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H H Goebel

Showing results (221-230 of 323) with videos related to

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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.
European Neurology|January 1, 1984
Centronuclear myopathy with special consideration of the adult formH H Goebel, H M Meinck, M Reinecke, et al.
Acta Neuropathologica|April 12, 1979
Becker's x-linked muscular dystrophy. Histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by BeckerH H Goebel, H Prange, F Gullotta, 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.
Pageof 33

Showing results (221-230 of 323) with videos related to

Sort By:
Pageof 33
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.
European Neurology|January 1, 1984
Centronuclear myopathy with special consideration of the adult formH H Goebel, H M Meinck, M Reinecke, et al.
Acta Neuropathologica|April 12, 1979
Becker's x-linked muscular dystrophy. Histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by BeckerH H Goebel, H Prange, F Gullotta, 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.
Pageof 33