gunn pupil. (1 November, 1996)

  J Pearce
• Local application of antimycotics in mucormycosis cerebri: a case report. (1 November, 1996)

  I Mohsenipour, M Schirmer, R Frank, F Geisen, E Semenitz, D zur Nedden, G Konwalinka
• Atypical dopa responsive parkinsonism in a patient with megalencephaly, midbrain Lewy body disease, and some pathological features of Hallervorden-Spatz disease. (1 November, 1996)

  P J Tuite, J P Provias, A E Lang
• Alexia without agraphia in multiple sclerosis. (1 November, 1996)

  C F Dogulu, T Kansu, R Karabudak
• Urinary retention in bilateral pontine tumour: evidence for a pontine micturition centre in humans. (1 November, 1996)

  G Manente, D Melchionda, A Uncini
• Chronic inflammatory demyelinating polyneuropathy with multifocal CNS demyelination in an Afrid. (1 November, 1996)

  P K Thomas, A Valentine, B D Youl
• Neurothekeoma of the cauda equina. (1 November, 1996)

  G F Kaar, S H Bashir, J M N'Dow, P V Best, L N Gomersall
• Voluntary facial palsy with a pontine lesion. (1 November, 1996)

  M Trepel, M Weller, J Dichgans, D Petersen
• Brainstem involvement in Leber's hereditary optic neuropathy: association with the 14,484 mitochondrial DNA mutation. (1 November, 1996)

  B Funalot, D Ranoux, J L Mas, C Garcia, J P Bonnefont
• Pure sensory deficit with crossed orocrural topography after pontine haemorrhage. (1 November, 1996)

  O Combarros, J Berciano, A Oterino
• Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A. (1 November, 1996)

  F Chapon, P Diraison, B Lechevalier, G Chazot, F Viader, C Bonnebouche, A Vandenberghe, V Timmerman, C Van Broeckhoven, A Vandenberghe