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Brain & Development|January 1, 1980
Congenital muscular dystrophies and unstructured congenital myopathiesH G Lenard, H H GoebelJournal of Neuropathology and Experimental Neurology|February 1, 1997
Apoptosis-related proteins in skeletal muscle fibers of spinal muscular atrophyD S Tews, H H GoebelAmerican Journal of Medical Genetics|June 5, 1995
Immunelectronmicroscopic characterization of T4 and T8 lymphocytes and natural killer cells in neuronal ceroid-lipofuscinosisB C Kieseier, H H GoebelClinical Immunology and Immunopathology|July 1, 1998
Cell death and oxidative damage in inflammatory myopathiesD S Tews, H H GoebelBrain Pathology (Zurich, Switzerland)|February 11, 1998
The neuronal ceroid-lipofuscinoses. Recent advancesH H Goebel, J D SharpHistopathology|January 20, 2005
Diagnostic immunohistochemistry in neuromuscular disordersD S Tews, H H GoebelActa Neuropathologica|January 1, 1993
Experimental emetine myopathy: enzyme histochemical, electron microscopic, and immunomorphological studiesN J Hopf, H H GoebelNeuromuscular Disorders : NMD|August 1, 1996
DNA fragmentation and BCL-2 expression in infantile spinal muscular atrophyD S Tews, H H GoebelZentralblatt Fur Allgemeine Pathologie U. Pathologische Anatomie|January 1, 1990
Amyloid-related neuropathiesH H Goebel, J Bohl, S StörkelNeuropathology and Applied Neurobiology|March 1, 1989
Mitochondria-related encephalomyopathiesH H Goebel, A Bornemann, H ReichmannPageof 38