Showing results (181-190 of 282) with videos related to
Sort By:
Pageof 29
Neurology|January 1, 1978
Juvenile Huntington chorea: clinical, ultrastructural, and biochemical studiesH H Goebel, R Heipertz, W Scholz, et al.Acta Neuropathologica|November 9, 2001
Neuronal ceroid lipofuscinosis: late infantile or Jansky Bielschowsky type--re-revisitedR B Wheeler, M Schlie, E Kominami, et al.Fortschritte Der Medizin|June 30, 1994
[Cell therapy and its risks]J R Bohl, H H Goebel, L Pötsch, et al.Journal of Child Neurology|October 1, 1990
Late-onset globoid cell leukodystrophy: unusual ultrastructural pathology and subtotal beta-galactocerebrosidase deficiencyH H Goebel, K Harzer, J P Ernst, et al.European Neurology|January 1, 1984
Centronuclear myopathy with special consideration of the adult formH H Goebel, H M Meinck, M Reinecke, et al.Brain & Development|January 1, 1983
A morphological study of non-Japanese congenital muscular dystrophy associated with cerebral lesionsH H Goebel, A Fidzianska, H G Lenard, et al.European Journal of Pediatrics|November 1, 1979
Clinical, morphological, and biochemical investigations on a patient with an unusual form of neuronal ceroid-lipofuscinosisK Becker, H H Goebel, L Svennerholm, et al.Dementia and Geriatric Cognitive Disorders|February 20, 1998
Reduced intraneuronal lipofuscin content in dementia with Lewy bodies compared with Alzheimer's disease and controlsL M Drach, J Bohl, S Wach, et al.American Journal of Medical Genetics|June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosisH H Goebel, F Gullotta, T Bajanowski, et al.Neuromuscular Disorders : NMD|May 1, 1997
Congenital myopathy with excess of thin myofilamentsH H Goebel, J R Anderson, C Hübner, et al.Pageof 29