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Muscle & Nerve
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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
Archives of Neurology
|
September 1, 1978
Elevations of hemopexin levels in neuromuscular disease
B T Adornato, W K Engel, M Foidart-Desalle
Journal of Chemotherapy (Florence, Italy)
|
July 1, 1989
Comparative clinical and pharmacokinetic aspects of cefotetan versus cefoxitin plus metronidazole in vaginal hysterectomy
K Engel, W Schmidt, H G Sonntag, et al.
Page
of 78
Search research articles
Search
Showing results (241-250 of 780) with videos related to
Sort By:
Page
of 78
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
Archives of Neurology
|
September 1, 1978
Elevations of hemopexin levels in neuromuscular disease
B T Adornato, W K Engel, M Foidart-Desalle
Journal of Chemotherapy (Florence, Italy)
|
July 1, 1989
Comparative clinical and pharmacokinetic aspects of cefotetan versus cefoxitin plus metronidazole in vaginal hysterectomy
K Engel, W Schmidt, H G Sonntag, et al.
Page
of 78