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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
Morphological studies on CLN2H H Goebel, E Kominami, E Neuen-Jacob, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|June 14, 2001
[Keratopathy as a sign of multifocal congenital sensory polyneuropathy. A case report]U Kottler, O Schwenn, H H Goebel, et al.
Acta Neuropathologica|January 1, 1981
Fingerprint profiles in lymphocytic vacuoles of mucopolysaccharidoses I-H, II, III-A, and III-BH H Goebel, K Ikeda, F Schulz, et al.
American Journal of Medical Genetics|February 15, 1992
Incidence of neuronal ceroid-lipofuscinoses in West Germany: variation of a method for studying autosomal recessive disordersM Claussen, P Heim, J Knispel, et al.
European Neurology|January 1, 1980
Adult metachromatic leukodystrophy. III. Clinical course, final stages and first biochemical resultsD Seidel, R Heipertz, H H Goebel, et al.
Neuropathology and Applied Neurobiology|May 1, 1978
Fatty acid composition of myelin lipids (cerebrosides, sulphatides and sphingomyelin) from normal human sural nerve, and changes in peripheral neuropathyR Heipertz, H Pilz, D Seidel, et al.
European Neurology|January 1, 1980
Adult metachromatic leukodystrophy. IV. Ultrastructural studies on the central and peripheral nervous systemH H Goebel, A Argyrakis, K Shimokawa, et al.
Brain : a Journal of Neurology|January 16, 2004
Desmin myopathyL G Goldfarb, P Vicart, H H Goebel, et al.
Brain & Development|January 1, 1986
Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome)R Heyer, J Ehrich, H H Goebel, et al.
Archives of Oto-Rhino-Laryngology|January 1, 1984
Esthesioneuroblastoma: ultrastructural, immunohistological and biochemical investigation of one caseM Vollrath, M Altmannsberger, D H Hunneman, et al.
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