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Nature Genetics
|
May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
A Bolino, M Muglia, F L Conforti, et al.
Genomics
|
February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22
A Bolino, E R Levy, M Muglia, et al.
Neurology
|
January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy
M Muglia, M Zappia, V Timmerman, et al.
Neurology
|
August 12, 2004
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL
R Mazzei, F L Conforti, P L Lanza, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis
F L Conforti, W Sproviero, I L Simone, et al.
Neuromuscular Disorders : NMD
|
August 21, 2007
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy
F L Conforti, T Sprovieri, R Mazzei, et al.
Neurogenetics
|
December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus
M Muglia, C Criscuolo, A Magariello, et al.
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Search research articles
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Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Nature Genetics
|
May 10, 2000
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
A Bolino, M Muglia, F L Conforti, et al.
Genomics
|
February 16, 2000
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22
A Bolino, E R Levy, M Muglia, et al.
Neurology
|
January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy
M Muglia, M Zappia, V Timmerman, et al.
Neurology
|
August 12, 2004
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL
R Mazzei, F L Conforti, P L Lanza, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis
F L Conforti, W Sproviero, I L Simone, et al.
Neuromuscular Disorders : NMD
|
August 21, 2007
A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy
F L Conforti, T Sprovieri, R Mazzei, et al.
Neurogenetics
|
December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus
M Muglia, C Criscuolo, A Magariello, et al.
Page
of 4