VITIELLO, LIBERO

VITIELLO, LIBERO  

Dipartimento di Biologia - DiBio  

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Risultati 1 - 20 di 101 (tempo di esecuzione: 0.036 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Diagnosis and treatment of cardiac involvement in Becker muscular dystrophy 1991 MELACINI, PAOLAFANIN, MARINAVITIELLO, LIBEROPEGORARO, ELENAANGELINI, CORRADO + ACTA CARDIOMIOLOGICA - -
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients. 1992 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + JOURNAL OF MEDICAL GENETICS - -
A 3′ consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions 1992 VITIELLO, LIBERO + HUMAN MOLECULAR GENETICS - -
Prevalence of dystrophin-positive fibers in 85 duchenne muscular dystrophy patients 1992 FANIN, MARINADANIELI, GIAN ANTONIOVITIELLO, LIBEROANGELINI, CORRADO + NEUROMUSCULAR DISORDERS - -
A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions. 1992 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISA + HUMAN MOLECULAR GENETICS - -
Patterns of deletions of the dystrophin gene in different European populations. 1993 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISA + HUMAN GENETICS - -
Cardiac involvement in Becker muscular dystrophy 1993 MELACINI, PAOLAFANIN, MARINADANIELI, GIAN ANTONIOFASOLI, GIUSEPPEANGELINI, CORRADOVITIELLO, LIBEROBUJA, GIANFRANCOMOSTACCIUOLO, MARIA LUISAPEGORARO, ELENADALLA VOLTA, SERGIO + JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY - -
DXS997 localized to intron 48 of dystrophin 1993 VITIELLO, LIBERODANIELI, GIAN ANTONIO + HUMAN MOLECULAR GENETICS - -
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis. 1993 MOSTACCIUOLO, MARIA LUISAPEGORARO, ELENAVITIELLO, LIBEROANGELINI, CORRADO + NEUROEPIDEMIOLOGY - -
Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP). 1993 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISA + PCR METHODS AND APPLICATIONS - -
A novel nonsense mutation in the human dystrophin gene 1993 VITIELLO, LIBERO + HUMAN MUTATION - -
A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intron. 1994 VITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISAANGELINI, CORRADO + HUMAN GENETICS - -
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy. 1994 MOSTACCIUOLO, MARIA LUISAVITIELLO, LIBERORampazzo AANGELINI, CORRADO + AMERICAN JOURNAL OF MEDICAL GENETICS - -
A study on duplications of the dystrophin gene: Evidence of a geographical difference in the distribution of breakpoints by intron 1994 DANIELI, GIAN ANTONIOVITIELLO, LIBEROMOSTACCIUOLO, MARIA LUISAAngelini C. + HUMAN GENETICS - -
Corrigenda: DXS997 localized to intron 48 of dystrophin (Human Molecular Genetics (1993) 2 (2199)) 1994 VITIELLO, LIBERODANIELI, GIAN ANTONIO + HUMAN MOLECULAR GENETICS - -
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study. 1994 MOSTACCIUOLO, MARIA LUISAVITIELLO, LIBERO + GENE GEOGRAPHY - -
Genomic organization of the human dystrophin gene across the major deletion hot spot & the 3' region 1995 VITIELLO, LIBERO + GENOMICS - -
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family 1995 VITIELLO, LIBERODANIELI, GIAN ANTONIO + NEUROMUSCULAR DISORDERS - -
Dystrophin-positive fibers in duchenne dystrophy: Origin and correlation to clinical course 1995 FANIN, MARINADANIELI, GIAN ANTONIOVITIELLO, LIBEROANGELINI, CORRADO + MUSCLE & NERVE - -
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size? 1996 FANIN, MARINAVITIELLO, LIBERODANIELI, GIAN ANTONIOPEGORARO, ELENAANGELINI, CORRADO + MUSCLE & NERVE - -