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Julia F Paim

Showing results (1-10 of 4) with videos related to

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Journal of Molecular Medicine (Berlin, Germany)|February 1, 2007
A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of delta-SG proteinTelma L F Gouveia, Patrícia M Kossugue, Julia F Paim, et al.
Journal of Molecular Neuroscience : MN|August 15, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial VariabilityAna Cotta, Julia F Paim, Elmano Carvalho, et al.
Journal of Molecular Neuroscience : MN|March 13, 2013
Muscle phenotypic variability in limb girdle muscular dystrophy 2 GJulia F Paim, Ana Cotta, Antonio P Vargas, et al.
JIMD Reports|July 21, 2020
Early-onset coenzyme Q10 deficiency associated with ataxia and respiratory chain dysfunction due to novel pathogenic <i>COQ8A</i> variants, including a large intragenic deletionAna Cotta, Charlotte L Alston, Sidney Baptista-Junior, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Journal of Molecular Medicine (Berlin, Germany)|February 1, 2007
A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of delta-SG proteinTelma L F Gouveia, Patrícia M Kossugue, Julia F Paim, et al.
Journal of Molecular Neuroscience : MN|August 15, 2019
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial VariabilityAna Cotta, Julia F Paim, Elmano Carvalho, et al.
Journal of Molecular Neuroscience : MN|March 13, 2013
Muscle phenotypic variability in limb girdle muscular dystrophy 2 GJulia F Paim, Ana Cotta, Antonio P Vargas, et al.
JIMD Reports|July 21, 2020
Early-onset coenzyme Q10 deficiency associated with ataxia and respiratory chain dysfunction due to novel pathogenic <i>COQ8A</i> variants, including a large intragenic deletionAna Cotta, Charlotte L Alston, Sidney Baptista-Junior, et al.
Pageof 1