Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Mateddu

Showing results (1-10 of 14) with videos related to

Pageof 2
Sort By:
Neuromuscular Disorders : NMD|January 1, 1991
Passive avoidance behaviour deficit in the mdx mouseF Muntoni, A Mateddu, G Serra
Journal of the Neurological Sciences|December 1, 1993
Muscular weakness in the mdx mouseF Muntoni, A Mateddu, F Marchei, et al.
Neuromuscular Disorders : NMD|July 17, 1999
X-linked dilated cardiomyopathy and the dystrophin geneA Ferlini, C Sewry, M A Melis, et al.
Human Mutation|January 8, 2000
Two novel mutations (10410 T-->G; 10296 del C) at carboxy-terminus of the dystrophin gene associated with mental retardation. Mutations in brief no. 149. OnlineM Cau, A Cao, D Loi, et al.
Developmental Medicine and Child Neurology|January 1, 1993
Diagnosis of DMD carrier status in a family with no known affected malesF Muntoni, A Mateddu, M Cau, et al.
Cardiologia (Rome, Italy)|December 25, 2002
Dilated cardiomyopathy and muscular dystrophies: which lesson can be learned?F Muntoni, A Ferlini, C Sewry, et al.
Clinical Genetics|July 1, 1992
Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrierF Muntoni, A Mateddu, M G Marrosu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
Human Mutation|February 6, 1998
Novel nonsense mutation (C-->A nt 10512) in exon 72 of dystrophin gene leading to exon skipping in a patient with a mild dystrophinopathyM A Melis, F Muntoni, M Cau, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Neuromuscular Disorders : NMD|January 1, 1991
Passive avoidance behaviour deficit in the mdx mouseF Muntoni, A Mateddu, G Serra
Journal of the Neurological Sciences|December 1, 1993
Muscular weakness in the mdx mouseF Muntoni, A Mateddu, F Marchei, et al.
Neuromuscular Disorders : NMD|July 17, 1999
X-linked dilated cardiomyopathy and the dystrophin geneA Ferlini, C Sewry, M A Melis, et al.
Human Mutation|January 8, 2000
Two novel mutations (10410 T-->G; 10296 del C) at carboxy-terminus of the dystrophin gene associated with mental retardation. Mutations in brief no. 149. OnlineM Cau, A Cao, D Loi, et al.
Developmental Medicine and Child Neurology|January 1, 1993
Diagnosis of DMD carrier status in a family with no known affected malesF Muntoni, A Mateddu, M Cau, et al.
Cardiologia (Rome, Italy)|December 25, 2002
Dilated cardiomyopathy and muscular dystrophies: which lesson can be learned?F Muntoni, A Ferlini, C Sewry, et al.
Clinical Genetics|July 1, 1992
Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrierF Muntoni, A Mateddu, M G Marrosu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
Human Mutation|February 6, 1998
Novel nonsense mutation (C-->A nt 10512) in exon 72 of dystrophin gene leading to exon skipping in a patient with a mild dystrophinopathyM A Melis, F Muntoni, M Cau, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.
Pageof 2