Journal of the Neurological Sciences 1997: Vol 151 Index

7 Pages·1997·2 MB·English

JOURNOAF LTH E
NEUROLOGICAL
SCIENCES
Journal of Neurological Sciences 151 (1997) 235-237
Author Index Volume 151
Abe, K., see Hayashi, T. (151) 107 Hamada, T., see Matsuura, T. (151) 65
Adelmann, M., see Dotsch, J. (151) 185 Hamano, T., see Hirayama, M. (151) 23
Aikawa, Y., see Kojima, T. (151) 141 Hinze, J., see Détsch, J. (151) 185
Aita, T., see Hirayama, M. (151) 23 Hara, H., see Yamamoto, A. (151) 121
Al Bunyan, M., see Al-Zahraa Omar, F. (151) 213 Harkness, W., see Harris, C.M. (151) 111
Al-Zahraa Omar, F. and Al Bunyan, M. Harris, C.M., Boyd, S., Chong, K., Harkness, W. and Neville, B.G.R.
Severe hyponatremia as poor prognostic factor in childhood Epileptic nystagmus in infancy (151) 111
neurologic diseases (151) 213 Hartard, C., see Wicklein, E.M. (151) 227
Antia, N.H., see Singh, N. (151) 13 Hayashi, M., see Waragai, M. (151) 93
Arimura, K., see Yamano, Y. (151) 163 Hayashi, T., Onodera, J., Mochizuki, H., Onodera, H., Abe, K. and
Itoyama, Y.
Baur, X., see Sindern, E. (151) 29 Primary central nervous system leukemia with a novel
Bianco, N., see Roche, P.-H. (151) 127 chromosomal translocation (151) 107
Birdi, T.J., see Singh, N. (151) 13 Hildebrand, J., see Manto, M. (151) 169
Blum, W.F., see Détsch,-J. (151) 185 Hildebrand, J., see van Blercom, N. (151) 71
Blumenfeld, A., see Korn-Lubetzki, I. (151) 57 Hirayama, M., Hamano, T., Shiratori, M., Mutoh, T., Kumano, T.,
Boyd, S., see Harris, C.M. (151) 111 Aita, T. and Kuriyama, M.
Brooks, D.J., see Jenkins, I.H. (151) 195 Chorea-acanthocytosis with polyclonal antibodies to ganglioside
GMI (151) 23
Chandrashekar, S., see Singh, N. (151) 13
Chiba, S., see Tachi, N. (151) 25 Ijichi, S., see Yamano, Y. (151) 163
Choksi, R., see Lopate, G. (151) 189 Inoue, K., see Kaida, K.-i. (151) 103
Chong, K., see Harris, C.M. (151) 111 Ishida, K., Kaneko, K., Kubota, T., Itoh, Y., Miyatake, T., Matsushita,
Collan, Y., see Ma, S.Y. (151) 83 M. and Yamada, M.
Comi, G., see Filippi, M. (151) 79 Identification and characterization of an anti-glial fibrillary acidic
protein antibody with a unique specificity in a demented patient
Daniel, L., see Roche, P.-H. (151) 127 with an autoimmune disorder (151) 41
Datti, A., see Orlacchio, A. (151) 177 Itoh, Y., see Ishida, K. (151) 41
Dotsch, A., see Dotsch, J. (151) 185 Itoyama, Y., see Hayashi, T. (151) 107
Détsch, J., Adelmann, M., Englaro, P., Détsch, A., Hinze, J., Blum, Iwasaki, Y., Shiojima, T. and Kinoshita, M.
W.F., Kiess, W. and Rascher, W. $1008 prevents the death of motor neurons in newborn rats after
Relation of leptin and neuropeptide Y in human blood and sciatic nerve section (151) 7
cerebrospinal fluid (151) 185
Duval, D., see Moumen, R. (151) 35 Jacquy, J., see Manto, M. (151) 169
Jacquy, J., see van Blercom, N. (151) 71
Englaro, P., see Dotsch, J. (151) 185 Jenkins, I.H., Passingham, R.E. and Brooks, D.J.
