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Journal of Neuropathology and Experimental Neurology
|
May 1, 1996
Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases
S Nakano, A G Engel, A J Waclawik, et al.
Muscle & Nerve
|
December 1, 1993
Congenital myasthenic syndromes: II. Syndrome attributed to abnormal interaction of acetylcholine with its receptor
O Uchitel, A G Engel, T J Walls, et al.
Neurology
|
December 1, 1994
1,1'-Ethylidenebis[tryptophan] induces pathologic alterations in muscle similar to those observed in the eosinophilia-myalgia syndrome
A M Emslie-Smith, A N Mayeno, S Nakano, et al.
Journal of Neuropathology and Experimental Neurology
|
August 14, 1999
Myopathy, myasthenic syndrome, and epidermolysis bullosa simplex due to plectin deficiency
B L Banwell, J Russel, T Fukudome, et al.
Annals of the New York Academy of Sciences
|
June 21, 1993
Congenital myasthenic syndrome associated with paucity of synaptic vesicles and reduced quantal release
T J Walls, A G Engel, A S Nagel, et al.
The Journal of General Physiology
|
June 1, 1997
Mutation in the M1 domain of the acetylcholine receptor alpha subunit decreases the rate of agonist dissociation
H L Wang, A Auerbach, N Bren, et al.
The Journal of Experimental Medicine
|
September 1, 1976
Pathological mechanisms in experimental autoimmune myasthenia gravis. II. Passive transfer of experimental autoimmune myasthenia gravis in rats with anti-acetylcholine recepotr antibodies
J M Lindstrom, A G Engel, M E Seybold, et al.
Annals of Neurology
|
August 26, 1998
Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptor
K Ohno, B Anlar, E Ozdirim, et al.
Annals of Internal Medicine
|
March 1, 1980
Azathioprine with prednisone for polymyositis. A controlled, clinical trial
T W Bunch, J W Worthington, J J Combs, et al.
The Journal of Clinical Investigation
|
January 1, 1995
Patients with congenital myasthenia associated with end-plate acetylcholinesterase deficiency show normal sequence, mRNA splicing, and assembly of catalytic subunits
S Camp, S Bon, Y Li, et al.
Page
of 25
Search research articles
Search
Showing results (191-200 of 242) with videos related to
Sort By:
Page
of 25
Journal of Neuropathology and Experimental Neurology
|
May 1, 1996
Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and electron microscopy analysis of 10 cases
S Nakano, A G Engel, A J Waclawik, et al.
Muscle & Nerve
|
December 1, 1993
Congenital myasthenic syndromes: II. Syndrome attributed to abnormal interaction of acetylcholine with its receptor
O Uchitel, A G Engel, T J Walls, et al.
Neurology
|
December 1, 1994
1,1'-Ethylidenebis[tryptophan] induces pathologic alterations in muscle similar to those observed in the eosinophilia-myalgia syndrome
A M Emslie-Smith, A N Mayeno, S Nakano, et al.
Journal of Neuropathology and Experimental Neurology
|
August 14, 1999
Myopathy, myasthenic syndrome, and epidermolysis bullosa simplex due to plectin deficiency
B L Banwell, J Russel, T Fukudome, et al.
Annals of the New York Academy of Sciences
|
June 21, 1993
Congenital myasthenic syndrome associated with paucity of synaptic vesicles and reduced quantal release
T J Walls, A G Engel, A S Nagel, et al.
The Journal of General Physiology
|
June 1, 1997
Mutation in the M1 domain of the acetylcholine receptor alpha subunit decreases the rate of agonist dissociation
H L Wang, A Auerbach, N Bren, et al.
The Journal of Experimental Medicine
|
September 1, 1976
Pathological mechanisms in experimental autoimmune myasthenia gravis. II. Passive transfer of experimental autoimmune myasthenia gravis in rats with anti-acetylcholine recepotr antibodies
J M Lindstrom, A G Engel, M E Seybold, et al.
Annals of Neurology
|
August 26, 1998
Myasthenic syndromes in Turkish kinships due to mutations in the acetylcholine receptor
K Ohno, B Anlar, E Ozdirim, et al.
Annals of Internal Medicine
|
March 1, 1980
Azathioprine with prednisone for polymyositis. A controlled, clinical trial
T W Bunch, J W Worthington, J J Combs, et al.
The Journal of Clinical Investigation
|
January 1, 1995
Patients with congenital myasthenia associated with end-plate acetylcholinesterase deficiency show normal sequence, mRNA splicing, and assembly of catalytic subunits
S Camp, S Bon, Y Li, et al.
Page
of 25