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Muscle & Nerve|January 1, 1978
Autosomal dominant "spheroid body myopathy"H H Goebel, J Muller, H W Gillen, et al.
Ophthalmic Paediatrics and Genetics|February 1, 1985
Ultrastructural study of primary canine and human pigmentary retinopathyH H Goebel, K Ikeda, W Eichholtz, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiencyH Porschke, W Kress, H Reichmann, et al.
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.
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