Escandon, S.L., see O’ Neill, B.J. (151) 223 The effect of movement frequency on cerebral activation: a
positron emission tomography study (151) 195
Figarella-Branger, D., see Roche, P.-H. (151) 127
Filippi, M. and Comi, G. Kaida, K.-i., Kamakura, K., Masaki, T., Okano, M., Nagata, N. and
Magnetization transfer ratio changes in a symptomatic lesion of a Inoue, K.
patient at presentation with possible multiple sclerosis (151) 79 Painful small-fibre multifocal mononeuropathy and local myositis
Flanders, A.E., see O’ Neill, B.J. (151) 223 following influenza B infection (151) 103
Fuchigami, Y., see Kaneko, K. (151) 217 Kamakura, K., see Kaida, K.-i. (151) 103
Funakawa, I. and Terao, A. Kamimura, S., see Tachi, N. (151) 25
Leber’s ‘plus’ (151) 115 Kaneko, K., see Ishida, K. (151) 41
Furuya, T., see Shirabe, S. (151) 97 Kaneko, K., Kawai, S., Taguchi, T., Fuchigami, Y., Morita, H., Ofuji,
A. and Yonemura, H.
Gallai, V., see Orlacchio, A. (151) 177 Spatial distribution of corticospinal potentials following
Gilman, S., see Vilensky, J.A. (151) 149 transcranial electric and magnetic stimulation in human spinal cord
Godaux, E., see Manto, M. (151) 169 (151) 217
Gomori, J.M., see Korn-Lubetzki, I. (151) 57 Katayama, S., see Noda, K. (151) 89
Goto, H., see Shirabe, S. (151) 97 Kawabata, M., see Yamano, Y. (151) 163
236 Author Index Volume 151
Kawai, S., see Kaneko, K. (151) 217 system atrophy: quantitative comparison with Parkinson’s disease
Kiess, W., see Dotsch, J. (151) 185 and amyotrophic lateral sclerosis (151) 89
Kinoshita, M., see Iwasaki, Y. (151) 7 Nouvelot, A., see Moumen, R. (151) 35
Kobayashi, T., see Yamamoto, A. (151) 121
Kojima, T., Tanuma, N., Aikawa, Y., Shin, T., Sasaki, A. and Ofuji, A., see Kaneko, K. (151) 217
Matsumoto, Y. Ohya, K., see Tachi, N. (151) 25
Myosin-induced autoimmune polymyositis in the rat (151) 141 Okano, M., see Kaida, K.-i. (151) 103
Kokai, M., see Ueki, A. (151) 1 O'Neill, B.J., Flanders, A.E., Escandon, S.L. and Tahmoush, A.J.
Kornberg, A.J., see Lopate, G. (151) 189 Treatable lumbosacral polyradiculitis masquerading as diabetic
Korn-Lubetzki, I., Blumenfeld, A., Gomori, J.M., Soffer, D. and amyotrophy (151) 223
Steiner, I. Onodera, H., see Hayashi, T. (151) 107
Progressive dystonia with optic atrophy in a Jewish—Iraqi family Onodera, J., see Hayashi, T. (151) 107
(151) 57 Oreja-Guevara, C., see Sindern, E. (151) 29
Kubota, T., see Ishida, K. (151) 41 Orlacchio, A., Sarchielli, P., Gallai, V., Datti, A., Saccardi, C. and
Kumano, T., see Hirayama, M. (151) 23 Palmerini, C.A.
Kunze, K., see Wicklein, E.M. (151) ) 227 Activity levels of a B1,6 N-acetylglucosaminyltransferase in
Kuriyama, M., see Hirayama, M. (151) 22 lymphomonocytes from multiple sclerosis patients (151) 177
Osame, M., see Yamano, Y. (151) 163
Lechevalier, B., see Moumen, R. (151) 35
Link, H., see Weissert, R. (151) 49 Palmerini, C.A., see Orlacchio, A. (151) 177
Lopate, G., Pestronk, A., Kornberg, A.J., Yue, J. and Choksi, R. Passingham, R.E., see Jenkins, I.H. (151) 195
IgM anti-sulfatide autoantibodies: Patterns of binding to Pellet, W., see Roche, P.-H. (151) 127
cerebellum, dorsal root ganglion and peripheral nerve (151) 189 Pellissier, J.-F., see Roche, P.-H. (151) 127
Pestronk, A., see Lopate, G. (151) 189
Ma, S.Y., Royttaé, M., Rinne, J.O., Collan, Y. and Rinne, U.K. Pfeiffer, G., see Wicklein, E.M. (151) 227
Correlation between neuromorphometry in the substantia nigra and
clinical features in Parkinson’s disease using disector counts (151) Rascher, W., see Dotsch, J. (151) 185
83 Raulf-Heimsoth, M., see Sindern, E. (151) 29
Machigashira, K., see Yamano, Y. (151) 163 Rice, R.R., see Thaut, M.H. (151) 207
Malin, J.P., see Sindern, E. (151) 29 Rinne, J.0., see Ma, S.Y. (151) 83
Mally, J., Szalai, G. and Stone, T.W. Rinne, U.K., see Ma, S.Y. (151) 83
Changes in the concentration of amino acids in serum and Roche, P.-H., Figarella-Branger, D., Daniel, L., Bianco, N., Pellet, W.
cerebrospinal fluid of patients with Parkinson’s disease (151) 159 and Pellissier, J.-F.
