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Blood
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April 1, 1980
The molecular mechanism of the inherited phosphofructokinase deficiency associated with hemolysis and myopathy
S Vora, L Corash, W K Engel, et al.
The American Journal of Pathology
|
January 1, 1994
Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau
V Askanas, W K Engel, M Bilak, et al.
Neuroreport
|
June 1, 1993
beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle
E Sarkozi, V Askanas, S A Johnson, et al.
Annals of Neurology
|
September 1, 1981
Lysosomal abnormalities in cultured schwann cells from a patient with peripheral neuropathy and continuous muscle fiber activity
V Askanas, W K Engel, V M Berginer, et al.
The Journal of Laboratory and Clinical Medicine
|
November 1, 1983
Hemopexin metabolism in patients with altered serum levels
M Foidart, H H Liem, B T Adornato, et al.
Lancet (London, England)
|
December 19, 2001
Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis
G Vattemi, W K Engel, J McFerrin, et al.
Archives of Neurology
|
December 1, 1978
Reincarnation in cultured muscle of mitochondrial abnormalities. Two patients with epilepsy and lactic acidosis
V Askanas, W K Engel, D E Britton, et al.
Neuroreport
|
October 25, 1993
Prion protein is abnormally accumulated in inclusion-body myositis
V Askanas, M Bilak, W K Engel, et al.
Journal of the Neurological Sciences
|
May 1, 1981
Immunocytochemical localization of thymosin-alpha 1 in thymic epithelial cells of normal and myasthenia gravis patients and in thymic cultures
M C Dalakas, W K Engel, J E McClure, et al.
Annals of the New York Academy of Sciences
|
January 1, 1981
Identification of human thymic epithelial cells with antibodies to thymosin alpha 1 in myasthenia gravis
M C Dalakas, W K Engel, J E McClure, et al.
Page
of 19
Search research articles
Search
Showing results (141-150 of 189) with videos related to
Sort By:
Page
of 19
Blood
|
April 1, 1980
The molecular mechanism of the inherited phosphofructokinase deficiency associated with hemolysis and myopathy
S Vora, L Corash, W K Engel, et al.
The American Journal of Pathology
|
January 1, 1994
Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau
V Askanas, W K Engel, M Bilak, et al.
Neuroreport
|
June 1, 1993
beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle
E Sarkozi, V Askanas, S A Johnson, et al.
Annals of Neurology
|
September 1, 1981
Lysosomal abnormalities in cultured schwann cells from a patient with peripheral neuropathy and continuous muscle fiber activity
V Askanas, W K Engel, V M Berginer, et al.
The Journal of Laboratory and Clinical Medicine
|
November 1, 1983
Hemopexin metabolism in patients with altered serum levels
M Foidart, H H Liem, B T Adornato, et al.
Lancet (London, England)
|
December 19, 2001
Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis
G Vattemi, W K Engel, J McFerrin, et al.
Archives of Neurology
|
December 1, 1978
Reincarnation in cultured muscle of mitochondrial abnormalities. Two patients with epilepsy and lactic acidosis
V Askanas, W K Engel, D E Britton, et al.
Neuroreport
|
October 25, 1993
Prion protein is abnormally accumulated in inclusion-body myositis
V Askanas, M Bilak, W K Engel, et al.
Journal of the Neurological Sciences
|
May 1, 1981
Immunocytochemical localization of thymosin-alpha 1 in thymic epithelial cells of normal and myasthenia gravis patients and in thymic cultures
M C Dalakas, W K Engel, J E McClure, et al.
Annals of the New York Academy of Sciences
|
January 1, 1981
Identification of human thymic epithelial cells with antibodies to thymosin alpha 1 in myasthenia gravis
M C Dalakas, W K Engel, J E McClure, et al.
Page
of 19