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V Campuzano

Showing results (11-20 of 19) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutationsM Cossée, M Schmitt, V Campuzano, et al.
Molecular & General Genetics : MGG|July 28, 1995
Isolation, characterization and transformation, by autonomous replication, of Mucor circinelloides OMPdecase-deficient mutantsE P Benito, V Campuzano, M A Lŏpez-Matas, et al.
The New England Journal of Medicine|October 17, 1996
Clinical and genetic abnormalities in patients with Friedreich's ataxiaA Dürr, M Cossee, Y Agid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2000
Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical featuresM L McCormack, R P Guttmann, M Schumann, et al.
American Journal of Human Genetics|November 1, 1995
The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13L Montermini, F Rodius, L Pianese, et al.
Human Molecular Genetics|September 25, 1997
Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranesV Campuzano, L Montermini, Y Lutz, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
British Journal of Haematology|September 18, 2023
Immune thrombotic thrombocytopenic purpura in older patients: Results from the Spanish TTP Registry (REPTT)I Gómez-Seguí, E Francés Aracil, M E Mingot-Castellano, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1997
Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutationsM Cossée, M Schmitt, V Campuzano, et al.
Molecular & General Genetics : MGG|July 28, 1995
Isolation, characterization and transformation, by autonomous replication, of Mucor circinelloides OMPdecase-deficient mutantsE P Benito, V Campuzano, M A Lŏpez-Matas, et al.
The New England Journal of Medicine|October 17, 1996
Clinical and genetic abnormalities in patients with Friedreich's ataxiaA Dürr, M Cossee, Y Agid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 15, 2000
Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical featuresM L McCormack, R P Guttmann, M Schumann, et al.
American Journal of Human Genetics|November 1, 1995
The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13L Montermini, F Rodius, L Pianese, et al.
Human Molecular Genetics|September 25, 1997
Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranesV Campuzano, L Montermini, Y Lutz, et al.
Nature Genetics|April 1, 1997
Frataxin fracasM Cossée, V Campuzano, H Koutnikova, et al.
Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.
British Journal of Haematology|September 18, 2023
Immune thrombotic thrombocytopenic purpura in older patients: Results from the Spanish TTP Registry (REPTT)I Gómez-Seguí, E Francés Aracil, M E Mingot-Castellano, et al.
Pageof 2