Manto, M., Godaux, E., Hildebrand, J., Van Naemen, J. and Jacquy, J. Expression of cell adhesion molecules in normal nerves, chronic
Analysis of single-joint rapid movements in patients with sporadic axonal neuropathies and Schwann cell tumors (151) 127
olivopontocerebellar atrophy (151) 169 Roytta, M., see Ma, S.Y. (151) 83
Manto, M., see van Blercom, N. (151) 71
Masaki, T., see Kaida, K.-i. (151) 103 Saccardi, C., see Orlacchio, A. (151) 177
Matsumoto, Y., see Kojima, T. (151) 141 Sarchielli, P., see Orlacchio, A. (151) 177
Matsushita, M., see Ishida, K. (151) 41 Sasaki, A., see Kojima, T. (151) 141
Matsuura, T., Sasaki, H., Wakisaka, A., Hamada, T., Moriwaka, F. and Sasaki, H., see Matsuura, T. (151) 65
Tashiro, K. Sasaki, K., see Tachi, N. (151) 25
Autosomal dominant spastic paraplegia linked to chromosome 2p: Shin, T., see Kojima, T. (151) 141
clinical and genetic studies of a large Japanese pedigree (151) 65 Shinjo, H., see Ueki, A. (151) 1
McIntosh, G.C., see Thaut, M.H. (151) 207 Shiojima, T., see Iwasaki, Y. (151) 7
Melms, A., see Weissert, R. (151) 49 Shirabe, S., Nakamura, T., Tsujino, A., Nishiura, Y., Furuya, T., Goto,
Miranda, A.F., see Walker, U.A. (151) 135 H., Suenaga, A., Nakane, S., Yoshimura, T. and Nagataki, S.
Miwa, C., see Ueki, A. (151) 1 Successful application of pentoxifylline in the treatment of HTLV-I
Miyatake, T., see Ishida, K. (151) 41 associated myelopathy (151) 97
Mochizuki, H., see Hayashi, T. (151) 107 Shiratori, M., see Hirayama, M. (151) 23
Morita, H., see Kaneko, K. (151) 217 Sindern, E., Oreja-Guevara, C., Raulf-Heimsoth, M., Baur, X. and
Morita, Y., see Ueki, A. (151) 1 Malin, J.P.
Moriwaka, F., see Matsuura, T. (151) 65 A longitudinal study of circulating lymphocyte subsets in the
Moumen, R., Nouvelot, A., Duval, D., Lechevalier, B. and Viader, F. peripheral blood during the acute stage of Guillain-Barré
Plasma superoxide dismutase and glutathione peroxidase activity syndrome (151) 29
in sporadic amyotrophic lateral sclerosis (151) 35 Singh, N., Birdi, T.J., Chandrashekar, S. and Antia, N.H.
Mutoh, T., see Hirayama, M. (151) 23 Schwann cell extracellular matrix protein production is modulated
by Mycobacterium leprae and macrophage secretory products
Nagata, N., see Kaida, K.-i. (151) 103 (151) 13
Nagataki, S., see Shirabe, S. (151) 97 Soffer, D., see Korn-Lubetzki, I. (151) 57
Nakamura, S., see Noda, K. (151) 89 Steiner, I., see Korn-Lubetzki, I. (151) 57
Nakamura, T., see Shirabe, S. (151) 97 Stone, T.W., see Mally, J. (151) 159
Nakane, S., see Shirabe, S. (151) 97 Suenaga, A., see Shirabe, S. (151) 97
Neville, B.G.R., see Harris, C.M. (151) 111 Szalai, G., see Mally, J. (151) 159
Nishiura, Y., see Shirabe, S. (151) 97
Noda, K., Katayama, S., Watanabe, C., Yamamura, Y. and Nakamura, Tachi, N., Kamimura, S., Ohya, K., Chiba, S. and Sasaki, K.
S. Congenital muscular dystrophy with partial deficiency of merosin
Decrease of neurons in the medullary arcuate nucleus of multiple (151) 25
Author Index Volume 151
Taguchi, T., see Kaneko, K. (151) 217 Walker, W.F., see Walker, U.A. (151) 135
Tahmoush, A.J., see O'Neill, BJ. (151) 223 Waragai, M., Takaya, Y. and Hayashi, M.
