DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 02 · Volume 16 · Mai 1985 DOI: 10.1055/s-002-10749

ORIGINAL ARTICLES

59
Meencke, H. J.; Gerhard, C.: Morphological Aspects of Aetiology and the Course of Infantile Spasms (West-Syndrome)1

67
Wolburg-Buchholz, Karen; Schlote, W.; Baumkötter, J.; Cantz, M.; Holder, H.; Harzer, K.: Familial Lysosomal Storage Disease with Generalized Vacuolization and Sialic Aciduria. Sporadic Salla Disease
76
Takashima, S.; Mito, T.; Becker, L. E.: Neuronal Development in the Medullary Reticular Formation in Sudden Infant Death Syndrome and Premature Infants
80
Baier, W. K.; Doose, H.: Petit Mal-Absences of Childhood Onset: Familial Prevalences of Migraine and Seizures*
84
Baier, W. K.: Genetics of Migraine and Migraine Accompagneé: A Study of Eighty-One Children and Their Families*
92
Behbehani, A. W.: Termination of Strict Diet Therapy in Phenylketonuria* A Study on EEG Sleep Patterns and Computer Spectral Analysis
106
Simmonds, H. A.; Webster, D. R.; Lingam, S.; Wilson, J.: An Inborn Error of Purine Metabolism, Deafness and Neurodevelopmental Abnormality
109
Yamano, T.; Shimada, M.; Sugino, H.; Dezawa, T.; Koike, M.; Okada, S.; Yabuuchi, H.: Ultrastructural Study on a Severe Infantile Sialidosis (β-Galactosidase - α-Neuraminidase Deficiency)

CASE REPORTS

98
Wisniewski, K.; Rudelli, R.; Laure-Kamionowska, M.; Sklower, S.; Houck, G. E.; Kieras Jr, F.; Ramos, P.; Wisniewski, H. M.; Braak, H.: Sanfilippo Disease, Type A with some Features of Ceroid Lipofuscinosis