Neuropediatrics

Issue 03 · June 2000

Recommend Journal

Short Communication
100
Topçu, M.; Saatci, I.; Anil Apak, R.; Söylemezoglu, F.:
A Case of Leukoencephalopathy with Vanishing White Matter

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141
Akaboshi, Shinjiro; Yoshimura, Masaki; Hara, Toshiro; Kageyama, Hiroko; Nishikwa, Ken-ichi; Kawakami, Tetsuo; Ieshima, Atsushi; Takeshita, Kenzo:
A Case of Høyeraal-Hreidarsson Syndrome: Delayed Myelination and Hypoplasia of Corpus Callosum are Other Important Signs

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145
Ramelli, G. P.; Vella, S.; Lövblad, K.; Remonda, L.; Vassella, F.:
Swelling of the Third Nerve in a Child with Transient Oculomotor Paresis: A Possible Cause of Ophthalmoplegic Migraine

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148
Polo, A.; Aldegheri, R.; Bongiovanni, L. G.; Cavallaro, T.; Rizzuto, N.:
Painless Fractures and Thermoregulation Disturbances in Sensory-Autonomic Neuropathy: Electrophysiological Abnormalities and Sural Nerve Biopsy

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151
Dörfler, A.; Wanke, I.; Wiedemayer, H.; Weber, J.; Forsting, M.:
Endovascular Treatment of a Giant Aneurysm of the Internal Carotid Artery in a Child with Visual Loss: Case Report

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155
Dale, R. C.; Ping Tang, S.; Heckmatt, J. Z.; Tatnall, M. F.:
Familial Systemic Lupus Erythematosus and Congenital Infection-Like Syndrome

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Editorial Annotation
113
Aicardi, J.; Goutières, Françoise:
Systemic Lupus Erythematosus or Aicardi-Goutières Syndrome?

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Original Article
114
Rubio-Gozalbo, M. E.; Sengers, R. C. A.; Trijbels, M. J. F.; Doesburg, W. H.; Janssen, M. A. J.; Verbeek, M. A. L.; Smeitink, M. J. A.:
A Prognostic Index as Diagnostic Strategy in Children Suspected of Mitochondriocytopathy

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122
Boor, R.; Miebach, E.; Brühl, K.; Beck, M.:
Abnormal Somatosensory Evoked Potentials Indicate Compressive Cervical Myelopathy in Mucopolysaccharidoses

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128
Sie, L. T. L.; van der Knaap, M. S.; Oosting, J.; de Vries, L. S.; Lafeber, H. N.; Valk, J.:
MR Patterns of Hypoxic-Ischemic Brain Damage After Prenatal, Perinatal or Postnatal Asphyxia

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137
Muntau, Ania C.; Röschinger, W.; Merkenschlager, A.; van der Knaap, M. S.; Jakobs, C.; Duran, M.; Hoffmann, G. F.; Roscher, A. A.:
Combined D-2- and L-2-Hydroxyglutaric Aciduria with Neonatal Onset Encephalopathy: A Third Biochemical Variant of 2-Hydroxyglutaric Aciduria?

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Letter to the Editor
159
Huisman, T. A. G.; Brandner, S.; Niggli, F.; Betts, D. R.; Boltshauser, E.; Martin, E.:
Malignant Rhabdoid Tumor of the Brain: Quantitative ¹H MR-Spectroscopy and Cytogenetics

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162
Nagdyman, N.; Behse, F.; Schülke, M.:
A Rare Variant of Guillain-Barré Syndrome with Acute Motor Axonal Neuropathy (AMAN) in a Caucasian Boy

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164
De Brasi, D.; Della Casa, R.; Titomanlio, L.; D'Agostino, A.; Perone, L.; Andria, G.:
Mental Retardation, Tall Stature and Minor Phenotypic Abnormalities Associated with a de novo Complex Chromosome Rearrangement

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