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Neuropediatrics|August 1, 1981
Neuromyopathy and vitamin E deficiency in manU Burck, H H Goebel, H D Kuhlendahl, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1973
Altered enzymes in drug-resistant variants of mammalian tissue culture cellsJ D Sharp, N E Capecchi, M R CapecchiBrain & Development|January 1, 1992
A mild juvenile variant of type IV glycogenosisE Reusche, F Aksu, H H Goebel, et al.Prenatal Diagnosis|April 1, 1989
Probable exclusion of juvenile neuronal ceroid lipofuscinosis in a fetus at risk: an interim reportA Kohlschütter, R Rauskolb, H H Goebel, et al.Muscle & Nerve|February 1, 1986
Sural nerve biopsy studies in Leigh's subacute necrotizing encephalomyelopathyH H Goebel, A Bardosi, R L Friede, et al.Journal of Neuropathology and Experimental Neurology|March 1, 1990
Polyneuropathy due to acute arsenic intoxication: biopsy studiesH H Goebel, P F Schmidt, J Bohl, et al.Molecular Genetics and Metabolism|April 7, 1999
Progress in neuropathology of the neuronal ceroid lipofuscinosesH H Goebel, S S Schochet, M Jaynes, et al.Muscle & Nerve|March 1, 1983
Mallory body-like inclusions in a hereditary congenital neuromuscular diseaseA Fidzianska, H H Goebel, M Osborn, et al.Revue Neurologique|June 1, 1994
Immunohistologic and electron microscopic abnormalities of desmin and dystrophin in familial cardiomyopathy and myopathyH H Goebel, T Voit, I Warlo, et al.Clinical Neuropathology|January 1, 1982
Morphologic studies on adult neuronal-ceroid lipofuscinosis (NCL)H H Goebel, H Braak, D Seidel, et al.Pageof 29