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H Goebel

Showing results (311-320 of 483) with videos related to

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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.
Scientific Reports|September 7, 2016
A novel algorithm for a precise analysis of subchondral bone alterationsLiang Gao, Patrick Orth, Lars K H Goebel, et al.
Zeitschrift Fur Urologie Und Nephrologie|November 1, 1977
[Problems in the determination of pathogens in prostatovesiculitis]D Wachtel, W Pfister, H Goebel, 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.
Disease Models & Mechanisms|May 6, 2018
Subchondral drilling for articular cartilage repair: a systematic review of translational researchLiang Gao, Lars K H Goebel, Patrick Orth, et al.
American Journal of Medical Genetics|June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosisH H Goebel, F Gullotta, T Bajanowski, et al.
Pageof 49

Showing results (311-320 of 483) with videos related to

Sort By:
Pageof 49
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.
Scientific Reports|September 7, 2016
A novel algorithm for a precise analysis of subchondral bone alterationsLiang Gao, Patrick Orth, Lars K H Goebel, et al.
Zeitschrift Fur Urologie Und Nephrologie|November 1, 1977
[Problems in the determination of pathogens in prostatovesiculitis]D Wachtel, W Pfister, H Goebel, 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.
Disease Models & Mechanisms|May 6, 2018
Subchondral drilling for articular cartilage repair: a systematic review of translational researchLiang Gao, Lars K H Goebel, Patrick Orth, et al.
American Journal of Medical Genetics|June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosisH H Goebel, F Gullotta, T Bajanowski, et al.
Pageof 49