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Histochemistry
|
January 1, 1990
Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscle
N Romero, C Marsac, M Fardeau, et al.
Revue Neurologique
|
January 1, 1980
[Inclusion body myositis: clinical, morphological and virological study of a new case associated with scleroderma and Klinefelter's syndrome (author's transl)]
J Salama, F M Tomé, P Lebon, et al.
Annales De Medecine Interne
|
October 1, 1978
[Atypical diffuse interstitial calcinosis]
G Cremer, M Fardeau, J J D'Izarn, et al.
Neuroradiology
|
January 1, 1991
Intracranial arachnoid cysts in myotonic dystrophy
M Fiorelli, D Duboc, S Pappatà, et al.
Electrodiagnostic-Therapie
|
January 1, 1980
[Electromyographic and histopathological study of the Lambert-Eaton myasthenia syndrome. Apropos of a case]
P Dudognon, H P Cathala, M Fardeau, et al.
Annales De Medecine Interne
|
August 1, 1976
[Neuropathy due to chloroquine in lupus erythematosus. 2 recent cases, emphasizing the necessity for ultrastructural study of the muscle biopsy]
P Godeau, G Herreman, H Himmich, et al.
Seminars in Neurology
|
March 11, 2000
Oculopharyngeal muscular dystrophy
B Brais, G A Rouleau, J P Bouchard, et al.
Biochemical and Biophysical Research Communications
|
June 9, 1997
Glycogen-storage disease type II (acid maltase deficiency): identification of a novel small deletion (delCC482+483) in French patients
M Nicolino, J P Puech, F Letourneur, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 15, 1987
Physical state abnormality of erythrocyte membrane in myotonic dystrophy: a spin label study
M A Thomas, E Lamas, D Daveloose, et al.
Acta Neuropathologica
|
January 1, 1991
Skeletal muscle involvement in human immunodeficiency virus infection
D Hantaï, J G Fournier, R Vazeux, et al.
Page
of 29
Search research articles
Search
Showing results (121-130 of 289) with videos related to
Sort By:
Page
of 29
Histochemistry
|
January 1, 1990
Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscle
N Romero, C Marsac, M Fardeau, et al.
Revue Neurologique
|
January 1, 1980
[Inclusion body myositis: clinical, morphological and virological study of a new case associated with scleroderma and Klinefelter's syndrome (author's transl)]
J Salama, F M Tomé, P Lebon, et al.
Annales De Medecine Interne
|
October 1, 1978
[Atypical diffuse interstitial calcinosis]
G Cremer, M Fardeau, J J D'Izarn, et al.
Neuroradiology
|
January 1, 1991
Intracranial arachnoid cysts in myotonic dystrophy
M Fiorelli, D Duboc, S Pappatà, et al.
Electrodiagnostic-Therapie
|
January 1, 1980
[Electromyographic and histopathological study of the Lambert-Eaton myasthenia syndrome. Apropos of a case]
P Dudognon, H P Cathala, M Fardeau, et al.
Annales De Medecine Interne
|
August 1, 1976
[Neuropathy due to chloroquine in lupus erythematosus. 2 recent cases, emphasizing the necessity for ultrastructural study of the muscle biopsy]
P Godeau, G Herreman, H Himmich, et al.
Seminars in Neurology
|
March 11, 2000
Oculopharyngeal muscular dystrophy
B Brais, G A Rouleau, J P Bouchard, et al.
Biochemical and Biophysical Research Communications
|
June 9, 1997
Glycogen-storage disease type II (acid maltase deficiency): identification of a novel small deletion (delCC482+483) in French patients
M Nicolino, J P Puech, F Letourneur, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 15, 1987
Physical state abnormality of erythrocyte membrane in myotonic dystrophy: a spin label study
M A Thomas, E Lamas, D Daveloose, et al.
Acta Neuropathologica
|
January 1, 1991
Skeletal muscle involvement in human immunodeficiency virus infection
D Hantaï, J G Fournier, R Vazeux, et al.
Page
of 29