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A Pizzuti

Showing results (51-60 of 117) with videos related to

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Journal of Medical Genetics|April 5, 2003
Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12E Flex, M Mangino, M Mazzoli, et al.
Applied Neurophysiology|January 1, 1988
Primary cultures of human caudate nucleusV Silani, G Pezzoli, E Motti, et al.
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology|October 26, 2001
[Cardiovascular risk factors in a community in Piedmont: changes after 11 years and a comparison with other regional and national data]A Pizzuti, R Gnavi, M A Testa, et al.
Giornale Italiano Di Cardiologia|August 1, 1997
[Anticoagulation and electrical cardioversion of chronic atrial fibrillation: proposal for an abbreviated protocol]E Antonielli, A Pizzuti, N Gandolfo, et al.
Human Mutation|April 11, 2001
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT)M D Cappellini, F Martinez di Montemuros, D Tavazzi, et al.
Bollettino Della Societa Italiana Di Cardiologia|January 1, 1980
[Detection with the Holter method of asymptomatic arrhythmias and silent ischemias in myocardial infarct patients transferred from the coronary unit]M Abrate, G C Bulgarelli, A Pizzuti, et al.
Bollettino Della Societa Italiana Di Cardiologia|January 1, 1981
[HDL-cholesterol in coronary disease in the acute phase]M Abrate, A Pizzuti, F Bernardi, et al.
Journal of Medical Genetics|February 27, 2004
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13F Brancati, E M Valente, A Sarkozy, et al.
Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.
Journal of Neurology|June 1, 1995
Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in spermA Massari, M Gennarelli, E Menegazzo, et al.
Pageof 12

Showing results (51-60 of 117) with videos related to

Sort By:
Pageof 12
Journal of Medical Genetics|April 5, 2003
Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12E Flex, M Mangino, M Mazzoli, et al.
Applied Neurophysiology|January 1, 1988
Primary cultures of human caudate nucleusV Silani, G Pezzoli, E Motti, et al.
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology|October 26, 2001
[Cardiovascular risk factors in a community in Piedmont: changes after 11 years and a comparison with other regional and national data]A Pizzuti, R Gnavi, M A Testa, et al.
Giornale Italiano Di Cardiologia|August 1, 1997
[Anticoagulation and electrical cardioversion of chronic atrial fibrillation: proposal for an abbreviated protocol]E Antonielli, A Pizzuti, N Gandolfo, et al.
Human Mutation|April 11, 2001
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT)M D Cappellini, F Martinez di Montemuros, D Tavazzi, et al.
Bollettino Della Societa Italiana Di Cardiologia|January 1, 1980
[Detection with the Holter method of asymptomatic arrhythmias and silent ischemias in myocardial infarct patients transferred from the coronary unit]M Abrate, G C Bulgarelli, A Pizzuti, et al.
Bollettino Della Societa Italiana Di Cardiologia|January 1, 1981
[HDL-cholesterol in coronary disease in the acute phase]M Abrate, A Pizzuti, F Bernardi, et al.
Journal of Medical Genetics|February 27, 2004
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13F Brancati, E M Valente, A Sarkozy, et al.
Human Genetics|April 6, 1999
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibilityS Semprini, F Capon, S Bovolenta, et al.
Journal of Neurology|June 1, 1995
Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in spermA Massari, M Gennarelli, E Menegazzo, et al.
Pageof 12