Search Results - Zapata-Aldana, E

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  1. 1
    NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY

    NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY by Zapata-Aldana, E., Campbell, C.

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  2. 2
    NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.378Clinical nonsense mutations in neuromuscular disorders

    NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY: P.378Clinical nonsense mutations in neuromuscular disorders by Zapata-Aldana, E., Campbell, C.

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  3. 3
    Predictors of ambulation in patients with Duchene muscular dystrophy

    Predictors of ambulation in patients with Duchene muscular dystrophy by Zapata Aldana, E., Eltayeb, N., Miller, M., Campbell, C.

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  4. 4
    P.8 - Predictors of ambulation in patients with Duchene muscular dystrophy

    P.8 - Predictors of ambulation in patients with Duchene muscular dystrophy by Zapata Aldana, E., Eltayeb, N., Miller, M., Campbell, C.

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  5. 5
    P.218Utility based health related quality of life in children and adolescents with spinal muscular atrophy

    P.218Utility based health related quality of life in children and adolescents with spinal muscular atrophy by Love, D., Hicks, R., Wei, Y., Zapata Aldana, E., Almobarak, S., Campbell, C.

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  6. 6
    PERINATAL FINDINGS IN A CONGENITAL MYOTONIC DYSTROPHY COHORT

    PERINATAL FINDINGS IN A CONGENITAL MYOTONIC DYSTROPHY COHORT by Ceballos-Saenz, D, Zapata-Aldana, E, Hicks, R, Campbell, C

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  7. 7
    A.01 The relationship between fatigue and health-related quality of life in a clinical trial population of Duchenne muscular dystrophy patients

    A.01 The relationship between fatigue and health-related quality of life in a clinical trial population of Duchenne muscular dystrophy patients by Wei, Y, El-Aloul, B, Nguyen, C, Zapata-Aldana, E, Campbell, C

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  8. 8
    P.077 Utility of a next generation sequencing in the diagnosis of Congenital Myasthenic Syndromes

    P.077 Utility of a next generation sequencing in the diagnosis of Congenital Myasthenic Syndromes by Zapata-Aldana, E, Nguyen, CE, Nicolle, MW, Carere, DA, Stuart, A, Campbell, C, Sadikovic, B

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  9. 9
    B.07 Review of patients with Spinal Muscular Atrophy treated with Nusinersen in Ontario

    B.07 Review of patients with Spinal Muscular Atrophy treated with Nusinersen in Ontario by Remtulla, S, Zapata-Aldana, E, Gonorazky, H, Boyd, J, Scholtes, C, Hicks, R, Leung, A, Dowling, J, Vajsar, J, McMillan, H, Tarnopolsky, M, Campbell, C

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  10. 10
    FACTORS ASSOCIATED WITH HEALTH-RELATED QUALITY OF LIFE IN CHILDREN WITH CONGENITAL MYOTONIC DYSTROPHY

    FACTORS ASSOCIATED WITH HEALTH-RELATED QUALITY OF LIFE IN CHILDREN WITH CONGENITAL MYOTONIC DYSTROPHY by Rogers, S, Hicks, R, Bax, K, Ceballos-Saenz, D, El-Aloul, B, Dibella, D, Pucillo, E, Johnson, N, Campbell, C, Zapata-Aldana, E

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  11. 11
    Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1

    Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1 by Johnson, Nicholas E, Aldana, Eugenio Zapata, Angeard, Nathalie, Ashizawa, Tetsuo, Berggren, Kiera N, Marini-Bettolo, Chiara, Duong, Tina, Ekström, Anne-Berit, Sansone, Valeria, Tian, Cuixia, Hellerstein, Leah, Campbell, Craig

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