Publications by authors named "S Raynaud"

Introduction: Dimethyl fumarate (DMF) has demonstrated a favorable benefit-risk profile in patients with relapsing-remitting multiple sclerosis (RRMS) in clinical and real-world studies. The ESTEEM study (NCT02047097) was conducted to assess the long-term safety and effectiveness of delayed-release DMF in patients with relapsing forms of MS in routine clinical practice. We report final outcomes from ESTEEM with up to 6.

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Introduction: Nusinersen clinical trials have limited data on adolescents and adults with 5q-associated spinal muscular atrophy (SMA). We conducted a systematic literature review (SLR) and meta-analysis to assess effectiveness of nusinersen in adolescents and adults with SMA in clinical practice.

Methods: Our search included papers published 12/23/2016 through 07/01/2022 with ≥ 5 individuals ≥ 13 years of age and with ≥ 6 months' data on ≥ 1 selected motor function outcomes [Hammersmith Functional Motor Scale-Expanded (HFMSE), Revised Upper Limb Module (RULM), and Six-Minute Walk Test (6MWT)].

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Bacterial regulatory RNAs (sRNAs) are important players to control gene expression. In , SprC is an antivirulent -acting sRNA known to base-pair with the major autolysin mRNA, preventing its translation. Using MS2-affinity purification coupled with RNA sequencing, we looked for its sRNA-RNA interactome and identified 14 novel mRNA targets.

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Nusinersen, administered by intrathecal injection at a dose of 12 mg, is indicated across all ages for the treatment of spinal muscular atrophy (SMA). Evidence on real-world healthcare resource use (HRU) and costs among patients taking nusinersen remains limited. This study aimed to evaluate real-world HRU and costs associated with nusinersen use through US claims databases.

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Article Synopsis
  • The study explored how genetic changes impact prognosis in chronic lymphocytic leukemia (CLL) patients, focusing on the role of immunoglobulin heavy variable (IGHV) status.
  • In 536 patients undergoing first-line therapies, specific genetic abnormalities like unmutated IGHV and complex karyotype were linked to shorter progression-free survival (PFS).
  • The effects of these genetic factors varied based on whether patients had mutated (M-IGHV) or unmutated (UM-IGHV) IGHV, emphasizing the importance of considering IGHV status in prognosis assessments for CLL.
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