Author Results for "Marie,Suely Kazue"

Marie,Suely Kazue Nagahashi
Oba-Shinjo,Sueli Mieko
Scaff,Milberto
Reed,Umbertina Conti
Carvalho,Mary Souza
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Resende,Maria Bernadete Dutra
Shinjo,Samuel Katsuyuki
Silva,Roseli da
Teixeira,Manoel Jacobsen
Conforto,Adriana Bastos

Showing 1 - 20 results of 36 for search '"Marie,Suely Kazue"', query time: 0.09s Refine Results
  1. 1
    Challenges to understand the mitochondrial respiratory diseases caused by mitochondrial DNA mutations
    by Marie,Suely Kazue Nagahashi
    Published 2015
    Digital revista
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  2. 2
    Mitochondriopathies: contribution to the study of mitochondrial DNA mutations
    by Nagahashi-Marie,Suely Kazue
    Published 1997
    Digital revista
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  3. 3
    Pompe disease: further challenges to pursue
    by Marie,Suely Kazue Nagahashi
    Published 2013
    Digital revista
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  4. 4
    The study of central nervous system involvement in mithochondrial disorders with mitochondrial DNA mutation
    by Marie,Suely Kazue Nagahashi
    Published 2002
    Digital revista
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  5. 5
    Metabolism and brain cancer
    Digital revista
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  6. 6
    Relevant coexpression of STMN1, MELK and FOXM1 in glioblastoma and review of the impact of STMN1 in cancer biology
    Digital revista
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  7. 7
    The expression of gene ANKRD1 correlates with hypoxia status in muscle biopsies of treatment-näive adult dermatomyositis
    Digital revista
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  8. 8
    Skeletal muscle major histocompatibility complex class I and II expression differences in adult and juvenile dermatomyositis
    Digital revista
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  9. 9
    Facial sensory symptoms in medullary infarcts
    Digital revista
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  10. 10
    Effects of yoga breathing exercises on pulmonary function in patients with Duchenne muscular dystrophy: an exploratory analysis,
    Digital revista
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  11. 11
    The expression of the aminoacid transporters ASCT2 (SLC1A5) and LAT1 (SLC7A5) in astrocytomas
    Digital revista
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  12. 12
    Comparison of motor strength and function in patients with Duchenne muscular dystrophy with or without steroid therapy
    Digital revista
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  13. 13
    Homozygotic intronic GAA mutation in three siblings with late-onset Pompe's disease
    Digital revista
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  14. 14
    Emery-Dreifuss muscular dystrophy: anatomical-clinical correlation (case report)
    Digital revista
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  15. 15
    Effects of somatosensory stimulation on the excitability of the unaffected hemisphere in chronic stroke patients
    Digital revista
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  16. 16
    Phenotypic and immunohistochemical characterization of sarcoglycanopathies
    Digital revista
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  17. 17
    The prevalence of mitochondrial DNA mutations in Leigh syndrome in a Brazilian series
    Digital revista
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  18. 18
    Ullrich congenital muscular dystrophy and bethlem myopathy: clinical and genetic heterogeneity
    Digital revista
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  19. 19
    Dystrophin-glycoproteins associated in congenital muscular dystrophy: immunohistochemical analysis of 59 Brazilian cases
    Digital revista
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  20. 20
    King-Denborough Syndrome: report of two Brazilian cases
    Digital revista
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