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Y Nevo

Showing results (41-50 of 53) with videos related to

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American Journal of Medical Genetics|February 5, 1998
SMA type 2 unrelated to chromosome 5q13Y Nevo, U Kramer, C Legum, et al.
Current Biology : CB|October 26, 1999
The COP9 signalosome is essential for development of Drosophila melanogasterS Freilich, E Oron, Y Kapp, et al.
Pediatric Neurology|July 31, 1999
Mutation analysis in Emery-Dreifuss muscular dystrophyY Nevo, M Al-Lozi, A S Parsadanian, et al.
Clinical and Experimental Rheumatology|July 15, 2000
A case of Bartter's syndrome, gout and Becker's muscular dystrophyB Fishel, G Zhukovsky, C Legum, et al.
Pediatric Neurology|October 1, 1995
Unprovoked seizures and developmental disabilities: clinical characteristics of children referred to a child development centerY Nevo, S Shinnar, E Samuel, et al.
Seizure|June 17, 1998
Neuroimaging of children with partial seizuresU Kramer, Y Nevo, I Reider-Groswasser, et al.
Neurology|July 1, 1996
Childhood chronic inflammatory demyelinating neuropathies: clinical course and long-term follow-upY Nevo, A Pestronk, A J Kornberg, et al.
Pediatric Neurology|November 1, 1996
Clinical characteristics of children referred to a child development center for evaluation of speech, language, and communication disordersS Harel, Y Greenstein, U Kramer, et al.
Neuropediatrics|November 10, 2004
Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thriveP J Lamont, D R Thorburn, V Fabian, et al.
European Journal of Neurology|April 8, 2009
Multicenter long-term follow-up of children with idiopathic West syndrome: ACTH versus vigabatrinS Cohen-Sadan, U Kramer, B Ben-Zeev, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|February 5, 1998
SMA type 2 unrelated to chromosome 5q13Y Nevo, U Kramer, C Legum, et al.
Current Biology : CB|October 26, 1999
The COP9 signalosome is essential for development of Drosophila melanogasterS Freilich, E Oron, Y Kapp, et al.
Pediatric Neurology|July 31, 1999
Mutation analysis in Emery-Dreifuss muscular dystrophyY Nevo, M Al-Lozi, A S Parsadanian, et al.
Clinical and Experimental Rheumatology|July 15, 2000
A case of Bartter's syndrome, gout and Becker's muscular dystrophyB Fishel, G Zhukovsky, C Legum, et al.
Pediatric Neurology|October 1, 1995
Unprovoked seizures and developmental disabilities: clinical characteristics of children referred to a child development centerY Nevo, S Shinnar, E Samuel, et al.
Seizure|June 17, 1998
Neuroimaging of children with partial seizuresU Kramer, Y Nevo, I Reider-Groswasser, et al.
Neurology|July 1, 1996
Childhood chronic inflammatory demyelinating neuropathies: clinical course and long-term follow-upY Nevo, A Pestronk, A J Kornberg, et al.
Pediatric Neurology|November 1, 1996
Clinical characteristics of children referred to a child development center for evaluation of speech, language, and communication disordersS Harel, Y Greenstein, U Kramer, et al.
Neuropediatrics|November 10, 2004
Nemaline rods and complex I deficiency in three infants with hypotonia, motor delay and failure to thriveP J Lamont, D R Thorburn, V Fabian, et al.
European Journal of Neurology|April 8, 2009
Multicenter long-term follow-up of children with idiopathic West syndrome: ACTH versus vigabatrinS Cohen-Sadan, U Kramer, B Ben-Zeev, et al.
Pageof 6