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Neurology
|
November 1, 1994
Polymorphonuclear leukocyte functions in multiple sclerosis
M Mayer
Neurology
|
June 1, 1970
Evidence for peripheral neurotoxic effect of trichloroethylene
R G Feldman, R M Mayer, A Taub
Neurology
|
January 1, 1992
Brain MRI and electrophysiologic abnormalities in preclinical and clinical adrenomyeloneuropathy
P Aubourg, C Adamsbaum, M C Lavallard-Rousseau, et al.
Neurology
|
November 19, 2008
Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype
E Matthews, A Guet, M Mayer, et al.
Neurology
|
April 27, 2005
Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 children
M Henneke, N Preuss, V Engelbrecht, et al.
Neurology
|
May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy
B Eymard, N B Romero, F Leturcq, et al.
Neurology
|
December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
P Richard, K Gaudon, H Haddad, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Neurology
|
November 1, 1994
Polymorphonuclear leukocyte functions in multiple sclerosis
M Mayer
Neurology
|
June 1, 1970
Evidence for peripheral neurotoxic effect of trichloroethylene
R G Feldman, R M Mayer, A Taub
Neurology
|
January 1, 1992
Brain MRI and electrophysiologic abnormalities in preclinical and clinical adrenomyeloneuropathy
P Aubourg, C Adamsbaum, M C Lavallard-Rousseau, et al.
Neurology
|
November 19, 2008
Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype
E Matthews, A Guet, M Mayer, et al.
Neurology
|
April 27, 2005
Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 children
M Henneke, N Preuss, V Engelbrecht, et al.
Neurology
|
May 1, 1997
Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy
B Eymard, N B Romero, F Leturcq, et al.
Neurology
|
December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
P Richard, K Gaudon, H Haddad, et al.
Page
of 1