Journal of the Neurological Sciences

Neurotoxicity of isolated limb perfusion with tumor necrosis factor
pp. 1-4(4)
Authors: Drory V.E.; Lev D.; Groozman G.B.; Gutmann M.; Klausner J.M.

Decade of the brain: neurological advances
pp. 5-14(10)
Author: Walton of Detchant L.

Lack of specific association of presenilin 1 (PS-1) protein with plaques and tangles in Alzheimer's disease
pp. 15-23(9)
Authors: Xia M.-Q.; Berezovska O.; Kim T.-W.; Xia W.-M.; Liao A.; Tanzi R.E.; Selkoe D.; Hyman B.T.

Mitochondrial function, GSH and iron in neurodegeneration and Lewy body diseases
pp. 24-29(6)
Authors: Gu M.; Owen A.D.; Toffa S.E.K.; Cooper J.M.; Dexter D.T.; Jenner P.; Marsden C.D.; Schapira A.H.V.

Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): Clinical and neuropathological features of a Japanese family
pp. 30-37(8)
Authors: Sekijima Y.; Ohara S.; Nakagawa S.; Tabata K.; Yoshida K.; Ishigame H.; Shimizu Y.; Yanagisawa N.

Genetic polymorphism and Parkinson's disease in Taiwan: Study of debrisoquine 4-hydroxylase (CYP2D6)
pp. 38-42(5)
Authors: Lo H.-S.; Chen C.-H.; Hogan E.L.; Kao K.-P.; Wang V.; Yan S.-H.

Molecular analysis of the SMN and NAIP genes in Saudi spinal muscular atrophy patients
pp. 43-46(4)
Authors: Al Rajeh S.; Majumdar R.; Awada A.; Adeyokunnu A.; Al Jumah M.; Al Bunyan M.; Snellen A.

Copper, iron and zinc in Alzheimer's disease senile plaques
pp. 47-52(6)
Authors: Lovell M.A.; Robertson J.D.; Teesdale W.J.; Campbell J.L.; Markesbery W.R.

Transglutaminase activity in serum and cerebrospinal fluid in sporadic amyotrophic lateral sclerosis: A possible use as an indicator of extent of the motor neuron loss
pp. 53-57(5)
Authors: Fujita K.; Honda M.; Hayashi R.; Ogawa K.; Ando M.; Yamauchi M.; Nagata Y.

Cerebral blood flow and oxygen metabolism before and after a stroke-like episode in patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
pp. 58-64(7)
Authors: Takahashi S.; Tohgi H.; Yonezawa H.; Obara S.; Nagane Y.

Etiological spectrum of symptomatic localization related epilepsies: A study from South India
pp. 65-70(6)
Authors: Murthy J.M.K.; Yangala R.

A comparative study of abnormal prion protein isoforms between Gerstmann-Straussler-Scheinker syndrome and Creutzfeldt-Jakob disease
pp. 71-75(5)
Authors: Furukawa H.; Doh-ura K.; Kikuchi H.; Tateishi J.; Iwaki T.

Centronuclear myopathy: Clinical aspects of ten Brazilian patients with childhood onset
pp. 76-82(7)
Authors: Zanoteli E.; Oliveira A.S.B.; Schmidt B.; Gabbai A.A.

Dopaminergic influences on the P300 abnormality in Parkinson's disease
pp. 83-87(5)
Authors: Sohn Y.H.; Kim G.W.; Huh K.; Kim J.-S.

Different types of cerebellar hypometria associated with a distinct topography of the lesion in cerebellum
pp. 88-95(8)
Authors: Manto M.-U.; Setta F.; Jacquy J.; Godaux E.; Hildebrand J.; Roland H.; Blum S.; Brohee P.

Objective evaluation of fatigue by event-related potentials
pp. 96-100(5)
Authors: Kaseda Y.; Jiang C.; Kurokawa K.; Mimori Y.; Nakamura S.

Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression
pp. 101-105(5)
Authors: Verhagen W.I.M.; Bartels R.H.A.M.; Fransen E.; van Camp G.; Renier W.O.; Grotenhuis J.A.

A case of Kearns-Sayre syndrome showing a constant proportion of deleted mitochondrial DNA in blood cells during 6 years of follow-up
pp. 106-109(4)
Authors: Mohri I.; Taniike M.; Fujimura H.; Matsuoka T.; Inui K.; Nagai T.; Okada S.

No association between apolipoprotein E alleles and olivopontocerebellar atrophy
pp. 110-112(3)
Authors: Toji H.; Kawakami H.; Kawarai T.; Nakayama T.; Komure O.; Kuno S.; Nakamura S.

Rapidly deteriorating polyneuropathy associated with osteosclerotic myeloma responsive to intravenous immunoglobulin and radiotherapy
pp. 113-117(5)
Authors: Benito-Leon J.; Lopez-Ros F.; Rodrguez-Martn F.J.; Madero S.; Ruiz J.