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M Pandolfo

Showing results (71-80 of 116) with videos related to

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Neurology|August 26, 1998
Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsyF Zara, M Labuda, P G Garofalo, et al.
Acta Neurologica|August 1, 1992
Friedreich's disease. A linkage study in southern and central ItalyF Cavalcanti, S Cocozza, A Filla, et al.
Genomics|January 1, 1990
Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23M Smith, S Smalley, R Cantor, et al.
Neurology|August 1, 1992
Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseasesA E Lehesjoki, M Koskiniemi, M Pandolfo, et al.
The EMBO Journal|September 1, 1986
Mammalian single-stranded DNA binding protein UP I is derived from the hnRNP core protein A1S Riva, C Morandi, P Tsoulfas, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
Isolation of a new gene in the Friedreich ataxia candidate region on human chromosome 9 by cDNA direct selectionM Pandolfo, A Pizzuti, E Redolfi, et al.
Neurology|November 24, 1999
A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesisK Ohshima, N Sakamoto, M Labuda, et al.
Neurology|March 27, 2002
Spinocerebellar ataxia type 10 is rare in populations other than MexicansT Matsuura, L P W Ranum, V Volpini, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2000
Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1B M Ross, K Eder, A Moszczynska, et al.
American Journal of Human Genetics|December 1, 1995
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndromeS H Elsea, R C Juyal, S Jiralerspong, et al.
Pageof 12

Showing results (71-80 of 116) with videos related to

Sort By:
Pageof 12
Neurology|August 26, 1998
Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsyF Zara, M Labuda, P G Garofalo, et al.
Acta Neurologica|August 1, 1992
Friedreich's disease. A linkage study in southern and central ItalyF Cavalcanti, S Cocozza, A Filla, et al.
Genomics|January 1, 1990
Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23M Smith, S Smalley, R Cantor, et al.
Neurology|August 1, 1992
Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseasesA E Lehesjoki, M Koskiniemi, M Pandolfo, et al.
The EMBO Journal|September 1, 1986
Mammalian single-stranded DNA binding protein UP I is derived from the hnRNP core protein A1S Riva, C Morandi, P Tsoulfas, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
Isolation of a new gene in the Friedreich ataxia candidate region on human chromosome 9 by cDNA direct selectionM Pandolfo, A Pizzuti, E Redolfi, et al.
Neurology|November 24, 1999
A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesisK Ohshima, N Sakamoto, M Labuda, et al.
Neurology|March 27, 2002
Spinocerebellar ataxia type 10 is rare in populations other than MexicansT Matsuura, L P W Ranum, V Volpini, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2000
Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1B M Ross, K Eder, A Moszczynska, et al.
American Journal of Human Genetics|December 1, 1995
Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndromeS H Elsea, R C Juyal, S Jiralerspong, et al.
Pageof 12