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M Pandolfo

Showing results (51-60 of 116) with videos related to

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Neurology|July 6, 2000
Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansionM Labuda, D Labuda, C Miranda, et al.
Molecular Cell|May 7, 1999
Sticky DNA: self-association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich's ataxiaN Sakamoto, P D Chastain, P Parniewski, et al.
Neurology|September 26, 2001
Unverricht-Lundborg disease in a five-generation Arab family: instability of dodecamer repeatsA Mazarib, L Xiong, M Y Neufeld, et al.
Neurology|October 27, 1997
Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxiaD H Geschwind, S Perlman, W W Grody, et al.
Revue Medicale De Bruxelles|February 15, 2003
[The neurology department]M Pandolfo, S Blecic, N Mavroudakis, et al.
Journal of Nephrology|November 30, 2007
Urinary excretion of low molecular weight proteins in patients with pure monoclonal light chain proteinuriaL Madalena, M L Facio, M Angerosa, et al.
Human Molecular Genetics|June 1, 1993
A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1M Pandolfo, M Munaro, S Cocozza, et al.
Human Genetics|March 1, 1991
Localization of DNA probes tightly linked to the Friedreich's ataxia locus by in situ hybridization in a case of pericentric inversion of chromosome 9E Raimondi, P Bernasconi, D Moralli, et al.
Neurology|March 27, 2002
The cerebellum may be directly involved in cognitive functionsM Vokaer, J C Bier, S Elincx, et al.
Science (New York, N.Y.)|June 13, 1997
Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxinM Babcock, D de Silva, R Oaks, et al.
Pageof 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
Neurology|July 6, 2000
Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansionM Labuda, D Labuda, C Miranda, et al.
Molecular Cell|May 7, 1999
Sticky DNA: self-association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich's ataxiaN Sakamoto, P D Chastain, P Parniewski, et al.
Neurology|September 26, 2001
Unverricht-Lundborg disease in a five-generation Arab family: instability of dodecamer repeatsA Mazarib, L Xiong, M Y Neufeld, et al.
Neurology|October 27, 1997
Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxiaD H Geschwind, S Perlman, W W Grody, et al.
Revue Medicale De Bruxelles|February 15, 2003
[The neurology department]M Pandolfo, S Blecic, N Mavroudakis, et al.
Journal of Nephrology|November 30, 2007
Urinary excretion of low molecular weight proteins in patients with pure monoclonal light chain proteinuriaL Madalena, M L Facio, M Angerosa, et al.
Human Molecular Genetics|June 1, 1993
A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1M Pandolfo, M Munaro, S Cocozza, et al.
Human Genetics|March 1, 1991
Localization of DNA probes tightly linked to the Friedreich's ataxia locus by in situ hybridization in a case of pericentric inversion of chromosome 9E Raimondi, P Bernasconi, D Moralli, et al.
Neurology|March 27, 2002
The cerebellum may be directly involved in cognitive functionsM Vokaer, J C Bier, S Elincx, et al.
Science (New York, N.Y.)|June 13, 1997
Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxinM Babcock, D de Silva, R Oaks, et al.
Pageof 12