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M Mayer

Neurology

Showing results (1-10 of 7) with videos related to

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Neurology|November 1, 1994
Polymorphonuclear leukocyte functions in multiple sclerosisM Mayer
Neurology|June 1, 1970
Evidence for peripheral neurotoxic effect of trichloroethyleneR G Feldman, R M Mayer, A Taub
Neurology|January 1, 1992
Brain MRI and electrophysiologic abnormalities in preclinical and clinical adrenomyeloneuropathyP Aubourg, C Adamsbaum, M C Lavallard-Rousseau, et al.
Neurology|November 19, 2008
Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotypeE Matthews, A Guet, M Mayer, et al.
Neurology|April 27, 2005
Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 childrenM 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 dystrophyB 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 AfricaP Richard, K Gaudon, H Haddad, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Neurology|November 1, 1994
Polymorphonuclear leukocyte functions in multiple sclerosisM Mayer
Neurology|June 1, 1970
Evidence for peripheral neurotoxic effect of trichloroethyleneR G Feldman, R M Mayer, A Taub
Neurology|January 1, 1992
Brain MRI and electrophysiologic abnormalities in preclinical and clinical adrenomyeloneuropathyP Aubourg, C Adamsbaum, M C Lavallard-Rousseau, et al.
Neurology|November 19, 2008
Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotypeE Matthews, A Guet, M Mayer, et al.
Neurology|April 27, 2005
Cystic leukoencephalopathy without megalencephaly: a distinct disease entity in 15 childrenM 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 dystrophyB 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 AfricaP Richard, K Gaudon, H Haddad, et al.
Pageof 1