Takaya, Y., see Waragai, M. (151) 93 Serial MR findings of chronic idiopathic ataxic neuropathy (151)
Tanuma, N., see Kojima, T. (151) 141 93
Tashiro, K., see Matsuura, T. (151) 65 Watanabe, C., see Noda, K. (151) 89
Terao, A., see Funakawa, I. (151) 115 Weissert, R., Melms, A. and Link, H.
Thaut, M.H., McIntosh, G.C. and Rice, R.R. Altered tumor growth factor 8 mRNA expression is associated
Rhythmic facilitation of gait training in hemiparetic stroke with thymectomy-related clinical remission in myasthenia gravis
rehabilitation (151) 207 (151) 49
Tsujino, A., see Shirabe, S. (151) 97 Wicklein, E.M., Pfeiffer, G., Yuki, N., Hartard, C. and Kunze, K.
Prominent sensory ataxia in Guillain-Barré syndrome associated
Ueki, A., Miwa, C., Shinjo, H., Kokai, M. and Morita, Y. with IgG anti-GDI1b antibody (151) 227
Synapse alteration in hippocampal CA3 field following entorhinal
cortex lesion (151) | Yamada, M., see Ishida, K. (151) 41
Usuku, K., see Yamano, Y. (151) 163 Yamamoto, A., Hara, H. and Kobayashi, T.
Induction of the expression of gag protein in HTLV-I infected
Van Blercom, N., Manto, M., Jacquy, J. and Hildebrand, J. lymphocytes by anti-ICAM | antibody in vitro (151) 121
Dissociation in the neural control of single-joint and multi-joint Yamamura, Y., see Noda, K. (151) 89
movements in the thalamic ataxia syndrome (151) 71 Yamano, Y., Machigashira, K., ljichi, S., Usuku, K., Kawabata, M.,
Van Naemen, J., see Manto, M. (151) 169 Arimura, K. and Osame, M.
Viader, F., see Moumen, R. (151) 35 Alteration of cytokine levels by fosfomycin and prednisolone in
Vilensky, J.A. and Gilman, S. spontaneous proliferation of cultured lymphocytes from patients
Positive and negative factors in movement control. A current with HTLV-I-associated myelopathy (HAM/TSP) (151) 163
review of Denny-Brown’s hypothesis (151) 149 Yonemura, H., see Kaneko, K. (151) 217
Yoshimura, T., see Shirabe, S. (151) 97
Wakisaka, A., see Matsuura, T. (151) 65 Yue, J., see Lopate, G. (151) 189
Walker, U.A., Walker, W.F. and Miranda, A.F. Yuki, N., see Wicklein, E.M. (151) 227
Mitochondrial mobility in differentiating muscle heterokaryons
(151) 135

JOURNOAF LTH E
NEUROLOGICAL
SCIENCES
ELSEVIER
Journal of Neurological Sciences 151 (1997) 239-240
Subject Index Volume 151
Acute sensory neuropathy (151) 227 Fibronectin (151) 13
Alzheimer’s disease (151) 1, 41 Flow cytometry (151) 29
Amino acids (151) 159 Food intake (151) 185
Amyotrophic lateral sclerosis (151) 35, 89 Fosfomycin (151) 163
Anticipation (151) 65
Anti-ganglioside antibody (151) 227 Gadolinium MRI (151) 223
Anti-GD1b antibody (151) 227 Gag (151) 121
Anti-GFAP antibody (151) 41 Gait (151) 207
Ataxia (151) 71 Ganglionopathy (151) 103
Auditory rhythm (151) 207 Genetic heterogeneity (151) 65
Autoantibodies (151) 189 Glutamate (151) 159
Autoimmune disorder (151) 41 Glutamine (151) 159
Autoimmunity (151) 49 Glutathione peroxidase (151) 35
Autosomal dominant spastic paraplegia (ADSP) (151) 65 Grasp reflex (151) 149
Avoiding (151) 149 Guillain-Barré syndrome (151) 29, 227
Axotomy (151) 7
Hereditary (151) 57
Ballistic movements (151) 71 Hippocampal CA3 field (151) 1
Brain damage (151) 149 HTLV-I (151) 121
HTLV-I associated myelopathy (151) 97
Campylobacter jejuni (151) 29 HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP)
CD8 cytotoxic T lymphocytes (151) 29 (151) 163
cDNA cloning (151) 41 Human T lymphotropic virus type I (HTLV-I) (151) 163
Cerebellar atrophy (151) 115 Hypermetria (151) 169
