Neuromuscular disorders : NMD - JoVE Visualize

Showing results (1721-1730 of 3,402) with videos related to

Pageof 341

Sort By:

Neuromuscular Disorders : NMD|April 30, 1999

Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy studyA L Taratuto, F Lubieniecki, D Díaz, et al.

Neuromuscular Disorders : NMD|April 30, 1999

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardationT Voit, R D Cohn, J Sperner, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Efficient non-viral DNA-mediated gene transfer to human primary myoblasts using electroporationE Espinos, J H Liu, C R Bader, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophyY K Hayashi, Z Tezak, T Momoi, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Regulation of alpha7 integrin by mechanical stress during skeletal muscle regenerationM Kääriäinen, T Liljamo, M Pelto-Huikko, et al.

Neuromuscular Disorders : NMD|May 23, 2001

A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsiesJ Meuleman, A Pou-Serradell, A Löfgren, et al.

Neuromuscular Disorders : NMD|June 19, 2001

Reference values of maximum isometric muscle force obtained in 270 children aged 4-16 years by hand-held dynamometryE A Beenakker, J H van der Hoeven, J M Fock, et al.

Neuromuscular Disorders : NMD|June 19, 2001

Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositisM F van der Meulen, J E Hoogendijk, K G Moons, et al.

Neuromuscular Disorders : NMD|June 19, 2001

The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocityO Dubourg, S Tardieu, N Birouk, et al.

Neuromuscular Disorders : NMD|June 19, 2001

A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNAT Nagashima, H Kato, S Maguchi, et al.

Pageof 341

Showing results (1721-1730 of 3,402) with videos related to

Sort By:

Pageof 341

Neuromuscular Disorders : NMD|April 30, 1999

Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy studyA L Taratuto, F Lubieniecki, D Díaz, et al.

Neuromuscular Disorders : NMD|April 30, 1999

Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardationT Voit, R D Cohn, J Sperner, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Efficient non-viral DNA-mediated gene transfer to human primary myoblasts using electroporationE Espinos, J H Liu, C R Bader, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophyY K Hayashi, Z Tezak, T Momoi, et al.

Neuromuscular Disorders : NMD|May 23, 2001

Regulation of alpha7 integrin by mechanical stress during skeletal muscle regenerationM Kääriäinen, T Liljamo, M Pelto-Huikko, et al.

Neuromuscular Disorders : NMD|May 23, 2001

A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsiesJ Meuleman, A Pou-Serradell, A Löfgren, et al.

Neuromuscular Disorders : NMD|June 19, 2001

Reference values of maximum isometric muscle force obtained in 270 children aged 4-16 years by hand-held dynamometryE A Beenakker, J H van der Hoeven, J M Fock, et al.

Neuromuscular Disorders : NMD|June 19, 2001

Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositisM F van der Meulen, J E Hoogendijk, K G Moons, et al.

Neuromuscular Disorders : NMD|June 19, 2001

The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocityO Dubourg, S Tardieu, N Birouk, et al.

Neuromuscular Disorders : NMD|June 19, 2001

A mitochondrial encephalo-myo-neuropathy with a nucleotide position 3271 (T-C) point mutation in the mitochondrial DNAT Nagashima, H Kato, S Maguchi, et al.

Pageof 341