Search Results - "Toro, W."

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    Rare primary leiomyosarcoma of the internal jugular vein with cervical extravascular extension by Moreno-Sánchez, M, González-García, R, Moreno-García, C, Toro, W, Monje, F

    “…Abstract Leiomysarcoma of intravascular origin is a rare malignant tumour of the soft tissue. We present what is, to our knowledge, the first example of one…”
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    Journal Article
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    165P Health Care Resource Use (HCRU) for patients with spinal muscular atrophy (SMA) Types 2 or 3 in the UK by Reyna, S., Toro, W., Patel, A., Saleh, S., Dabbous, O.

    Published in Neuromuscular disorders : NMD (01-10-2024)
    “…Data on HCRU for patients with SMA types 2 (SMA2) and 3 (SMA3) are sparse. To our knowledge, no studies address costs from the HCP perspective. We assessed…”
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    Journal Article
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    164P Meta-analysis of clinical impact of onasemnogene abeparvovec treatment of spinal muscular atrophy patients by Reyna, S., Dabbous, O., Wallach, S., Patel, A., Toro, W., Ritter, S.

    Published in Neuromuscular disorders : NMD (01-10-2024)
    “…Spinal muscular atrophy (SMA) is a severe genetic neuromuscular disease that is caused by a defect in the survival motor neuron 1 (SMN1) gene, leading to rapid…”
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    Journal Article
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    P231 Early intervention and speed-to-effect in spinal muscular atrophy type 1 following onasemnogene abeparvovec gene replacement therapy by Toro, W., Reyna, S., Ritter, S., Patel, A., Mumneh, N., Dabbous, O.

    Published in Neuromuscular disorders : NMD (01-10-2023)
    “…Spinal muscular atrophy (SMA) type 1 is a severe genetic neuromuscular disease that is caused by a defect in the survival motor neuron 1 (SMN1) gene, and that…”
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    Journal Article
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    P79 Real-world outcomes of disease-modifying treatment for patients with spinal muscular atrophy: findings from a global retrospective chart review by Dabbous, O., LaMarca, N., Toro, W., Wallach, S., Mumneh, N., Aassi, M., O'Brien, E., Baranello, G., Reyna, S.

    Published in Neuromuscular disorders : NMD (01-10-2023)
    “…Disease-modifying treatments (DMTs; nusinersen, onasemnogene abeparvovec [OA], and risdiplam), have substantially improved prognoses for patients with spinal…”
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    Journal Article
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