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Journal of Child Neurology
|
October 1, 1990
Late-onset globoid cell leukodystrophy: unusual ultrastructural pathology and subtotal beta-galactocerebrosidase deficiency
H H Goebel, K Harzer, J P Ernst, et al.
European Neurology
|
January 1, 1984
Centronuclear myopathy with special consideration of the adult form
H 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 Becker
H 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 lesions
H 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-lipofuscinosis
K Becker, H H Goebel, L Svennerholm, et al.
Scientific Reports
|
September 7, 2016
A novel algorithm for a precise analysis of subchondral bone alterations
Liang 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 controls
L 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 research
Liang Gao, Lars K H Goebel, Patrick Orth, et al.
American Journal of Medical Genetics
|
June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosis
H H Goebel, F Gullotta, T Bajanowski, et al.
Page
of 49
Search research articles
Search
Showing results (311-320 of 483) with videos related to
Sort By:
Page
of 49
Journal of Child Neurology
|
October 1, 1990
Late-onset globoid cell leukodystrophy: unusual ultrastructural pathology and subtotal beta-galactocerebrosidase deficiency
H H Goebel, K Harzer, J P Ernst, et al.
European Neurology
|
January 1, 1984
Centronuclear myopathy with special consideration of the adult form
H 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 Becker
H 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 lesions
H 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-lipofuscinosis
K Becker, H H Goebel, L Svennerholm, et al.
Scientific Reports
|
September 7, 2016
A novel algorithm for a precise analysis of subchondral bone alterations
Liang 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 controls
L 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 research
Liang Gao, Lars K H Goebel, Patrick Orth, et al.
American Journal of Medical Genetics
|
June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosis
H H Goebel, F Gullotta, T Bajanowski, et al.
Page
of 49