Search Results - "Dwinnell, S."

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    Sildenafil citrate therapy for severe early‐onset intrauterine growth restriction by von Dadelszen, P, Dwinnell, S, Magee, LA, Carleton, BC, Gruslin, A, Lee, B, Lim, KI, Liston, RM, Miller, SP, Rurak, D, Sherlock, RL, Skoll, MA, Wareing, MM, Baker, PN

    “…Please cite this paper as: von Dadelszen P, Dwinnell S, Magee LA, Carleton BC, Gruslin A, Lee B, Lim KI, Liston RM, Miller SP, Rurak D, Sherlock RL, Skoll MA,…”
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    Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations by PILLERS, D.-A. M, FITZGERALD, K. M, WELEBER, R. G, DUNCAN, N. M, RASH, S. M, WHITE, R. A, DWINNELL, S. J, POWELL, B. R, SCHNUR, R. E, RAY, P. N, CIBIS, G. W

    Published in Human genetics (01-07-1999)
    “…The dark-adapted electroretinogram (ERG) of patients with Duchenne and Becker muscular dystrophy (DMD/BMD) shows a marked reduction in b-wave amplitude…”
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    Normal cochlear function in mdx and mdx(Cv3) Duchenne muscular dystrophy mouse models by Pillers, D A, Duncan, N M, Dwinnell, S J, Rash, S M, Kempton, J B, Trune, D R

    Published in The Laryngoscope (01-08-1999)
    “…Sensorineural hearing loss has been found in association with inherited muscular dystrophies in humans and in mouse models. An increased brainstem auditory…”
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    Normal Cochlear Function in mdx and mdxCv3 Duchenne Muscular Dystrophy Mouse Models by Pillers, De-Ann M., Duncan, Nancy M., Dwinnell, Shannon J., Rash, Sean M., Kempton, J. Beth, Trune, Dennis R.

    Published in The Laryngoscope (01-08-1999)
    “…Objectives/Hypothesis: Sensorineural hearing loss has been found in association with inherited muscular dystrophies in humans and in mouse models. An increased…”
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  9. 9

    Hearing loss in the laminin-deficient dy mouse model of congenital muscular dystrophy by Pillers, De-Ann M, Kempton, J.Beth, Duncan, Nancy M, Pang, Jiaqing, Dwinnell, Shannon J, Trune, Dennis R

    Published in Molecular genetics and metabolism (01-07-2002)
    “…Sensorineural hearing loss is found in many inherited forms of muscular dystrophy. We investigated the dy mouse model, which has congenital muscular dystrophy…”
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