Rita C.M. Pavanello

The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females

Mayana Zatz, Suely Kazue Nagahashi Marie, Antonia Cerqueira et al. · American Journal of Medical Genetics · 1998 · 156 citations

Life Sciences, Genetics, Molecular Genetics +14

Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)

Maria Manuela O. Tonini, Maria Rita Passos‐Bueno, A. H. Cerqueira et al. · Neuromuscular Disorders · 2003 · 143 citations

Life Sciences, Endocrinology, Genetics +8

A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G)

Natássia M. Vieira, Michel Satya Naslavsky, Luciana Licínio et al. · Human Molecular Genetics · 2014 · 121 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population

Mariz Vainzof, Maria Rita Passos-Bueno, Rita C.M. Pavanello et al. · Journal of the Neurological Sciences · 1999 · 98 citations

Life Sciences, Genetics, Molecular Genetics +9

Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies

Mariz Vainzof, Louise V.B. Anderson, Elizabeth M. McNally et al. · Journal of Molecular Neuroscience · 2001 · 85 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +13