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Brain : a Journal of Neurology|January 16, 2004
Desmin myopathyL G Goldfarb, P Vicart, H H Goebel, et al.Neuropediatrics|August 1, 1992
Sudden loss of hearing and vestibular function, muscular weakness, and multiple white matter lesions in preschool childrenH G Lenard, T Voit, A Lamprecht, et al.Neuropediatrics|April 29, 1998
Clinical and genetic aspects of X-linked adrenoleukodystrophyJ Gärtner, A Braun, A Holzinger, et al.Pediatric Dermatology|July 1, 1997
Gianotti-Crosti syndrome associated with Epstein-Barr virus infectionB Hofmann, H C Schuppe, O Adams, et al.Brain & Development|January 1, 1986
Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome)R Heyer, J Ehrich, H H Goebel, et al.Archives of Oto-Rhino-Laryngology|January 1, 1984
Esthesioneuroblastoma: ultrastructural, immunohistological and biochemical investigation of one caseM Vollrath, M Altmannsberger, D H Hunneman, et al.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.Pageof 33