Cerebello-thalamic projections (151) 71 Hyponatremia (151) 213
Cerebellum (151) 169, 189, 195
Cerebral blood flow (151) 195 Ibotenic acid (151) 1
Cerebrospinal fluid (151) 185 ICAM | (151) 121
Chromosomal translocation (151) 107 Immunocytochemistry (151) 189
Chronic idiopathic ataxic neuropathy (151) 93 Immunohistochemistry (151) 141
Clinical features (151) 83 Inertial loads (151) 169
Collagens (151) 13 Infant vision (151) 111
Congenital muscular dystrophy (151) 25 Influenza B (151) 103
Correlation (151) 83 Integrins (151) 127
Cortex (151) 111 Isoelectric point (151) 41
Cortical cerebellar atrophy (151) 169
Cytokine (151) 49 Kearns-Sayre syndrome (151) 135
Cytomegalovirus (151) 29
Laminin (151) 13
Diabetic amyotrophy (151) 223 Leber’s ‘plus’ (151) 115
Disability (151) 79 Leber’s hereditary optic neuropathy (151) 115
Disector counts (151) 83 Leptin (151) 185
Dorsal root ganglia (151) 189 Leukemia (151) 107
Dystonia (151) 57 Lewis rat (151) 141
Linkage analysis (151) 65
EMG triphasic pattern (151) 169 Lymphocyte proliferation (151) 163
Encephalomyopathies (151) 135 Lymphomonocytes (151) 177
Entorhinal cortex (151) 1
Enzyme assay (151) 177 Macrophages (151) 13
Epilepsy (151) 111 Magnetic resonance imaging (151) 93
Epithelial cadherin (151) 127 Magnetization transfer imaging (151) 79
Evoked spinal cord potentials (151) 217 Malone dialdehyde (151) 35
Experimental autoimmune myositis (151) 141 Medullary arcuate nucleus (151) 89
240 Subject Index Volume 151
Mitochondria (151) 135 Putaminal atrophy (151) 57
Mitochondrial disease (151) 57 Pyramidal tract (151) 217
Mitochondrial DNA (151) 135
Motor behavior (151) 149 Quantitative study (151) 89
Motor cortex (151) 195
Motor neuron (151) 7 Ragged-red fiber (151) 135
Motor neuron disease (151) 7 Rehabilitation (151) 207
Multifocal mononeuropathy (151) 103 Release phenomenon (151) 149
Multiple sclerosis (151) 79, 177
Multiple system atrophy (151) 89 $1008 (151) 7
Muscle cell fusion (151) 135 Schwann cells (151) 13, 127
Myasthenia gravis (151) 49 Schwannoma (151) 127
Mycobacterium leprae (151) 13 SIADH (151) 213
Myosin (151) 141 Small fibre neuropathy (151) 103
Smooth pursuit (151) 111
N-Acetylglucosaminyltransferase (151) 177 SPG4 locus on chromosome 2p (151) 65
Neoplastic meningitis (151) 107 Spinal cord (151) 93
Neural cell adhesion molecule (151) 127 Spontaneous lymphocyte proliferation (151) 97
Neuralgic amyotrophy (151) 103 Striatum (151) 195
NPY (151) 185 Stroke (151) 207
Substantia nigra (151) 83
Obesity (151) 185 Sulfatide (151) 189
Ob-Product (151) 185 Superoxide dismutase (151) 35
Olivopontocerebellar atrophy (151) 169 Supplementary motor area (151) 195
Optic atrophy (151) 57 Sural nerve biopsy (151) 103
Optokinetic nystagmus (151) 111 Synaptophysin (151) 1
Parkinsonism (151) 149 T cell (151) 49
Parkinson’s disease (151) 83, 89, 159 TGF-B (151) 49
Partial deficiency of merosin (151) 25 Thymus (151) 49
Pediatric neurology (151) 213 TNF-a (151) 97
Pentoxifylline (151) 97 Transcranial electrical stimulation corticospinal tract (151) 217
Peripheral nerve (151) 189 Transcranial magnetic stimulation (151) 217
Perivascular infiltrates (151) 223 Tremor (151) 159
Phenotype variation (151) 65 Trophic factor (151) 7
Polyneuropathy (151) 189 Two-dimensional gel electrophoresis (151) 41
Polyradiculitis (151) 223
Positron emission tomography (151) 195 Vascular dementia (151) 41
Posterior column (151) 93 Vasculopathy (151) 223
Prefrontal cortex (151) 195 Visual development (151) 111
Premotor cortex (151) 195
Prognosis (151) 213