Mariz Vainzof
Human Genome Sciences (United States)(US)Universidade de São Paulo(BR)Human Stem Cells Institute PJSC (Russia)(RU)Institute of Human Genetics(PL)Stem Cell Institute(PA)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Cardiomyopathy and Myosin Studies, Neurogenetic and Muscular Disorders Research, Tissue Engineering and Regenerative Medicine
Most-Cited Works
- → Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene(1996)422 cited
- → Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin(2000)333 cited
- → Approach to the diagnosis of congenital myopathies(2013)318 cited
- → The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies(1996)190 cited
- → Consensus Statement on Standard of Care for Congenital Myopathies(2012)187 cited
- → Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy(1991)158 cited