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The American Journal of Pathology
|
July 1, 1992
Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis
V Askanas, W K Engel, R B Alvarez
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
November 1, 1978
Histochemistry of rat intrafusal muscle fibers and their motor innervation
J Kucera, K Dorovini-Zis, W K Engel
Muscle & Nerve
|
March 1, 1993
Calf muscle hypertrophy, complex repetitive discharges and spinal stenosis
S R Beydoun, C Shapiro, W K Engel
Neuropathology and Applied Neurobiology
|
July 15, 2010
In sporadic inclusion body myositis muscle fibres TDP-43-positive inclusions are less frequent and robust than p62 inclusions, and are not associated with paired helical filaments
C D'Agostino, A Nogalska, W K Engel, et al.
Archives of Neurology
|
June 1, 1981
Poly ICLC in the treatment of postinfectious demyelinating encephalomyelitis
A M Salazar, W K Engel, H B Levy
Developmental Neuroscience
|
January 1, 1988
Age-dependent requirements of cultured spinal cord neurons
G Micaglio, V Askanas, F Moriwaka, et al.
Neurology
|
October 1, 1974
Pyruvate oxidation in neuromuscular diseases. Evidence of a genetic defect in two families with the clinical syndrome of Friedreich's ataxia
R A Kark, J P Blass, W K Engel
Neurology
|
October 1, 1974
Effect of lactate infusions on patients with myasthenia gravis
B M Patten, K L Oliver, W K Engel
Lancet (London, England)
|
March 4, 1978
Polyinosinic-polycytidylic acid treatment of neuropathy
W K Engel, R A Cuneo, H B Levy
Archives of Neurology
|
April 1, 1977
Amyloidosis with plasma cell dyscrasia. An overlooked caused of adult onset sensorimotor neuropathy
J L Trotter, W K Engel, F I Ignaczak
Page
of 33
Search research articles
Search
Showing results (131-140 of 326) with videos related to
Sort By:
Page
of 33
The American Journal of Pathology
|
July 1, 1992
Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis
V Askanas, W K Engel, R B Alvarez
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
November 1, 1978
Histochemistry of rat intrafusal muscle fibers and their motor innervation
J Kucera, K Dorovini-Zis, W K Engel
Muscle & Nerve
|
March 1, 1993
Calf muscle hypertrophy, complex repetitive discharges and spinal stenosis
S R Beydoun, C Shapiro, W K Engel
Neuropathology and Applied Neurobiology
|
July 15, 2010
In sporadic inclusion body myositis muscle fibres TDP-43-positive inclusions are less frequent and robust than p62 inclusions, and are not associated with paired helical filaments
C D'Agostino, A Nogalska, W K Engel, et al.
Archives of Neurology
|
June 1, 1981
Poly ICLC in the treatment of postinfectious demyelinating encephalomyelitis
A M Salazar, W K Engel, H B Levy
Developmental Neuroscience
|
January 1, 1988
Age-dependent requirements of cultured spinal cord neurons
G Micaglio, V Askanas, F Moriwaka, et al.
Neurology
|
October 1, 1974
Pyruvate oxidation in neuromuscular diseases. Evidence of a genetic defect in two families with the clinical syndrome of Friedreich's ataxia
R A Kark, J P Blass, W K Engel
Neurology
|
October 1, 1974
Effect of lactate infusions on patients with myasthenia gravis
B M Patten, K L Oliver, W K Engel
Lancet (London, England)
|
March 4, 1978
Polyinosinic-polycytidylic acid treatment of neuropathy
W K Engel, R A Cuneo, H B Levy
Archives of Neurology
|
April 1, 1977
Amyloidosis with plasma cell dyscrasia. An overlooked caused of adult onset sensorimotor neuropathy
J L Trotter, W K Engel, F I Ignaczak
Page
of 33