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Brain & Development|January 1, 1980
A form of congenital muscular dystrophyH H Goebel, H G Lenard, U Langenbeck, et al.
European Journal of Pediatrics|April 25, 1979
The development of skeletal muscles in premature infants. I. Fibre size and histochemical differentiationH Schloon, J Schlottmann, H G Lenard, et al.
Brain : a Journal of Neurology|June 1, 1987
A morphometric study on sural nerves in metachromatic leucodystrophyA Bardosi, R L Friede, S Ropte, et al.
Acta Anatomica|December 1, 1998
Ultrastructure of the retina in adult neuronal ceroid lipofuscinosisH H Goebel, S S Schochet, M Jaynes, et al.
Der Nervenarzt|June 12, 2003
[Fabry's disease: new therapeutic options for this lysosomal storage disorder]A J Grau, M Schwaninger, H H Goebel, et al.
Acta Neurologica Scandinavica|January 13, 2009
Congenital myopathies--a comprehensive update of recent advancementsM C Sharma, D Jain, C Sarkar, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1987
Chemical heterogeneity of amyloid in the carpal tunnel syndromeK Stein, S Störkel, R P Linke, et al.
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.
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