Neuropediatrics
Issue 02 · April 1999
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The Peter Emil Becker Award Lecture 1998
55
Tomé, F. M. S.:
The Saga of Congenital Muscular Dystrophy
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Original articles
66
Saito, Y.; Ito, M.; Hanaoka, S.; Ohama, E.; Akaboshi, S.; Takashima, S.:
Dopamine Receptor Upregulation in Lesch-Nyhan Syndrome: A Postmortem Study
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72
Alikaşifoǧlu, M.; Topaloǧlu, H.; Tunçbilek, E.; Ceviz, N.; Anar, B.; Demir, E.; Özme, Ş:
Clinical and Genetic Correlate in Childhood Onset Friedreich Ataxia
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77
Stieh, J.; Kramer, H. H.; Harding, P.; Fischer, G.:
Gross and Fine Motor Development is Impaired in Children with Cyanotic Congenital Heart Disease
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83
Mercuri, E.; Guzzetta, A.; Haataja, L.; Cowan, F.; Rutherford, M.; Counsell, S.; Papadimitriou, M.; Cioni, G.; Dubowitz, L.:
Neonatal Neurological Examination in Infants with Hypoxic Ischaemic Encephalopathy: Correlation with MRI Findings
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90
Stibler, H.; Gylje, H.; Uller, A.:
A Neurodystrophic Syndrome Resembling Carbohydrate-Deficient Glycoprotein Syndrome Type III
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Short communications
93
de Koning, T. J.; de Vries, L. S.; Groenendaal, F.; Ruitenbeek, W.; Jansen, G. H.; Poll-The, B. T.; Barth, P. G.:
Pontocerebellar Hypoplasia Associated with Respiratory-Chain Defects
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96
Kiechl-Kohlendorfer, U.; Ellemunter, H.; Kiechl, S.:
Chorea as the Presenting Clinical Feature of Primary Antiphospholipid Syndrome in Childhood
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99
Giordano, L.; Accorsi, P.; Valseriati, D.; Tiberti, A.; Menegati, E.; Zara, F.; Vignolio, A.; Vigevano, F.:
Benign Infantile Familial Convulsions: Natural History of a Case and Clinical Characteristics of a Large Italian Family
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Letters to the editor
102
Hanefeld, F. A.:
Oligogyric Microcephaly
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104
Dobyns, W. B.; Barkovich, A. J.:
Microcephaly with Simplified Gyral Pattern (Oligogyric Microcephaly) and Microlissencephaly
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107
Lenard, H.-G.:
Dacrystic Seizures Reconsidered
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108
Dan, B.; Boyd, S. G.:
Dacrystic Seizures Reconsidered: Reply
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